(Q35928277)

English

Neutral sphingomyelinase (SMPD3) deficiency causes a novel form of chondrodysplasia and dwarfism that is rescued by Col2A1-driven smpd3 transgene expression

scientific article published in July 2007

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Neutral sphingomyelinase (SMPD3) deficiency causes a novel form of chondrodysplasia and dwarfism that is rescued by Col2A1-driven smpd3 transgene expression (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Sphingomyelin phosphodiesterase 3, neutral

1 reference

GOA release 2020-03-11

author name string

Wilhelm Stoffel

1

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Britta Jenke

2

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Barbara Holz

3

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Erika Binczek

4

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Robert Heinz Günter

5

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Jutta Knifka

6

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Jürgen Koebke

7

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Anja Niehoff

8

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

language of work or name

0 references

publication date

1 July 2007

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

The American Journal of Pathology

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

171

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

153-161

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Neutral sphingomyelinase 2 (smpd3) in the control of postnatal growth and development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

Matrilin-3 is dispensable for mouse skeletal growth and development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

Neutral sphingomyelinase 1 deficiency in the mouse causes no lipid storage disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

Stage-and tissue-specific expression of a Col2a1-Cre fusion gene in transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

The somatomedin hypothesis: 2001.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

Cloning and characterization of the mammalian brain-specific, Mg2+-dependent neutral sphingomyelinase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

Characterization and subcellular localization of murine and human magnesium-dependent neutral sphingomyelinase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

Cloned mammalian neutral sphingomyelinase: functions in sphingolipid signaling?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

Primary structure of matrilin‐3, a new member of a family of extracellular matrix proteins related to cartilage matrix protein (matrilin‐1) and von Willebrand factor1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

Differential effects of insulin-like growth factor I and growth hormone on developmental stages of rat growth plate chondrocytes in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

Characterization of human and mouse cartilage oligomeric matrix protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

Osteopontin--a possible anchor of osteoclasts to bone

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

2 October 2017

Acid sphingomyelinase-deficient mice mimic the neurovisceral form of human lysosomal storage disease (Niemann-Pick disease)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

11 July 2018

COMP (cartilage oligomeric matrix protein) is structurally related to the thrombospondins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

11 July 2018

Effects of Igf1 gene deletion on postnatal growth patterns.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

24 September 2018

Developmental expression of a type II collagen/beta-galactosidase fusion gene in transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

24 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1941606

24 September 2018

Fragilitas ossium: a new autosomal recessive mutation in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/17591962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morphological and biochemical studies of a mouse mutant (fro/fro) with bone fragility

1 reference

https://pubmed.ncbi.nlm.nih.gov/17591962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/17591962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragilitas ossium (fro/fro) in the mouse: a model for a recessively inherited type of osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/17591962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cartilage oligomeric matrix protein (COMP) is an abundant component of tendon

1 reference

https://pubmed.ncbi.nlm.nih.gov/17591962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.2353/AJPATH.2007.061285

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

release_xcyfrsydmje35erfj6kxdmvwu4

1 reference

https://api.fatcat.wiki/v0/release/xcyfrsydmje35erfj6kxdmvwu4

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

ResearchGate publication ID

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