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Research 31–60 of 1000+
- Novel TMEM173 Mutation and the Role of Disease Modifying Alleles
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Pinkie, the First Viable Germline Hypomorph Allele of Retinoid X Receptor Alpha, Reveals an Important Role for RXRa in Th2 Development.
- Functional Characterization of<i>fer-ts</i>, a Temperature-Sensitive FERONIA Mutant Allele That Alters Root Hair Growth
- Gene-wide association study between the aromatase gene (<i>CYP19A1</i>) and female pattern hair loss
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Genetic analysis of interleukin 18 gene polymorphisms in alopecia areata
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
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- Application of PCR Technique to Detect Polymorphism of the KRTAP1.1 Gene in Three Sheep Breeds - A Review
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Investigation of Vaspin and Visfatin -4689G/T Gene Polymorphisms in Alopecia Areata Patients
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- An evaluation of the RapidHIT™ ID system for hair roots stained with Diamond™ Nucleic Acid Dye
- Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis
- Clinical Snippets
- Clinical Snippets
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog