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Research 601–630 of 1000+
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Case Report: Disorder of Sexual Development in a Chinese Crested Dog With XX/XY Leukocyte Chimerism and Mixed Cell Testicular Tumors
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- BIPHENOTYPIC LEUKAEMIA
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Sex differences in the hypothalamic–pituitary–adrenal axis’ response to stress: an important role for gonadal hormones
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Genetic mechanism of androgenic alopecia
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Male androgenetic alopecia (Part II)
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Fertility and Sterility Vol 101 No 4, April 2014
- Cutaneous signals of immune system disease
- Depression from a physical symptom.
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene