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Research 391–420 of 1000+
- 67 Patterns of clinical response in patients with alopecia areata (AA) treated with ritlecitinib in the ALLEGRO phase 2b/3 and ongoing, phase 3, ALLEGRO-LT studies
- Optimal processing for proteomic genotyping of single human hairs
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- Alopecia: Association with Resistance to Thyroid Hormones
- 0441 Systemic autoimmune comorbidity in alopecia totalis and universalis compared with patchy alopecia areata: A retrospective cohort study
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Hair Anomalies in a 6-Year-Old Girl
- Iron Chelators in the Management of Autoimmune-Induced Alopecia: A Focus on Hypoxia-Inducible Factor 1 Modulation and Hair Restoration
- Litigation associated with 5-alpha-reductase-inhibitor use: A Canadian legal database review.
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Epigenetics of Colorectal Cancer
- Basal cell carcinomas in mice arise from hair follicle stem cells and multiple epithelial progenitor populations
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Mettl3-catalyzed m <sup>6</sup> A regulates histone modifier and modification expression in self-renewing somatic tissue
- Human skin color: Origin, variation and significance
- Heat treatment increases the incidence of alopecia areata in the C3H/HeJ mouse model
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Tumor suppressor identity can contribute to heterogeneity of phenotype in hair follicle stem cell‐induced squamous cell carcinoma
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Exploiting the origins of Ras mediated squamous cell carcinoma to develop novel therapeutic interventions
- A comprehensive genome-wide analysis for signatures of selection in goat (genus Capra) revealed new candidate genes for environmental adaptation and productive traits
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Keratin 15 promotes a progenitor cell state in basal keratinocytes of skin epidermis
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Dermatological diseases from a genetic perspective
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- UTX (KDM6A) promotes differentiation noncatalytically in somatic self-renewing epithelia
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders