A single point-mutation within the melanophilin gene causes the lavender plumage colour dilution phenotype in the chicken (Q33314967)

25 July 2017

A single point-mutation within the melanophilin gene causes the lavender plumage colour dilution phenotype in the chicken (English)

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25 July 2017

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Michèle Tixier-Boichard

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Terry Burke

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object named as

Terry Burke

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25 July 2017

Mohsen Vaez

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25 July 2017

Sarah A Follett

2

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25 July 2017

David Gourichon

4

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25 July 2017

15 January 2008

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25 July 2017

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25 July 2017

9

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25 July 2017

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https://scigraph.springernature.com/pub.10.1186/1471-2156-9-7

25 July 2017

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cites work

A noncoding melanophilin gene (MLPH) SNP at the splice donor of exon 1 represents a candidate causal mutation for coat color dilution in dogs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Evolution of an avian pigmentation gene correlates with a measure of sexual selection

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

A homozygous single-base deletion in MLPH causes the dilute coat color phenotype in the domestic cat.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Pigment Cells: A Model for the Study of Organelle Transport

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Characterization of the molecular defects in Rab27a, caused by RAB27A missense mutations found in patients with Griscelli syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

A family of Rab27-binding proteins. Melanophilin links Rab27a and myosin Va function in melanosome transport

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Melanophilin, the product of the leaden locus, is required for targeting of myosin-Va to melanosomes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Identification of an organelle receptor for myosin-Va

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

The leaden gene product is required with Rab27a to recruit myosin Va to melanosomes in melanocytes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Primer3 on the WWW for general users and for biologist programmers

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

The mottling gene, the basis of six plumage color patterns in the domestic fowl

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Novel myosin heavy chain encoded by murine dilute coat colour locus

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Mapping of the silver gene in mink and its association with the dilution gene in dog.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Testing homology of loci for two plumage colors, "lavender" and "recessive white," with chicken and Japanese quail hybrids.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Covariation of GC content and the silent site substitution rate in rodents: implications for methodology and for the evolution of isochores.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Maltese dilution of domestic cats. A generalized cutaneous albinism lacking ocular involvement.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253553

Adendritic melanocytes: a mutation in linkage group II of the fowl

31 October 2018

1 reference

12 December 2020

Treatment of hemophagocytic lymphohistiocytosis with chemotherapy and bone marrow transplantation: a single-center study of 22 cases

1 reference

12 December 2020

Myosin V in the brain: mutations lead to neurological defects

1 reference

12 December 2020

Embryonal feather growth in the chicken

1 reference

12 December 2020

Recessive "lavender" in the Muscovy duck

1 reference

12 December 2020

Lavender, a chick melanocyte mutant with defective melanosome translocation: a possible role for 10 nm filaments and microfilaments but not microtubules

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2156-9-7

1 reference

Dimensions Publication ID

25 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2156-9-7

9 September 2019

1 reference

25 July 2017

1 reference