(Q47624116)

English

Metaphyseal chondrodysplasia type Schmid mutations are predicted to occur in two distinct three-dimensional clusters within type X collagen NC1 domains that retain the ability to trimerize

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

Metaphyseal chondrodysplasia type Schmid mutations are predicted to occur in two distinct three-dimensional clusters within type X collagen NC1 domains that retain the ability to trimerize (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

2

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

4

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

author name string

Marks DS

1

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

Wallis GA

3

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

Kadler KE

5

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

Boot-Handford RP

6

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

language of work or name

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publication date

1 February 1999

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Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

number of pages

10

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Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

274

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Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

6

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Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

3632-3641

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

Immunohistochemical localization of short chain cartilage collagen (type X) in avian tissues

1 reference

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The human collagen X gene: complete primary sequence and re-expression in osteoarthritis

1 reference

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21 January 2018

The human collagen X gene. Complete primary translated sequence and chromosomal localization

1 reference

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Macromolecular organization of chicken type X collagen in vitro

1 reference

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Characterization of human type X procollagen and its NC-1 domain expressed as recombinant proteins in HEK293 cells.

1 reference

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The fibrillar collagens, collagen VIII, collagen X and the C1q complement proteins share a similar domain in their C-terminal non-collagenous regions

1 reference

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Isolation, sequence analysis and characterization of cDNA clones coding for the C chain of mouse C1q. Sequence similarity of complement subcomponent C1q, collagen type VIII and type X and precerebellin

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Molecular cloning of rat cerebellin-like protein cDNA which encodes a novel membrane-associated glycoprotein

1 reference

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21 January 2018

Precerebellin is a cerebellum-specific protein with similarity to the globular domain of complement C1q B chain

1 reference

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A Novel Serum Protein Similar to C1q, Produced Exclusively in Adipocytes

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Abnormal compartmentalization of cartilage matrix components in mice lacking collagen X: implications for function

1 reference

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21 January 2018

A type X collagen mutation causes Schmid metaphyseal chondrodysplasia

1 reference

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21 January 2018

Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasia

1 reference

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21 January 2018

The C-propeptide domain of procollagen can be replaced with a transmembrane domain without affecting trimer formation or collagen triple helix folding during biosynthesis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3632

21 January 2018

Site-directed mutagenesis of human type X collagen. Expression of alpha1(X) NC1, NC2, and helical mutations in vitro and in transfected cells

1 reference

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21 January 2018

A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasia

1 reference

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21 January 2018

The crystal structure of a complement-1q family protein suggests an evolutionary link to tumor necrosis factor

1 reference

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21 January 2018

Rapid and sensitive sequence comparison with FASTP and FASTA

1 reference

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21 January 2018

Methods for assessing the statistical significance of molecular sequence features by using general scoring schemes

1 reference

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21 January 2018

Amino acid substitution matrices from protein blocks

1 reference

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21 January 2018

Multiple sequence alignment with hierarchical clustering

1 reference

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21 January 2018

Approaches to DNA mutagenesis: an overview

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21 January 2018

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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The alpha1(VIII) and alpha2(VIII) chains of type VIII collagen can form stable homotrimeric molecules

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Aromatic-aromatic interaction: a mechanism of protein structure stabilization

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Design, structure and stability of a hyperthermophilic protein variant

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Spondylometaphyseal dysplasia in mice carrying a dominant negative mutation in a matrix protein specific for cartilage-to-bone transition

1 reference

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21 January 2018

Immunolocalization of type X collagen in normal fetal and adult osteoarthritic cartilage with monoclonal antibodies

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Normal long bone growth and development in type X collagen-null mice

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Identifiers

10.1074/JBC.274.6.3632

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 February 2018

http://europepmc.org/abstract/MED/9920912

ResearchGate publication ID

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