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Research 271–300 of 1000+
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Association of Androgen Receptor CAG Repeat Length with Polycystic Ovary Syndrome in an Iranian Female Population
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Genetic and Environmental Factors Affecting Hair Density in East Asian Populations
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia
- Effects of <i>KISS1</i> structural polymorphism on the risk of polycystic ovary syndrome and reproductive hormones in Iraqi women who take metformin
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq
- 177 The Striatin-Interacting Phosphatase And Kinases complex is important for skin epidermal differentiation and barrier formation
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1, TACR3 and SPPL2C associated with Alzheimer’s disease
- WNT10B (wingless-type MMTV integration site family)
- 268 Male-pattern baldness and its association with coronary heart disease
- 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- AKT2 Gene Polymorphisms, sRANKL/OPG and Hormone Measurements in Polycystic Ovarian Syndrome (PCOS) Women
- Decision letter: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- BJD Editor's Choice
- 9. Immunology and Genetics
- 14. Wound Healing; Cutaneous Therapy; Hair
- Registrars’ Symposium: Summaries of Papers
- Genetics of Diabetes in Childhood
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Beyond Appearances: The Hidden Coat Diversity of the Sicilian Mastiff Revealed by Integrated Phenotypic and Genetic Analyses
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Research Snippets
- Association of psoriasis and psoriatic arthritis with human leukocyte antigen and killer cell immunoglobulin–like receptor gene frequency: A multiethnic population study
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- Study on genetic polymorphisms of androgen receptor gene and 5α-reductase genes of Han men with androgenetic alopecia in the Eastern China