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Research 301–330 of 1000+
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Alopezien und Hypotrichosen im Kindesalter
- Effect of Oral Minoxidil on Monilethrix
- Gsdma3 is required for hair follicle differentiation in mice
- Dynamic analysis of skin transcriptome in Xinjiang goats and functional verification of ELOVL3 in dermal papilla cell proliferation
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Table 5_Molecular mechanisms underlying cashmere quality differences between Jiangnan cashmere goats and Changthangi pashmina goats.docx
- Table 3_Molecular mechanisms underlying cashmere quality differences between Jiangnan cashmere goats and Changthangi pashmina goats.xlsx
- Table 1_Molecular mechanisms underlying cashmere quality differences between Jiangnan cashmere goats and Changthangi pashmina goats.xlsx
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- 545 Skin Organoids derived from NCSTN mutated patient-induced pluripotent stem cells recapitulate Hidradenitis Suppurativa pathogenic hallmarks
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- 백모 모구의 유전자 발현 프로파일링을 통한 백모화 기전 분석
- A nonsense variant in <i>KRT31</i> is associated with autosomal-dominant monilethrix
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Construction and Verification of Recombinant Follicle-specific Expression Vector
- GWAS Identifies Three Susceptibility Loci for Trichilemmal Cysts
- Papular atrichia
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Generation of folliculogenic human epithelial stem cells from induced pluripotent stem cells
- Biomarkers of alopecia areata disease activity and response to corticosteroid treatment
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle