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Research 241–270 of 1000+
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- The biology and genetics of curly hair
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin
- BJD Editor's Choice
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Dietary and Genetic Aspects of Polycystic Ovary Syndrome (PCOS) in Polish Women-Part II: Association of
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Hepatitis C virus: host, environmental and viral factors promoting spontaneous clearance
- Pharmacotherapy for Keloids and Hypertrophic Scars
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Resurgent Clinical Science (and it's all about Health)
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata
- Genetics of Diabetes in Childhood
- ENZYMES
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- A missense mutation in Lama3 causes androgen alopecia
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- Proceedings of the Ninth World Congress for Hair Research (2015)