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Research 301–330 of 1000+
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- Recurrent Pregnancy Loss Associated Cytogenetic and Genetic Anomalies – Study from Eastern India
- Análise de esteróides em extratos vegetais e estudo fitoquímico e biológico preliminar de Brunfelsia uniflora.
- Buschke-Ollendorff syndrome
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- Intermittent nitrate transdermal therapy
- A Scoping Review of Pharmacotherapy, Complementary, and Alternative Medicine (CAM), and Surgical Therapies for Androgenic Alopecia
- The Off-Label Use of Selective Serotonin Reuptake Inhibitors for Sexual Behavior Management: Risks and Considerations
- Fractional erbium-doped yttrium aluminum garnet laser 2940 nm-assisted delivery of topical timolol solution for the treatment of histiocytoid hemangioma
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- <i>Hoxc13</i> mutant mice lack external hair
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- NUDT15 polymorphism explains serious toxicity to azathioprine in Indian patients with chronic immune thrombocytopenia and autoimmune hemolytic anemia: a case series
- Le gène<i>hairless</i>de la souris
- Standardizing the Nomenclature of Grafts
- Association of Cyp11a Gene with Polycystic Ovarian Syndrome Patients in Lahore, Pakistan
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Oncogenes and morphogens: intricacies of targeted therapy in cutaneous basal cell carcinoma
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Development of a Chitosan Nanofibrillar Scaffold for Skin Repair and Regeneration
- Antioxidants in dermatology
- New lifestyle drugs and somatoform disorders in dermatology
- Clinical Management in Psychodermatology
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- Learning from nudity: lessons from the nude phenotype
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Alopecia areata: An update
- Cutaneous and Mucosal Manifestations Associated with Celiac Disease
- Nonclassic adrenal hyperplasia