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論文 - 一覧

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  • 検索条件 : 絞込み (MeSH = Homozygote)
生物種 リソース名 タイトル
ヒト・動物細胞 Hep G2(RCB0459) Infrequent alterations of the p16INK4A gene in liver cancer.
実験動物マウス RBRC01615 Diverse dystonin gene mutations cause distinct patterns of Dst isoform deficiency and phenotypic heterogeneity in Dystonia musculorum mice.
ショウジョウバエ DGRC#118827 Genetic dissection of Nucleoporin 160 (Nup160), a gene involved in multiple phenotypes of reproductive isolation in Drosophila.
ヒト・動物細胞 HSC-3(RCB1975) , SAS(RCB1974) , 293T(RCB2022) , MRC-5 Insufficiency of hepatocyte growth factor activator inhibitor-1 confers lymphatic invasion of tongue carcinoma cells.
ヒト・動物細胞 GCIY(RCB0555) , TGBC11TKB(RCB1148) Alterations and hypermethylation of the p14(ARF) gene in gastric cancer.
ショウジョウバエ 1063R-2 Predicting novel candidate human obesity genes and their site of action by systematic functional screening in Drosophila.
ヒト・動物細胞 NALM-6(RCB1933) RAG1 splicing mutation causes enhanced B cell differentiation and autoantibody production.
遺伝子材料 CS-CDF-CG-PRE (RDB04379) , pCMV-VSV-G-RSV-Rev (RDB04393) , pCAG-HIVgp (RDB04394) The polymicrogyria-associated GPR56 promoter preferentially drives gene expression in developing GABAergic neurons in common marmosets.
トマト TOMJPF00001(Micro-Tom) Efficient base editing in tomato using a highly expressed transient system.
ヒト・動物細胞 CW-2(RCB0778) Functional characterization of SMARCA4 variants identified by targeted exome-sequencing of 131,668 cancer patients.
ヒト・動物細胞 409B2(HPS0076) Synergistic gene editing in human iPS cells via cell cycle and DNA repair modulation.
ニワトリ・ウズラ JB , GSP/Cp Combined deletions of IHH and NHEJ1 cause chondrodystrophy and embryonic lethality in the Creeper chicken.
ショウジョウバエ Studying Nonproliferative Roles for Egfr Signaling in Tissue Morphogenesis Using Dorsal Closure of the Drosophila Embryo.
遺伝子材料 MSM Mouse BAC clone (RDB04214) MSMg01-526L10 Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function.
線虫 tm373 Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization.
ゼブラフィッシュ Tg(vglut2a:loxP-DsRed-loxP-GFP) The dual developmental origin of spinal cerebrospinal fluid-contacting neurons gives rise to distinct functional subtypes.
遺伝子材料 Human HLA cDNA HLA-C*04:01:01 (RDB02886) , HLA-C*15:02:01 (RDB03379) , HLA-C*01:02 (RDB02883) , CS-UbC-RfA-IRES2-Venus (RDB08255). NK Cell Alloreactivity against KIR-Ligand-Mismatched HLA-Haploidentical Tissue Derived from HLA Haplotype-Homozygous iPSCs.
遺伝子材料 , ヒト・動物細胞 pSpCas9-mGli3-exon2_sgRNA (RDB15037) , pSpCas9-mGli3-exon3_sgRNA (RDB15038) , pCMV-3xFLAG-mGli3_WT (RDB15039) , pCMV-3xFLAG-mGli3_WT-HA (RDB15040) , pCMV-3xFLAG-mGli3_del97G-HA (RDB15041) , pCMV-3xFLAG-mGli3_insGafter97G-HA (RDB15042). , NIH/3T3(RCB2767) Illegitimate translation causes unexpected gene expression from on-target out-of-frame alleles created by CRISPR-Cas9.
コムギ LPGKU2271(Norin 61) , KT001-001 , KT003-005 Loss-of-Function Mutations in Three Homoeologous PHYTOCLOCK 1 Genes in Common Wheat Are Associated with the Extra-Early Flowering Phenotype.
遺伝子材料 Genome Network Project Human cDNA IRAL058O23 (HGY103559). Identification of Novel Mutations in the LRR-Cap Domain of C21orf2 in Japanese Patients With Retinitis Pigmentosa and Cone-Rod Dystrophy.