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Research 841–870 of 1000+
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Hair Follicle: A Novel Source of Multipotent Stem Cells for Tissue Engineering and Regenerative Medicine
- Perspectives of Kennedy's disease
- The population dynamics of cancer: a Darwinian perspective
- Polycystic Ovaries Are Inherited as an Autosomal Dominant Trait: Analysis of 29 Polycystic Ovary Syndrome and 10 Control Families
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Frontal Fibrosing Alopecia: An Update on Pathogenesis, Diagnosis, and Treatment
- Acne keloidalis nuchae: prevalence, impact, and management challenges
- Lineage Analysis of Epidermal Stem Cells
- Alopecia areata: What’s new in epidemiology, pathogenesis, diagnosis, and therapeutic options?
- Skin grafting for the treatment of chronic leg ulcers – a systematic review in evidence‐based medicine
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Skin Keratins
- Functional enhancement strategies for immunomodulation of mesenchymal stem cells and their therapeutic application
- Bioengineered Plants Can Be a Useful Source of Omega-3 Fatty Acids
- An Overview of Alopecias
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- How to diagnose a lipodystrophy syndrome
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Alopecia Areata
- Do Changes in Chromosomes Cause Aging?
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Optimal Management of Hair Loss (Alopecia) in Children
- Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness
- Association between the D19S884 marker at the insulin receptor gene locus and polycystic ovary syndrome
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis