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Research 151–180 of 1000+
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Molecular genetics of androgen insensitivity
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Clinico-investigative profile of patients of hirsutism in a tertiary level institution
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Treatment-resistant Schizophrenia and Global Cortical Atrophy in a Patient with Turner Syndrome
- FLCN regulates transferrin receptor 1 transport and iron homeostasis
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Loss of the Y Chromosome: A Review of Molecular Mechanisms, Age Inference, and Implications for Men’s Health
- Identification of the Ovine Keratin-Associated Protein 26-1 Gene and Its Association with Variation in Wool Traits
- Sex-limited chromosomes and non-reproductive traits
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Susceptibility variants for male-pattern baldness on chromosome 20p11
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11*1
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability