(Q21283794)

4 July 2017

Polymorphisms within the canine MLPH gene are associated with dilute coat color in dogs (English)

1 reference

4 July 2017

8

Tosso Leeb

Tosso

Leeb

1 reference

4 July 2017

5

Emmanuel Mignot

Emmanuel

Mignot

1 reference

4 July 2017

Ute Philipp

1

Ute

Philipp

1 reference

4 July 2017

Henning Hamann

2

Henning

Hamann

1 reference

4 July 2017

Lars Mecklenburg

3

Lars

Mecklenburg

1 reference

4 July 2017

Seiji Nishino

4

Seiji

Nishino

1 reference

4 July 2017

Anne-Rose Günzel-Apel

6

Anne-Rose

Günzel-Apel

1 reference

4 July 2017

Sheila M Schmutz

7

Sheila M

Schmutz

1 reference

4 July 2017

language of work or name

English

0 references

publication date

16 June 2005

1 reference

4 July 2017

1 reference

4 July 2017

6

1 reference

4 July 2017

34

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2156-6-34

4 July 2017

1

0 references

exact match

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1471-2156-6-34

cites work

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

Black hair follicular dysplasia, an autosomal recessive condition in dogs

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

dsu functions in a MYO5A-independent pathway to suppress the coat color of dilute mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

A mutation in Rab27a causes the vesicle transport defects observed in ashen mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

Novel myosin heavy chain encoded by murine dilute coat colour locus

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

Bayesian haplotype inference for multiple linked single-nucleotide polymorphisms

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

Construction and characterization of an eightfold redundant dog genomic bacterial artificial chromosome library

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

The actin-binding domain of Slac2-a/melanophilin is required for melanosome distribution in melanocytes

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

Chromosome-specific single-locus FISH probes allow anchorage of an 1800-marker integrated radiation-hybrid/linkage map of the domestic dog genome to all chromosomes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

Chromosomal assignment of the canine melanophilin gene (MLPH): a candidate gene for coat color dilution in Pinschers.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

TYRP1 and MC1R genotypes and their effects on coat color in dogs

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

[Coat color in dogs. 2: Clinical significance].

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1183202

Follicular dysplasia in five Weimaraners

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15960853

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2156-6-34

1 reference

Dimensions Publication ID

4 July 2017

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1471-2156-6-34

PMCID

1183202

1 reference

4 July 2017

1 reference