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Research 661–690 of 1000+
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Non‐biologic immunosuppressive drugs for inflammatory and autoimmune skin diseases
- E-Poster
- Current understanding and treatment of sex hormone-related hair diseases
- Examining the Effect of Notocactus ottonis Cold Vacuum Isolated Plant Cell Extract on Hair Growth in C57BL/6 Mice Using a Combination of Physiological and OMICS Analyses
- Association of Acne Tarda with Endocrinological Disorders
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- DNA Microarray and Bioinformatic Analysis Reveals the Potential of Whale Oil in Enhancing Hair Growth in a C57BL/6 Mice Dorsal Skin Model
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
- An Update of Congenital Adrenal Hyperplasia
- Methimazole, Carbimazole, and Congenital Skin Defects
- Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Congenital ptosis: Long-term outcome of frontalis suspension using autogenous temporal fascia or fascia lata in children
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- An overview on congenital alopecia in domestic animals
- Congenital alopecia areata
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- Lash Ptosis in Congenital and Acquired Blepharoptosis
- Congenital adrenal hyperplasia
- Eyelash trichomegaly: review of congenital, acquired, and drug‐associated etiologies for elongation of the eyelashes
- Ocular involvement caused by the accumulation of porphyrins in a patient with congenital erythropoietic porphyria