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Research 451–480 of 1000+
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Utilising SNP Association Analysis as a Prospective Approach for Personalising Androgenetic Alopecia Treatment
- Causal Effects of Lipids-Related Metabolites on Androgenic Alopecia: A Mendelian Randomization Study
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Chronic overlapping pain conditions and nociplastic pain
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Pharmacotherapy of plexiform neurofibromas in patients with neurofibromatosis type 1. Possible adverse events and their management
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Association of early-onset androgenetic alopecia with metabolic syndrome: A case–control study on 46 patients in a tertiary care hospital in South India
- Nanozyme Catalysis Restores Hair Follicle Integrity by Reversing Peroxisomal Collapse.
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Medical Dermatology
- Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep