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Research 691–720 of 1000+
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Enhanced Insights into Frontal Fibrosing Alopecia: Advancements in Pathogenesis Understanding and Management Strategies
- Potential therapeutic applications of mesenchymal stem cell-derived extracellular vesicles
- Androgen receptor gene polymorphism and biological age markers in men
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Nevus Sebaceus With Novel HRAS Sequence Variant Mutation Misdiagnosed as Alopecia Areata
- Hair loss in children.
- Diagnosis and treatments of hirsutism: where are we?
- Dermatologic therapy: December 1986 to December 1987
- Identification of genes and proteins associated with anagen wool growth
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Interleukin 15 Gene Polymorphism in patients with Alopecia Areata
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Intraovarian platelet-rich plasma administration could improve blastocyst euploidy rates in women undergoing in vitro fertilization
- Association between angiotensin‐converting enzyme gene insertion deletion polymorphism and androgenetic alopecia susceptibility among Egyptian patients: A preliminary case‐controlled study
- Decreased Serum Ferritin is Associated With Alopecia in Women
- Cutaneous Reactions in Patients with Chronic Hepatitis C Treated with Peginterferon and Ribavirin
- Electrophoretic analysis of human hair keratins
- CCDC22 and CCDC93, two potential retriever-interacting proteins, are required for root and root hair growth in Arabidopsis
- Effects and Mechanism of Nutrients on Root Hair Growth
- Comments concerning the real risk of sexual adverse events secondary to the use of 5-ARIs
- Metformin therapy for the reproductive and metabolic consequences of polycystic ovary syndrome
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats