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Research 31–60 of 1000+
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Patched1 Functions as a Gatekeeper by Promoting Cell Cycle Progression
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Severe Hypernatremia as Presentation of Netherton Syndrome
- Obesity and the skin
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Cronkhite–Canada syndrome: from clinical features to treatment
- Skin Development and Disease: A Molecular Perspective
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- Author Response: Touch receptor end-organ innervation and function require sensory neuron expression of the transcription factor Meis2
- Alk1 acts in non-endothelial VE-cadherin+ perineurial cells to maintain nerve branching during hair homeostasis
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- British Society for Dermatopathology: Summaries of Papers
- Identification of the cell lineage at the origin of basal cell carcinoma
- Finasteride-induced gynecomastia
- CPC12 Coinheritance of <i>BRCA2</i> and <i>CYLD</i> germline pathogenic variants associated with targetable metastatic malignant cylindroma