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Research 241–270 of 1000+
- Characterisation of the Ovine KRTAP36-1 Gene in Chinese Tan Lambs and Its Impact on Selected Wool Traits
- Landmark native breed of the Orenburg goats: progress in its breeding and genetics and future prospects
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Pitfalls of PCR-Based Strategy for Genotyping <i>Cre-Loxp</i> Mice
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Finding bald spots on chromosome 20p11
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Registrars’ Symposium: Summaries of Papers
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Divergent roles of HDAC1 and HDAC2 in the regulation of epidermal development and tumorigenesis
- What may be the markers of the male equivalent of polycystic ovary syndrome?
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- BJD Editor's Choice
- 14. Wound Healing; Cutaneous Therapy; Hair
- Somatostatin Expression in Human Hair Follicles and Its Potential Role in Immune Privilege
- POS0080 TOFACITINIB TREATMENT IN CHILDREN WITH RHEUMATIC DISEASES: SINGLE-CENTER EXPERIENCE
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Research Snippets
- WNT10B (wingless-type MMTV integration site family)
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- 9. Immunology and Genetics
- Intermittent nitrate transdermal therapy
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Regulation of Mitochondrial Oxidative Metabolism by Tumor Suppressor FLCN
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Common Variants in the Sex Hormone-Binding Globulin (SHBG) Gene Influence SHBG Levels in Women with Polycystic Ovary Syndrome
- Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots