about
Acute multi-sgRNA knockdown of KEOPS complex genes reproduces the microcephaly phenotype of the stable knockout zebrafish model.Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasia.Knockdown of Laminin gamma-3 (Lamc3) impairs motoneuron guidance in the zebrafish embryo.Fishing for histamine H3 receptor functions.Genetic compensation triggered by actin mutation prevents the muscle damage caused by loss of actin protein.Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus.Pseudopodium-enriched atypical kinase 1 mediates angiogenesis by modulating GATA2-dependent VEGFR2 transcription.Planar cell polarity signalling coordinates heart tube remodelling through tissue-scale polarisation of actomyosin activity.An optimised pipeline for parallel image-based quantification of gene expression and genotyping after in situ hybridisation.Genetics of Cardiovascular Disease: Fishing for Causality.Fish mutant, where is thy phenotype?Role of Calcium-Sensing Receptor in Mechanotransducer-Channel-Mediated Ca2+ Influx in Hair Cells of Zebrafish Larvae.Depdc5 knockdown causes mTOR-dependent motor hyperactivity in zebrafish.Craniofacial genetics: Where have we been and where are we going?Zebrafish Models of Rare Hereditary Pediatric Diseases.Preclinical Animal Models for Dravet Syndrome: Seizure Phenotypes, Comorbidities and Drug Screening.Zebrafish as a Model for Drug Screening in Genetic Kidney Diseases.Genetic Renal Diseases: The Emerging Role of Zebrafish ModelsZebrafish Models of Neurodevelopmental Disorders: Past, Present, and FuturePGE production at sites of tissue injury promotes an anti-inflammatory neutrophil phenotype and determines the outcome of inflammation resolution in vivoBMP- and neuropilin 1-mediated motor axon navigation relies on spastin alternative translationZebrafish snai2 mutants fail to phenocopy morphant phenotypesCXCL12 and MYC control energy metabolism to support adaptive responses after kidney injuryRare Genetic Blood Disease Modeling in Zebrafish
P2860
Q47561032-CE77413C-78BA-4DA3-93E3-1F34EFED19C2Q48232072-D08E573E-D032-4296-813F-DF63D71ACD65Q49435329-34B2157E-DAB3-4A35-828C-ECC2D4156940Q49910549-ED9CB0C9-A3EF-46D5-863D-AA988F94C83BQ50114679-09A4B0EB-0C82-4413-AB17-B890998982F1Q50421956-F001EE16-5C3F-444A-9528-07F0DF24AFE5Q54959791-296EA66C-0634-4D2B-ACE0-A96A061D6DADQ55007691-0594CD9C-4179-480F-8500-69231BD743D5Q55014350-D4679580-9D9F-4529-9820-DF875FC986AEQ55137371-36DB8A18-037B-4696-88A5-73116836EF99Q55250191-9EAFC4FF-B146-44D9-B2C9-9F849F015C12Q55266700-9755F951-C2CA-48E7-A8FE-6779A557D176Q55397465-689D29CE-4BD9-4120-8AB4-3E5C2824FF21Q55429704-6716ED4B-D888-44A4-A840-585801B44DADQ55429803-B5CF834A-F2FC-4F84-A795-BC0BF417456CQ55471525-EB2F17F4-1BBA-491F-AFA7-F965A901B597Q55689509-F3E82A8D-FBBC-4E9F-83CB-F9619F06638FQ56992139-77049EC5-3B23-412F-9679-D35219C92E45Q57166914-9A39DBBF-409B-43F7-9AD5-9F12AD81CF09Q57628803-12063AC9-DDC5-45EA-A00F-65FDEE15713AQ58746716-C8EAEE65-3B20-4DC1-8F42-6D8F1EBD872BQ58747994-F886CEB4-3491-4813-AF6D-79B0EA0EC4AFQ58756005-9F44DB96-D7A3-416B-8595-A52002DB4320Q58780870-14AED06A-EEDE-4122-86B0-5F753F05A756
P2860
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
@zh
2017年學術文章
@zh-hant
name
Guidelines for morpholino use in zebrafish.
@en
Guidelines for morpholino use in zebrafish.
@nl
type
label
Guidelines for morpholino use in zebrafish.
@en
Guidelines for morpholino use in zebrafish.
@nl
prefLabel
Guidelines for morpholino use in zebrafish.
@en
Guidelines for morpholino use in zebrafish.
@nl
P2093
P2860
P50
P1433
P1476
Guidelines for morpholino use in zebrafish
@en
P2093
Anming Meng
Brant M Weinstein
Cecilia B Moens
Deborah Yelon
Lalita Ramakrishnan
Nathan D Lawson
Pertti Panula
Rebecca D Burdine
Sharon L Amacher
Stefan Schulte-Merker
P2860
P304
P356
10.1371/JOURNAL.PGEN.1007000
P50
P577
2017-10-19T00:00:00Z