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Research 211–240 of 1000+
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Changes in the PCOS phenotype with age
- 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
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- Role of Phenylalanine and Its Metabolites in Health and Neurological Disorders
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Metabolic aspects of different phenotypes of polycystic ovary syndrome: Iranian PCOS Prevalence Study
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- [4-t-Butylphenyl]-N-(4-imidazol-1-yl phenyl)sulfonamide (ISCK03) inhibits SCF/c-kit signaling in 501mel human melanoma cells and abolishes melanin production in mice and brownish guinea pigs
- Multiomics-empowered Deep Phenotyping of Ulcerative Colitis Identifies Biomarker Signatures Reporting Functional Remission States
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Persistently curly hair phenotype with the use of nivolumab for squamous cell lung cancer
- Observation of phenotypic variation among Indian women with polycystic ovary syndrome (PCOS) from Delhi and Srinagar
- The hair eclipse phenomenon: sharpening the focus on the hair cycle chronobiology
- Increased anxiety‐like phenotype in female guinea pigs following reduced neurosteroid exposure <i>in utero</i>
- 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
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- “Osler’s phenomenon”: misdiagnosing Cushing’s 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
- Embryonic-like regenerative phenomenon: wound-induced hair follicle neogenesis
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- The Graying Phenomenon An Unusual Manifestation of Alopecia Areata