| scholarly article | Q13442814 |
| P50 | author | Jan Lammerding | Q48134943 |
| P2093 | author name string | Chieh-Ren Hsia | |
| Alexandra Lynn McGregor | |||
| P2860 | cites work | Intravital third harmonic generation microscopy of collective melanoma cell invasion: Principles of interface guidance and microvesicle dynamics. | Q55019659 |
| Comparison of neutrophil and capillary diameters and their relation to neutrophil sequestration in the lung | Q72913006 | ||
| Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins | Q24298586 | ||
| Coupling of the nucleus and cytoplasm: role of the LINC complex | Q24299991 | ||
| Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C | Q24310845 | ||
| LINC complexes form by binding of three KASH peptides to domain interfaces of trimeric SUN proteins | Q24336621 | ||
| When lamins go bad: nuclear structure and disease | Q26827624 | ||
| Actomyosin networks and tissue morphogenesis | Q27010487 | ||
| Non-muscle myosin IIB is critical for nuclear translocation during 3D invasion. | Q27310111 | ||
| Chemotaxis of cell populations through confined spaces at single-cell resolution | Q27310963 | ||
| Continual cell deformation induced via attachment to oriented fibers enhances fibroblast cell migration | Q27312477 | ||
| Design of a microfluidic device to quantify dynamic intra-nuclear deformation during cell migration through confining environments | Q27334775 | ||
| Nuclear mechanotransduction: forcing the nucleus to respond | Q28085113 | ||
| Structural organization of the human gene (LMNB1) encoding nuclear lamin B1 | Q28115157 | ||
| Tumor cell interactions with the extracellular matrix during invasion and metastasis | Q28258256 | ||
| A perspective on cancer cell metastasis | Q28307891 | ||
| Compensation mechanism in tumor cell migration: mesenchymal-amoeboid transition after blocking of pericellular proteolysis | Q29615193 | ||
| Rapid leukocyte migration by integrin-independent flowing and squeezing | Q29620345 | ||
| Power-law rheology of isolated nuclei with deformation mapping of nuclear substructures | Q30476785 | ||
| An open access microfluidic device for the study of the physical limits of cancer cell deformation during migration in confined environments | Q30488379 | ||
| Dynein drives nuclear rotation during forward progression of motile fibroblasts | Q30493073 | ||
| Kinesin 3 and cytoplasmic dynein mediate interkinetic nuclear migration in neural stem cells | Q30498808 | ||
| Opposing microtubule motors drive robust nuclear dynamics in developing muscle cells | Q30527771 | ||
| Physical limits of cell migration: control by ECM space and nuclear deformation and tuning by proteolysis and traction force | Q30540882 | ||
| Water permeation drives tumor cell migration in confined microenvironments | Q30629758 | ||
| Mechanical interplay between invadopodia and the nucleus in cultured cancer cells | Q30633015 | ||
| Lamin A/C is a risk biomarker in colorectal cancer | Q33361579 | ||
| Abnormal development of the cerebral cortex and cerebellum in the setting of lamin B2 deficiency. | Q33740216 | ||
| Isolated nuclei adapt to force and reveal a mechanotransduction pathway in the nucleus. | Q33859070 | ||
| Nuclear lamins and neurobiology | Q34056472 | ||
| Lamin B1 overexpression increases nuclear rigidity in autosomal dominant leukodystrophy fibroblasts | Q34072629 | ||
| The nuclear envelope environment and its cancer connections | Q34254678 | ||
| Constitutive nuclear lamina-genome interactions are highly conserved and associated with A/T-rich sequence | Q34309873 | ||
| Nuclear deformability constitutes a rate-limiting step during cell migration in 3-D environments | Q34568577 | ||
| Nuclear mechanics during cell migration. | Q34777149 | ||
| Biophysical regulation of histone acetylation in mesenchymal stem cells | Q34800912 | ||
| Accessorizing and anchoring the LINC complex for multifunctionality | Q34825870 | ||
| Mechanical integration of actin and adhesion dynamics in cell migration | Q34990511 | ||
| Multifunctional polymer scaffolds with adjustable pore size and chemoattractant gradients for studying cell matrix invasion | Q35020911 | ||
| Matrix elasticity regulates lamin-A,C phosphorylation and turnover with feedback to actomyosin. | Q35216800 | ||
| Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction. | Q35632054 | ||
| Direct inhibition of myosin II effectively blocks glioma invasion in the presence of multiple motogens. | Q35756665 | ||
| Nonpolarized signaling reveals two distinct modes of 3D cell migration | Q35925311 | ||
| Lamins at a glance | Q36010368 | ||
| Physical plasticity of the nucleus in stem cell differentiation | Q36023764 | ||
| The cellular mastermind(?)-mechanotransduction and the nucleus | Q36113002 | ||
| Nuclear mechanics in cancer | Q36116300 | ||
| Mechanics of the nucleus | Q36144966 | ||
| Fibroblasts Lead the Way: A Unified View of 3D Cell Motility | Q36236775 | ||
| Physical confinement alters tumor cell adhesion and migration phenotypes. | Q36252334 | ||
| Differential basal-to-apical accessibility of lamin A/C epitopes in the nuclear lamina regulated by changes in cytoskeletal tension | Q36305787 | ||
| Mechanical activation of cells induces chromatin remodeling preceding MKL nuclear transport | Q36318027 | ||
| Structural organization of nuclear lamins A, C, B1, and B2 revealed by superresolution microscopy | Q36455433 | ||
| Lamin A/C deficiency reduces circulating tumor cell resistance to fluid shear stress | Q36498071 | ||
| Mechanical regulation of nuclear structure and function. | Q36617270 | ||
| Nuclear envelope composition determines the ability of neutrophil-type cells to passage through micron-scale constrictions. | Q36708649 | ||
| Nuclear positioning | Q36765676 | ||
| Cell geometric constraints induce modular gene-expression patterns via redistribution of HDAC3 regulated by actomyosin contractility | Q37010867 | ||
| The A- and B-type nuclear lamin networks: microdomains involved in chromatin organization and transcription | Q37023583 | ||
| Nesprin-3 connects plectin and vimentin to the nuclear envelope of Sertoli cells but is not required for Sertoli cell function in spermatogenesis | Q37056635 | ||
| Elucidating mechanical transition effects of invading cancer cells with a subnucleus-scaled microfluidic serial dimensional modulation device | Q37113994 | ||
| Influence of lamin A on the mechanical properties of amphibian oocyte nuclei measured by atomic force microscopy | Q37265569 | ||
| cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins | Q37397300 | ||
| Actomyosin pulls to advance the nucleus in a migrating tissue cell | Q37533446 | ||
| Collagen-based cell migration models in vitro and in vivo | Q37580117 | ||
| Generation of compartmentalized pressure by a nuclear piston governs cell motility in a 3D matrix | Q37596116 | ||
| Nuclear lamin stiffness is a barrier to 3D migration, but softness can limit survival. | Q37614860 | ||
| Broken nuclei--lamins, nuclear mechanics, and disease. | Q37678536 | ||
| Nuclear lamin-A scales with tissue stiffness and enhances matrix-directed differentiation | Q37686106 | ||
| Microfabricated devices for cell biology: all for one and one for all. | Q38063651 | ||
| Do lamins influence disease progression in cancer? | Q38190516 | ||
| Leukocyte migration in the interstitial space of non-lymphoid organs. | Q38193988 | ||
| How to Measure Molecular Forces in Cells: A Guide to Evaluating Genetically-Encoded FRET-Based Tension Sensors | Q38387139 | ||
| Microfluidics: reframing biological enquiry. | Q38571113 | ||
| Migration in Confined 3D Environments Is Determined by a Combination of Adhesiveness, Nuclear Volume, Contractility, and Cell Stiffness | Q38838700 | ||
| Microconstriction arrays for high-throughput quantitative measurements of cell mechanical properties | Q38855502 | ||
| Confinement and low adhesion induce fast amoeboid migration of slow mesenchymal cells | Q38909995 | ||
| Role of suspended fiber structural stiffness and curvature on single-cell migration, nucleus shape, and focal-adhesion-cluster length | Q38932800 | ||
| Differential nuclear shape dynamics of invasive andnon-invasive breast cancer cells are associated with actin cytoskeleton organization and stability | Q38972545 | ||
| The effect of fibrillar matrix architecture on tumor cell invasion of physically challenging environments | Q38994423 | ||
| Cell jamming: collective invasion of mesenchymal tumor cells imposed by tissue confinement. | Q39005469 | ||
| Nuclear deformation during breast cancer cell transmigration. | Q39302311 | ||
| Cytoplasmic intermediate filaments mediate actin-driven positioning of the nucleus. | Q39580612 | ||
| Inhibition of hsp90 compromises the DNA damage response to radiation | Q40230441 | ||
| An alternative splicing product of the lamin A/C gene lacks exon 10. | Q41205134 | ||
| Dynamic force-induced direct dissociation of protein complexes in a nuclear body in living cells. | Q42223382 | ||
| Cancer cell migration in 3D tissue: negotiating space by proteolysis and nuclear deformability | Q42250953 | ||
| Hutchinson-Gilford progeria syndrome alters nuclear shape and reduces cell motility in three dimensional model substrates | Q42826076 | ||
| Mechanical stress-induced DNA damage and rac-p38MAPK signal pathways mediate p53-dependent apoptosis in vascular smooth muscle cells | Q44120985 | ||
| Loss of lamin A/C expression in stage II and III colon cancer is associated with disease recurrence | Q44551732 | ||
| Identification and cloning of an mRNA coding for a germ cell-specific A-type lamin in mice | Q48081964 | ||
| Cloning and sequencing of cDNA clones encoding chicken lamins A and B1 and comparison of the primary structures of vertebrate A- and B-type lamins | Q48290157 | ||
| A second higher vertebrate B-type lamin. cDNA sequence determination and in vitro processing of chicken lamin B2. | Q48290261 | ||
| A close-up view of migrating Langerhans cells in the skin. | Q49023130 | ||
| The nuclear envelope lamina network has elasticity and a compressibility limit suggestive of a molecular shock absorber. | Q50671769 | ||
| LBR and lamin A/C sequentially tether peripheral heterochromatin and inversely regulate differentiation. | Q52633974 | ||
| The clinicopathological significance of lamin A/C, lamin B1 and lamin B receptor mRNA expression in human breast cancer. | Q53080649 | ||
| Lamins A and C but not lamin B1 regulate nuclear mechanics. | Q53613002 | ||
| Lamin A/C deficiency is an independent risk factor for cervical cancer. | Q53784074 | ||
| P304 | page(s) | 32-40 | |
| P577 | publication date | 2016-02-16 | |
| P1433 | published in | Current Opinion in Cell Biology | Q13505682 |
| P1476 | title | Squish and squeeze-the nucleus as a physical barrier during migration in confined environments | |
| P478 | volume | 40 |
| Q90706142 | A coupled approach for fluid saturated poroelastic media and immersed solids for modeling cell-tissue interactions |
| Q48247179 | Aggressive prostate cancer cell nuclei have reduced stiffness. |
| Q92983627 | An endocytic-secretory cycle participates in Toxoplasma gondii in motility |
| Q90478522 | Apicomplexan F-actin is required for efficient nuclear entry during host cell invasion |
| Q39154257 | Are cancer cells really softer than normal cells? |
| Q55223163 | Automated analysis of cell migration and nuclear envelope rupture in confined environments. |
| Q38891711 | Causes and consequences of nuclear envelope alterations in tumour progression |
| Q92732420 | Cell migration through three-dimensional confining pores: speed accelerations by deformation and recoil of the nucleus |
| Q41958762 | Connecting the plasma membrane to the nucleus by intermediate filaments |
| Q59794703 | Cytoskeletal control of nuclear migration in neurons and non-neuronal cells |
| Q91869885 | Extracellular matrix alignment dictates the organization of focal adhesions and directs uniaxial cell migration |
| Q57050077 | Fibroblasts lacking nuclear lamins do not have nuclear blebs or protrusions but nevertheless have frequent nuclear membrane ruptures |
| Q58745588 | G9a Correlates with VLA-4 Integrin and Influences the Migration of Childhood Acute Lymphoblastic Leukemia Cells |
| Q92708952 | Genome organization in immune cells: unique challenges |
| Q90325049 | High-throughput microfluidic micropipette aspiration device to probe time-scale dependent nuclear mechanics in intact cells |
| Q50618815 | Increased chromatin plasticity supports enhanced metastatic potential of mouse melanoma cells. |
| Q48357964 | Lamin A and microtubules collaborate to maintain nuclear morphology |
| Q38698252 | Lamins in the nuclear interior - life outside the lamina |
| Q47262581 | Mechanoreciprocity in cell migration. |
| Q94544802 | Mechanosensing of Mechanical Confinement by Mesenchymal-Like Cells |
| Q55516137 | Micro and Nanofabrication methods to control cell-substrate interactions and cell behavior: A review from the tissue engineering perspective. |
| Q92451167 | Migration through physical constraints is enabled by MAPK-induced cell softening via actin cytoskeleton re-organization |
| Q92183061 | Modelling actin polymerization: the effect on confined cell migration |
| Q64951524 | Multicompartment cell-based modeling of confined migration: regulation by cell intrinsic and extrinsic factors. |
| Q38809211 | Multiple mechanisms of 3D migration: the origins of plasticity |
| Q64038729 | Non-canonical processes that shape the cell migration landscape |
| Q104073521 | Nonlinear mechanics of lamin filaments and the meshwork topology build an emergent nuclear lamina |
| Q92341904 | Novel K6-K14 keratin fusion enhances cancer stemness and aggressiveness in oral squamous cell carcinoma |
| Q36319488 | Nuclear Membrane-Targeted Gold Nanoparticles Inhibit Cancer Cell Migration and Invasion |
| Q37727547 | Nuclear morphologies: their diversity and functional relevance |
| Q92781335 | Nup93 regulates breast tumor growth by modulating cell proliferation and actin cytoskeleton remodeling |
| Q97530366 | Persistence of a regeneration-associated, transitional alveolar epithelial cell state in pulmonary fibrosis |
| Q47133845 | Persistent inhibition of pore-based cell migration by sub-toxic doses of miuraenamide, an actin filament stabilizer |
| Q57283064 | Physical confinement alters sarcoma cell cycle progression and division |
| Q64882883 | Precise cell behaviors manipulation through light-responsive nano-regulators: recent advance and perspective. |
| Q58786959 | Quantitative phase imaging unravels new insight into dynamics of mesenchymal and amoeboid cancer cell invasion |
| Q91811377 | Recapitulation of molecular regulators of nuclear motion during cell migration |
| Q38768262 | Recent advances in understanding nuclear size and shape |
| Q47433774 | Regulation of genome organization and gene expression by nuclear mechanotransduction |
| Q59800862 | Role of Mechanotransduction and Tension in T Cell Function |
| Q64981806 | Shape and Size Control of Artificial Cells for Bottom-Up Biology. |
| Q58740843 | Skeletal Muscle Dystrophy mutant of lamin A alters the structure and dynamics of the Ig fold domain |
| Q33725650 | The "inherent vice" in the anti-angiogenic theory may cause the highly metastatic cancer to spread more aggressively. |
| Q96304809 | The Emerging Roles of Heterochromatin in Cell Migration |
| Q38998765 | The Mechanics of Single Cell and Collective Migration of Tumor Cells |
| Q59128386 | The Role of Melanoma Cell-Stroma Interaction in Cell Motility, Invasion, and Metastasis |
| Q48060921 | The nucleus is irreversibly shaped by motion of cell boundaries in cancer and non-cancer cells. |
| Q50732844 | Unbiased High-Precision Cell Mechanical Measurements with Microconstrictions. |
| Q63407154 | WDR5 modulates cell motility and morphology and controls nuclear changes induced by a 3D environment |
Search more.