Related references
Note: Only part of the references are listed.A Third MLPH Variant Causing Coat Color Dilution in Dogs
Samantha L. Van Buren et al.
GENES (2020)
A comprehensive biomedical variant catalogue based on whole genome sequences of 582 dogs and eight wolves
V Jagannathan et al.
ANIMAL GENETICS (2019)
A novel MLPH variant in dogs with coat colour dilution
A. Bauer et al.
ANIMAL GENETICS (2018)
DoGSD: the dog and wolf genome SNP database
Bing Bai et al.
NUCLEIC ACIDS RESEARCH (2015)
Melanosome transfer: it is best to give and receive
Xufeng Wu et al.
CURRENT OPINION IN CELL BIOLOGY (2014)
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3
Pablo Cingolani et al.
FLY (2012)
Myosin-Va transports the endoplasmic reticulum into the dendritic spines of Purkinje neurons
Wolfgang Wagner et al.
NATURE CELL BIOLOGY (2011)
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna et al.
GENOME RESEARCH (2010)
Whole-Genome SNP Association in the Horse: Identification of a Deletion in Myosin Va Responsible for Lavender Foal Syndrome
Samantha A. Brooks et al.
PLOS GENETICS (2010)
Griscelli syndrome type 1: a report of two cases and review of the literature
Ellen R. Thomas et al.
CLINICAL DYSMORPHOLOGY (2009)
MLPH Genotype-Melanin Phenotype Correlation in Dilute Dogs
M. Welle et al.
JOURNAL OF HEREDITY (2009)
The tail that wags the dog: the globular tail domain defines the function of myosin V/XI
Jian-Feng Li et al.
TRAFFIC (2008)
A Noncoding melanophilin gene (MLPH) SNP at the splice donor of Exon 1 represents a candidate causal mutation for coat color dilution in dogs
Cord Drogemueller et al.
JOURNAL OF HEREDITY (2007)
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)
G Ménasché et al.
JOURNAL OF CLINICAL INVESTIGATION (2003)
Griscelli syndrome types 1 and 2
G Ménasché et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
The dilute locus and Griscelli syndrome:: Gateways towards a better understanding of melanosome transport
W Westbroek et al.
PIGMENT CELL RESEARCH (2001)
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome
G Ménasché et al.
NATURE GENETICS (2000)
Share Paper
