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Research 451–480 of 712
- Genetic basis of polycystic ovary syndrome
- A comparative analysis of immune privilege in pregnancy and cancer in the context of checkpoint blockade immunotherapy
- Prevalence of vitamin D deficiency in Slovak women with polycystic ovary syndrome and its relation to metabolic and reproductive abnormalities
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- Androgen Receptor (<i>AR</i>) Gene (CAG)n and (GGN)n Length Polymorphisms and Symptoms in Young Males With Long-Lasting Adverse Effects After Finasteride Use Against Androgenic Alopecia
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- The Significance of Scalp Involvement in Pemphigus: A Literature Review
- Trichoscopy - a useful tool in the preliminary differential diagnosis of autoimmune bullous diseases
- Dermoscopy of discoid lupus erythematosus: Report of two cases
- Development of a Doxazosin and Finasteride Transdermal System for Combination Therapy of Benign Prostatic Hyperplasia
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations
- Upregulation of interfollicular epidermal and hair infundibulum β-catenin expression in Gsdma3 mutant mice
- Androgens and hair: a biological paradox
- A systematic review of dermatologic manifestations among adult patients with COVID‐19 diagnosis
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Cutaneous Manifestations in COVID-19: Report on 31 Cases from Five Countries
- The role of aquaporins in polycystic ovary syndrome – A way towards a novel drug target in PCOS
- Disease causing homozygous variants in the human hairless gene
- Kerion Celsi due to <i>Microsporum canis</i> in an Adult Woman, Treated Successfully with Fosravuconazole
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia
- Pharmacological Options for Treatment of Hyperandrogenic Disorders
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- Pruritic urticarial papules and plaques of pregnancy
- Dermatologic Conditions of the Early Post-Transplant Period in Hematopoietic Stem Cell Transplant Recipients
- Association of a polymorphism in the ornithine decarboxylase gene with male androgenetic alopecia
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- After‐Rinsing Hair Growth Promotions of Hinokitiol‐Containing Vesicles and Emulsions