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Research 271–300 of 1000+
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene
- Image 1_Resident T cell activation leads to human hair follicle immune privilege loss ex vivo, which is prevented by the DHODH inhibitor farudodstat: relevance for alopecia areata.pdf
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Genomic Portraiture: The Science and Ethics of DNA Phenotyping in Identity Prediction
- The biochemical and phenotypic characterization of females homozygous for 5 alpha-reductase-2 deficiency.
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- MOESM1 of A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- ATP6AP1‐CDG: Follow‐up and female phenotype
- Alopecia Areata With an FFA ‐Like Phenotype: Clinicopathologic Features and Treatment Outcomes in a Prospective Cohort
- [The complex detection of AB(O)-system antigens and of keratin polymorphism in the forensic medical study of hair].
- Restoring neuropetide Y levels in the hypothalamus ameliorates premature aging phenotype in mice
- The Cutaneous Epidermal Growth Factor Network: Can it be Translated Clinically to Stimulate Hair Growth? - eScholarship
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- MmuPV1 infection and tumor development of T cell-deficient mice is prevented by passively transferred hyperimmune sera from normal congenic mice immunized with MmuPV1 virus-like particles (VLPs)
- EVALUATION OF ASSOCIATION OF ANTHROPOMETRIC INDICES WITH STRESS RESPONSE IN PCOS POPULATION
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- 加齢に伴うミトコンドリア枯渇は皮膚老化と肥満を加速する
- 1379 Cell of origin contributes to the melanoma diversity
- Itpr3 Is Responsible for the Mouse Tufted (tf) Locus
- 52711 Benefit of a Selenium Disulfide-based shampoo in subjects of any phototype and hair type presenting with dandruff
- Trichoscopy of Dark Scalp
- Defects in mitochondrial DNA replication and oxidative damage in muscle of mtDNA mutator mice
- THERAPY OF ENDOCRINE DISEASE: Treatment of hirsutism in the polycystic ovary syndrome