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Research 631–660 of 1000+
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep
- miR-200a Targets PITX2 to Mediate Goose Fibroblast Proliferation Through the Wnt Pathway
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Effects of KRTAP20-1 Gene Variation on Wool Traits in Chinese Tan Sheep
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Upregulation of genes orchestrating keratinocyte differentiation, including the novel marker gene <i>ID2</i>, by contact sensitizers in human bulge‐derived keratinocytes
- COLLAB: A Global Survey of Clinical and Laboratory Assessment in Alopecia Areata by Hair Specialists
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Intraovarian platelet-rich plasma administration could improve blastocyst euploidy rates in women undergoing in vitro fertilization
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- PA33 When bones speak through nails: insights from a paediatric case series
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Current evaluation of amenorrhea
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Hair Follicle Signaling Networks: A Dermal Papilla–Centric Approach
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- A Genetically Defined Male Counterpart of Polycystic Ovary Syndrome: Evidence for Ovarian-Independent Pathogenesis
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Advancing skin model development: A focus on a self-assembled, induced pluripotent stem cell-derived, xeno-free approach
- Light-Emitting Hair Follicles: Studying Skin Regeneration With In Vivo Imaging
- 080 Mouse models of alopecia areata: C3H/HeJ mice versus the humanized AA mouse model
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses