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Research 901–930 of 1000+
- The Frequency of Metabolic Syndrome is Higher Among PCOS Brazilian Women With Menstrual Irregularity Plus Hyperandrogenism
- Single-Cell RNA Sequencing Reveals Cellular and Transcriptional Changes Associated With M1 Macrophage Polarization in Hidradenitis Suppurativa
- 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
- Effective holistic characterization of small molecule effects using heterogeneous biological networks
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- MOESM1 of A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
- Basal cell carcinomas in mice arise from hair follicle stem cells and multiple epithelial progenitor populations
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- CSI on steroids
- Hair metal dysregulation in Parkinson’s disease: Implications for diagnosis and gut-brain axis involvement
- Caractérisation des Réactions Paradoxales Psoriasiformes Alopéciantes Induites par les Anti-TNFα chez des Patients Atteints de Maladies Inflammatoires Chroniques de l’Intestin
- Effect of Topical Gel Administration of Secretome Hypoxia Mesenchymal Stem Cells (SH-MSCs) on IL-10 and TNF- α Gene Expression (In Vivo Experimental Study in Male Rats of Wistar Strains Model of Fluconazole-Induced Alopecia)
- Ethnicity, obesity and the prevalence of impaired glucose tolerance and type 2 diabetes in PCOS: a systematic review and meta-regression
- The evolutionary impact of androgen levels on prostate cancer in a multi-scale mathematical model
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Developmental and functional roles of androgen and interactive signals for external genitalia and erectile tissues
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Polycystic ovarian morphology in Thai women of reproductive age with polycystic ovary syndrome
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Auxin Input Pathway Disruptions Are Mitigated by Changes in Auxin Biosynthetic Gene Expression in Arabidopsis
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- Clinical characteristics of polycystic ovary syndrome: investigating differences in White and South Asian women
- The Molecular Basis of Androgen Insensitivity
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Antimüllerian hormone to determine polycystic ovarian morphology