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Research 571–600 of 1000+
- Application of big data analytics in minoxidil drug development: a data-driven model for predicting efficacy and side effect risks
- Understanding Polycystic Ovary Syndrome: A Comprehensive Guide
- POLYCYSTIC OVARY SYNDROME (PCOS): DIAGNOSIS, PATHOPHYSIOLOGY AND CONTEMPORARY THERAPEUTIC APPROACHES
- Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
- Androgens/Androgen Receptor in the Management of Skin Diseases
- Exploring the role of CYP19A1 single nucleotide polymorphisms in the pathogenesis of female pattern hair loss
- Topical Finasteride: A Comprehensive Review of Androgenetic Alopecia Management for Men and Women
- Epidemiology, diagnosis, and management of polycystic ovary syndrome
- Vaccines, adjuvants and autoimmunity
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- FGF5 is a crucial regulator of hair length in humans
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Noggin overexpression inhibits eyelid opening by altering epidermal apoptosis and differentiation
- Androgen Action in the Ovary
- Integrated analysis of long non-coding RNA and mRNA expression in different colored skin of koi carp
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Pathomechanisms of immune-mediated alopecia
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- The influence of interferon on healthy and diseased skin
- Sarcoptic mange outbreak decimates South American wild camelid populations in San Guillermo National Park, Argentina
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Engineering molecular imaging strategies for regenerative medicine
- Anti-Müllerian Hormone and Polycystic Ovary Syndrome in Women and Its Male Equivalent
- Transcriptomic regulation of seasonal coat color change in hares
- Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing
- Skin Development and Disease: A Molecular Perspective
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- Association of atopic dermatitis with autoimmune diseases: A bidirectional and multivariable two-sample mendelian randomization study