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Research 181–210 of 705
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Pica for Uncooked Basmati Rice in Two Women with Iron Deficiency and a Review of Ryzophagia
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- Azathioprine‐induced severe myelosuppression accompanied by massive hair loss and painful oral ulcer in an autoimmune hepatitis patient with <i>NUDT15</i> minor variant: A case report
- Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis
- Mitochondrial DNA Variation in Human Hair Shafts Influenced by Physical Characteristics: A Massively Parallel Sequencing Analysis
- Comprehensive Genomic Profiling of Cutaneous Adnexal Carcinomas: A Genomic Landscape Study
- MITF E318K naevus phenotype: the modifying role of MC1R Red Hair Variants
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Causal relationship between gut microbiota and androgenic alopecia A mendelian randomization analysis
- Do Alopecia Areata and Hair Colour Have a Shared Genetic Component?
- Developmental genetics of color pattern establishment in cats
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- The RpoS Gatekeeper in Borrelia burgdorferi: An Invariant Regulatory Scheme That Promotes Spirochete Persistence in Reservoir Hosts and Niche Diversity
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Control by a hair’s breadth: the role of microRNAs in the skin
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue