Results 51 to 60 of about 880 (178)
Striking contiguous depigmentation across the lower limbs in piebaldism and its implications for understanding melanocytic migration and development [PDF]
, 2019 Piebaldism is a rare autosomal dominant disorder of pigmentation that is characterized by variable patches of depigmentation on the face, chest, abdomen, and extremities. We describe two cases of piebaldism, in whom the remarkable asymmetric distribution
Kinsler, VA +5 more
core +1 more source
G3: Genes, Genomes, Genetics, 2020 The body coloration of animals is due to pigment cells derived from neural crest cells, which are multipotent and differentiate into diverse cell types.
Yuji Otsuki +3 more
doaj +1 more source
Twenty years of cucurbit breeding research at the World Vegetable Center
Crop Science, Volume 65, Issue 6, November/December 2025.Abstract The contribution of cucurbit crops to global food and nutrition security is immense. They are economically and nutritionally important to smallholder farmers in Asia, who account for 81% of global cucurbit production. World Vegetable Center (WorldVeg) has been focused for 20 years on four species: bitter gourd (Momordica charantia), ridge ...
Narinder Pal Singh Dhillon
wiley +1 more source
Ecology and Evolution, Volume 15, Issue 11, November 2025.This article provides the first known scientific record of albinism in a New Zealand fur seal pup. We describe the individual with a particular focus on its sensory abilities. This individual's birth at a central mainland colony may permit continued study throughout his life, unlike many records of similar conditions in other species.
Alasdair A. Hall +2 more
wiley +1 more source
Analogs of human genetic skin disease in domesticated animals
International Journal of Women's Dermatology, 2017 Genetic skin diseases encompass a vast, complex, and ever expanding field. Recognition of the features of these diseases is important to ascertain a correct diagnosis, initiate treatment, consider genetic counseling, and refer patients to specialists ...
Justin Finch, MD +2 more
doaj +1 more source
Piebaldism: A familial case report [Piebaldizm: Ailesel bir olgu sunumu] [PDF]
, 2013 Piebaldism is a rare autosomal dominant skin disease presented with white forelock and depigmented patches. It is characterized by congenital absence of melanocytes and caused by mutation of KIT-proto-oncogene.
Acer, Ersoy +4 more
core
The Southern Journal of Philosophy, Volume 63, Issue 3, Page 429-443, September 2025.Abstract We all have experiences in which it “seems clear” to us that something is true. This kind of clear experience can play significant roles in determining whether we believe something to be true. But what are the significant roles? So far, the literature has focused on optimal cases where a person's clear experience might provide prima facie ...
Chenwei Nie
wiley +1 more source
, 1993 Piebaldism is an autosomal dominant genetic disorder of pigmentation characterized by congenital patches of white skin and hair that lack melanocytes.
Holmes, Stuart A. +3 more
core +1 more source
Donor to recipient ratios in the surgical treatment of vitiligo and piebaldism: a systematic review
, 2021 Stabilized vitiligo resistant to conventional therapy (e.g. segmental vitiligo) and piebaldism lesions can be treated with autologous cellular grafting techniques, such as non-cultured cell suspension transplantation (NCST) and cultured melanocyte ...
van Geel, Nanja +16 more
core +1 more source
Você conhece esta síndrome? Do you know this syndrome?
Anais Brasileiros de Dermatologia, 2007 Na síndrome de Waardenburg, genodermatose autossômica dominante, distúrbios da pigmentação (hipo ou acromia de pele e cabelos, heterocromia da íris) podem se associar a surdez, distopia do canto interno do olho e, eventualmente, outras malformações de ...
Erick Dancuart Omar +2 more
doaj +1 more source