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Research 601–630 of 1000+
- Endocrine disorders and hormonal therapy for adolescent acne
- Polycystic Ovary Syndrome (PCOS): From Diagnosis to Treatment
- A Comparative Analysis of Serum Irisin Levels and Body Composition Indices in Women With and Without Polycystic Ovary Syndrome (PCOS)
- Cysteine and Glutamine level in hair shaft fractures patients
- Cardiometabolic and neuroimaging correlates of cognitive function in polycystic ovary syndrome
- Spectrum and signals of medication-associated cognitive disorder: a comprehensive disproportionality analysis with cross-database validation
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Relationship of Serum Prostate Specific Antigen with Hirsutism in Women Having Polycystic Ovary Syndrome Belonging to the Province of Khyber Pakhtunkhwa, Pakistan
- Effect of decellularisation methods on methacryloyl-substituted placental ECM hydrogels
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- Historical Archives
- Approach to the adult female patient with diffuse nonscarring alopecia
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Investigation of Insulin-Like Growth Factor 1 Receptor Expression in Cases of Sacrococcygeal Pilonidal Sinus
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- Perbandingan Kadar Transforming Growth Factor-Beta 1 pada Platelet Rich Plasma dengan Metode Pure dan Buffy Coat pada Populasi Individu Sehat
- Molecular mechanisms of androgenetic alopecia
- Regulatory T-Cells: Potential Regulator of Tissue Repair and Regeneration
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Wnt signaling in skin organogenesis
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- Idiopathic Hirsutism*
- Short anagen syndrome
- The Basic Science of Hair Biology
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Understanding Polycystic Ovary Syndrome
- The human keratins: biology and pathology