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Paper Citation Record · LEDGER

Learning via mechanosensitivity and activity in cytoskeletal networks

As of 23 August 2026, this Paper Citation Record lists 49 of 49 outbound references and 0 inbound Pith citation observations for arXiv:2504.15107.

A citation records a reference. It does not transfer a finding from one paper to another.

pith.paper-citation-record.v1
2504.15107 v1

Coverage vector

measured 49 of 49 reference resolution

Typed states for the displayed outbound observations.

Source: paper_references, paper_reference_links, observed 2026-08-16T11:40:52.516640Z

measured 49 of 49 standing notices

One-hop event checks from named stored sources.

Source: scholarly_work_events, retraction_status_cache, observed 2026-08-22T06:32:14.747728+00:00

measured 0 of 0 inbound itemization

Pith citing papers itemized under the disclosed page cap.

Source: paper_references, paper_reference_links

measured 0 of 1 external citation measurements

A source-named dated measurement, never combined with another source.

Source: cited_works

Reference resolution

49 of 49 outbound references displayed

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  • verified fuzzy48
  • unresolved1
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External citation measurements

No source-named external measurement is stored.

Outbound references

Observation 897e8004-c985-425d-b0a1-7e68eeaa627b · outbound

This paper cites Disordered actomyosin networks are sufficient to produce cooperative and telescopic contractility.

Learning via mechanosensitivity and activity in cytoskeletal networks Disordered actomyosin networks are sufficient to produce cooperative and telescopic contractility

Reference 13

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 4806aa21-ace2-4e2d-b35f-36b90101fb8a · outbound

This paper cites Directional cell migration guided by a strain gradient.

Learning via mechanosensitivity and activity in cytoskeletal networks Directional cell migration guided by a strain gradient

Reference 30

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation c429a319-3208-4180-8b5a-b28dec15c1cb · outbound

This paper cites Mechanical stability of the cell nucleus–roles played by the cytoskeleton in nuclear deformation and strain recovery.

Learning via mechanosensitivity and activity in cytoskeletal networks Mechanical stability of the cell nucleus–roles played by the cytoskeleton in nuclear deformation and strain recovery

Reference 43

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation fe580d1a-6b57-4511-8111-724623b890be · outbound

This paper cites Cytoskeletal remodeling of the airway smooth muscle cell: a mechanism for adaptation to mechanical forces in the lung.

Learning via mechanosensitivity and activity in cytoskeletal networks Cytoskeletal remodeling of the airway smooth muscle cell: a mechanism for adaptation to mechanical forces in the lung

Reference 47

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation f238bc37-9336-4b45-bf0c-3341e594e610 · outbound

This paper cites Decoupling the roles of cell shape and mechanical stress in orienting and cueing epithe- lial mitosis.

Learning via mechanosensitivity and activity in cytoskeletal networks Decoupling the roles of cell shape and mechanical stress in orienting and cueing epithe- lial mitosis

Reference 48

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation e79e6c3c-01f0-4446-9764-5406d14e0a66 · outbound

This paper cites Mechanics of epithelial tissue homeostasis and morphogenesis.

Learning via mechanosensitivity and activity in cytoskeletal networks Mechanics of epithelial tissue homeostasis and morphogenesis

Reference 49

Resolution
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no resolver link, observed 2026-08-16T11:40:52.265497Z

Source-reported events for the cited work

Unavailable: canonical work link unavailable.

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Observation 9058c542-808a-4951-9e96-09a09aef7170 · outbound

This paper cites Rigidity of epithelial tissues as a double optimization problem.

Learning via mechanosensitivity and activity in cytoskeletal networks Rigidity of epithelial tissues as a double optimization problem

Reference 50

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 747507ab-acf8-4716-8fe5-2e8b95195356 · outbound

This paper cites A minimal vertex model explains how the amnioserosa avoids fluidization during drosophila dorsal closure.

Learning via mechanosensitivity and activity in cytoskeletal networks A minimal vertex model explains how the amnioserosa avoids fluidization during drosophila dorsal closure

Reference 51

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation b973edae-8ee9-497d-adcd-0664347e941b · outbound

This paper cites The actin cortex acts as a mechanical memory of morphology in confined migrating cells.

Learning via mechanosensitivity and activity in cytoskeletal networks The actin cortex acts as a mechanical memory of morphology in confined migrating cells

Reference 52

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 4eee8da2-2b5f-4936-862a-f3679c5ec945 · outbound

This paper cites Active shape programming drives drosophila wing disc eversion.

Learning via mechanosensitivity and activity in cytoskeletal networks Active shape programming drives drosophila wing disc eversion

Reference 53

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation fe429aed-673e-4736-b639-94e0353935b4 · outbound

This paper cites Learning without neurons in physical systems.

Learning via mechanosensitivity and activity in cytoskeletal networks Learning without neurons in physical systems

Reference 54

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 64d85cce-0f5e-40da-81be-0d211ba1133f · outbound

This paper cites Designing allostery-inspired response in mechanical networks.

Learning via mechanosensitivity and activity in cytoskeletal networks Designing allostery-inspired response in mechanical networks

Reference 55

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 839d1d2e-ab10-4b58-970c-f4cc309c66be · outbound

This paper cites Directed aging, memory, and nature’s greed.

Learning via mechanosensitivity and activity in cytoskeletal networks Directed aging, memory, and nature’s greed

Reference 56

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 472c3ec5-08e7-4b97-a92f-0aa677b979e8 · outbound

This paper cites Supervised learning in physical networks: From machine learning to learning machines.

Learning via mechanosensitivity and activity in cytoskeletal networks Supervised learning in physical networks: From machine learning to learning machines

Reference 57

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 49d18d77-ccdd-45d4-94b7-06da169c6eb8 · outbound

This paper cites Temporal contrastive learning through implicit non-equilibrium memory.

Learning via mechanosensitivity and activity in cytoskeletal networks Temporal contrastive learning through implicit non-equilibrium memory

Reference 58

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.979654Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 4e16a969-a0e6-4311-b4ce-429584422439 · outbound

This paper cites Disordered actomyosin networks are sufficient to produce 17 cooperative and telescopic contractility.

Learning via mechanosensitivity and activity in cytoskeletal networks Disordered actomyosin networks are sufficient to produce 17 cooperative and telescopic contractility

Reference 59

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 604daba7-792b-4945-9931-d0b6440337ce · outbound

This paper cites Molecular motors stiffen non-affine semiflexible polymer networks.

Learning via mechanosensitivity and activity in cytoskeletal networks Molecular motors stiffen non-affine semiflexible polymer networks

Reference 60

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 724c6c19-c1f2-4be0-b3bb-16c4f70cafe4 · outbound

This paper cites Modeling semiflexible polymer networks.

Learning via mechanosensitivity and activity in cytoskeletal networks Modeling semiflexible polymer networks

Reference 61

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation d7361182-b627-4fe6-ae53-69510f01df31 · outbound

This paper cites Dynamic reorientation of cultured cells and stress fibers under mechanical stress from periodic stretching.

Learning via mechanosensitivity and activity in cytoskeletal networks Dynamic reorientation of cultured cells and stress fibers under mechanical stress from periodic stretching

Reference 62

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation b8703ff0-c50f-4b00-b083-5a94c6ba2d76 · outbound

This paper cites Active tension network model suggests an exotic mechanical state realized in epithelial tissues.

Learning via mechanosensitivity and activity in cytoskeletal networks Active tension network model suggests an exotic mechanical state realized in epithelial tissues

Reference 63

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 4dccb316-c03e-4169-b790-a1a0793d1301 · outbound

This paper cites Adaptive response of actin bundles under mechanical stress.

Learning via mechanosensitivity and activity in cytoskeletal networks Adaptive response of actin bundles under mechanical stress

Reference 64

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.908740Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 6a72b56b-8ceb-4044-a1aa-eeb5ceecf165 · outbound

This paper cites Rhoa medi- ates epithelial cell shape changes via mechanosensitive endocytosis.

Learning via mechanosensitivity and activity in cytoskeletal networks Rhoa medi- ates epithelial cell shape changes via mechanosensitive endocytosis

Reference 65

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 1916c237-72e3-4d46-bf5b-e4ee7e9411e8 · outbound

This paper cites Mechanosen- sitive junction remodeling promotes robust epithelial morphogenesis.

Learning via mechanosensitivity and activity in cytoskeletal networks Mechanosen- sitive junction remodeling promotes robust epithelial morphogenesis

Reference 66

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 728c1e79-fb7d-4723-a9a3-3a44ec1835b6 · outbound

This paper cites Lim domain proteins in cell mechanobiology.

Learning via mechanosensitivity and activity in cytoskeletal networks Lim domain proteins in cell mechanobiology

Reference 67

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 57d339d7-3268-4076-9b30-1464081753e1 · outbound

This paper cites Quantitative proteomics of the integrin adhesome show a myosin ii-dependent recruitment of lim domain proteins.

Learning via mechanosensitivity and activity in cytoskeletal networks Quantitative proteomics of the integrin adhesome show a myosin ii-dependent recruitment of lim domain proteins

Reference 68

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.859518Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.330870Z digest=sha256:e31689c0129a5cb6c8d702eb26d9641523105bc5c25dd3453f40332553da3c48

Observation 5caa0a55-dfd9-4d39-acea-75deca1a466f · outbound

This paper cites Mechan- ical forces alter zyxin unbinding kinetics within focal adhesions of living cells.

Learning via mechanosensitivity and activity in cytoskeletal networks Mechan- ical forces alter zyxin unbinding kinetics within focal adhesions of living cells

Reference 69

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.847411Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.334309Z digest=sha256:efbcc12fc7229ad5c5e5e63a6013a7ae6a390a44227f919d231558aa5767ce31

Observation d4601307-d61e-4445-8f71-4a9493cd608f · outbound

This paper cites Lim proteins in actin cytoskeleton mechanoresponse.

Learning via mechanosensitivity and activity in cytoskeletal networks Lim proteins in actin cytoskeleton mechanoresponse

Reference 70

Resolution
verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.337548Z digest=sha256:c8f592fcea49f5d6024c0183d870cd5a838aaec96e07eafcc4dd2cb1fd09b65f

Observation e4eab9ac-3fee-4fad-8858-f46f458f2529 · outbound

This paper cites Strain hardening of actin filament networks: regulation by the dynamic cross-linking protein α-actinin.

Learning via mechanosensitivity and activity in cytoskeletal networks Strain hardening of actin filament networks: regulation by the dynamic cross-linking protein α-actinin

Reference 71

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.824575Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 5ffce2f2-57d9-4886-81af-55b6221c19c5 · outbound

This paper cites The mechanical properties of actin gels.

Learning via mechanosensitivity and activity in cytoskeletal networks The mechanical properties of actin gels

Reference 72

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.812654Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 14a94384-7592-4f4e-8251-e806c1e0a557 · outbound

This paper cites Strategies for cellular decision-making.

Learning via mechanosensitivity and activity in cytoskeletal networks Strategies for cellular decision-making

Reference 73

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.799837Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.347273Z digest=sha256:e67df7215da87bae3a80f47da8eeed40f59521957523b22ac5acc09185e8cdaf

Observation c352bedb-01bd-49e1-a668-462ef367fcdb · outbound

This paper cites Growth factors, matrices, and forces combine and control stem cells.

Learning via mechanosensitivity and activity in cytoskeletal networks Growth factors, matrices, and forces combine and control stem cells

Reference 74

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.789305Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.350492Z digest=sha256:f466058825ee59568c17e22036f32a35fe8c5c1b58c6ebee35b53ca2dc5e3e84

Observation a5dd4cc2-79ba-48ab-9f10-d704c14eae2a · outbound

This paper cites A synthetic protein-level neural network in mammalian cells.

Learning via mechanosensitivity and activity in cytoskeletal networks A synthetic protein-level neural network in mammalian cells

Reference 75

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.777035Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.353769Z digest=sha256:5812f047dc5cc30f75d393923d592d94b61ae118a5920a0e0279fd0ebec06927

Observation 6e3d6a3c-fc23-4b7d-b716-fdf3e3c45035 · outbound

This paper cites Directional cell migration guided by a strain gradient.

