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Research 91–120 of 1000+
- Practical approaches to medical and cosmetic dermatology in skin of color patients
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Ferreting out stem cells from their niches
- Congenital atrichia and hypotrichosis
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Acne
- The Role of Histone Demethylases in Disease
- Genetic mechanism of androgenic alopecia
- The clinicopathological spectrum of trichoepitheliomas: a retrospective descriptive study
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- ENZYMES
- Alopecias
- Guidelines for the management of androgenetic alopecia (2010)
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Non polycystic ovary syndrome–related endocrine disorders associated with hirsutism
- Genetically-manipulated adult stem cells as therapeutic agents and gene delivery vehicle for wound repair and regeneration
- Molecular mapping of lymph node metastases by real-time reverse transcription polymerase chain reaction in two melanoma patients
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.