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Research 301–330 of 1000+
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Human Wharton’s Jelly Mesenchymal Stem Cells Plasticity Augments Scar-Free Skin Wound Healing with Hair Growth
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- Dermal lymphatic dilation in a mouse model of alopecia areata
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Single-Cell Transcriptomic Identification of a Proliferative Intermediate State During Early Anagen Hair Follicle Regeneration
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Direct cellular reprogramming enables development of viral T antigen–driven Merkel cell carcinoma in mice
- Induced pluripotent stem cell line MUSIi006-A derived from hair follicle keratinocytes as a non-invasive somatic cell source
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Acne
- Does Complement Have a Role in the Pathogenesis of Alopecia Areata?
- Familial congenital generalized hypertrichosis
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- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Social selection favours offspring prone to the development of androgenetic alopecia.
- Notch signaling is significantly suppressed in basal cell carcinomas and activation induces basal cell carcinoma cell apoptosis
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- The Roles of EDA2R in Ageing and Disease
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Genetic and molecular aspects of androgenetic alopecia