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Research 451–480 of 1000+
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Characterization of transport systems for cysteine, lysine, alanine, and leucine in wool follicles of sheep
- The role of AUTS2 in neurodevelopment and human evolution
- Susceptibility variants for male-pattern baldness on chromosome 20p11
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- P448: Identification of a novel RPS6KA3 variant in a female child with features of Coffin-Lowry syndrome: A case study
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Gain‐of‐function variants in the <i>ODC1</i> gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Optimal processing for proteomic genotyping of single human hairs
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- A second <i>KRT</i>71 allele in curly coated dogs
- Disease causing homozygous variants in the human hairless gene
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners.
- Baldness and the androgen receptor: the AR polyglycine repeat polymorphism does not confer susceptibility to androgenetic alopecia
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Genetic Defects of Female Sexual Differentiation
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria