Related references
Note: Only part of the references are listed.Basement membrane stiffness determines metastases formation
Raphael Reuten et al.
NATURE MATERIALS (2021)
Aberrant splicing as potential modifier of the phenotype of junctional epidermolysis bullosa
R. Mittwollen et al.
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY (2020)
Laminin N-terminus α31 protein distribution in adult human tissues
Lee D. Troughton et al.
PLOS ONE (2020)
Laminin-deficient muscular dystrophy: Molecular pathogenesis and structural repair strategies
Peter D. Yurchenco et al.
MATRIX BIOLOGY (2018)
Chimeric protein identification of dystrophic, Pierson and other laminin polymerization residues
Karen K. McKee et al.
MATRIX BIOLOGY (2018)
LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypes
Jorge Oliveira et al.
HUMAN MUTATION (2018)
Differential Distribution of Laminin N-Terminus α31 Across the Ocular Surface: Implications for Corneal Wound Repair
Valentina Barrera et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2018)
Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix
Simone Sampaolo et al.
JOURNAL OF MEDICAL GENETICS (2017)
Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in mice
Judith R. Reinhard et al.
SCIENCE TRANSLATIONAL MEDICINE (2017)
Increased Expression of Laminin Subunit Alpha 1 Chain by dCas9-VP160
Arnaud Perrin et al.
MOLECULAR THERAPY-NUCLEIC ACIDS (2017)
Structural decoding of netrin-4 reveals a regulatory function towards mature basement membranes
Raphael Reuten et al.
NATURE COMMUNICATIONS (2016)
Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data
M. Saad et al.
GENES BRAIN AND BEHAVIOR (2015)
Distinct functions of the laminin β LN domain and collagen IV during cardiac extracellular matrix formation and stabilization of alary muscle attachments revealed by EMS mutagenesis in Drosophila
Dominik Hollfelder et al.
BMC DEVELOPMENTAL BIOLOGY (2014)
High creatine kinase levels and white matter changes: Clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency
Maria de los Angeles Beytia et al.
MOLECULAR AND CELLULAR PROBES (2014)
Limb girdle muscular dystrophy due to LAMA2 mutations: Diagnostic difficulties due to associated peripheral neuropathy
Sophelia H. S. Chan et al.
NEUROMUSCULAR DISORDERS (2014)
Biologically-active laminin-111 fragment that modulates the epithelial-to-mesenchymal transition in embryonic stem cells
Christine-Maria Horejs et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Laminin 332 processing impacts cellular behavior
Patricia Rousselle et al.
CELL ADHESION & MIGRATION (2013)
Laminins in basement membrane assembly
Erhard Hohenester et al.
CELL ADHESION & MIGRATION (2013)
Functional Diversity of Laminins
Anna Domogatskaya et al.
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 28 (2012)
Origin and Evolution of Laminin Gene Family Diversity
Bryony Fahey et al.
MOLECULAR BIOLOGY AND EVOLUTION (2012)
Crystal Structures of the Network-Forming Short-Arm Tips of the Laminin β1 and γ1 Chains
Federico Carafoli et al.
PLOS ONE (2012)
Determinants of laminin polymerization revealed by the structure of the α5 chain amino-terminal region
Sadaf-Ahmahni Hussain et al.
EMBO REPORTS (2011)
CLINICAL AND MOLECULAR CHARACTERIZATION OF LIMB-GIRDLE MUSCULAR DYSTROPHY DUE TO LAMA2 MUTATIONS
Bruno F. Gavassini et al.
MUSCLE & NERVE (2011)
A Novel Mutation of LAMB2 in a Multigenerational Mennonite Family Reveals a New Phenotypic Variant of Pierson Syndrome
Brian G. Mohney et al.
OPHTHALMOLOGY (2011)
Mutations in the Human Laminin β2 (LAMB2) Gene and the Associated Phenotypic Spectrum
Verena Matejas et al.
HUMAN MUTATION (2010)
Observations of Skin Grafts Derived from Keratinocytes Expressing Selectively Engineered Mutant Laminin-332 Molecules
Noriyasu Sakai et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2010)
Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations
Fatemeh Geranmayeh et al.
NEUROMUSCULAR DISORDERS (2010)
Ophthalmological aspects of Pierson syndrome
Cecilie Bredrup et al.
AMERICAN JOURNAL OF OPHTHALMOLOGY (2008)
LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients
J. Oliveira et al.
CLINICAL GENETICS (2008)
A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination
Bruce L. Patton et al.
JOURNAL OF CELL SCIENCE (2008)
Variable phenotype of Pierson syndrome
Hyun Jin Choi et al.
PEDIATRIC NEPHROLOGY (2008)
A milder variant of Pierson syndrome
Mikhail Kagan et al.
PEDIATRIC NEPHROLOGY (2008)
The coiled-coil structure potential of the laminin LCC domain is very fragmented and does not differentiate between natural and non-detected isoforms
Tahl Zimmerman et al.
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2007)
The congenital muscular dystrophies:: Recent advances and molecular insights
Jerry R. Mendell et al.
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY (2006)
A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2
Verena Matejas et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION (2006)
Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders
K. Hasselbacher et al.
KIDNEY INTERNATIONAL (2006)
Ligand-binding specificities of laminin-binding integrins:: A comprehensive survey of laminin-integrin interactions using recombinant α3β1, α6β1, α7β1 and α6β4 integrins
R Nishiuchi et al.
MATRIX BIOLOGY (2006)
Distribution of laminins in the developing human eye
B Byström et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
LAMA2 gene analysis in congenital muscular dystrophy - New mutations, prenatal diagnosis, and founder effect
C Di Blasi et al.
ARCHIVES OF NEUROLOGY (2005)
A simplified laminin nomenclature
M Aumailley et al.
MATRIX BIOLOGY (2005)
Laminin-sulfatide binding initiates basement membrane assembly and enables receptor signaling in Schwann cells and fibroblasts
SH Li et al.
JOURNAL OF CELL BIOLOGY (2005)
Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
M Zenker et al.
HUMAN MOLECULAR GENETICS (2004)
Assembly and tissue functions of early embryonic laminins and netrins
PD Yurchenco et al.
CURRENT OPINION IN CELL BIOLOGY (2004)
UCSF chimera - A visualization system for exploratory research and analysis
EF Pettersen et al.
JOURNAL OF COMPUTATIONAL CHEMISTRY (2004)
The congenital muscular dystrophies in 2004: a century of exciting progress
F Muntoni et al.
NEUROMUSCULAR DISORDERS (2004)
Targeted inactivation of murine laminin γ2-chain gene recapitulates human junctional epidermolysis bullosa
XM Meng et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2003)
Matrix assembly, regulation, and survival functions of laminin and its receptors in embryonic stem cell differentiation
S Li et al.
JOURNAL OF CELL BIOLOGY (2002)
Identification of homologous biologically active sites on the N-terminal domain of laminin alpha chains
M Nomizu et al.
BIOCHEMISTRY (2001)
The expanding phenotype of laminin α2 chain (merosin) abnormalities:: case series and review
KJ Jones et al.
JOURNAL OF MEDICAL GENETICS (2001)
An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy
J Moll et al.
NATURE (2001)
Glycosaminoglycan-binding properties and secondary structure of the C-terminus of netrin-1
J Kappler et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2000)
Share Paper
