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  • Search Condition : Filter (MeSH = Mutation*)
Species Resource Title
Human and Animal Cells MtT/S(RCB0528) , MtT/SM(RCB0530) Infrequent detectable somatic mutations of the RET and glial cell line-derived neurotrophic factor (GDNF) genes in human pituitary adenomas.
Human and Animal Cells MC3T3-E1(RCB1126) Transcriptional activation of the wild-type and mutant vitamin D receptors by vitamin D3 analogs.
Human and Animal Cells TGBC1TKB(RCB1129) , TGBC2TKB(RCB1130) Therapeutic efficacy of G207, a conditionally replicating herpes simplex virus type 1 mutant, for gallbladder carcinoma in immunocompetent hamsters.
Human and Animal Cells TGBC24TKB(RCB1196) , TGBC1TKB(RCB1129) , TGBC11TKB(RCB1148) , RCC10RGB(RCB1151) Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer.
Human and Animal Cells B901L(RCB3530) MALDI mass spectrometry imaging of erlotinib administered in combination with bevacizumab in xenograft mice bearing B901L, EGFR-mutated NSCLC cells.
Human and Animal Cells HuCCT1(RCB1960) , G-415(RCB2640) , RBE(RCB1292) , SSP-25(RCB1293) , TFK-1(RCB2537) , TGBC14TKB(RCB1186) , YSCCC(RCB1549) , TKKK(RCB1907) Isocitrate Dehydrogenase Mutations Confer Dasatinib Hypersensitivity and SRC Dependence in Intrahepatic Cholangiocarcinoma.
Human and Animal Cells Ba/F3(RCB0805) Emergence of CTNNB1 mutation at acquired resistance to KIT inhibitor in metastatic melanoma.
Rats GRY/Idr (StrainID=498) Poor mother-offspring relationships in rats with Cacna1a mutation.
Drosophila Glial cell lineage expression of mutant ataxin-1 and huntingtin induces developmental and late-onset neuronal pathologies in Drosophila models.
Zebrafish Tg(chx10:Gal4) Augmentation of spinal cord glutamatergic synaptic currents in zebrafish primary motoneurons expressing mutant human TARDBP (TDP-43).
Human and Animal Cells Ba/F3(RCB0805) Mutant-Selective Irreversible EGFR Inhibitor, Naquotinib, Inhibits Tumor Growth in NSCLC Models with EGFR-Activating Mutations, T790M Mutation, and AXL Overexpression.
Yeast BY3072, BY22441, BYP558, BYP556 Meiotic chromosomal recombination defect in sake yeasts.
Yeast BY3072 , BY22441 , BYP558 , BYP556 Meiotic chromosomal recombination defect in sake yeasts.
C.elegans tm2149 , tm1297 Forward Genetic Screen for Caenorhabditis elegans Mutants with a Shortened Locomotor Healthspan.
C.elegans tm2508 An autism-causing calcium channel variant functions with selective autophagy to alter axon targeting and behavior.
C.elegans tm760 , tm4525 Mitochondrial unfolded protein response transcription factor ATFS-1 promotes longevity in a long-lived mitochondrial mutant through activation of stress response pathways.
C.elegans tm9602 Pathogenetic basis of Takenouchi-Kosaki syndrome: Electron microscopy study using platelets in patients and functional studies in a Caenorhabditis elegans model.
C.elegans tm4374 , tm2862 , tm6691 AP endonuclease EXO-3 deficiency causes developmental delay and abnormal vulval organogenesis, Pvl, through DNA glycosylase-initiated checkpoint activation in Caenorhabditis elegans.
Drosophila DGRC#150122 Mutations in mxc Tumor-Suppressor Gene Induce Chromosome Instability in Drosophila Male Meiosis.
Prokaryotes B. subtilis BKE library Expansion of the Spore Surface Polysaccharide Layer in Bacillus subtilis by Deletion of Genes Encoding Glycosyltransferases and Glucose Modification Enzymes.