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Research 31–60 of 1000+
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- 036 Expanded T cells under lymphopenic condition exhibit memory phenotype and infiltrate around hair follicle
- 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
- White and yellow dots as new trichoscopic signs of severe female androgenetic alopecia in dark skin phototypes
- 43687 Fitzpatrick Skin Phototypes: More than Just Skin Deep
- 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
- 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 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
- 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
- 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
- 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>
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome