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生物種
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リソース名
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RRC ID
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タイトル
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ジャーナル
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公開日
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外部リンク
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メダカ
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MT147
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87810
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A genetic model of congenital intestinal atresia implicates Mypt1 in epithelial organisation.
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Dis Model Mech |
2026-2-1 |
Pubmed
Full text
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線虫
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tm3410
,
tm515
,
tm1978
,
tm2318
,
tm3262
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84028
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Regulatory mechanism of cold-inducible diapause in Caenorhabditis elegans.
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Nat Commun |
2024-7-10 |
Pubmed
Full text
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線虫
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tm872
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53965
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The Coding Regions of Germline mRNAs Confer Sensitivity to Argonaute Regulation in C. elegans.
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Cell Rep |
2018-2-27 |
Pubmed
Full text
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原核生物(枯草菌)
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MBS662
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53802
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Isolation and characterization of sporulation-initiation mutation in the Bacillus subtilis prfB gene.
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Biosci Biotechnol Biochem |
2007-2-1 |
Pubmed
Full text
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線虫
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tm1153
,
tm849
,
tm5409
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46490
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RNA surveillance is required for endoplasmic reticulum homeostasis.
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Proc Natl Acad Sci U S A |
2012-5-22 |
Pubmed
Full text
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ショウジョウバエ
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32398
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Genome features of "Dark-fly", a Drosophila line reared long-term in a dark environment.
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PLoS One |
2012-3-14 |
Pubmed
Full text
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メダカ
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MT326
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30897
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Filamin C plays an essential role in the maintenance of the structural integrity of cardiac and skeletal muscles, revealed by the medaka mutant zacro.
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Dev Biol |
2012-1-1 |
Pubmed
Full text
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オオムギ
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Full length cDNA
,
Haruna Nijo
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21551
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A physical, genetic and functional sequence assembly of the barley genome.
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Nature |
2012-11-29 |
Pubmed
Full text
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実験動物マウス
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RBRC01680
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11864
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SMOC1 is essential for ocular and limb development in humans and mice.
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Am J Hum Genet |
2011-1-7 |
Pubmed
Full text
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ラット
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F344.CVD-Unc5ccvd/Kyo(strainID=153)
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97
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Rat neurological mutations cerebellar vermis defect and hobble are caused by mutations in the netrin-1 receptor gene Unc5h3.
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Brain Res Mol Brain Res |
2004-3-30 |
Pubmed
Full text
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ラット
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KZC/Tky(strainID=20)
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77
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Rat neurological disease creeping is caused by a mutation in the reelin gene.
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Brain Res Mol Brain Res |
2003-4-10 |
Pubmed
Full text
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