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Research 931–960 of 1000+
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Approaching fertility in congenital adrenal hyperplasia: exploring P30L mutation-induced 21-hydroxylase deficiency with a presentation between non-classical and simple virilizing phenotypes. A case report
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- Commentary 2
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- The Relation of the SHBG Gene Polymorphism (rs1799941) with PCOS in a Group of Iraqi Women
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- Defects in mitochondrial DNA replication and oxidative damage in muscle of mtDNA mutator mice
- TREATMENT OF KERATOSIS PILARIS: A NARRATIVE LITERATURE REVIEW OF TOPICAL, PROCEDURAL, AND VARIANT-SPECIFIC THERAPIES
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Pathology of Mouse Models of Accelerated Aging
- Molecular and physiological mechanisms underlying the antifungal and nutrient acquisition activities of beneficial microbes
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies?
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Effects of the bovine slick mutation on heat stress responses and hair growth in mice
- Auxin Input Pathway Disruptions Are Mitigated by Changes in Auxin Biosynthetic Gene Expression in Arabidopsis
- Association between <i>IL16</i> gene polymorphisms and susceptibility to alopecia areata in the Korean population