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Research 121–150 of 1000+
- Identification and characterization of Birt–Hogg–Dubé associated renal carcinoma
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Establishment of Tsc2-deficient rat embryonic stem cells
- Management of Colorectal Cancer Using Nanocarriers-based Drug Delivery for Herbal Bioactives: Current and Emerging Approaches
- Comprehensive Genomic Profiling of Cutaneous Adnexal Carcinomas: A Genomic Landscape Study
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- The Case | Bilateral kidney tumors and lung cysts
- Flavonoids as Potential Wound-Healing Molecules: Emphasis on Pathways Perspective
- Frizzled Receptors in Development and Disease
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Odontogenic Keratocysts Arise from Quiescent Epithelial Rests and Are Associated with Deregulated Hedgehog Signaling in Mice and Humans
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Atrichia with papular lesions
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Joint Public Review: Touch receptor end-organ innervation and function require sensory neuron expression of the transcription factor Meis2
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- TRANSMEDCON 2022: E-Poster Abstracts
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Sox2-positive dermal papilla cells specify hair follicle type in mammalian epidermis
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1