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Research 361–390 of 1000+
- Dermatological diseases from a genetic perspective
- Upregulation of the truncated basic hair keratin 1(hHb1‐ΔN) in carcinoma cells by Epstein‐Barr virus (EBV)
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- The role of AUTS2 in neurodevelopment and human evolution
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- URB expression in human dermal papilla cells
- Synaptic processes and immune-related pathways implicated in Tourette Syndrome
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- BJD Editor's Choice
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Functional Characterization of<i>fer-ts</i>, a Temperature-Sensitive FERONIA Mutant Allele That Alters Root Hair Growth
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Host Genetic Susceptibility and Impacts of Dietary Factors on Covid-19
- Clinical Snippets
- Clinical Snippets
- Identification of a Novel MPL Loss of Function Mutation in a Patient with Cyclic Thrombocytopenia and Characterization of This Syndrome
- Hypomyelinating leukodystrophy-10 presenting with an additional atypical feature of increased body hair and Mongolian spots
- Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Characterisation of Four New Genes in the Ovine KAP19 Family
- ASPCR‐ASDR 2013
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Glucocorticoid Receptor Mutants Demonstrate Increased Motility Inside the Nucleus of Living Cells: Time of Fluorescence Recovery After Photobleaching (FRAP) Is an Integrated Measure of Receptor Function