Increased Hemichannel Activity Displayed by a Connexin43 Mutation Causing a Familial Connexinopathy Exhibiting Hypotrichosis with Follicular Keratosis and Hyperostosis [PDF]
, 2023 Olivia E. Crouthamel +3 more
openalex +1 more source
Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
, 2000 K. Kánai +8 more
openalex +2 more sources
Overexpression of Hr links excessive induction of Wnt signaling to Marie Unna hereditary hypotrichosis [PDF]
, 2009 Jeong-Ki Kim +11 more
openalex +1 more source
A novel heterozygous missense variant in ribosomal protein L21 associated with familial hypotrichosis simplex [PDF]
, 2023 Tuntas Rayinda +8 more
openalex +1 more source
A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis [PDF]
, 2018 Chen, Fuyin +9 more
core +2 more sources
Autosomal recessive hypotrichosis with loose anagen hairs associated with TKFC mutations* [PDF]
, 2020 Alexandros Onoufriadis +13 more
openalex +1 more source
Hypotrichosis with juvenile macular dystrophy with novel mutations in CDH3 gene [PDF]
, 2023 Yuanxiang Liu +5 more
openalex +1 more source
Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
, 2000 G.P. Sreekumar +4 more
openalex +1 more source
Hypotrichosis with juvenile macular dystrophy: Portuguese case [PDF]
, 2020 Fatima Zahra Elfatoiki +4 more
openalex +1 more source