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Research 631–660 of 1000+
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Genetic Hair Disorders: A Review
- Developmental genetics of color pattern establishment in cats
- Engineering molecular imaging strategies for regenerative medicine
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Enriching Proteolysis Targeting Chimeras with a Second Modality: When Two Are Better Than One
- Extracellular vesicles in age-related diseases: disease pathogenesis, intervention, and biomarker
- Inhibition of the CoREST Repressor Complex Promotes Wound Re-Epithelialization through the Regulation of Keratinocyte Migration
- Deciphering the molecular drivers for cashmere/pashmina fiber production in goats: a comprehensive review
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- A Chemically Defined Culture for Tooth Reconstitution
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Spontaneous fertility in a male patient with testotoxicosis despite suppression of FSH levels
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- The Mechanisms of Fur Development and Color Formation in American Mink Revealed Using Comparative Transcriptomics
- When bugs and drugs conspire: driving acneiform skin toxicity
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Research progress and strategies for the biosynthesis of keratinocyte growth factor-2 (KGF-2) in <i>Arabidopsis thaliana</i>
- Evolution of long scalp hair in humans