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Research 721–750 of 1000+
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Sequence, expression, and evolutionary conservation of a gene encoding a glycine/tyrosine-rich keratin-associated protein of hair.
- Structure of human type II 5 alpha-reductase gene
- Long-Term Differential Changes in Mouse Intestinal Metabolomics after γ and Heavy Ion Radiation Exposure
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Evolution of Trichocyte Keratins
- Identification of dual-purpose therapeutic targets implicated in aging and glioblastoma multiforme using PandaOmics - an AI-enabled biological target discovery platform
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle
- Modulation of genomic and postgenomic alterations in noncancer diseases and critical periods of life
- 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
- 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
- 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