Organization and chromosomal localization of the mouse gene, distance between human COL13A1 and prolyl 4-hydroxylase a-subunit genes, and generation of mice expressing an N-terminally altered type XIII collagen.

No abstract is available for this paper.

• Publication year

  1999

• Venue

  Unknown venue

• Publication date

  Unknown publication date

• Fields of study

  Not labeled

• Identifiers

  No identifiers available.

• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• Molecular Cloning: A Laboratory Manual

  2001influential reference
• A heterozygous splice site mutation in COL6A1 leading to an in-frame deletion of the alpha1(VI) collagen chain in an italian family affected by bethlem myopathy.

  1999cited by this paper
• Structure and function of hemidesmosomes: more than simple adhesion complexes.

  1999cited by this paper
• A dup(17)(p11.2p11.2) detected by fluorescence in situ hybridization in a boy with Alport syndrome.

  1999cited by this paper
• Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy.

  1998cited by this paper
• Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.

  1998cited by this paper
• Complete primary structure of two variant forms of human type XVIII collagen and tissue-specific differences in the expression of the corresponding transcripts.

  1998cited by this paper
• Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy.

  1998cited by this paper
• Mutation of the type X collagen gene (COL10A1) causes spondylometaphyseal dysplasia.

  1998cited by this paper
• Analysis of the COL1A1 and COL1A2 genes by PCR amplification and scanning by conformation-sensitive gel electrophoresis identifies only COL1A1 mutations in 15 patients with osteogenesis imperfecta type I: identification of common sequences of null-allele mutations.

  1998cited by this paper
• Reduced collagen VI causes Bethlem myopathy: a heterozygous COL6A1 nonsense mutation results in mRNA decay and functional haploinsufficiency.

  1998cited by this paper
• Genetic heterogeneity in Miyoshi-type distal muscular dystrophy.

  1998cited by this paper
• Human COL9A1 and COL9A2 genes. Two genes of 90 and 15 kb code for similar polypeptides of the same collagen molecule.

  1998cited by this paper
• Ultrastructural, physiological, and molecular defects in the inner ear of a gene-knockout mouse model for autosomal Alport syndrome.

  1998cited by this paper
• The short and long forms of type XVIII collagen show clear tissue specificities in their expression and location in basement membrane zones in humans.

  1998cited by this paper
• Collagen types VIII and X, two non-fibrillar, short-chain collagens. Structure homologies, functions and involvement in pathology.

  1997cited by this paper
• Abnormal Compartmentalization of Cartilage Matrix Components in Mice Lacking Collagen X: Implications for Function

  1997cited by this paper
• GeneCards: integrating information about genes, proteins and diseases.

  1997cited by this paper
• Complete Primary Structure of Two Splice Variants of Collagen XII, and Assignment of α1(XII) Collagen (COL12A1), α1(IX) Collagen (COL9A1), and α1(XIX) Collagen (COL19A1) to Human Chromosome 6q12–q13

  1997cited by this paper
• Type VI Collagen Anchors Endothelial Basement Membranes by Interacting with Type IV Collagen*

  1997cited by this paper
• Differential expression of collagens XII and XIV in human skin and in reconstructed skin.

  1997cited by this paper
• Type III collagen is crucial for collagen I fibrillogenesis and for normal cardiovascular development.

  1997cited by this paper
• Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion

  1997cited by this paper
• Cloning of the human type XVII collagen gene (COL17A1), and detection of novel mutations in generalized atrophic benign epidermolysis bullosa.

  1997cited by this paper
• Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II.

  1997cited by this paper
• Mutations in fibrillar collagens (types I, II, III, and XI), fibril‐associated collagen (type IX), and network‐forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vessels

  1997cited by this paper
• Localization of a Binding Site for the Proteoglycan Decorin on Collagen XIV (Undulin)*

  1997cited by this paper
• Type IIA Procollagen Amino Propeptide Is Localized in Human Embryonic Tissues

  1997cited by this paper
• Human Gene Mutation Database

  1996cited by this paper
• Genes and gene regulation of extracellular matrix proteins: an introduction.

  1996cited by this paper
• The mouse col11a2 gene. Some transcripts from the adjacent rxr-beta gene extend into the col11a2 gene.

  1996cited by this paper
• Visual mapping by high resolution FISH.