Learning via mechanosensitivity and activity in cytoskeletal networks Directional cell migration guided by a strain gradient

Reference 76

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.560146Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.357160Z digest=sha256:784e31b5d8da42077c9e391f3dccd5d7b05b4bc8ca7134da4be781b046e218b6

Observation 43ebfd7e-0537-456a-a790-4cb7697e271a · outbound

This paper cites Extra-embryonic tissue spreading directs early embryo morphogenesis in killifish.

Learning via mechanosensitivity and activity in cytoskeletal networks Extra-embryonic tissue spreading directs early embryo morphogenesis in killifish

Reference 77

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.753140Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.360626Z digest=sha256:e7b8053874cbc5f9df20441ff71fef380aca2857af39d91fa33dbbac070fd1c7

Observation 4b07ea4a-e020-459d-804a-c28384ac1dce · outbound

This paper cites Actin filaments function as a tension sensor by tension-dependent binding of cofilin to the filament.

Learning via mechanosensitivity and activity in cytoskeletal networks Actin filaments function as a tension sensor by tension-dependent binding of cofilin to the filament

Reference 78

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.741500Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.364034Z digest=sha256:5e1a1d3ade6af8c2654637c92a5cb8d897ba69280d0f4cc82d3791b7b983c68c

Observation 55cae1b3-6c6a-43b8-baa0-3cb16aac8184 · outbound

This paper cites Quantitative evaluation of threshold fiber strain that induces reorganization of cytoskeletal actin fiber structure in osteoblastic cells.

Learning via mechanosensitivity and activity in cytoskeletal networks Quantitative evaluation of threshold fiber strain that induces reorganization of cytoskeletal actin fiber structure in osteoblastic cells

Reference 79

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.729895Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.367511Z digest=sha256:6417ca79a5054af7623c06741820e8f3082cb5e31824e981916d80057e3b3a0c

Observation 9f701a3e-e349-4754-9fd0-46f8bd749115 · outbound

This paper cites Pulsed contractions of an actin–myosin network drive apical constriction.

Learning via mechanosensitivity and activity in cytoskeletal networks Pulsed contractions of an actin–myosin network drive apical constriction

Reference 80

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.718654Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.370848Z digest=sha256:4ffa74fcc06fd8d5c1b1e5f0baefd452a0f2586935e9d7a66e279160fa8c4a71

Observation 60329e72-654f-4518-a001-affbaeadcb00 · outbound

This paper cites A self-organized biomechanical network drives shape changes during tissue morphogenesis.

Learning via mechanosensitivity and activity in cytoskeletal networks A self-organized biomechanical network drives shape changes during tissue morphogenesis

Reference 81

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.706128Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.374115Z digest=sha256:da2afb917880b93d8743238cde36dc2141c42c9f3d2e911d9d99aea36b9f8a0a

Observation 7db74493-3b9b-44a1-a61d-6aa2e4e8b59b · outbound

This paper cites Actomyosin pulsation and flows in an active elastomer with turnover and network remodeling.

Learning via mechanosensitivity and activity in cytoskeletal networks Actomyosin pulsation and flows in an active elastomer with turnover and network remodeling

Reference 82

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.694554Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.377393Z digest=sha256:1320917a434cf9d3cf867c69f825cd9e4fa944a5419dbec9e4287874bd212519

Observation 100afbf1-7fec-4926-aace-968983f3d815 · outbound

This paper cites Waves of change: Dynamic actomyosin networks in embryonic development.

Learning via mechanosensitivity and activity in cytoskeletal networks Waves of change: Dynamic actomyosin networks in embryonic development

Reference 83

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.682165Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.380516Z digest=sha256:820d2f73c03ccd9c0754b88c0cdd29c13904f3bfb9bb40d0357f0161968300f5

Observation 0b985df7-5c0c-493d-bfe3-f81845e8eb36 · outbound

This paper cites Learning outside the brain: Inte- grating cognitive science and systems biology.

