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Research 511–540 of 1000+
- Quantitation of human mitochondrial DNA and whole mtGenomes sequencing of fingernail/hair shaft samples
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Connexin 26 (<i>GJB2</i>) mutations in keratitis–ichthyosis–deafness syndrome presenting with squamous cell carcinoma
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Identification of Somatic <i>KRAS</i> Mutation in a Korean Baby with Nevus Sebaceus Syndrome
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Lung Cancer Awareness Symposium Highlights Necessary Focus Areas for Research
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Synaptic processes and immune-related pathways implicated in Tourette syndrome
- Cutaneous Ultrastructural Features of the Flaky Skin (<i>fsn</i>) Mouse Mutation
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Evaluating the Causal Relationship Between Human Blood Metabolites and the Susceptibility to Alopecia Areata
- Gene expression patterns during palatal shelf fusion
- A glutathione-dependent control of the indole butyric acid pathway supports Arabidopsis root system adaptation to phosphate deprivation
- MobiMed: Framework for Rapid Application Development of Medical Mobile Apps
- Steroidogenic factor-1 lineage origin of skin lesions in Carney complex syndrome
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- HAIR KERATINIZATION IN HEALTH AND DISEASE
- Identification of the cell lineage at the origin of basal cell carcinoma
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Functional Interpretation of Genome-Wide Association Study Evidence in Alopecia Areata
- Uncharted waters
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Parental Uveitis Influences Offspring With an Increased Susceptibility to the Experimental Autoimmune Uveitis