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Research 211–240 of 1000+
- Variation in the ovine trichohyalin gene and its association with wool curvature
- A newborn presenting with congenital blistering
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- Pseudofolliculitis barbae; current treatment options
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Recurrent Pregnancy Loss Associated Cytogenetic and Genetic Anomalies – Study from Eastern India
- A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA
- Phosphate starvation alters calcium signalling in roots of Arabidopsis thaliana
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Interleukin 15 Gene Polymorphism in patients with Alopecia Areata
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Genome-Wide Association Studies for Immunoglobulin Concentrations in Colostrum and Serum in Chinese Holstein
- Histology and ultrastructure of canine hair follicle stem cells (cHFSCs)
- Polymorphism of Exon V of prolactin gene and its association with Cashmere traits in Changthangi Pashmina goats
- Cloning and sequence analysis of KAP 6.1 gene in Xinjiang fine-wool sheep
- Localizing the ROS Signal
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Failure of Fresh Plasma in Leiner Disease
- Analysis of 1,25-Dihydroxyvitamin D3 Receptors (VDR. in Basal Cell Carcinomas
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- NUDT15 polymorphism explains serious toxicity to azathioprine in Indian patients with chronic immune thrombocytopenia and autoimmune hemolytic anemia: a case series
- Physiology and Medical Treatments for Alopecia
- Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- A Preview of Selected Articles
- Posters Presented at the 19th Joint Meeting of the International Society of Dermatopathology, March 2–3, 2016, Hilton Crystal City at Washington Reagan National Airport, Arlington, Virginia, USA