Results 51 to 60 of about 401 (136)
The FASEB Journal, Volume 35, Issue 4, April 2021., 2021 Abstract Intracellular adaptor proteins are indispensable for the transduction of receptor‐derived signals, as they recruit and connect essential downstream effectors. The SLy/SASH1‐adaptor family comprises three highly homologous proteins, all of them sharing conserved structural motifs. The initial characterization of the first member SLy1/SASH3 (SH3
Jennifer Jaufmann +8 more
wiley +1 more source
Dyschromatosis universalis hereditaria: report of six cases from a family [PDF]
, 2016 Dyschromatosis universalis hereditaria (DUH) is a rare pigmentary disorder characterized by the presence of mottled hyperpigmented and hypopigmented macules over the trunk, extremities, and face.
Das, Anupam +2 more
core +2 more sources
A woman with hyperpigmented macules and papules
, 2021 JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 19, Issue 11, Page 1656-1660, November 2021.
Viktor Schnabel +5 more
wiley +1 more source
Eine Frau mit hyperpigmentierten Maculae und Papeln
, 2021 JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 19, Issue 11, Page 1655-1659, November 2021.
Viktor Schnabel +5 more
wiley +1 more source
A rare association of dyschromatosis universalis hereditaria and bilateral corneal ulcer
Indian Journal of Ophthalmology. Case Reports, 2022 Dyschromatosis universalis hereditaria (DUH) is a rare entity in the Indian subcontinent presenting with generalized pigmented macule all over the body.
Mamta Singh +2 more
doaj +1 more source
Dyschromatosis Universalis Hereditaria
The Nishinihon Journal of Dermatology, 1982 NISHIJIMA, Setsuko +2 more
openaire +3 more sources
An inventory of lysosomal ABC transporters
FEBS Letters, Volume 594, Issue 23, Page 3965-3985, December 2020., 2020 ABC transporters fulfill diverse physiological functions in different cellular localizations ranging from the plasma membrane to intracellular membranous compartments. Several ABC transporters have been spotted in the endolysosomal system, which consists of endosomes, autophagosomes, lysosomes, and lysosome‐related organelles.
Gergely Szakacs, Rupert Abele
wiley +1 more source
Reticulate Pigmentary Disorders: a review
Pigment International, 2019 Reticulate pigmentary disorders include presentations with “net-like,” “sieve-like,” or “chicken wire” configuration of the skin lesions. Various congenital and acquired dermatoses, as well as few systemic diseases, are present with this pattern of skin ...
Surabhi Sinha, Anita Kulhari
doaj +1 more source
Biology of Heme in Mammalian Erythroid Cells and Related Disorders
BioMed Research International, Volume 2015, Issue 1, 2015., 2015 Heme is a prosthetic group comprising ferrous iron (Fe2+) and protoporphyrin IX and is an essential cofactor in various biological processes such as oxygen transport (hemoglobin) and storage (myoglobin) and electron transfer (respiratory cytochromes) in addition to its role as a structural component of hemoproteins.
Tohru Fujiwara +2 more
wiley +1 more source
Dyschromatosis Symmetrica Hereditaria of Late Onset?
Case Reports in Dermatological Medicine, Volume 2014, Issue 1, 2014., 2014 Dyschromatosis symmetrica hereditaria (DSH), also known as reticulated acropigmentation of Dohi, is an autosomal dominant disease with high penetrance, characterized by hypo‐ and hyperpigmented macules of varying sizes on the dorsal of the extremities with reticulated pattern.
Caroline Balvedi Gaiewski +5 more
wiley +1 more source