Results 31 to 40 of about 880 (178)

Retraction: Piebaldism: A Brief Report and Review of the Literature [PDF]

Indian Dermatology Online Journal
doaj   +2 more sources

Anomalous Coloration of Indo-Pacific Humpback Dolphins off Southern China

Journal of Marine Science and Engineering, 2023
The Indo-Pacific humpback dolphin is characterized by a particular ontogenic change in body color from dark gray at birth to pure white (or with a few dark-gray spots) after reaching adulthood.
Wenzhi Lin, Shenglan Chen, Ruiqiang Zheng, Agathe Serres, Binshuai Liu, Mingli Lin, Mingming Liu, Songhai Li   +7 more
doaj   +1 more source

Molecular Dynamics Simulation of KIT Mutation in a Patient wıth Piebaldism, Congenital Cataract and Aphakic Glaucoma

Journal of Biochemical and Clinical Genetics, 2023
Background: Piebaldism (OMIM #172800) is a rare autosomal dominant genodermatosis characterized by congenital poliosis and stable patches of leucoderma. Piebaldism is caused by mutations in the KIT and SNAI2 genes.
Fahrettin Duymus, Banu Bozkurt, Ali Sahin, Huseyin Babayev, Sibel Ersoy Evans, Betul Saylik, Tulin Cora   +6 more
doaj   +1 more source

Piebaldism.

Archives of dermatology, 1988
D B, Mosher, T B, Fitzpatrick
core   +4 more sources

Piebaldism in To Balo, South Sulawesi: Brief Report and Literature Review [PDF]

, 2019
Piebaldism is an autosomal dominant congenital disorder in pigment as a result of mutations in KIT gene, mapped on the long arm of chromosome 4. To Balo lived as a carrier of piebaldism genes.
Aziz, Isna Rasdianah, Muthiadin, Cut
core   +3 more sources

The first record of a piebald common bottlenose dolphin (Tursiops truncatus) in offshore waters of the north-western Black Sea

Theriologia Ukrainica, 2020
Piebaldism is one of three types of hypopigmentation of animals, when some areas on the skin have no pigments. Anomalously white cetaceans are rare, although they have been reported in more than 20 different cetacean species, including the common ...
Oksana Savenko
doaj   +1 more source

YY1 regulates melanocyte development and function by cooperating with MITF. [PDF]

PLoS Genetics, 2012
Studies of coat color mutants have greatly contributed to the discovery of genes that regulate melanocyte development and function. Here, we generated Yy1 conditional knockout mice in the melanocyte-lineage and observed profound melanocyte deficiency and
Juying Li, Jun S Song, Robert J A Bell, Thanh-Nga T Tran, Rizwan Haq, Huifei Liu, Kevin T Love, Robert Langer, Daniel G Anderson, Lionel Larue, David E Fisher   +10 more
doaj   +1 more source

A PIEBALD FAMILY [PDF]

Biometrika, 1914
n ...
openaire   +2 more sources

Naa12 compensates for Naa10 in mice in the amino-terminal acetylation pathway

eLife, 2021
Amino-terminal acetylation is catalyzed by a set of N-terminal acetyltransferases (NATs). The NatA complex (including X-linked Naa10 and Naa15) is the major acetyltransferase, with 40–50% of all mammalian proteins being potential substrates. However, the
Hyae Yon Kweon, Mi-Ni Lee, Max Dorfel, Seungwoon Seo, Leah Gottlieb, Thomas PaPazyan, Nina McTiernan, Rasmus Ree, David Bolton, Andrew Garcia, Michael Flory, Jonathan Crain, Alison Sebold, Scott Lyons, Ahmed Ismail, Elaine Marchi, Seong-keun Sonn, Se-Jin Jeong, Sejin Jeon, Shinyeong Ju, Simon J Conway, Taesoo Kim, Hyun-Seok Kim, Cheolju Lee, Tae-Young Roh, Thomas Arnesen, Ronen Marmorstein, Goo Taeg Oh, Gholson J Lyon   +28 more
doaj   +1 more source

Piebaldism: a case report [PDF]

Journal of Korean Medical Science, 1996
We report a familial case of piebaldism affecting a 33-year-old man and his 3-month-old son. Typical skin findings, white forelock and amelanotic white macules containing hyperpigmented macules, were characteristically presented on both patients.
S M, Hwang, S K, Ahn, W S, Lee, M S, Yoo, E H, Choi   +4 more
openaire   +2 more sources