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Research 211–240 of 1000+
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Pangenome and genome variation analyses of pigs unveil genomic facets for their adaptation and agronomic characteristics
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Epidemiologic Study of Gene Distribution in Romanian and Brazilian Patients with Non-Cicatricial Alopecia
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Skin diseases associated with atopic dermatitis
- Association analysis of oestrogen receptor beta gene ( <i>ESR2</i> ) polymorphisms with female pattern hair loss
- In vivo reflectance confocal microscopy: usefulness for diagnosing hair diseases
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- RETRACTED: Explore the genetic exposure to alopecia areata
- Genetic diversity of Armillaria spp. symbiotic with Polyporus umbellatus in China
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- Integrated multiomics analysis reveals the molecular features and crucial regulators of hair follicles in yak (Bos grunniens)
- The genetic basis of dermatophytosis skin infection susceptibility
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Generic vs. Disease-Specific Patient Reported Outcome (PRO) Instruments for Assessing HRQoL Burden Among Patients Diagnosed with Alopecia Areata: Evidence from TARGET-DERM AA
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Exploring the overlap between alopecia areata and major depressive disorder: Epidemiological and genetic perspectives
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Proteome Analysis of Human Hair Shaft
- Integrated analysis of long non-coding RNA and mRNA expression in different colored skin of koi carp
- Integrated analysis of lncRNAs and mRNAs by RNA-Seq in secondary hair follicle development and cycling (anagen, catagen and telogen) of Jiangnan cashmere goat (Capra hircus)
- Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay