Pages that link to "Q24536147"
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The following pages link to Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4 (Q24536147):
Displaying 50 items.
- albinism (Q81867) (← links)
- What Controls Variation in Human Skin Color? (Q21092842) (← links)
- A partial gene deletion of SLC45A2 causes oculocutaneous albinism in Doberman pinscher dogs (Q21132281) (← links)
- Oculocutaneous albinism (Q21202962) (← links)
- The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild (Q21266671) (← links)
- Mutational analysis of oculocutaneous albinism: a compact review (Q21284502) (← links)
- Genetic architecture of skin and eye color in an African-European admixed population (Q21563358) (← links)
- Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan (Q24534208) (← links)
- Predicting phenotype from genotype: normal pigmentation (Q24633905) (← links)
- Melanosomes--dark organelles enlighten endosomal membrane transport (Q24647195) (← links)
- A genomewide association study of skin pigmentation in a South Asian population (Q24648719) (← links)
- The Development of Sugar-Based Anti-Melanogenic Agents (Q26752370) (← links)
- DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnostics (Q26864287) (← links)
- Understanding the evolution of human pigmentation: recent contributions from population genetics (Q27008258) (← links)
- The Genetics of Human Pigmentary Disorders (Q27008379) (← links)
- BLOC-2 targets recycling endosomal tubules to melanosomes for cargo delivery (Q27310758) (← links)
- Identification of Aim-1 as the underwhite mouse mutant and its transcriptional regulation by MITF (Q28204392) (← links)
- The etiology of oculocutaneous albinism (OCA) type II: the pink protein modulates the processing and transport of tyrosinase (Q28218945) (← links)
- Update on the regulation of mammalian melanocyte function and skin pigmentation (Q28237643) (← links)
- Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4 (Q28238670) (← links)
- Nitisinone improves eye and skin pigmentation defects in a mouse model of oculocutaneous albinism (Q28249590) (← links)
- Population differences of two coding SNPs in pigmentation-related genes SLC24A5 and SLC45A2 (Q28252679) (← links)
- Analysis of cultured human melanocytes based on polymorphisms within the SLC45A2/MATP, SLC24A5/NCKX5, and OCA2/P loci (Q28288300) (← links)
- Promoter polymorphisms in the MATP (SLC45A2) gene are associated with normal human skin color variation (Q28292797) (← links)
- Proton-associated sucrose transport of mammalian solute carrier family 45: an analysis in Saccharomyces cerevisiae (Q28595094) (← links)
- Identification of genes associated with shell color in the black-lipped pearl oyster, Pinctada margaritifera (Q28645914) (← links)
- Oculocutaneous albinism type 1: link between mutations, tyrosinase conformational stability, and enzymatic activity. (Q30394454) (← links)
- Synteny and candidate gene prediction using an anchored linkage map of Astyanax mexicanus (Q30485549) (← links)
- The Concise Guide to PHARMACOLOGY 2013/14: transporters (Q30486743) (← links)
- Vitamin D status and risk for malignant cutaneous melanoma: recent advances. (Q30490787) (← links)
- A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation (Q33335147) (← links)
- Homozygosity Mapping and Whole-Exome Sequencing to Detect SLC45A2 and G6PC3 Mutations in a Single Patient with Oculocutaneous Albinism and Neutropenia (Q33395814) (← links)
- Environmental and phenotype-related risk factors for owner-reported allergic/atopic skin symptoms and for canine atopic dermatitis verified by veterinarian in a Finnish dog population (Q33752006) (← links)
- Delineating the genetic heterogeneity of OCA in Hungarian patients (Q33815046) (← links)
- Myotis rufoniger genome sequence and analyses: M. rufoniger's genomic feature and the decreasing effective population size of Myotis bats (Q33874135) (← links)
- A customized pigmentation SNP array identifies a novel SNP associated with melanoma predisposition in the SLC45A2 gene. (Q33894967) (← links)
- Relationship between foveal cone specialization and pit morphology in albinism (Q33901490) (← links)
- MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2) (Q33906371) (← links)
- Signaling pathways in melanosome biogenesis and pathology (Q33913618) (← links)
- The interplay between natural selection and susceptibility to melanoma on allele 374F of SLC45A2 gene in a South European population. (Q34004833) (← links)
- Mutation of melanosome protein RAB38 in chocolate mice (Q34048569) (← links)
- Spectrum of candidate gene mutations associated with Indian familial oculocutaneous and ocular albinism (Q34079314) (← links)
- Prediction of eye color from genetic data using Bayesian approach (Q34175078) (← links)
- Characterization of the human RAB38 and RAB7 genes: exclusion of new major pathological loci for Japanese OCA. (Q34212647) (← links)
- Does levodopa improve vision in albinism? Results of a randomized, controlled clinical trial. (Q34214644) (← links)
- Diversity of human hair pigmentation as studied by chemical analysis of eumelanin and pheomelanin (Q34231940) (← links)
- Sequences associated with human iris pigmentation. (Q34287539) (← links)
- MATP polymorphisms in Germans and Japanese: the L374F mutation as a population marker for Caucasoids (Q34354119) (← links)
- A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population (Q34354851) (← links)
- Slc15a4, AP-3, and Hermansky-Pudlak syndrome proteins are required for Toll-like receptor signaling in plasmacytoid dendritic cells (Q34359204) (← links)