A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells
about
The histone demethylase Jarid1b ensures faithful mouse development by protecting developmental genes from aberrant H3K4me3MEGF8 is a modifier of BMP signaling in trigeminal sensory neuronsDisruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases.Cyclin-dependent kinase 16/PCTAIRE kinase 1 is activated by cyclin Y and is essential for spermatogenesisUncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndromeSemaphorin 7A promotes axon outgrowth through integrins and MAPKsThe tumor susceptibility gene TMEM127 is mutated in renal cell carcinomas and modulates endolysosomal functionDisruption of the langerin/CD207 gene abolishes Birbeck granules without a marked loss of Langerhans cell functionNociceptor-specific gene deletion reveals a major role for Nav1.7 (PN1) in acute and inflammatory painDisruption of the mouse mTOR gene leads to early postimplantation lethality and prohibits embryonic stem cell developmentEssential role for mitochondrial thioredoxin reductase in hematopoiesis, heart development, and heart functionMaspin is not required for embryonic development or tumour suppressionThe miR-144/451 locus is required for erythroid homeostasisLrp5 functions in bone to regulate bone massTargeted disruption of SPI3/Serpinb6 does not result in developmental or growth defects, leukocyte dysfunction, or susceptibility to strokeTargeted transgenesisCaspase-2 activation in the absence of PIDDosome formationDual functions for the endoplasmic reticulum calcium sensors STIM1 and STIM2 in T cell activation and toleranceCalcitonin receptor plays a physiological role to protect against hypercalcemia in miceEssential function of p300 acetyltransferase activity in heart, lung and small intestine formationDeletion of calcineurin and myocyte enhancer factor 2 (MEF2) binding domain of Cabin1 results in enhanced cytokine gene expression in T cellsInterference with immunoglobulin (Ig)alpha immunoreceptor tyrosine-based activation motif (ITAM) phosphorylation modulates or blocks B cell development, depending on the availability of an Igbeta cytoplasmic tailHepatic cholesterol metabolism and resistance to dietary cholesterol in LXRbeta-deficient miceIdentification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging techniqueExtended Synaptotagmin (ESyt) Triple Knock-Out Mice Are Viable and Fertile without Obvious Endoplasmic Reticulum DysfunctionAndrogen receptor (AR) pathophysiological roles in androgen-related diseases in skin, bone/muscle, metabolic syndrome and neuron/immune systems: lessons learned from mice lacking AR in specific cellsStrategies to achieve conditional gene mutation in miceA Mouse Model for Imprinting of the Human Retinoblastoma GeneRgnef (p190RhoGEF) knockout inhibits RhoA activity, focal adhesion establishment, and cell motility downstream of integrinsTRIM3 regulates the motility of the kinesin motor protein KIF21BComparison of phenotypes between different vangl2 mutants demonstrates dominant effects of the Looptail mutation during hair cell developmentThe Mammalian Orthologs of Drosophila Lgd, CC2D1A and CC2D1B, Function in the Endocytic Pathway, but Their Individual Loss of Function Does Not Affect Notch SignallingThe circadian clock coordinates ribosome biogenesisA hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal systemA critical function of Mad2l2 in primordial germ cell development of miceDeregulation of the protocadherin gene FAT1 alters muscle shapes: implications for the pathogenesis of facioscapulohumeral dystrophyPancreatic cancer modeling using retrograde viral vector delivery and in vivo CRISPR/Cas9-mediated somatic genome editing.A causative link between inner ear defects and long-term striatal dysfunction.Conditional disruption of IkappaB kinase 2 fails to prevent obesity-induced insulin resistanceLiver disintegration in the mouse embryo caused by deficiency in the RNA-editing enzyme ADAR1
P2860
Q21092410-2C766AF5-94F4-4C30-A844-4B7F33AA7440Q21128782-A703220D-A455-4B87-9269-60E116BE5FFFQ22255523-C08D6F84-174C-4507-801D-9EEBBA9EE307Q24300150-C178D22E-6DA1-4E89-87F0-D28E70A80C3DQ24301073-B84EE874-F6C6-4C7F-A42A-B75C49B19A55Q24310744-4DA76F53-3DA9-4CFE-B7E7-F2999FD2D8ECQ24312781-64DA1F0E-595F-4163-9317-402EE6F19EA7Q24558690-4D12070F-63B5-48FC-B89B-78DDCAAEF749Q24562888-3E0AEC44-DB64-4C43-90AB-FB4F3FEABF6CQ24563399-F41AC0CE-2578-4138-94FA-DD9C68D1BE1EQ24563493-BE038145-65B7-4DBD-AF36-1404C6A6B051Q24612315-08538746-A8AA-4069-82F0-9DD71C63FF0BQ24615624-BC7591BF-DED0-4C8D-8434-A3CE6B513B68Q24615653-3CF58167-D3A1-48E9-BB0B-C29D8B67FB94Q24623219-411FD220-7684-46DA-B1B3-95F79EDEA4C8Q24631266-F3A035C1-E905-438B-8ED4-750558F88B03Q24641934-8AD9B597-9F8D-477D-A688-C25CCD66DA72Q24642248-B2AC43D2-0DB6-420B-9FAB-73B9DC53E46EQ24646547-61AFD4DE-CD2B-45D7-BE19-B2DF75C09759Q24672302-17C45D46-4604-4FB7-8A6F-9ED9D6B18A32Q24674634-5D154878-B8F5-424F-B881-9D5F255FA780Q24675475-52A3AD56-D698-4D29-A66D-2B849E96707EQ24681140-BF3E73DB-5F87-473E-AC6E-845D0E7F2592Q24808964-3B3E1A70-ECD5-4BDB-9E0B-F055B7F1D9C8Q26269815-AA2171BE-A0AA-45BB-8F7E-F98EB94E258AQ27013914-5B6CCFE5-4F35-4A2B-A1FE-62BF878BC8CCQ27023444-8CDB6245-F163-410A-AC47-73FE456A86E8Q27301081-6930CBD3-9D94-4D0B-BB4F-0CBE1A3783B3Q27302153-BA6BFCC2-E0C8-4B76-A1BD-08AD26BBDEA3Q27305209-6BF0FA18-6DA6-4317-94EA-0CBCE6FDD0C3Q27308779-14FDAAE4-E9E9-4D34-8A17-7365C381D2F3Q27309437-B980DBC3-52E9-46A5-ADE4-9B945AC1E70DQ27318396-DA11CDFF-BBC8-4D8B-BE44-3E9055DA47A8Q27318572-B988A109-5EE3-4D22-9C05-2EDEA7882D21Q27320769-D56113AC-C0CA-4365-87FC-B4A8FB6CFCCCQ27322323-B868E203-3C52-4539-B851-35243CDFDC41Q27322787-B3DA5E53-8990-4FAE-84C4-EDB13FE154C4Q27331947-4AFE4FF1-D3FB-4448-A583-D0487DA8499BQ28167026-871FE9A1-DA88-46E1-B133-BF8FE2F2422EQ28184194-F212DA2B-2498-40A2-98AE-ECF88C3EA9C5
P2860
A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells
description
1995 nî lūn-bûn
@nan
1995 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
A cre-transgenic mouse strain ...... cluding deletion in germ cells
@ast
A cre-transgenic mouse strain ...... cluding deletion in germ cells
@en
type
label
A cre-transgenic mouse strain ...... cluding deletion in germ cells
@ast
A cre-transgenic mouse strain ...... cluding deletion in germ cells
@en
prefLabel
A cre-transgenic mouse strain ...... cluding deletion in germ cells
@ast
A cre-transgenic mouse strain ...... cluding deletion in germ cells
@en
P2860
P3181
P356
P1476
A cre-transgenic mouse strain ...... cluding deletion in germ cells
@en
P2093
P2860
P304
P3181
P356
10.1093/NAR/23.24.5080
P407
P577
1995-12-25T00:00:00Z