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Research 211–240 of 1000+
- Adnexotropic Variants of the Interface Dermatitides: A Review
- Transient CD44 Variant Isoform Expression and Reduction in CD4+/CD25+ Regulatory T Cells in C3H/HeJ Mice with Alopecia Areata
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Correlation between Androgenetic Alopecia and Severe Acute Respiratory Syndrome Coronavirus 2 Omicron Variant Infection in China
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Melanotrichoblastoma: A Histopathological Case Report of a Rare Pigmented Variant of Trichoblastoma
- Nevus Comedonicus (Blaschkoid Variant)
- ADAM17 variant causes hair loss via ubiquitin ligase TRIM47 mediated degradation
- Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with <i>MCHR2</i>
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- MITF E318K naevus phenotype: the modifying role of MC1R Red Hair Variants
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Food Administration and Not Genetic Variants Causes Pharmacokinetic Variability of Tadalafil and Finasteride
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Top 10 Facts: Common Hair Loss Causes and Management in Patients
- GENOTYPE ? PHENOTYPE CORRELATIONS IN CUTANEOUS MELANOMA PATIENTS CARRIER OF THE MITF p.E318K PATHOGENIC VARIANT
- Ovine KRT81 Variants and Their Influence on Selected Wool Traits of Commercial Value
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Circumferential acute limited exanthematous pustulosis
- Polycystic ovary syndrome: a common reproductive syndrome with long-term metabolic consequences
- Linear Alopecia Areata in a 4-year-old Patient: A Rare Clinical Variant