Mouse Samd9l is not a functional paralogue of the human SAMD9, the gene mutated in normophosphataemic familial tumoral calcinosis (Q36054790)

11 August 2017

Mouse Samd9l is not a functional paralogue of the human SAMD9, the gene mutated in normophosphataemic familial tumoral calcinosis (English)

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11 August 2017

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8

Jouni Uitto

1 reference

11 August 2017

Qiaoli Li

1

1 reference

11 August 2017

Haitao Guo

2

1 reference

11 August 2017

Hirotaka Matsui

3

1 reference

11 August 2017

Hiroaki Honda

4

1 reference

11 August 2017

Toshiya Inaba

5

1 reference

11 August 2017

John P Sundberg

6

1 reference

11 August 2017

Eli Sprecher

7

1 reference

11 August 2017

1 July 2012

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11 August 2017

Experimental Dermatology

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11 August 2017

21

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11 August 2017

554-556

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11 August 2017

7

1 reference

The Samd9L gene: transcriptional regulation and tissue-specific expression in mouse development

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3381902

Pseudoxanthoma elasticum: molecular genetics and putative pathomechanisms

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3381902

Familial tumoral calcinosis: from characterization of a rare phenotype to the pathogenesis of ectopic calcification

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3381902

The mineralization phenotype in Abcc6 ( -/- ) mice is affected by Ggcx gene deficiency and genetic background--a model for pseudoxanthoma elasticum

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3381902

Normophosphatemic familial tumoral calcinosis is caused by deleterious mutations in SAMD9, encoding a TNF-alpha responsive protein

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3381902

Ectopic mineralization of connective tissue in Abcc6-/- mice: effects of dietary modifications and a phosphate binder--a preliminary study

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3381902

Human sterile alpha motif domain 9, a novel gene identified as down-regulated in aggressive fibromatosis, is absent in the mouse

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3381902

A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3381902

Targeted ablation of the abcc6 gene results in ectopic mineralization of connective tissues

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3381902

Expression of the Abca-subfamily of genes in Abcc6-/- mice--upregulation of Abca4.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3381902

Aberrant mineralization of connective tissues in a mouse model of pseudoxanthoma elasticum: systemic and local regulatory factors

11 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22716256

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/J.1600-0625.2012.01524.X

1 reference

11 August 2017

1 reference

11 August 2017

1 reference