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Research 271–300 of 1000+
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- Evaluation of the phenotypic, proliferative and secretory profile of mesenchymal stem cells from adipose tissue captured by laser-assisted liposuction
- Analysis of the phenotypic variants of polycystic ovarian syndrome in women of reproductive age group
- Forensic DNA Phenotyping
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Clinicopathological insights into the phenotypic variation of autosomal recessive hypotrichosis/wooly hair by c.736T>A LIPH mutation
- Location and phenotype of human adult keratinocyte stem cells of the skin
- Metabolic risk in PCOS: phenotype and adiposity impact
- Changes in the PCOS phenotype with age
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- 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
- Increased anxiety‐like phenotype in female guinea pigs following reduced neurosteroid exposure <i>in utero</i>
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- The ‘bald’ phenotype (androgenetic alopecia) is caused by the high glycaemic, high cholesterol and low mineral ‘western diet’
- The Frequency of Various Phenotypes of Polycystic Ovarian Syndrome in Adolescents, Based on Rotterdam Criteria
- Forensic DNA Phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Minoxidil Regulates Aging-Like Phenotypes in Rat Cortical Astrocytes <i>In Vitro</i>
- Multi-omics empowered deep phenotyping of ulcerative colitis
- Beyond Hirsutism: Hair Phenotypes as Clinical Signals for the Recognition of Polyendocrine Metabolic Ovarian Syndrome (PMOS): A Scoping Review Protocol
- Male Senescence Phenotypes Include Hair Loss and Hair Gain
- 0439 Temporal–phenotype signatures of alopecia associated with GLP-1–based therapies: A PRISMA-ScR scoping review
- Forensic DNA phenotyping: the need for proportionate regulation and judicial clarity in law enforcement
- Acquired Progressive Kinking of the Hair: A Narrative Review of the Androgen‐Dependent Phenotype
- 0877 Activated wound phenotype and microbial dysbiosis are driven by AhR suppression in hidradenitis suppurativa tunnels