| scholarly article | Q13442814 |
| P356 | DOI | 10.1083/JCB.139.6.1507 |
| P953 | full work available at URL | http://jcb.rupress.org/content/139/6/1507.full.pdf |
| https://europepmc.org/articles/PMC2132624 | ||
| https://europepmc.org/articles/PMC2132624?pdf=render | ||
| https://rupress.org/jcb/article-pdf/139/6/1507/1488192/12517.pdf | ||
| P3181 | OpenCitations bibliographic resource ID | 2007759 |
| P932 | PMC publication ID | 2132624 |
| P698 | PubMed publication ID | 9396756 |
| P5875 | ResearchGate publication ID | 277510407 |
| P2093 | author name string | J. H. Miner | |
| J. R. Sanes | |||
| A. Y. Chiu | |||
| B. L. Patton | |||
| P2860 | cites work | Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere | Q24298375 |
| Distribution and isolation of four laminin variants; tissue restricted distribution of heterotrimers assembled from five different subunits | Q24304482 | ||
| Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy | Q24308817 | ||
| Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy | Q24310537 | ||
| Merosin, a tissue-specific basement membrane protein, is a laminin-like protein | Q24323587 | ||
| The laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoform | Q24678511 | ||
| A new nomenclature for the laminins | Q28238308 | ||
| A laminin-like adhesive protein concentrated in the synaptic cleft of the neuromuscular junction | Q28284633 | ||
| The renal glomerulus of mice lacking s-laminin/laminin beta 2: nephrosis despite molecular compensation by laminin beta 1 | Q28585172 | ||
| 43K protein and acetylcholine receptors colocalize during the initial stages of neuromuscular synapse formation in vivo | Q28589038 | ||
| Aberrant differentiation of neuromuscular junctions in mice lacking s-laminin/laminin beta 2 | Q28591375 | ||
| Collagen IV alpha 3, alpha 4, and alpha 5 chains in rodent basal laminae: sequence, distribution, association with laminins, and developmental switches | Q28592655 | ||
| Expression and in vitro function of beta 1-integrin laminin receptors in the developing avian ciliary ganglion. | Q30439162 | ||
| Quantitation of junctional and extrajunctional acetylcholine receptors by electron microscope autoradiography after 125I-alpha-bungarotoxin binding at mouse neuromuscular junctions | Q31126900 | ||
| Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development | Q33557296 | ||
| Laminin–a glycoprotein from basement membranes | Q34083862 | ||
| Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene | Q34319775 | ||
| An L1-like molecule, the 8D9 antigen, is a potent substrate for neurite extension | Q34361199 | ||
| Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse | Q35493060 | ||
| Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein. | Q35882763 | ||
| Expression of several adhesive macromolecules (N-CAM, L1, J1, NILE, uvomorulin, laminin, fibronectin, and a heparan sulfate proteoglycan) in embryonic, adult, and denervated adult skeletal muscle | Q36214328 | ||
| Distribution of N-CAM in synaptic and extrasynaptic portions of developing and adult skeletal muscle | Q36214493 | ||
| Neurite outgrowth on cryostat sections of innervated and denervated skeletal muscle | Q36217190 | ||
| Selective immunoreactivities of kidney basement membranes to monoclonal antibodies against laminin: localization of the end of the long arm and the short arms to discrete microdomains | Q36222348 | ||
| Merosin and laminin in myogenesis; specific requirement for merosin in myotube stability and survival | Q36237447 | ||
| Molecular and functional defects in kidneys of mice lacking collagen alpha 3(IV): implications for Alport syndrome | Q36237693 | ||
| Native chick laminin-4 containing the beta 2 chain (s-laminin) promotes motor axon growth | Q36257741 | ||
| The histogenesis of rat intercostal muscle | Q36574088 | ||
| Properties of a basement membrane-related glycoprotein synthesized in culture by a mouse embryonal carcinoma-derived cell line | Q39553287 | ||
| Neuromuscular transmission in dystrophic mice | Q40085315 | ||
| Histometric and electron cytochemical study of muscle in the dystrophic mouse | Q40608304 | ||
| Reinnervation of muscle fiber basal lamina after removal of myofibers. Differentiation of regenerating axons at original synaptic sites | Q40682942 | ||
| The fine structure of motor endplate morphogenesis | Q41106850 | ||
| Expression of laminin isoforms in mouse myogenic cells in vitro and in vivo. | Q41262845 | ||
