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Research 241–270 of 1000+
- 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
- From Wound to Hair Follicle: Unravelling the Mechanisms and Molecular Networks in Wound‐Induced Hair Follicle Neogenesis
- 0882 Patterning and regional specification of hairy skin
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Dermoscopy findings of the axilla of women with frontal fibrosing alopecia
- A missense mutation in Lama3 causes androgen alopecia
- 画像解析による抗がん剤脱毛頭皮の形態構造の検証
- Alopecia totalis in an infant
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Acne/Folliculitis Keloidalis
- Papular atrichia
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene