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Research 961–990 of 1000+
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Prepregnancy Phenotype and Physiological Characteristics in PCOS
- MON-218 Inflammatory Role of Sex Steroids in Hidradenitis Suppurativa: An Androgenic Phenotype
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- 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)
- 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
- Shared Phenotypes Among Segmental Progeroid Syndromes Suggest Underlying Pathways of Aging
- KERATIN PHENOTYPES IN BASAL-CELL CARCINOMAS OF THE SKIN
- Arrhythmia phenotypes in hair-loss therapies: insights from minoxidil and finasteride reports in eudravigilance
- Inheritance of Some Electrophoretic Phenotypes of Human Hair
- Location and phenotype of human adult keratinocyte stem cells of the skin
- Metabolic risk in PCOS: phenotype and adiposity impact
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Changes in the PCOS phenotype with age
- 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
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- 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’
- Body Composition and Characterization of Skinfold Thicknesses from Polycystic Ovary Syndrome Phenotypes. A Preliminar Case-Control Study
- The Frequency of Various Phenotypes of Polycystic Ovarian Syndrome in Adolescents, Based on Rotterdam Criteria
- Polycystic Ovary Syndrome Phenotypes and Infertility Treatment