| A synaptic localization domain in the synaptic cleft protein laminin beta 2 (s-laminin) | Q41323947 | ||
| Gated migration: neurons migrate on but not onto substrates containing S-laminin | Q41371550 | ||
| Expression of laminin chains during myogenic differentiation. | Q41479944 | ||
| The anchoring filament protein kalinin is synthesized and secreted as a high molecular weight precursor | Q41603554 | ||
| Purification and lectin-binding properties of s-laminin, a synaptic isoform of the laminin B1 chain | Q41615229 | ||
| Monoclonal antibodies against laminin A chain fragment E3 and their effects on binding to cells and proteoglycan and on kidney development | Q41615287 | ||
| Synthesis and assembly of the synaptic cleft protein S-laminin by cultured cells | Q41643294 | ||
| Activity-dependent accumulation of basal lamina by cultured rat myotubes | Q42454621 | ||
| Development of basal lamina in synaptic and extrasynaptic portions of embryonic rat muscle | Q42455556 | ||
| The basal lamina of the neuromuscular junction | Q42459543 | ||
| Aneural muscle cell cultures make synaptic basal lamina components | Q42467475 | ||
| Two components from eye tissue that differentially stimulate the growth and development of ciliary ganglion neurons in cell culture. | Q42472375 | ||
| Identification of a novel mutant transcript of laminin α2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice | Q42482053 | ||
| A motoneuron-selective stop signal in the synaptic protein S-laminin | Q42484054 | ||
| Primary sequence of a motor neuron-selective adhesive site in the synaptic basal lamina protein S-laminin | Q42495702 | ||
| Clonal derivation of a rat muscle cell strain that forms contraction-competent myotubes | Q42498457 | ||
| Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus | Q42501151 | ||
| Abnormal localization of laminin subunits in muscular dystrophies | Q42503064 | ||
| Different distributions of dystrophin and related proteins at nerve-muscle junctions | Q44300706 | ||
| Perineurium originates from fibroblasts: demonstration in vitro with a retroviral marker | Q45282105 | ||
| The ability of agrin to cluster AChRs depends on alternative splicing and on cell surface proteoglycans | Q46736156 | ||
| Developmental expression of nicein adhesion protein (laminin-5) subunits suggests multiple morphogenic roles. | Q48082007 | ||
| Differential expression of laminins and their integrin receptors in developing and adult human lung | Q52200561 | ||
| During secondary myotube formation, primary myotubes preferentially absorb new nuclei at their ends | Q53680848 | ||
| Roles for the integrin VLA-4 and its counter receptor VCAM-1 in myogenesis | Q57223535 | ||
| Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene | Q59053234 | ||
| Autosomal recessive Alport syndrome: Immunohistochemical study of type IV collagen chain distribution | Q59619363 | ||
| Distribution of the alpha 1 and alpha 2 chains of collagen IV and of collagens V and VI in Alport syndrome | Q68216629 | ||
| Transient and locally restricted expression of laminin A chain mRNA by developing epithelial cells during kidney organogenesis | Q68926908 | ||
| Distribution of Na+ channels and ankyrin in neuromuscular junctions is complementary to that of acetylcholine receptors and the 43 kd protein | Q69364556 | ||
| Basement membranes during development of human nerve: Schwann cells and perineurial cells display marked changes in their expression profiles for laminin subunits and beta 1 and beta 4 integrins | Q70671855 | ||
| Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin staining | Q71051488 | ||
| Ultrastructural changes in muscle and motor end-plate of the dystrophic mouse | Q71706061 | ||
| Increased laminin A expression in regenerating myofibers in neuromuscular disorders | Q71706133 | ||
| Expression of laminin subunits in congenital muscular dystrophy | Q71791408 | ||
| Collagen COL4A3 knockout: a mouse model for autosomal Alport syndrome | Q71864916 | ||
| Morphological changes of neuromuscular junctions in the dystrophic (dy) mouse: a scanning and transmission electron microscopic study | Q71997915 | ||
| Differential expression of laminin polypeptides in developing and adult human kidney | Q72283552 | ||
| Skeletal and Cardiac Myopathies in Mice Lacking Utrophin and Dystrophin: A Model for Duchenne Muscular Dystrophy | Q73677664 | ||
| The synaptic cleft of the neuromuscular junction | Q126261893 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Laminin, alpha 2 | Q21496568 |
| Laminin B1 | Q21983452 | ||
| Laminin, alpha 4 | Q21985625 | ||
| Laminin, alpha 5 | Q21985626 | ||
| Laminin, beta 2 | Q21985630 | ||
| Laminin subunit gamma-1 | Q21986087 | ||
| P304 | page(s) | 1507–1521 | |
| P577 | publication date | 1997-12-15 | |
| P1433 | published in | Journal of Cell Biology | Q1524550 |
| P1476 | title | Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant mice | |
| Distribution and Function of Laminins in the Neuromuscular System of Developing, Adult, and Mutant Mice | |||
| P478 | volume | 139 |
| Q34133690 | A laminin-2, dystroglycan, utrophin axis is required for compartmentalization and elongation of myelin segments |
| Q36291506 | A novel early onset phenotype in a zebrafish model of merosin deficient congenital muscular dystrophy |
| Q47835020 | A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5. |
| Q35097359 | A role for Galgt1 in skeletal muscle regeneration |
| Q59061359 | A synaptic laminin–calcium channel interaction organizes active zones in motor nerve terminals |
| Q36936640 | A synaptic nidogen: developmental regulation and role of nidogen-2 at the neuromuscular junction |
| Q64944865 | Abnormal reinnervation of skeletal muscle in a tenascin‐C‐deficient mouse |
| Q28594941 | Abnormalities in neural crest cell migration in laminin alpha5 mutant mice |
| Q77458773 | Accumulation of F-spondin in injured peripheral nerve promotes the outgrowth of sensory axons |
| Q42489528 | Active zones on motor nerve terminals contain alpha 3beta 1 integrin. |
| Q36378446 | Activity-dependent retrograde laminin A signaling regulates synapse growth at Drosophila neuromuscular junctions. |
| Q28276814 | Agrin Receptors at the Skeletal Neuromuscular Junction |
| Q28511069 | Agrin and Synaptic Laminin Are Required to Maintain Adult Neuromuscular Junctions |
| Q33951903 | Akt/PKB regulates laminin and collagen IV isotypes of the basement membrane |
| Q42514853 | Alpha7beta1 integrin is a receptor for laminin-2 on Schwann cells |
| Q43823933 | Alternative splice variants of alpha 7 beta 1 integrin selectively recognize different laminin isoforms. |
| Q28513062 | Alternatively spliced isoforms of nerve- and muscle-derived agrin: their roles at the neuromuscular junction |
| Q33922811 | Amelioration of laminin-alpha2-deficient congenital muscular dystrophy by somatic gene transfer of miniagrin |
| Q33999451 | An Antibody to the Lutheran Glycoprotein (Lu) Recognizing the LU4 Blood Type Variant Inhibits Cell Adhesion to Laminin α5 |
| Q34091913 | An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy. |
| Q46986553 | An extracellular pathway for dystroglycan function in acetylcholine receptor aggregation and laminin deposition in skeletal myotubes |
| Q41767641 | An immunohistochemical study of the sciatic nerve in a rat knee immobilization model |
| Q90245857 | An improved method for culturing myotubes on laminins for the robust clustering of postsynaptic machinery |
| Q40724184 | Analysis of basement membrane self-assembly and cellular interactions with native and recombinant glycoproteins. |
| Q39559269 | Angiotensin II type 1 receptor antagonists alleviate muscle pathology in the mouse model for laminin-α2-deficient congenital muscular dystrophy (MDC1A) |
| Q90522821 | Antioxidants Reduce Muscular Dystrophy in the dy2J/dy2J Mouse Model of Laminin α2 Chain-Deficient Muscular Dystrophy |
| Q47150601 | BDNF/trkB Induction of Calcium Transients through Cav2.2 Calcium Channels in Motoneurons Corresponds to F-actin Assembly and Growth Cone Formation on β2-Chain Laminin (221). |
| Q52655400 | Basal lamina remodeling at the skeletal muscle stem cell niche mediates stem cell self-renewal |
| Q92136801 | Basement membrane and blood-brain barrier |
| Q37772080 | Biological role of dystroglycan in Schwann cell function and its implications in peripheral nervous system diseases |
| Q37085050 | Biology of the striated muscle dystrophin-glycoprotein complex |
| Q41866964 | Both laminin and Schwann cell dystroglycan are necessary for proper clustering of sodium channels at nodes of Ranvier. |
| Q98464776 | Brain Dysfunction in LAMA2-Related Congenital Muscular Dystrophy: Lessons From Human Case Reports and Mouse Models |
| Q47991754 | CNS Neurons Deposit Laminin α5 to Stabilize Synapses |
| Q37044607 | Calcium Channels Link the Muscle-Derived Synapse Organizer Laminin β2 to Bassoon and CAST/Erc2 to Organize Presynaptic Active Zones |
| Q45990379 | Cardiomyopathy associated with microcirculation dysfunction in laminin alpha4 chain-deficient mice. |
| Q92014464 | Cell Biology of Intracellular Adaptation of Mycobacterium leprae in the Peripheral Nervous System |
| Q37188791 | Cell biology of embryonic migration |
| Q24641876 | Cell culture-based analysis of postsynaptic membrane assembly in muscle cells |
| Q42061880 | Cell elongation induces laminin alpha2 chain expression in mouse embryonic mesenchymal cells: role in visceral myogenesis |
| Q40748050 | Cell line-specific translation of two laminin 5 beta3 chain isoforms |
| Q35778393 | Changes in Laminin Expression Pattern during Early Differentiation of Human Embryonic Stem Cells. |
| Q33644573 | Characteristics of skeletal muscle in mdx mutant mice |
| Q34560210 | Clustering of nicotinic acetylcholine receptors: from the neuromuscular junction to interneuronal synapses |
| Q42157709 | Complete sequence, recombinant analysis and binding to laminins and sulphated ligands of the N-terminal domains of laminin alpha3B and alpha5 chains |
| Q40959219 | Constitutively active MuSK is clustered in the absence of agrin and induces ectopic postsynaptic-like membranes in skeletal muscle fibers. |
| Q38291309 | Contributions of the LG modules and furin processing to laminin-2 functions |
| Q36321400 | Coordinate control of axon defasciculation and myelination by laminin-2 and -8. |
| Q91906240 | Current understanding and treatment of cardiac and skeletal muscle pathology in laminin-α2 chain-deficient congenital muscular dystrophy |
| Q36167600 | Deletion of Galgt2 (B4Galnt2) reduces muscle growth in response to acute injury and increases muscle inflammation and pathology in dystrophin-deficient mice |
| Q40556372 | Deletion of integrin α7 subunit does not aggravate the phenotype of laminin α2 chain-deficient mice |
| Q28589136 | Deletion of the laminin alpha4 chain leads to impaired microvessel maturation |
| Q77468492 | Development of the neuromuscular junction: genetic analysis in mice |
| Q24608109 | Developmental and pathogenic mechanisms of basement membrane assembly |
| Q77195610 | Differential Heparin Sensitivity of α-Dystroglycan Binding to Laminins Expressed in Normal and dy/dy Mouse Skeletal Muscle |
| Q30718427 | Differential expression of gap junction proteins connexin26, 32, and 43 in normal and crush-injured rat sciatic nerves. Close relationship between connexin43 and occludin in the perineurium |
| Q34970248 | Disruption of basal lamina components in neuromotor synapses of children with spastic quadriplegic cerebral palsy |
| Q52536757 | Disruption of laminin beta2 chain production causes alterations in morphology and function in the CNS. |
| Q27323309 | Distinct roles for laminin globular domains in laminin alpha1 chain mediated rescue of murine laminin alpha2 chain deficiency |
| Q42479484 | Distribution of ten laminin chains in dystrophic and regenerating muscles |
| Q45713806 | Domain IV of mouse laminin beta1 and beta2 chains |
| Q45871995 | ECM-Related Myopathies and Muscular Dystrophies: Pros and Cons of Protein Therapies |
| Q90497140 | Early skeletal muscle pathology and disease progress in the dy3K/dy3K mouse model of congenital muscular dystrophy with laminin α2 chain-deficiency |
| Q52143200 | Electrical activity and postsynapse formation in adult muscle: gamma-AChRs are not required |
| Q36326348 | Endothelial cell laminin isoforms, laminins 8 and 10, play decisive roles in T cell recruitment across the blood-brain barrier in experimental autoimmune encephalomyelitis |
| Q30664059 | Endothelial podosome rosettes regulate vascular branching in tumour angiogenesis. |
| Q52047958 | Epithelial laminin alpha5 is necessary for distal epithelial cell maturation, VEGF production, and alveolization in the developing murine lung |
| Q47781683 | Expression of laminin receptors in schwann cell differentiation: evidence for distinct roles. |
| Q38264895 | Extracellular matrix control of dendritic spine and synapse structure and plasticity in adulthood |
| Q36957019 | Fak56 functions downstream of integrin alphaPS3betanu and suppresses MAPK activation in neuromuscular junction growth |
| Q33969539 | Fibrillin-2 is dispensable for peripheral nerve development, myelination and regeneration |
| Q36083438 | Fibroblast growth factor signaling and the function and assembly of basement membranes |
| Q89963758 | Fibrogenesis in LAMA2-Related Muscular Dystrophy Is a Central Tenet of Disease Etiology |
| Q35217074 | Forced expression of laminin β1 in podocytes prevents nephrotic syndrome in mice lacking laminin β2, a model for Pierson syndrome |
| Q22254277 | Form and function: the laminin family of heterotrimers |
| Q33734614 | Formation of the neuromuscular junction. Agrin and its unusual receptors |
| Q34387851 | Functional Consequences of Cell Type-Restricted Expression of Laminin α5 in Mouse Placental Labyrinth and Kidney Glomerular Capillaries |
| Q78872863 | Functional analysis of neurotransmission at beta2-laminin deficient terminals |
| Q33563640 | Functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression |
| Q43153801 | Functional in situ assessment of muscle contraction in wild-type and mdx mice |
| Q90218080 | Functionalization of hyaluronic acid hydrogels with ECM-derived peptides to control myoblast behavior |
| Q38317471 | Gene expression profiling of diaphragm muscle in alpha2-laminin (merosin)-deficient dy/dy dystrophic mice |
| Q37810689 | Genetic dissection of synaptic specificity |
| Q33348860 | Genetics and cell biology of building specific synaptic connectivity |
| Q28087402 | Hanging on for the ride: adhesion to the extracellular matrix mediates cellular responses in skeletal muscle morphogenesis and disease |
| Q41903504 | Hedgehog signaling and laminin play unique and synergistic roles in muscle development |
| Q30872188 | Heparan sulfate heterogeneity in skeletal muscle basal lamina: demonstration by phage display-derived antibodies. |
| Q33818891 | How does Mycobacterium leprae target the peripheral nervous system? |
| Q64248716 | Identification of Candidate Protein Markers in Skeletal Muscle of Laminin-211-Deficient CMD Type 1A-Patients |
| Q38312539 | Identification of a major heparin and cell binding site in the LG4 module of the laminin alpha 5 chain |
| Q43510805 | Identification of cell-binding sites on the Laminin alpha 5 N-terminal domain by site-directed mutagenesis |
| Q28203001 | Identification of the binding site for the Lutheran blood group glycoprotein on laminin alpha 5 through expression of chimeric laminin chains in vivo |
| Q96304536 | Impaired Regeneration in Dystrophic Muscle-New Target for Therapy |
| Q38882098 | Impaired fetal muscle development and JAK-STAT activation mark disease onset and progression in a mouse model for merosin-deficient congenital muscular dystrophy |
| Q42479958 | Induction of presynaptic differentiation in cultured neurons by extracellular matrix components |
| Q42493929 | Influence of laminin-2 on Schwann cell-axon interactions |
| Q35166258 | Integrated genomics and proteomics of the Torpedo californica electric organ: concordance with the mammalian neuromuscular junction |
| Q35829510 | Integrin alpha1beta1 and transforming growth factor-beta1 play distinct roles in alport glomerular pathogenesis and serve as dual targets for metabolic therapy |
| Q45288511 | Integrin repertoire on myogenic cells changes during the course of primary myogenesis in the mouse |
| Q37901445 | Integrins and the extracellular matrix: Key mediators of development and regeneration of the sensory nervous system |
| Q28359758 | Investigation into the mechanism of the loss of laminin 5 (alpha3beta3gamma2) expression in prostate cancer |
| Q73261177 | Involvement of alpha7beta1 integrin in the conditioning-lesion effect on sensory axon regeneration |
| Q94544460 | LAMA2 Neuropathies: Human Findings and Pathomechanisms From Mouse Models |
| Q36321567 | LL5beta: a regulator of postsynaptic differentiation identified in a screen for synaptically enriched transcripts at the neuromuscular junction |
| Q82081196 | Lack of collagen XV impairs peripheral nerve maturation and, when combined with laminin-411 deficiency, leads to basement membrane abnormalities and sensorimotor dysfunction |
| Q40300149 | Laminin alpha1 chain improves laminin alpha2 chain deficient peripheral neuropathy |
| Q52096064 | Laminin alpha2 is essential for odontoblast differentiation regulating dentin sialoprotein expression |
| Q28592227 | Laminin alpha5 is required for dental epithelium growth and polarity and the development of tooth bud and shape |
| Q37461843 | Laminin alters fyn regulatory mechanisms and promotes oligodendrocyte development |
| Q89963755 | Laminin and Integrin in LAMA2-Related Congenital Muscular Dystrophy: From Disease to Therapeutics |
