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Research 301–330 of 1000+
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- Biotin and biotinidase deficiency
- Overview of Alopecia Areata
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Androgenetic Alopecia
- Markers of Epidermal Stem Cell Subpopulations in Adult Mammalian Skin
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Apoptosis May Explain the Pharmacological Mode of Action and Adverse Effects of Isotretinoin, Including Teratogenicity
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Alopecia areata: What’s new in epidemiology, pathogenesis, diagnosis, and therapeutic options?
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- <i>NUDT15</i>,<i>FTO</i>, and<i>RUNX1</i>genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Madarosis
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Multifactorial Classification of Male and Female Androgenetic Alopecia
- Identifying genes associated with the development of human polycystic ovary syndrome
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Lifestyle and Physiological Factors Associated with Facial Wrinkling in Men and Women
- An epidemiological study of androgenic alopecia in 3114 Korean patients
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- The aetiology and pathogenesis of alopecia areata
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Alopecia in IL-10-deficient mouse pups is c-kit-dependent and can be triggered by iron deficiency
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- 4 Vitamin D resistance