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A curated gene list for expanding the horizons of pigmentation biology

Pigment cell and melanoma research, 2019-05, Vol.32 (3), p.348-358

2019

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TFAP2 paralogs regulate melanocyte differentiation in parallel with MITF

PLoS genetics, 2017-03, Vol.13 (3), p.e1006636

2017

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Identification and functional analysis of SOX10 phosphorylation sites in melanoma

PloS one, 2018-01, Vol.13 (1), p.e0190834-e0190834

2018

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Sox proteins in melanocyte development and melanoma

Pigment cell and melanoma research, 2010-08, Vol.23 (4), p.496-513

2010

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Multicenter Evaluation of the Novel ETEST Fosfomycin for Antimicrobial Susceptibility Testing of Enterobacterales, Enterococcus faecalis, and Staphylococcus Species

Journal of clinical microbiology, 2022-07, Vol.60 (7), p.e0002122

2022

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SOX10 Ablation Arrests Cell Cycle, Induces Senescence, and Suppresses Melanomagenesis

Cancer research (Chicago, Ill.), 2013-09, Vol.73 (18), p.5709-5718

2013

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Computational Investigation of the pH Dependence of Stability of Melanosome Proteins: Implication for Melanosome formation and Disease

International journal of molecular sciences, 2021-07, Vol.22 (15), p.8273

2021

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Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish

PLoS genetics, 2008-09, Vol.4 (9), p.e1000174-e1000174

2008

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Murine Model of Niemann-Pick C Disease: Mutation in a Cholesterol Homeostasis Gene

Science (American Association for the Advancement of Science), 1997-07, Vol.277 (5323), p.232-235

1997

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MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells

Epigenetics & chromatin, 2019-08, Vol.12 (1), p.50-50, Article 50

2019

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Frequent mutations in the MITF pathway in melanoma

Pigment cell and melanoma research, 2009-08, Vol.22 (4), p.435-444

2009

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The next generation of melanocyte data: Genetic, epigenetic, and transcriptional resource datasets and analysis tools

Pigment cell and melanoma research, 2018-05, Vol.31 (3), p.442-447

Loftus, Stacie K.

2018

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Mutation of Melanosome Protein RAB38 in chocolate Mice

Proceedings of the National Academy of Sciences - PNAS, 2002-04, Vol.99 (7), p.4471-4476

2002

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Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome

Nature genetics, 1996-02, Vol.12 (2), p.130-136

1996

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SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer

BMC developmental biology, 2011-06, Vol.11 (1), p.40-40, Article 40

2011

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A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation

Development (Cambridge), 2003-10, Vol.130 (19), p.4665-4672

2003

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A rare case of isolated traumatic avulsion of the pes anserinus tendon

Skeletal radiology, 2020-10, Vol.49 (10), p.1659-1662

2020

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Gpnmb is a melanoblast‐expressed, MITF‐dependent gene

Pigment cell and melanoma research, 2009-02, Vol.22 (1), p.99-110

2009

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Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B

American journal of human genetics, 2023-07, Vol.110 (7), p.1123-1137

2023

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Rescue of neurodegeneration in Niemann–Pick C mice by a prion-promoter-driven Npc1 cDNA transgene

Human molecular genetics, 2002-11, Vol.11 (24), p.3107-3114

2002

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Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes

Genome research, 2018-11, Vol.28 (11), p.1621-1635

2018

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Massively Parallel Sequencing of Exons on the X Chromosome Identifies RBM10 as the Gene that Causes a Syndromic Form of Cleft Palate

American journal of human genetics, 2010-05, Vol.86 (5), p.743-748

2010

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A custom capture sequence approach for oculocutaneous albinism identifies structural variant alleles at the OCA2 locus

Human mutation, 2021-10, Vol.42 (10), p.1239-1253

2021

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Complete tibial insertion of the biceps femoris tendon: an MRI-based study to assess the prevalence of this variant

Surgical and radiologic anatomy (English ed.), 2020-06, Vol.42 (6), p.661-665

2020

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A curated gene list for expanding the horizons of pigmentation biology

TFAP2 paralogs regulate melanocyte differentiation in parallel with MITF

A Polymorphism in IRF4 Affects Human Pigmentation through a Tyrosinase-Dependent MITF/TFAP2A Pathway

Identification and functional analysis of SOX10 phosphorylation sites in melanoma

Sox proteins in melanocyte development and melanoma

Multicenter Evaluation of the Novel ETEST Fosfomycin for Antimicrobial Susceptibility Testing of Enterobacterales, Enterococcus faecalis, and Staphylococcus Species

SOX10 Ablation Arrests Cell Cycle, Induces Senescence, and Suppresses Melanomagenesis

Computational Investigation of the pH Dependence of Stability of Melanosome Proteins: Implication for Melanosome formation and Disease

Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish

Murine Model of Niemann-Pick C Disease: Mutation in a Cholesterol Homeostasis Gene

MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells

Frequent mutations in the MITF pathway in melanoma

The next generation of melanocyte data: Genetic, epigenetic, and transcriptional resource datasets and analysis tools

Mutation of Melanosome Protein RAB38 in chocolate Mice

Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome

SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer

A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation

A rare case of isolated traumatic avulsion of the pes anserinus tendon

Gpnmb is a melanoblast‐expressed, MITF‐dependent gene

Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B

Rescue of neurodegeneration in Niemann–Pick C mice by a prion-promoter-driven Npc1 cDNA transgene

Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes

Massively Parallel Sequencing of Exons on the X Chromosome Identifies RBM10 as the Gene that Causes a Syndromic Form of Cleft Palate

A custom capture sequence approach for oculocutaneous albinism identifies structural variant alleles at the OCA2 locus

Complete tibial insertion of the biceps femoris tendon: an MRI-based study to assess the prevalence of this variant

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