  1996cited by this paper
• A chondroitin/dermatan sulfate form of CD44 is a receptor for collagen XIV (undulin).

  1996cited by this paper
• Collagen COL4A3 knockout: a mouse model for autosomal Alport syndrome.

  1996cited by this paper
• Type XV and XVIII collagens, a new subgroup within the family of collagens

  1996cited by this paper
• Biosynthesis and processing of type XVI collagen in human fibroblasts and smooth muscle cells.

  1996cited by this paper
• Fiber-FISH: experiences and a refined protocol.

  1996cited by this paper
• Targeted transgenesis.

  1996cited by this paper
• Transgenic animals

  1996cited by this paper
• Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

  1995cited by this paper
• Two new collagen subgroups: membrane-associated collagens and types XV and XVII.

  1995cited by this paper
• Mechanically stretched chromosomes as targets for high-resolution FISH mapping.

  1995cited by this paper
• Distribution of type XV collagen transcripts in human tissue and their production by muscle cells and fibroblasts.

  1995cited by this paper
• Identification of Three N-terminal Ends of Type XVIII Collagen Chains and Tissue-specific Differences in the Expression of the Corresponding Transcripts

  1995influential reference
• Predicting Pol II promoter sequences using transcription factor binding sites.

  1995cited by this paper
• The Human COL11A2 Gene Structure Indicates that the Gene Has Not Evolved with the Genes for the Major Fibrillar Collagens (*)

  1995cited by this paper
• Targeting the mouse genome: a compendium of knockouts (Part II)

  1995cited by this paper
• Gene knock-out technology: a methodological overview for the interested novice.

  1995cited by this paper
• Targeting the mouse genome

  1995cited by this paper
• Localization of the undulin gene (UND) to human chromosome band 8q23.

  1995cited by this paper
• Mouse Col18a1 is expressed in a tissue-specific manner as three alternative variants and is localized in basement membrane zones.

  1995cited by this paper
• Inducible gene targeting in mice

  1995cited by this paper
• A targeted mutation at the known collagenase cleavage site in mouse type I collagen impairs tissue remodeling

  1995cited by this paper
• Primary structure of the long and short splice variants of mouse collagen XII and their tissue‐specific expression during embryonic development

  1995cited by this paper
• Another look at collagen V and XI molecules.

  1995cited by this paper
• Molecular cloning, chromosomal assignment, and expression of the mouse aspartylglucosaminidase gene.

  1995cited by this paper
• Targeted mutation in the col5a2 gene reveals a regulatory role for type V collagen during matrix assembly

  1995cited by this paper
• Fast hybridization solution for the detection of immobilized nucleic acids.

  1995cited by this paper
• The complete cDNA coding sequence for the mouse proα1(I) chain of type I procollagen

  1995cited by this paper
• Head to tail organization of the human COL6A1 and COL6A2 genes by fiber-FISH.

  1995cited by this paper
• Targeting the mouse genome: a compendium of knockouts (Part III)

  1995cited by this paper
• Conservation of the sizes of 53 introns and over 100 intronic sequences for the binding of common transcription factors in the human and mouse genes for type II procollagen (COL2A1).

  1995cited by this paper
• Tissue distribution and developmental expression of type XVI collagen in the mouse.

  1994cited by this paper
• Alpha 1(XVIII), a collagen chain with frequent interruptions in the collagenous sequence, a distinct tissue distribution, and homology with type XV collagen.

  1994cited by this paper
• Phenotypic variability and incomplete penetrance of spontaneous fractures in an inbred strain of transgenic mice expressing a mutated collagen gene (COL1A1).

  1994cited by this paper
• The exon structure of the mouse alpha 2(IX) collagen gene shows unexpected divergence from the chick gene.

  1994cited by this paper
• Deletion of a DNA polymerase beta gene segment in T cells using cell type-specific gene targeting.

  1994cited by this paper
• Cloning of human type VII collagen. Complete primary sequence of the alpha 1(VII) chain and identification of intragenic polymorphisms.

  1994cited by this paper
• Alternative splicing of the NC1 domain of the human alpha 3(IV) collagen gene. Differential expression of mRNA transcripts that predict three protein variants with distinct carboxyl regions.

