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Research 571–600 of 1000+
- Activation of TRPV4 Induces Exocytosis and Ferroptosis in Human Melanoma Cells
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- An important role of podoplanin in hair follicle growth
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- LGR5 is a conserved marker of hair follicle stem cells in multiple species and is present early and throughout follicle morphogenesis
- COVID-19 Severity and Androgen Receptor Polymorphism
- Siberian cats help in solving part of the mystery surrounding golden cats
- Effect of CUX1 on the Proliferation of Hu Sheep Dermal Papilla Cells and on the Wnt/β-Catenin Signaling Pathway
- Hub biomarkers in ultrasound-guided bladder cancer and osteosarcoma: Myosin light chain kinase and caldesmon
- Cellular Senescence and Aging in Myotonic Dystrophy
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- TRPV3 Ion Channel: From Gene to Pharmacology
- Exome analysis for Cronkhite-Canada syndrome: A case report
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Canonical prolactin signaling and global mRNA expression in the skin of Holstein heifers carrying the SLICK1 allele of the prolactin receptor gene
- Steatocystoma Multiplex
- Food Administration and Not Genetic Variants Causes Pharmacokinetic Variability of Tadalafil and Finasteride
- Association between DNA Methylation in the Core Promoter Region of the CUT-like Homeobox 1 (CUX1) Gene and Lambskin Pattern in Hu Sheep
- Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Large-Scale, Multicenter, Prospective Registry Study of Ripretinib in Advanced GIST: A Real-World Study from China
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose