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Deletion of the Laminin α4 Chain Leads to Impaired Microvessel Maturation
47/47 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
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The 47 checked references that resolve
resolves10.1073/pnas.95.24.14389
Vascular endothelial growth factor C induces angiogenesis
<i>in vivo</i>
resolves10.1002/(SICI)1097-0177(200006)218:2<213::AID-DVDY1>3.0.CO;2-R
Form and function: The laminin family of heterotrimers
resolves10.1083/jcb.133.2.417
Inhibition of laminin alpha 1-chain expression leads to alteration of basement membrane assembly and cell differentiation.
resolves10.1111/j.1432-1033.1997.t01-1-00727.x
Cloning of the Mouse Laminin α4 cDNA. Expression in a Subset of Endothelium
resolves10.1006/excr.1999.4653
Blood Platelets Contain and Secrete Laminin-8 (α4β1γ1) and Adhere to Laminin-8 via α6β1 Integrin
resolves10.1016/S0945-053X(00)00056-1
Chain specificity assignment of monoclonal antibodies to human laminins by using recombinant laminin β1 and γ1 chains
resolves10.1111/j.1432-1033.1991.tb16358.x
Localization of a major nidogen‐binding site to domain III of laminin B2 chain
resolves10.1038/jid.1994.7
Junctional Epidermolysis Bullosis: Defects in Expression of Epiligrin/Nicein/Kalinin and Integrin ß4 That Inhibit Hemidesmosome Formation
resolves10.1038/ng1095-216
Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy
resolves10.1074/jbc.272.44.27862
Primary Structure, Developmental Expression, and Immunolocalization of the Murine Laminin α4 Chain
resolves10.1074/jbc.274.20.14107
Molecular Cloning and Tissue-specific Expression of a Novel Murine Laminin γ3 Chain
resolves10.1016/0014-5793(95)00462-I
Primary structure and expression of a novel human laminin α4 chain
resolves10.1016/0306-4522(95)00496-3
Laminin α2 is a component of brain capillary basement membrane: Reduced expression in dystrophic dy mice
resolves10.1093/hmg/4.5.959
A homozygous nonsense mutation in the 3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa
resolves10.1083/jcb.145.3.605
Characterization and Expression of the Laminin γ3 Chain: A Novel, Non-Basement Membrane–associated, Laminin Chain
resolves10.1128/MCB.21.20.7025-7034.2001
Perinatal Lethality and Endothelial Cell Abnormalities in Several Vessel Compartments of Fibulin-1-Deficient Mice
resolves10.1007/s003359900535
IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa
resolves10.1006/dbio.1999.9270
Developmental Expression and Cellular Origin of the Laminin α2, α4, and α5 Chains in the Intestine
resolves10.1016/0012-1606(80)90365-6
Appearance and distribution of collagens and laminin in the early mouse embryo
resolves10.1101/gad.8.16.1875
Mice deficient for PDGF B show renal, cardiovascular, and hematological abnormalities.
resolves10.1126/science.277.5323.242
Pericyte Loss and Microaneurysm Formation in PDGF-B-Deficient Mice
resolves10.1016/S0945-053X(96)90162-6
The complete cDNA coding sequence and tissue-specific expression of the mouse laminin α4 chain
resolves10.1083/jcb.143.6.1713
Roles for Laminin in Embryogenesis: Exencephaly, Syndactyly, and Placentopathy in Mice Lacking the Laminin α5 Chain
resolves10.1083/jcb.137.3.685
The Laminin α Chains: Expression, Developmental Transitions, and Chromosomal Locations of α1-5, Identification of Heterotrimeric Laminins 8–11, and Cloning of a Novel α3 Isoform
resolves10.1038/88414
Properly formed but improperly localized synaptic specializations in the absence of laminin α4
resolves10.1083/jcb.139.6.1507
Distribution and Function of Laminins in the Neuromuscular System of Developing, Adult, and Mutant Mice
resolves10.1002/j.1460-2075.1994.tb06683.x
Two non‐contiguous regions contribute to nidogen binding to a single EGF‐like motif of the laminin gamma 1 chain.
resolves10.1038/ng0394-293
Mutations in the γ2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa
resolves10.1006/geno.1994.1627
A Homozygous Nonsense Mutation in the β3 Chain Gene of Laminin 5 (LAMB3) in Herlitz Junctional Epidermolysis Bullosa
resolves10.1006/excr.1998.4244
Expression of Laminin α1, α2, α4, and α5 Chains, Fibronectin, and Tenascin-C in Skeletal Muscle of Dystrophic 129ReJdy/dyMice
resolves10.1083/jcb.145.6.1309
Targeted Disruption of the <i>LAMA3</i> Gene in Mice Reveals Abnormalities in Survival and Late Stage Differentiation of Epithelial Cells
resolves10.1242/jcs.108.12.3795
Expression of laminin isoforms in mouse myogenic cells in vitro and in vivo
resolves10.1083/jcb.153.5.933
Endothelial Cell Laminin Isoforms, Laminins 8 and 10, Play Decisive Roles in T Cell Recruitment across the Blood–Brain Barrier in Experimental Autoimmune Encephalomyelitis
resolves10.1083/jcb.144.1.151
Absence of Basement Membranes after Targeting the <i>LAMC1</i> Gene Results in Embryonic Lethality Due to Failure of Endoderm Differentiation
resolves10.1016/0014-4827(92)90357-E
Monoclonal antibodies against laminin A chain fragment E3 and their effects on binding to cells and proteoglycan and on kidney development
resolves10.1006/dbio.1997.8668
Developmental Regulation of the Laminin α5 Chain Suggests a Role in Epithelial and Endothelial Cell Maturation
resolves10.1074/jbc.M003261200
Structural and Functional Analysis of the Recombinant G Domain of the Laminin α4 Chain and Its Proteolytic Processing in Tissues
resolves10.1111/j.1460-9568.1996.tb01568.x
Dystroglycan in the Cerebellum is a Laminin α2‐chain Binding Protein at the Glial‐Vascular Interface and is Expressed in Purkinje cells
resolves10.1038/ng1194-297
Murine muscular dystrophy caused by a mutation in the laminin α2 (Lama2) gene
resolves10.1073/pnas.94.19.10189
The α chain of laminin-1 is independently secreted and drives secretion of its β- and γ-chain partners
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no DOI — not checkedR47
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