| Q39932939 | Laminin and integrin expression in the ventral ectodermal ridge of the mouse embryo: implications for regulation of BMP signalling. |
| Q44223039 | Laminin chains in rat and human peripheral nerve: distribution and regulation during development and after axonal injury |
| Q42693930 | Laminin deposition in the extracellular matrix: a complex picture emerges |
| Q42323278 | Laminin differentially regulates the stemness of type I and type II pericytes |
| Q53151357 | Laminin induced local axonal translation of β-actin mRNA is impaired in SMN-deficient motoneurons |
| Q52180212 | Laminin isoforms and epithelial development |
| Q36462201 | Laminin isoforms and lung development: all isoforms are not equal |
| Q36342173 | Laminin polymerization induces a receptor-cytoskeleton network |
| Q28821298 | Laminin targeting of a peripheral nerve-highlighting peptide enables degenerated nerve visualization |
| Q28087548 | Laminin therapy for the promotion of muscle regeneration |
| Q58108925 | Laminin α2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice |
| Q27336438 | Laminin α4 deficient mice exhibit decreased capacity for adipose tissue expansion and weight gain |
| Q36324334 | Laminin-1 redistributes postsynaptic proteins and requires rapsyn, tyrosine phosphorylation, and Src and Fyn to stably cluster acetylcholine receptors |
| Q33730495 | Laminin-11. |
| Q35952091 | Laminin-111 protein therapy reduces muscle pathology and improves viability of a mouse model of merosin-deficient congenital muscular dystrophy |
| Q37073808 | Laminin-111 restores regenerative capacity in a mouse model for alpha7 integrin congenital myopathy |
| Q28506713 | Laminin-121--recombinant expression and interactions with integrins |
| Q36531788 | Laminin-211 in skeletal muscle function |
| Q42501123 | Laminin-5 promotes neurite outgrowth from central and peripheral chick embryonic neurons |
| Q47345657 | Laminin-deficient muscular dystrophy: Molecular pathogenesis and structural repair strategies. |
| Q38815433 | Laminin: loss-of-function studies. |
| Q24302103 | Laminins 2 (alpha2beta1gamma1, Lm-211) and 8 (alpha4beta1gamma1, Lm-411) are synthesized and secreted by tooth pulp fibroblasts and differentially promote neurite outgrowth from trigeminal ganglion sensory neurons |
| Q34071975 | Laminins and human disease |
| Q36164129 | Laminins and their receptors in Schwann cells and hereditary neuropathies |
| Q36961190 | Laminins in peripheral nerve development and muscular dystrophy |
| Q33657773 | Laminins of the dermo-epidermal junction |
| Q34071971 | Laminins of the neuromuscular system |
| Q36890111 | Laminins promote postsynaptic maturation by an autocrine mechanism at the neuromuscular junction |
| Q92535136 | Linker Protein Repair of LAMA2 Dystrophic Neuromuscular Basement Membranes |
| Q36118063 | Linker molecules between laminins and dystroglycan ameliorate laminin-alpha2-deficient muscular dystrophy at all disease stages |
| Q47164258 | Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in mice. |
| Q28587935 | Localization of Lutheran, a novel laminin receptor, in normal, knockout, and transgenic mice suggests an interaction with laminin alpha5 in vivo |
| Q42520559 | Localization of the membrane-anchored MMP-regulator RECK at the neuromuscular junctions |
| Q86448489 | Loss of β2-laminin alters calcium sensitivity and voltage-gated calcium channel maturation of neurotransmission at the neuromuscular junction |
| Q21284413 | Lung development in laminin gamma2 deficiency: abnormal tracheal hemidesmosomes with normal branching morphogenesis and epithelial differentiation |
| Q28548194 | Magnetic Resonance Imaging Is Sensitive to Pathological Amelioration in a Model for Laminin-Deficient Congenital Muscular Dystrophy (MDC1A) |
| Q42485105 | Maturation and maintenance of the neuromuscular synapse: genetic evidence for roles of the dystrophin--glycoprotein complex |
| Q30501336 | Mesenchymal stem cells facilitate axon sorting, myelination, and functional recovery in paralyzed mice deficient in Schwann cell-derived laminin. |
| Q36027867 | Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A. |
| Q37472670 | Molecular Mechanism of Active Zone Organization at Vertebrate Neuromuscular Junctions |
| Q34137688 | Molecular basis for the peripheral nerve predilection of Mycobacterium leprae |
| Q40271963 | Molecular dissection of laminin alpha 5 in vivo reveals separable domain-specific roles in embryonic development and kidney function |
| Q34179309 | Molecules involved in the formation of synaptic connections in muscle and brain |
| Q51130563 | Muscular dystrophy meets protein biochemistry, the mother of invention |
| Q40925883 | Myoblast transplantations lead to the expression of the laminin alpha 2 chain in normal and dystrophic (dy/dy) mouse muscles |
| Q74139732 | Nerve terminals form but fail to mature when postsynaptic differentiation is blocked: in vivo analysis using mammalian nerve-muscle chimeras |
| Q45993052 | Neurite outgrowth and in vivo sensory innervation mediated by a Ca(V)2.2-laminin beta 2 stop signal. |
| Q44413786 | Neuromuscular synapses mediate motor axon branching and motoneuron survival during the embryonic period of programmed cell death |
| Q38254331 | Non-redundant function of dystroglycan and β1 integrins in radial sorting of axons |
| Q34340036 | Nonneuronal cellular prion protein |
| Q38911732 | Novel Acellular Scaffold Made from Decellularized Schwann Cell Sheets for Peripheral Nerve Regeneration |
| Q34103413 | Order and disorder: the role of extracellular matrix in epithelial cancer |
| Q35928246 | Overexpression of the cytotoxic T cell (CT) carbohydrate inhibits muscular dystrophy in the dyW mouse model of congenital muscular dystrophy 1A. |
| Q38563300 | Pathoproteomic profiling of the skeletal muscle matrisome in dystrophinopathy associated myofibrosis |
| Q38090267 | Peripheral axon regrowth: New molecular approaches |
| Q35030852 | Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy. |
| Q38597729 | Perisynaptic Schwann Cells at the Neuromuscular Synapse: Adaptable, Multitasking Glial Cells |
| Q38272679 | Pluripotent stem cells for Schwann cell engineering |
| Q30491552 | Podosomes are present in a postsynaptic apparatus and participate in its maturation. |
| Q35000938 | Presynaptic and postsynaptic interaction of the amyloid precursor protein promotes peripheral and central synaptogenesis. |
| Q42385886 | Presynaptic calcium channels and α3-integrins are complexed with synaptic cleft laminins, cytoskeletal elements and active zone components |
| Q52093729 | Presynaptic congenital myasthenic syndrome with a homozygous sequence variant in LAMA5 combines myopia, facial tics, and failure of neuromuscular transmission |
| Q73919999 | Properly formed but improperly localized synaptic specializations in the absence of laminin alpha4 |
| Q38160233 | Proregenerative properties of ECM molecules |
| Q54401460 | Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice |
| Q37479666 | Quantitative proteomic analysis of cultured skin fibroblast cells derived from patients with triglyceride deposit cardiomyovasculopathy |
| Q40599747 | Rac regulates integrin-mediated endothelial cell adhesion and migration on laminin-8. |
| Q24292239 | Recombinant human laminin-10 (alpha5beta1gamma1). Production, purification, and migration-promoting activity on vascular endothelial cells |
| Q41882498 | Regional differences in the expression of laminin isoforms during mouse neural tube development. |
| Q37273622 | Regulation of Schwann cell function by the extracellular matrix. |
| Q37895625 | Regulation of axonal outgrowth and pathfinding by integrin–ecm interactions |
| Q52163310 | Regulation of laminin-associated integrin subunit mRNAs in rat spinal motoneurons during postnatal development and after axonal injury |
| Q73295664 | Restricted distribution of laminin alpha1 chain in normal adult mouse tissues |
| Q36321503 | Role of extracellular matrix proteins and their receptors in the development of the vertebrate neuromuscular junction |
| Q36507175 | Role of integrins in peripheral nerves and hereditary neuropathies |
| Q38306604 | Role of the cell wall phenolic glycolipid-1 in the peripheral nerve predilection of Mycobacterium leprae |
| Q36255943 | Roles for laminin in embryogenesis: exencephaly, syndactyly, and placentopathy in mice lacking the laminin alpha5 chain |
| Q26825226 | Roles of the amyloid precursor protein family in the peripheral nervous system |
| Q37136844 | Scaffold-forming and Adhesive Contributions of Synthetic Laminin-binding Proteins to Basement Membrane Assembly |
| Q28212722 | Schwann Cell Adhesion to a Novel Heparan Sulfate Binding Site in the N-terminal Domain of α4 Type V Collagen Is Mediated by Syndecan-3 |
| Q42507557 | Schwann cell myelination occurred without basal lamina formation in laminin alpha2 chain-null mutant (dy3K/dy3K) mice |
| Q74316059 | Schwann cell type V collagen inhibits axonal outgrowth and promotes Schwann cell migration via distinct adhesive activities of the collagen and noncollagen domains |
| Q34806340 | Schwann cell-specific ablation of laminin gamma1 causes apoptosis and prevents proliferation |
| Q36459534 | Seeking long-term relationship: axon and target communicate to organize synaptic differentiation |
| Q44357337 | Sensory neuron subtypes have unique substratum preference and receptor expression before target innervation. |
| Q55001741 | Shaping Synapses by the Neural Extracellular Matrix |
| Q22001192 | Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies |
| Q91622135 | Soluble Heparin Binding Epidermal Growth Factor-Like Growth Factor Is a Regulator of GALGT2 Expression and GALGT2-Dependent Muscle and Neuromuscular Phenotypes |
| Q43581716 | Src, Fyn, and Yes are not required for neuromuscular synapse formation but are necessary for stabilization of agrin-induced clusters of acetylcholine receptors. |
| Q74582921 | Structural analysis and proteolytic processing of recombinant G domain of mouse laminin α2 chain |
| Q74241820 | Structural and functional alterations of neuromuscular junctions in NCAM-deficient mice |
| Q36951544 | Structure and function of basement membranes |
| Q38070755 | Synaptic basal lamina–associated congenital myasthenic syndromes |
| Q28585206 | Synaptic laminin prevents glial entry into the synaptic cleft |
| Q43159925 | The C-terminal region of laminin beta chains modulates the integrin binding affinities of laminins |
| Q64075376 | The Electrophysiology of Presynaptic Congenital Myasthenic Syndromes With and Without Facilitation: From Electrodiagnostic Findings to Molecular Mechanisms |
| Q52166178 | The Ets transcription factor GABP is required for postsynaptic differentiation in vivo. |
| Q42513999 | The Permissive Cue Laminin Is Essential for Growth Cone TurningIn Vivo |
| Q45066212 | The Structure of Human Neuromuscular Junctions: Some Unanswered Molecular Questions |
| Q35056186 | The basement membrane/basal lamina of skeletal muscle |
| Q42519963 | The critical role of basement membrane-independent laminin gamma 1 chain during axon regeneration in the CNS. |
| Q34352280 | The extracellular matrix of muscle--implications for manipulation of the craniofacial musculature |
| Q43708420 | The laminins in the murine inner ear: developmental transitions and expression in cochlear basement membranes |
| Q37218057 | The neuromuscular junction |
| Q42482793 | The presynaptic calcium channel is part of a transmembrane complex linking a synaptic laminin (alpha4beta2gamma1) with non-erythroid spectrin. |
| Q35123983 | The role of laminin in embryonic cell polarization and tissue organization |
| Q38950913 | The role of laminins in the organization and function of neuromuscular junctions |
| Q37361308 | The synaptic CT carbohydrate modulates binding and expression of extracellular matrix proteins in skeletal muscle: Partial dependence on utrophin |
| Q28141654 | The synaptic vesicle protein SV2 is complexed with an alpha5-containing laminin on the nerve terminal surface |
| Q57270383 | Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin α2-deficient mice |
| Q34343200 | Transgenic isolation of skeletal muscle and kidney defects in laminin beta2 mutant mice: implications for Pierson syndrome |
| Q35083466 | Transgenic overexpression of dystroglycan does not inhibit muscular dystrophy in mdx mice |
| Q42489627 | Transgenic overexpression of the α7 integrin reduces muscle pathology and improves viability in the dy(W) mouse model of merosin-deficient congenital muscular dystrophy type 1A. |
| Q30481597 | Transient axonal glycoprotein-1 (TAG-1) and laminin-alpha1 regulate dynamic growth cone behaviors and initial axon direction in vivo |
| Q30440403 | Trophoblast cells exhibit differential responses to laminin isoforms |
| Q33667939 | Unique expression pattern of the alpha6beta4 integrin and laminin-5 in human prostate carcinoma |
| Q35232779 | Wallerian degeneration: gaining perspective on inflammatory events after peripheral nerve injury |
| Q46784710 | Zebrafish bashful/laminin-alpha 1 mutants exhibit multiple axon guidance defects |
| Q36256527 | alpha-Dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability. |
| Q92345001 | rAAVrh74.MCK.GALGT2 Demonstrates Safety and Widespread Muscle Glycosylation after Intravenous Delivery in C57BL/6J Mice |
Search more.