Search
for
Sort by
Research 241–270 of 1000+
- Pathophysiology of the Burn Scar
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Pleiotropic effects of the nude mutation.
- Atrichia with papular lesions
- Alopecia: Association with Resistance to Thyroid Hormones
- Lectinhistochemistry of Dorsal Skin of Wistar-derived Hypotrichotic WBN/Ila-Ht Rats.
- Alopecia in children
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- In vitro skin permeation of hinokitiol loaded in vesicles composed of behenyltrimethylammonium chloride and stearic acid
- Congenital atrichia with papular lesions
- Another Way to Look at Donor Harvesting Effects with FUE
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Le gène<i>hairless</i>de la souris
- Werewolf, there wolf: variants in <i>Hairless</i> associated with hypotrichia and roaning in the lykoi cat breed
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Terapia por el arte
- Automated quantitative analysis of coat and skin coloration in laboratory animals
- Reply
- The accelerated aging skin in rhino‐like SHJH<sup><i>hr</i></sup> mice
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Stem Cells and their Niches
- Effect of gamma-ray exposure on the genome-editing efficiency of improved genome-editing via oviductal nucleic acids delivery (<i>i</i>-GONAD)
- A homozygous single T deletion found in the GGCX gene with PXE-like phenotypes
- The skin and vitamin D
- Genetics of Alopecia
- The skin and vitamin D
- The variable cell
- A novel finding of hair growth like vellus hairs on glabrous skin of distal phalanx of thumb in Vogt–Koyanagi–Harada disease: A case report