Learning via mechanosensitivity and activity in cytoskeletal networks Learning outside the brain: Inte- grating cognitive science and systems biology

Reference 84

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.670964Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.384502Z digest=sha256:b4687e94a34adf4f13d163639657f271abd3539e651fb20e887ec6613bd9b875

Observation 79058876-3f9c-4be9-bc08-58cb8704e6bf · outbound

This paper cites Extracellular forces cause the nucleus to deform in a highly controlled anisotropic manner.

Learning via mechanosensitivity and activity in cytoskeletal networks Extracellular forces cause the nucleus to deform in a highly controlled anisotropic manner

Reference 85

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.659752Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.388048Z digest=sha256:2e79f7547d5a1108501ee81496e8bc51f03147d92946bba6574bd6596f0d92ee

Observation 7d45676b-9d5f-4416-8b8b-bba5a8a6ef0b · outbound

This paper cites Nuclear deformation causes dna damage by increasing replication stress.

Learning via mechanosensitivity and activity in cytoskeletal networks Nuclear deformation causes dna damage by increasing replication stress

Reference 86

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.648300Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.391639Z digest=sha256:0d330baaaa51873361cf1ad62228ae408232d4f3a292626fad6783c8fc068865

Observation 9fc3623a-8143-45a5-bdef-44fbfc22ce2b · outbound

This paper cites Nuclear envelope rupture and repair during cancer cell migration.

Learning via mechanosensitivity and activity in cytoskeletal networks Nuclear envelope rupture and repair during cancer cell migration

Reference 87

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.638113Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.395456Z digest=sha256:78b3a49326e65dac7466a4f3a6e43f553aa1adbf31ea8dfb6949e19c0843bd0a

Observation 1ddb37e5-2f4f-4468-afb9-53eb63983ce0 · outbound

This paper cites Mechanical properties of the cell nucleus and the effect of emerin deficiency.

Learning via mechanosensitivity and activity in cytoskeletal networks Mechanical properties of the cell nucleus and the effect of emerin deficiency

Reference 88

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.626998Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.398959Z digest=sha256:bb76271cd86eafffb1f1207575c2e91ceb1dc1134e3ff71748870b819bd18e51

Observation f45f20eb-1ae2-453e-baec-51ff3a5d42bb · outbound

This paper cites Mechanical stability of the cell nucleus–roles played by the cytoskeleton in nuclear deformation and strain recovery.

Learning via mechanosensitivity and activity in cytoskeletal networks Mechanical stability of the cell nucleus–roles played by the cytoskeleton in nuclear deformation and strain recovery

Reference 89

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.549282Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.402178Z digest=sha256:b5de396ab5503d2440ac6a85337b2cc2ecc79cb74d3b0cb05cd228f40b24891f

Observation 3fe0d483-90a1-43ac-b21f-e4738c022039 · outbound

This paper cites How cells sense their own shape–mechanisms to probe cell geometry and their implications in cellular organization and function.

Learning via mechanosensitivity and activity in cytoskeletal networks How cells sense their own shape–mechanisms to probe cell geometry and their implications in cellular organization and function

Reference 90

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.605504Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.405474Z digest=sha256:0c50328cbd53084d3cd9993b3027b6ec415d1e84ecde9cb209d0f97a045ce731

Observation c4dcaea6-fe4a-4a6f-a882-907d634dbb4b · outbound

This paper cites The influence of cell mechanics, cell-cell interactions, and proliferation on epithelial packing.

Learning via mechanosensitivity and activity in cytoskeletal networks The influence of cell mechanics, cell-cell interactions, and proliferation on epithelial packing

Reference 91

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.593655Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.408774Z digest=sha256:03c6a7b1868b7c27df8042793c57506909153d67f56fd68433edb462af046d2f

Observation 5408598d-e2a1-4763-9d93-aea5108d8468 · outbound

This paper cites Vertex models: from cell mechanics to tissue morphogen- esis.

Learning via mechanosensitivity and activity in cytoskeletal networks Vertex models: from cell mechanics to tissue morphogen- esis

Reference 92

Resolution
verified fuzzy
raw_fallback, observed 2026-08-16T11:40:52.582211Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-16T11:40:52.516640Z digest=sha256:4ffd4562335bf0a724cad425442f23f447c429181a7cd01e94d6d78172c23a48

Pith citing papers

No inbound Pith citation observations are available.