Related references
Note: Only part of the references are listed.Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis
Cilla Soderhall et al.
PLOS BIOLOGY (2007)
Rocks and clocks: calibrating the Tree of Life using fossils and molecules
Philip C. J. Donoghue et al.
TRENDS IN ECOLOGY & EVOLUTION (2007)
Molecular recognition in the assembly of collagens: Terminal noncollagenous domains are key recognition modules in the formation of triple helical protomers
Jamshid Khoshnoodi et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Primate molecular divergence dates
Michael E. Steiper et al.
MOLECULAR PHYLOGENETICS AND EVOLUTION (2006)
The C5 domain of the collagen VI α3(VI) chain is critical for extracellular microfibril formation and is present in the extracellular matrix of cultured cells
Shireen R. Lamande et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
WARP is a novel multimeric component of the chondrocyte pericellular matrix that interacts with perlecan
JM Allen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathy
S Lucioli et al.
NEUROLOGY (2005)
Congenital muscular dystrophy: molecular and cellular aspects
C Jimenez-Mallebrera et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2005)
Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy
AK Lampe et al.
JOURNAL OF MEDICAL GENETICS (2005)
Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy
NL Baker et al.
HUMAN MOLECULAR GENETICS (2005)
Collagen VI related muscle disorders
AK Lampe et al.
JOURNAL OF MEDICAL GENETICS (2005)
Ullrich disease due to deficiency of collagen VI in the sarcolemma
H Ishikawa et al.
NEUROLOGY (2004)
Improved prediction of signal peptides: SignalP 3.0
JD Bendtsen et al.
JOURNAL OF MOLECULAR BIOLOGY (2004)
Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency
WA Irwin et al.
NATURE GENETICS (2003)
New molecular mechanism for Ullrich congenital muscular dystrophy:: A heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
TC Pan et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Structural basis of type VI collagen dimer formation
S Ball et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Discrete integration of collagen XVI into tissue-specific collagen fibrils or beaded microfibrils
A Kassner et al.
MATRIX BIOLOGY (2003)
Ullrich disease: Collagen VI deficiency: EM suggests a new basis for muscular weakness
H Ishikawa et al.
NEUROLOGY (2002)
Electron microscopic abnormalities of skeletal muscle in patients with collagen VI deficiency in Ullrich's disease
T Niiyama et al.
ACTA NEUROPATHOLOGICA (2002)
Constitutive expression of hZnT4 zinc transporter in human breast epithelial cells
AA Michalczyk et al.
BIOCHEMICAL JOURNAL (2002)
WARP is a new member of the von Willebrand factor A-domain superfamily of extracellular matrix proteins
J Fitzgerald et al.
FEBS LETTERS (2002)
Kinked collagen VI tetramers and reduced microfibril formation as a result of Bethlem myopathy and introduced triple helical glycine mutations
SR Lamandé et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
The role of the C1 and C2 A-domains in type VI collagen assembly
SG Ball et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
The N-terminal N5 subdomain of the α3(VI) chain is important for collagen VI microfibril formation
J Fitzgerald et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
The amino-terminal part of PRELP binds to heparin and heparan sulfate
E Bengtsson et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Share Paper
