Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations inKITLG-Reference-Cited by-同舟云学术

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Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations inKITLG

Published:2015-07-14 Issue:8 Volume:40 Page:860-864
ISSN:0307-6938
Container-title:Clinical and Experimental Dermatology
language:en
Short-container-title:Clin Exp Dermatol

Author:

Cuell A.¹,Bansal N.²,Cole T.³,Kaur M. R.²,Lee J.⁴,Loffeld A.²,Moss C.¹,O'Donnell M.³,Takeichi T.⁴,Thind C. K.¹,McGrath J. A.⁴

Affiliation:

1. Department of Dermatology; Birmingham Children's Hospital; NHS Foundation Trust; Birmingham UK

2. Department of Dermatology; Solihull Hospital; Heart of England NHS Foundation Trust; Solihull UK

3. Department of Clinical Genetics; Birmingham Women's Hospital; NHS Foundation Trust; Birmingham UK

4. Genetic Skin Disease Group; St John's Institute of Dermatology; King's College London; London UK

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ced.12702/fullpdf

Reference9 articles.

1. Hereditary congenital hypopigmented and hyperpigmented macules;Westerhof;Arch Dermatol,1978

2. KITLG mutations cause familial progressive hyper- and hypopigmentation;Amyere;J Invest Dermatol,2011

3. Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation;Wang;Am J Hum Genet,2009

4. Mutations in ABCB6 cause dyschromatosis universalis hereditaria;Zhang;J Invest Dermatol,2013

5. The genetic determination of skin pigmentation: KITLG and the KITLG/c-Kit pathway as key players in the onset of human familial pigmentary diseases;Picardo;J Invest Dermatol,2011

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1. Therapeutic modulation of KIT ligand in melanocytic disorders with implications for mast cell diseases;Experimental Dermatology;2024-05

2. Overexpression of KITLG predicts unfavorable clinical outcomes and promotes lymph node metastasis via the JAK/STAT pathway in nasopharyngeal carcinoma;Laboratory Investigation;2022-11

3. Genome-Wide Association Study Identifies Candidate Genes for Stripe Pattern Feather Color of Rhode Island Red Chicks;Genes;2022-08-24

4. De novo mutation in KITLG gene causes a variant of Familial Progressive Hyper‐ and Hypo‐pigmentation (FPHH);Molecular Genetics & Genomic Medicine;2021-10-30

5. Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation;BMC Medical Genomics;2021-01-06

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