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Research 301–330 of 1000+
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds
- Nonclassic adrenal hyperplasia
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- α3β1-integrin regulates hair follicle but not interfollicular morphogenesis in adult epidermis
- Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- The Mesenchymal Niche of the Hair Follicle Induces Regeneration by Releasing Primed Progenitors from Inhibitory Effects of Quiescent Stem Cells
- Sex dependent influence of a functional polymorphism in steroid 5‐α‐reductase type 2 (<i>SRD5A2</i>) on post‐traumatic stress symptoms
- Nonclassic congenital adrenal hyperplasia
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- Foliar and Root Applications of Vegetal-Derived Protein Hydrolysates Differentially Enhance the Yield and Qualitative Attributes of Two Lettuce Cultivars Grown in Floating System
- Runx1 Role in Epithelial and Cancer Cell Proliferation Implicates Lipid Metabolism and Scd1 and Soat1 Activity
- Is polycystic ovary syndrome a sexual conflict? A review
- Variation in the ovine keratin-associated protein 15-1 gene affects wool yield
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Cutaneous Reactions in Patients with Chronic Hepatitis C Treated with Peginterferon and Ribavirin
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Efficacy of metformin therapy in adolescent girls with androgen excess: relation to sex hormone–binding globulin and androgen receptor polymorphisms
- A novel calmodulin‐interacting Domain of Unknown Function 506 protein represses root hair elongation in <i>Arabidopsis</i>
- PR-independent neurosteroid regulation of α2-GABA-A receptors in the hippocampus subfields
- Context-dependent effect of sPLA2-IIA induced proliferation on murine hair follicle stem cells and human epithelial cancer
- Flightless I exacerbation of inflammatory responses contributes to increased colonic damage in a mouse model of dextran sulphate sodium-induced ulcerative colitis
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- Association of Gly972Arg variant of insulin receptor subtrate-1 and Gly1057Asp variant of insulin receptor subtrate-2 with polycystic ovary syndrome in the Chinese population
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation