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Research 121–150 of 1000+
- Wound Healing: A Cellular Perspective
- The Rotterdam Study: 2016 objectives and design update
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Immunological aspects and gender bias during respiratory viral infections including novel Coronavirus disease‐19 (COVID‐19): A scoping review
- Genetic prediction of male pattern baldness
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- Ovine KRT81 Variants and Their Influence on Selected Wool Traits of Commercial Value
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Associations between clinical data, vaccination status, antibody responses, and post-COVID-19 symptoms in Thais infected with SARS-CoV-2 Delta and Omicron variants: a 1-year follow-up study
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- Tru9I Variant as a Novel Genetic Marker for Vitamin D Deficiency in Alopecia Areata
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Finding bald spots on chromosome 20p11
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- Assessing protein sequencing in human single hair shafts of decreasing lengths
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Polycystic ovary syndrome is linked with the fat mass obesity (FTO) gene variants rs17817449 and rs1421085 in western Saudi Arabia