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Research 151–180 of 1000+
- Identification of the Ovine Keratin-Associated Protein 22-1 (KAP22-1) Gene and Its Effect on Wool Traits
- Recently Identified Forms of Epidermolysis Bullosa
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene on Fibre Traits in Inner Mongolia Cashmere Goats
- The pressing need for standardization in epidemiologic studies of PCOS across the globe
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Genetic analysis of interleukin 18 gene polymorphisms in alopecia areata
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Filaggrin mutations as an archetype for understanding the pathophysiology of atopic dermatitis
- Single nucleotide polymorphisms associated with elevated alanine aminotransferase in patients receiving asunaprevir plus daclatasvir combination therapy for chronic hepatitis C
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Análise dos níveis de metilação e de polimorfismos genéticos dos genes GSTP1, MGMT, VDR e AR em pacientes com câncer de próstata
- The Trotter collection: A review of Mildred Trotter's hair research and an update for studies of human variation
- The Association of Gene Expression and Single Nucleotide Polymorphism (rs 6152 SNP) in Androgen Receptor Gene with Recurrent Spontaneous Abortion (RSA) in Iraqi Women
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Evaluating HWE and Association in Genome Wide Association Studies: A Unified Procedure
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Prioritizing Susceptibility Genes for the Prognosis of Male-pattern Baldness with Transcriptome-wide Association Study
- Uncombable hair syndrome and beyond