The heterozygous disproportionate micromelia (dmm) mouse: morphological changes in fetal cartilage precede postnatal dwarfism and compared with lethal homozygotes can explain the mild phenotype (Q36942482)

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scientific article published on 04 August 2008

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English	The heterozygous disproportionate micromelia (dmm) mouse: morphological changes in fetal cartilage precede postnatal dwarfism and compared with lethal homozygotes can explain the mild phenotype	scientific article published on 04 August 2008

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scholarly article

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11 January 2020

The heterozygous disproportionate micromelia (dmm) mouse: morphological changes in fetal cartilage precede postnatal dwarfism and compared with lethal homozygotes can explain the mild phenotype (English)

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11 January 2020

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Laura C Bridgewater

3

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11 January 2020

author name string

Robert E Seegmiller

1

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11 January 2020

Brandon D Bomsta

2

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11 January 2020

Cindy M Niederhauser

4

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11 January 2020

Carolina Montaño

5

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11 January 2020

Sterling Sudweeks

6

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11 January 2020

David R Eyre

7

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11 January 2020

Russell J Fernandes

8

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11 January 2020

publication date

4 August 2008

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11 January 2020

Journal of Histochemistry and Cytochemistry

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11 January 2020

56

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11 January 2020

11

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11 January 2020

1003-1011

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11 January 2020

Protein consequences of the Col2a1 C-propeptide mutation in the chondrodysplastic Dmm mouse

1 reference

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29 September 2017

Developmental regulation of the growth plate

1 reference

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Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule.

1 reference

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Building collagen molecules, fibrils, and suprafibrillar structures.

1 reference

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

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29 September 2017

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29 September 2017

Inactivation of one allele of the type II collagen gene alters the collagen network in murine articular cartilage and makes cartilage softer

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29 September 2017

Hsp47: a molecular chaperone that interacts with and stabilizes correctly-folded procollagen

1 reference

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29 September 2017

Report of five novel and one recurrent COL2A1 mutations with analysis of genotype-phenotype correlation in patients with a lethal type II collagen disorder

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29 September 2017

Procollagen folding and assembly: the role of endoplasmic reticulum enzymes and molecular chaperones

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29 September 2017

Completion of the mouse aggrecan gene structure and identification of the defect in the cmd-Bc mouse as a near complete deletion of the murine aggrecan gene

1 reference

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29 September 2017

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

1 reference

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29 September 2017

Disproportionate micromelia (Dmm) in mice caused by a mutation in the C-propeptide coding region of Col2a1

1 reference

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29 September 2017

A specific collagen type II gene (COL2A1) mutation presenting as spondyloperipheral dysplasia

1 reference

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29 September 2017

Pulmonary hypoplasia associated with reduced thoracic space in mice with disproportionate micromelia (DMM)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569899

29 September 2017

Transgenic mice with targeted inactivation of the Col2 alpha 1 gene for collagen II develop a skeleton with membranous and periosteal bone but no endochondral bone

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569899

29 September 2017

Disproportionate micromelia (Dmm): an incomplete dominant mouse dwarfism with abnormal cartilage matrix

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569899

29 September 2017

A new chondrodystrophic mutant in mice. Electron microscopy of normal and abnormal chondrogenesis

1 reference

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29 September 2017

Histochemical, immunofluorescence, and ultrastructural differences in fetal cartilage among three genetically distinct chondrodystrophic mice

1 reference

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29 September 2017

Identification of the molecular defect in a family with spondyloepiphyseal dysplasia

1 reference

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29 September 2017

Differential growth by growth plates as a function of multiple parameters of chondrocytic kinetics.

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27 June 2018

Structure formation in the C terminus of type III collagen guides disulfide cross-linking.

1 reference

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4 September 2018

Altered mandibular development precedes the time of palate closure in mice homozygous for disproportionate micromelia: an oral clefting model supporting the Pierre-Robin sequence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569899

4 September 2018

Double heterozygosity for pseudoachondroplasia and spondyloepiphyseal dysplasia congenita.

1 reference

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4 September 2018

Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene.

1 reference

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4 September 2018

Premature osteoarthritis in the Disproportionate micromelia (Dmm) mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/18678883

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved cartilage fixation by ruthenium hexammine trichloride (RHT). A prerequisite for morphometry in growth cartilage

1 reference

https://pubmed.ncbi.nlm.nih.gov/18678883

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic stability of bovine articular chondrocytes after long-term culture in alginate beads

1 reference

https://pubmed.ncbi.nlm.nih.gov/18678883

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stickler syndrome. A mutation in the nonhelical 3' end of type II procollagen gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18678883

12 December 2020

based on heuristic

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Identifiers

10.1369/JHC.2008.951673

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11 January 2020

1 reference

Europe PubMed Central

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11 January 2020

1 reference

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11 January 2020

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