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Research 211–240 of 1000+
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)
- Inheritance of Some Electrophoretic Phenotypes of Human Hair
- 333 Poor perifollicular vascularization is associated with nutrient insufficiency and a quiescent metabolic phenotype in intermediate hair follicles from patients with female pattern hair loss
- The prevalence and phenotypic features of polycystic ovary syndrome: a systematic review and meta-analysis
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- The biochemical and phenotypic characterization of females homozygous for 5 alpha-reductase-2 deficiency.
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Insulin resistance and obesity among infertile women with different polycystic ovary syndrome phenotypes
- Modulation of the differentiated phenotype of keratinocytes of the hair follicle and from epidermis
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- Observation of phenotypic variation among Indian women with polycystic ovary syndrome (PCOS) from Delhi and Srinagar
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Body Composition and Characterization of Skinfold Thicknesses from Polycystic Ovary Syndrome Phenotypes. A Preliminar Case-Control Study
- Genomic and phenotypic characterization of Investigator Global Assessment (IGA) scale-based endotypes in atopic dermatitis
- Genetics underlying phenotypic diversity in South African sheep breeds
- The PCOS Phenotypes in Unselected Populations (P-PUP) study: participant clinical features and data harmonization on analysis of individual participant data
- 46, XY 5-Alpha Reductase Deficiency in a 36-Year-Old Phenotypic Female Patient
- Polycystic Ovary Syndrome Phenotypes and Infertility Treatment
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Exploring imputation performance of phenotype-associated SNPs for forensic prediction models
- MITF E318K naevus phenotype: the modifying role of MC1R Red Hair Variants