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Research 61–90 of 1000+
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Progressive Alopecia Reveals Decreasing Stem Cell Activation Probability during Aging of Mice with Epidermal Deletion of DNA Methyltransferase 1
- 666 Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in follicular dystrophy and primary cicatricial alopecia
- Homozygous K5Cre transgenic mice have wavy hair and accelerated malignant progression in a murine model of skin carcinogenesis
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Analysis of hairless corepressor mutants to characterize molecular cooperation with the vitamin D receptor in promoting the mammalian hair cycle
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- An in vivo method for the detection of somatic mutations at the cellular level in mice
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- Abstract 5357: Targeting mTORC1 suppresses proliferation of keratinocyte stem cells and inhibits skin tumor promotion in mice
- Suppression of hair follicle development inhibits induction of sonic hedgehog, patched, and patched-2 in hair germs in mice
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation.
- The transcriptional repressor CDP (Cutl1) is essential for epithelial cell differentiation of the lung and the hair follicle
- The Effect of Copper Supplementation on the Brindled Mouse
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- Hair follicle regeneration suppresses Ras-driven oncogenic growth
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Field Cancerization: From Molecular Basis to Selective Field-Directed Management of Actinic Keratosis
- 318 The Wnt-inhibitor Dkk4 is required for primary hair follicle induction and patterning
- The role of Pygo2 during intestinal tumor initiation and progression in vivo
- Neural crest cells give rise to non-myogenic mesenchymal tissue in the adult murid ear pinna
- 726 The Wnt-inhibitor Dkk4 is required for primary hair follicle induction and patterning
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype