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Research 781–810 of 1000+
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Genome-Wide Association Study for Body Conformation Traits in Kazakh Fat-Tailed Coarse-Wool Sheep
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep
- miR-200a Targets PITX2 to Mediate Goose Fibroblast Proliferation Through the Wnt Pathway
- Molecular mechanisms underlying cashmere quality differences between Jiangnan cashmere goats and Changthangi pashmina goats
- Correlation between Pilomatrixoma and Polycystic Ovary Syndrome (PCOS)
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- MINOXIDIL NA FARMÁCIA ESTÉTICA: ANÁLISE DA SUA EFICÁCIA NO TRATAMENTO DA ALOPECIA
- Genome-Wide Association Studies of Hair Whorl in Pigs
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Effects of KRTAP20-1 Gene Variation on Wool Traits in Chinese Tan Sheep
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- LBODP010 A Case of Glucocorticoid Resistance Syndrome
- CAQ Corner: Basic concepts of transplant immunology
- Drug points: Topical minoxidil for common baldness
- The Mechanism of Androgen Actions in PCOS Etiology
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy