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Research 30 of 914
- Clinical Impact of Molecular Diagnostics in Endocrinology
- Inflammatory and non-melanocytic tumoral pathology of the nail
- Management of a Refractory EIF3E-RSPO2 Fusion Positive Pilomatrical Cancer Patient with Encyclopedic Tumor Analysis Guided Treatment
- Genetics of thyroid lesions updated
- The Editor's Choice
- Natural Compounds Targeting MAPK, PI3K/Akt, and JAK/STAT Signaling in Papillary Thyroid Cancer
- Can you diagnose hair loss (Non-scarring alopecia)
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Expression patterns of the glial cell line–derived neurotrophic factor, neurturin, their cognate receptors GFRα-1, GFRα-2, and a common signal transduction element c-Ret in the human skin hair follicles
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Cutaneous gain-of-function mutation of LRIG3 leads to alopecia by upregulation of ERBB, PI3K/AKT, NOTCH1 signaling pathways
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Roles of tumor suppressors in regulating tumor-associated inflammation
- Progeroide Syndrome
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Somatic Mutations in Normal Tissues: New Perspectives on Early Carcinogenesis
- Clonal analysis of stem cells in differentiation and disease
- Woolly Antics between the Sheaths
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Alopezien und Hypotrichosen im Kindesalter
- Prostate Cancer Early Detection, Version 2.2015