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Research 961–990 of 1000+
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- ACE2 and TMPRSS2 Potential Involvement in Genetic Susceptibility to SARS-COV-2 in Cancer Patients
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Bone vs. fat: Embryonic origin of progenitors determines response to androgen in adipocytes and osteoblasts
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- The role of cathepsin E in terminal differentiation of keratinocytes
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Nonclassic 21-hydroxylase deficiency
- Horse Chestnut: Cultivation for Ornamental Purposes and Non-Food Crop Production
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Association between <i>IL16</i> gene polymorphisms and susceptibility to alopecia areata in the Korean population
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- The Tumor Suppressor Actions of the Vitamin D Receptor in Skin
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib
- Alopecia universalis following interferon alfa-2b and ribavirin treatment for hepatitis C.
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia
- Serum interleukin-37 and its gene polymorphism (rs3811047) in Egyptian patients with alopecia areata
- Hair phenotype diversity across Indriidae lemurs
- Genomic Analysis of Trichotillomania
- Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese
- Mechanisms of aluminium toxicity, tolerance and amelioration in wheat
- Evaluation of Susceptibility Genes/Loci Associated with Male Androgenetic Alopecia (MAGA) for Female-Pattern Hair Loss in a Chinese Han Population and a Brief Literature Review
- Iatrogenic Cushing Syndrome and Secondary Adrenal Insufficiency Due to an Interaction Between Fluticasone and Ritonavir
- Abstract 1835: Development of mammary hyperplasia, dysplasia, and invasive ductal carcinoma in transgenic mice expressing the 8p11 amplicon oncogene NSD3 (WHSC1L1)