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Research 301–330 of 1000+
- Revisiting Diffuse Unpatterned Alopecia: Reappraisal of a Controversial Diagnosis
- Bioinspired Antibacterial-Antioxidant Bioactive Hydrogel Synchronizes Immunomodulation-Microenvironment Remodeling for Infected Wound Regeneration
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Testosterone and doping control
- Exploring the Impact of the Microbiome on Neuroactive Steroid Levels in Germ-Free Animals
- 237 Unveiling Skin Cancers Pathophysiology via the Modeling of Xeroderma Pigmentosum Disease Modeling Using CRISPR-Cas9 Technology
- Cisd2 deficiency impairs neutrophil function by regulating calcium homeostasis via Calnexin and SERCA
- Polycystic ovary syndrome
- Current Guidelines for Diagnosing PCOS
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Triglycerides, independent of Ferriman Gallwey Score, is a main determinant of free testosterone index in PCOS
- Abstracts
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Beyond Wavy Hairs
- Actinic keratosis: a clinical and epidemiological revision
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- From Primary MSC Culture of Adipose Tissue to Immortalized Cell Line Producing Cytokines for Potential Use in Regenerative Medicine Therapy or Immunotherapy
- Making the head: Caspases in life and death
- Regulation and Role of GLI1 in Cutaneous Squamous Cell Carcinoma Pathogenesis
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Establishment of an in vitro hairless guinea pig dermal model
- Sexual Dysfunction in Polycystic Ovary Syndrome (PCOS): A Biopsychosocial Approach to Assessment and Management
- Endocrinology
- Criteria for Diagnosis of Polycystic Ovary Syndrome during Adolescence: Literature Review
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Prevalence and characteristics of polycystic ovary syndrome in Brazilian women: protocol for a nation-wide case–control study