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Research 811–840 of 1000+
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Future Directions: Gene Polymorphism Diagnostics Relevant to Hair
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Hair Diseases (Alopecia Areata and Androgenetic Alopecia)
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Androgen Receptor Copy Number Variation and Androgenetic Alopecia: A Case-Control Study
- Disease Prevention and Alleviation by Human Myoblast Transplantation
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- Role of MEG3-miRNAs in immune-inflammatory regulation in age-dependent wool follicle remodeling in Tan sheep
- Molecular Genetics of Human Hair Diseases
- Alopecia Areata: Updates from the Mouse Perspective
- Association between genetically predicted leukocyte telomere length and non-scarring alopecia: A two-sample Mendelian randomization study
- Regulation of somatic cell reprogramming through inducible mir-302 expression
- Serum interleukin-37 and its gene polymorphism (rs3811047) in Egyptian patients with alopecia areata
- Alopecia areata
- Male pattern hair loss
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- The analysis of genetics and associated autoimmune diseases in Chinese vitiligo patients
- Coming of Age of Melanogenesis-Related Proteins
- Ethanol intake patterns in female mice: Influence of allopregnanolone and the inhibition of its synthesis
- Hair Keratins and Hair Follicle–Specific Epithelial Keratins