  1994cited by this paper
• The mouse type-III procollagen-encoding gene: genomic cloning and complete DNA sequence.

  1994cited by this paper
• Structural organization of the human type VII collagen gene (COL7A1), composed of more exons than any previously characterized gene.

  1994cited by this paper
• Normal long bone growth and development in type X collagen-null mice

  1994cited by this paper
• Primary structure of the alpha 1 chain of human type XV collagen and exon-intron organization in the 3' region of the corresponding gene.

  1994cited by this paper
• The genes COL4A5 and COL4A6, coding for basement membrane collagen chains alpha 5(IV) and alpha 6(IV), are located head-to-head in close proximity on human chromosome Xq22 and COL4A6 is transcribed from two alternative promoters.

  1994cited by this paper
• An inbred line of transgenic mice expressing an internally deleted gene for type II procollagen (COL2A1). Young mice have a variable phenotype of a chondrodysplasia and older mice have osteoarthritic changes in joints.

  1993cited by this paper
• The carboxyl-terminal half of type VII collagen, including the non-collagenous NC-2 domain and intron/exon organization of the corresponding region of the COL7A1 gene.

  1993cited by this paper
• Physical and linkage mapping of the human and murine genes for the alpha 1 chain of type IX collagen (COL9A1).

  1993cited by this paper
• Chromosomal localization of mouse bullous pemphigoid antigens. BPAG1 and BPAG2: identification of a new region of homology between mouse and human chromosomes.

  1993cited by this paper
• Tissue‐specific expression of type XII collagen during mouse embryonic development

  1993cited by this paper
• Alternate exon usage is a commonly used mechanism for increasing coding diversity within genes coding for extracellular matrix proteins.

  1993influential reference
• Identification of a novel collagen chain represented by extensive interruptions in the triple-helical region.

  1993cited by this paper
• Human chromosome 21: genome mapping and exploration, circa 1993.

  1993cited by this paper
• Complete primary structure of chicken collagen XIV.

  1993cited by this paper
• Transgenic mice expressing a partially deleted gene for type I procollagen (COL1A1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineral.

  1993cited by this paper
• Type XIV collagen is encoded by alternative transcripts with distinct 5' regions and is a multidomain protein with homologies to von Willebrand's factor, fibronectin, and other matrix proteins.

  1993influential reference
• Osteoarthritis associated with mild chondrodysplasia in transgenic mice expressing α1 (IX) collagen chains with a central deletion

  1993cited by this paper
• cDNA cloning and chromosomal mapping of the mouse type VII collagen gene (Col7a1): evidence for rapid evolutionary divergence of the gene.

  1993influential reference
• Cloning of the human and mouse type X collagen genes and mapping of the mouse type X collagen gene to chromosome 10.

  1992cited by this paper
• Cloning and primary structural analysis of the bullous pemphigoid autoantigen BP180.

  1992cited by this paper
• A simple method for simultaneous R- or G-banding and fluorescence in situ hybridization of small single-copy genes.

  1992cited by this paper
• Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

  1992cited by this paper
• Sequence analysis of a full-length cDNA for the murine proα2(I) collagen chain: Comparison of the derived primary structure with human proα2(I) collagen

  1992cited by this paper
• Colocalization of the genes for the α3(IV) and α4(IV) chains of type IV collagen to chromosome 2 bands q35–q37

  1992cited by this paper
• Structural comparison of the chicken genes for α1(VI) and α2(VI) collagen

  1992cited by this paper
• Purification and characterization of native type XIV collagen.

  1992cited by this paper
• Location of the mouse complement factor H gene (cfh) by FISH analysis and replication R-banding.

  1992cited by this paper
• Molecular cloning and characterization of type VII collagen cDNA.

  1992cited by this paper
• Human alpha 2(VI) collagen gene. Heterogeneity at the 5'-untranslated region generated by an alternate exon.

  1992cited by this paper
• Type XIV collagen is a variant of undulin.

  1992cited by this paper
• Characterization of the spectrum of alternative splicing of alpha 1 (XIII) collagen transcripts in HT-1080 cells and calvarial tissue resulted in identification of two previously unidentified alternatively spliced sequences, one previously unidentified exon, and nine new mRNA variants.

  1992cited by this paper

• No citing papers are available for this paper.