Positional cloning of the gene LIMBIN responsible for bovine chondrodysplastic dwarfism (Q34075108)

30 July 2017

Positional cloning of the gene LIMBIN responsible for bovine chondrodysplastic dwarfism (English)

1 reference

30 July 2017

Haruko Takeda

1

1 reference

30 July 2017

Marika Takami

2

1 reference

30 July 2017

Tomoko Oguni

3

1 reference

30 July 2017

Takehito Tsuji

4

1 reference

30 July 2017

Kazuhiro Yoneda

5

1 reference

30 July 2017

Hiroaki Sato

6

1 reference

30 July 2017

Naoya Ihara

7

1 reference

30 July 2017

Tomohito Itoh

8

1 reference

30 July 2017

Srinivas R Kata

9

1 reference

30 July 2017

Yuji Mishina

10

1 reference

30 July 2017

James E Womack

11

1 reference

30 July 2017

Yasuo Moritomo

12

1 reference

30 July 2017

Yoshikazu Sugimoto

13

1 reference

30 July 2017

Tetsuo Kunieda

14

1 reference

30 July 2017

language of work or name

English

0 references

publication date

22 July 2002

1 reference

Proceedings of the National Academy of Sciences of the United States of America

30 July 2017

6

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

30 July 2017

99

1 reference

30 July 2017

16

1 reference

30 July 2017

10549-10554

1 reference

The Gene Resource Locator: gene locus maps for transcriptome analysis

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Establishment of a high throughput EST sequencing system using poly(A) tail-removed cDNA libraries and determination of 36,000 bovine ESTs

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

A common cis-acting sequence in the DiGeorge critical region regulates bi-directional transcription of UFD1L and CDC45L.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

PSORT: a program for detecting sorting signals in proteins and predicting their subcellular localization

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Construction of a bovine yeast artificial chromosome (YAC) library

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

A rank-based nonparametric method for mapping quantitative trait loci in outbred half-sib pedigrees: application to milk production in a granddaughter design.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

SMART, a simple modular architecture research tool: identification of signaling domains

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Characterization of 42 highly polymorphic bovine microsatellite markers.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

PTH/PTHrP receptor in early development and Indian hedgehog-regulated bone growth

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Fibroblast growth factor receptor 3 is a negative regulator of bone growth

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

A type X collagen mutation causes Schmid metaphyseal chondrodysplasia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Parathyroid hormone-related peptide-depleted mice show abnormal epiphyseal cartilage development and altered endochondral bone formation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Enrichment of microsatellites from the citrus genome using biotinylated oligonucleotide sequences bound to streptavidin-coated magnetic particles.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

A constitutively active mutant PTH-PTHrP receptor in Jansen-type metaphyseal chondrodysplasia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Identification of the molecular defect in a family with spondyloepiphyseal dysplasia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Morphological Changes of Epiphyseal Plate in the Long Bone of Chondrodysplastic Dwarfism in Japanese Brown Cattle

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Exogenous retinoic acid rapidly induces anterior ectopic expression of murine Hox-2 genes in vivo

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Glycine to serine substitution in the triple helical domain of pro-alpha 1 (II) collagen results in a lethal perinatal form of short-limbed dwarfism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=124971

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

28 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337899

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337899

A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337899

Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337899

Localization of a locus responsible for the bovine chondrodysplastic dwarfism (bcd) on chromosome 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337899

Association between homeobox-containing gene MSX1 and the occurrence of limb deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337899

Tensile stress induces bone morphogenetic protein 4 in preosteoblastic and fibroblastic cells, which later differentiate into osteoblasts leading to osteogenesis in the mouse calvariae in organ culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337899

A whole-genome radiation hybrid panel for bovine gene mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337899

Basic fibroblast growth factor binds to heparan sulfate in the extracellular matrix of rat growth plate chondrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.152337899

The current status of bovine dwarfism

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12136126

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.152337899

1 reference

30 July 2017

0 references

1 reference

30 July 2017

1 reference