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Research 61–90 of 1000+
- Delayed Wound Healing in Keratin 6a Knockout Mice
- Genetically separable determinants of hair keratin gene expression
- Bone Regeneration Is Regulated by Wnt Signaling
- ADAM17 variant causes hair loss via ubiquitin ligase TRIM47 mediated degradation
- Establishment of Tsc2-deficient rat embryonic stem cells
- 778 Designing and utilizing a c-Rel specific bioassay in drug repurposing screen for HNSCC
- Dissecting the bulge in hair regeneration
- The genetic evolution of skin squamous cell carcinoma: tumor suppressor identity matters
- Exploiting the origins of Ras mediated squamous cell carcinoma to develop novel therapeutic interventions
- Adipocyte Lineage Cells Contribute to the Skin Stem Cell Niche to Drive Hair Cycling
- Integrative Comparison of the Role of the PHOSPHATE RESPONSE1 Subfamily in Phosphate Signaling and Homeostasis in Rice
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- The Role of Vitamin D and Its Receptor in Hair Follicle Biology
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- Roles of the Hedgehog Signaling Pathway in Cutaneous Physiology and Oncology
- Localizing the ROS Signal
- Loss‐of‐function of Endothelin receptor type A results in Oro‐Oto‐Cardiac syndrome
- A protein kinase target of a PDK1 signalling pathway is involved in root hair growth in Arabidopsis
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- Targeted therapy in melanoma
- XEDAR activates the non-canonical NF-κB pathway
- OsUEV1B, an Ubc enzyme variant protein, is required for phosphate homeostasis in rice
- Acne-Associated Syndromes
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Hairless: A nuclear receptor corepressor essential for skin function
- Lentiginous melanoma. A clinically malignant entity that histopathologically seems benign. Case study harbouring BRAF V 600R mutation
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis