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Research 511–540 of 1000+
- Beyond Wavy Hairs
- Conserved γδ T cell selection by BTNL proteins limits progression of human inflammatory bowel disease
- Cutaneous gene therapy
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- SOX9 in organogenesis: shared and unique transcriptional functions
- Sox2 in the dermal papilla regulates hair follicle pigmentation
- Transglutaminase Activity Is Conserved in Stratified Epithelia and Skin Appendages of Mammals and Birds
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Ear pinna growth and differentiation is conserved in murids and requires BMP signaling for chondrocyte proliferation
- <i>PIK3CA</i> gain-of-function mutation in Schwann cells leads to severe neuropathy and aerobic glycolysis through a non-cell autonomous effect
- Intercellular junctions in normal epidermis
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- A Transition State Analogue of 5′-Methylthioadenosine Phosphorylase Induces Apoptosis in Head and Neck Cancers
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- Myotonic Dystrophy—A Progeroid Disease?
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Molecular determinants for the chemical activation of the warmth-sensitive TRPV3 channel by the natural monoterpenoid carvacrol
- Relevance of the Axis Spermidine/eIF5A for Plant Growth and Development
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- miR-129-5p Participates in Hair Follicle Growth by Targeting HOXC13 in Rabbit
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Regulation of Hair Follicle Growth and Development by Different Alternative Spliceosomes of FGF5 in Rabbits
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans