Results 31 to 40 of about 1,435 (174)
Ultraviolet radiation and melanogenesis [PDF]
Light radiation is a part of the electromagnetic radiation, and it consists of the ultraviolet (UV) radiation, visible light, and infrared radiation.
Jovanović Dragan L. +3 more
core +1 more source
Primer registro de albinismo y piebaldismo en atelognathus patagonicus Gallardo, 1962 (Anura: Batrachylidae), Parque Nacional Laguna Blanca, Patagonia Argentina [PDF]
Entre los distintos tipos de anomalías pigmentarias, el albinismo es la más frecuente en anfibios. La Críticamente Amenazada ranita patagónica (Atelognathus patagonicus) es endémica del noroeste de la Patagonia Argentina, donde habita pequeñas lagunas ...
Calvo, Rodrigo +10 more
core +1 more source
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
O piebaldismo é uma genodermatose rara onde as lesões acrômicas não respondem aos tratamentos tópico e fototerápico. Este artigo tem como objetivo demonstrar a importância do transplante de melanócitos, usando a técnica de minigrafting no tratamento do ...
Daniela Rezende Neves +4 more
doaj +1 more source
Naa12 compensates for Naa10 in mice in the amino-terminal acetylation pathway
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 +28 more
doaj +1 more source
Video institucional donde presenta la situación actual de la Universidad Militar Nueva Granada, conociendo su misión, programas académicos e ...
Emanuel, Janet Rettig
core +1 more source
Piebaldism-Moebius and prenatal exposure to misoprostol: a case report
Piebaldism is a rare congenital disease with prevalence of 1/100.000, characterized by patchy depigmentation of the skin and the presence of a white forelock. Its course is static and otherwise patients are healthy.
Mendoza-Urbano, Diana Marcela +2 more
doaj +1 more source
Congenital sensorineural hearing loss may occur in association with inborn pigmentary defects of the iris, hair, and skin. These conditions, named auditory-pigmentary disorders (APDs), represent extremely heterogeneous hereditary diseases, including ...
Laura Cristina Gironi +10 more
doaj +1 more source
SLUG in cancer development [PDF]
The SNAIL-related zinc-finger transcription factor, SLUG (SNAI2), is critical for the normal development of neural crest-derived cells and loss-of-function SLUG mutations have been proven to contribute to piebaldism and Waardenburg syndrome type 2 in a ...
Flores, Teresa +8 more
core +2 more sources

