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Research 601–630 of 1000+
- The First Visit: Consult and Workup Before Sperm Banking
- Trichorrhexis Invaginata and Netherton’s Syndrome
- Medical Management Options for Hair Loss
- A single type of progenitor cell maintains normal epidermis
- Hyperpigmentation and Melasma
- The role of keratin proteins and their genes in the growth, structure and properties of hair
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Abstracts
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Male fertility and skin diseases
- 원저 : 유전성 안드로겐탈모증의 임상적 고찰(제6보)
- Congenital atrichia and hypotrichosis
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Down Syndrome and Autoimmune Disease
- Loss‐of‐function of Endothelin receptor type A results in Oro‐Oto‐Cardiac syndrome
- Update on Melasma—Part I: Pathogenesis
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Whole blood transcriptome profiling identifies candidate genes associated with alopecia in male giant pandas (Ailuropoda melanoleuca)
- Research Snippets
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Adult Acne
- Adrenal causes of endocrine hypertension in childhood or adolescence
- PCOS in Adolescence and Type 2 Diabetes
- Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss
- Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Identification of Potential Hub Genes in Alopecia Areata