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Research 91–120 of 1000+
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Transcriptome Sequencing and Mass Spectrometry Reveal Genes Involved in the Non-mendelian Inheritance-Mediated Feather Growth Rate in Chicken
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Inherited Epidermolysis Bullosa: A Clinical Case
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Monilethrix – Case report of a rare disease
- Monilethrix in three generations
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Familial Frontal Fibrosing Alopecia
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Diagnostic approach to low‐renin hypertension
- The Genetics of Human Skin Disease
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Ectodermal Dysplasia: Variable Expressions
- Frontal Fibrosing Alopecia: A Comprehensive Review with Recent Updates
- AN UPDATE OF HAIR SHAFT DISORDERS
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Central centrifugal cicatricial alopecia: retrospective case-control study of 54 patients from a tertiary care center
- Sebaceous adenitis in Swedish dogs, a retrospective study of 104 cases
- Bioengineering the Hair Follicle