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Results 1 to 25 of 556

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Inversion-induced disruption of the Hoxd cluster leads to the partition of regulatory landscapesSPITZ, Francois; HERKENNE, Carole; MORRIS, Michael A et al.Nature genetics. 2005, Vol 37, Num 8, pp 889-893, issn 1061-4036, 5 p.Article

To knockout in 129 or in C57BL/6: that is the questionSEONG, Eunju; SAUNDERS, Thomas L; STEWART, Colin L et al.Trends in genetics (Regular ed.). 2004, Vol 20, Num 2, pp 59-62, issn 0168-9525, 4 p.Article

Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null allelesWESTMAN, Julia S; HELLBERG, Asa; PEYRARD, Thierry et al.Transfusion (Philadelphia, PA). 2014, Vol 54, Num 7, pp 1831-1835, issn 0041-1132, 5 p.Article

Functional muscle analysis of the Tcap knockout mouseMARKERT, C. D; MEANEY, M. P; BROWN, M et al.Human molecular genetics (Print). 2010, Vol 19, Num 11, pp 2268-2283, issn 0964-6906, 16 p.Article

Generation of C57BL/6 knockout mice using C3H × BALB/c blastocystsPACHOLCZYK, Gabriela; SUHAG, Rupali; MAZUREK, Magdalena et al.BioTechniques. 2008, Vol 44, Num 3, issn 0736-6205, 413-416 [3 p.]Article

Branching and nucleokinesis defects in migrating interneurons derived from Doublecortin knockout miceKAPPELER, Caroline; SAILLOUR, Yoann; FRANCIS, Fiona et al.Human molecular genetics (Print). 2006, Vol 15, Num 9, pp 1387-1400, issn 0964-6906, 14 p.Article

AP-2α knockout mice exhibit optic cup patterning defects and failure of optic stalk morphogenesisBASSETT, Erin A; WILLIAMS, Trevor; ZACHARIAS, Amanda L et al.Human molecular genetics (Print). 2010, Vol 19, Num 9, pp 1791-1804, issn 0964-6906, 14 p.Article

Complexin 1 knockout mice exhibit marked deficits in social behaviours but appear to be cognitively normalDREW, Cheney J. G; KYD, Rachel J; MORTON, A. Jennifer et al.Human molecular genetics (Print). 2007, Vol 16, Num 19, pp 2288-2305, issn 0964-6906, 18 p.Article

Altered visual function and interneuron survival in Atrx knockout mice : inference for the human syndromeMEDINA, Chantal F; MAZEROLLE, Chantal; YAPING WANG et al.Human molecular genetics (Print). 2009, Vol 18, Num 5, pp 966-977, issn 0964-6906, 12 p.Article

An Actn3 knockout mouse provides mechanistic insights into the association between α-actinin-3 deficiency and human athletic performanceMACARTHUR, Daniel G; SETO, Jane T; COONEY, Gregory J et al.Human molecular genetics (Print). 2008, Vol 17, Num 8, pp 1076-1086, issn 0964-6906, 11 p.Article

The JR blood group system (ISBT 032): molecular characterization of three new null allelesHUE-ROYE, Kim; LOMAS-FRANCIS, Christine; COGHLAN, Gail et al.Transfusion (Philadelphia, PA). 2013, Vol 53, Num 7, pp 1575-1579, issn 0041-1132, 5 p.Article

ABCG2 null alleles define the Jr(a―) blood group phenotypeZELINSKI, Teresa; COGHLAN, Gail; LIU, Xiao-Qing et al.Nature genetics. 2012, Vol 44, Num 2, pp 131-132, issn 1061-4036, 2 p.Article

Less Is More: Unveiling the Functional Core of Hematopoietic Stem Cells through Knockout MiceROSSI, Lara; LIN, Kuanyin K; BOLES, Nathan C et al.Cell stem cell. 2012, Vol 11, Num 3, pp 302-317, issn 1934-5909, 16 p.Article

Multiple knockout analysis of genetic robustness in the yeast metabolic networkDEUTSCHER, David; MEILIJSON, Isaac; KUPIEC, Martin et al.Nature genetics. 2006, Vol 38, Num 9, pp 993-998, issn 1061-4036, 6 p.Article

Direct detection of null alleles in SNP genotyping dataCARLSON, Christopher S; SMITH, Joshua D; STANAWAY, Ian B et al.Human molecular genetics (Print). 2006, Vol 15, Num 12, pp 1931-1937, issn 0964-6906, 7 p.Article

Changes in neuronal migration in neocortex of connexin43 null mutant miceFUSHIKI, Shinji; PEREZ VELAZQUEZ, Jose Luis; LIANG ZHANG et al.Journal of neuropathology and experimental neurology. 2003, Vol 62, Num 3, pp 304-314, issn 0022-3069, 11 p.Article

Discovery of a null mutation in a human trace amine receptor geneVANTI, William B; MUGLIA, Pierandrea; NGUYEN, Tuan et al.Genomics (San Diego, Calif.). 2003, Vol 82, Num 5, pp 531-536, issn 0888-7543, 6 p.Article

Essential roles of Jab1 in cell survival, spontaneous DNA damage and DNA repairTIAN, L; PENG, G; LOZANO, G et al.Oncogene (Basingstoke). 2010, Vol 29, Num 46, pp 6125-6137, issn 0950-9232, 13 p.Article

Yeast knockout-and-rescue system for identification of eIF4E-family members possessing eIE4E-activityJOSHI, Bhavesh; ROBALINO, Javier; SCHOTT, Eric J et al.BioTechniques. 2002, Vol 33, Num 2, pp 392-401, issn 0736-6205, 8 p.Article

Quenching accumulation of toxic galactose-1-phosphate as a system to select disruption of protein-protein interactions in vivoGUNDE, Tea; TANNER, Stefan; AUF DER MAUR, Adrian et al.BioTechniques. 2004, Vol 37, Num 5, pp 844-852, issn 0736-6205, 9 p.Article

P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems : Twenty Years since the Cloning of the Blood Group GenesWESTMAN, Julia S; HELLBERG, Asa; PEYRARD, Thierry et al.Transfusion (Philadelphia, PA). 2013, Vol 53, Num 11, pp 2928-2939, issn 0041-1132, 12 p., 2Article

Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiPLIHONG ZHAO; LONGO-GUESS, Chantal; HARRIS, Belinda S et al.Nature genetics. 2005, Vol 37, Num 9, pp 974-979, issn 1061-4036, 6 p.Article

Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cellsGARCIA AROCENA, Dolores; IWAHASHI, Christine K; WON, Nelly et al.Human molecular genetics (Print). 2005, Vol 14, Num 23, pp 3661-3671, issn 0964-6906, 11 p.Article

Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycleTHOMPSON, Debra A; JANECKE, Andreas R; AYUSO, Carmen et al.Human molecular genetics (Print). 2005, Vol 14, Num 24, pp 3865-3875, issn 0964-6906, 11 p.Article

Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivoMIENTJES, Edwin J; WILLEMSEN, Rob; NELSON, David L et al.Human molecular genetics (Print). 2004, Vol 13, Num 13, pp 1291-1302, issn 0964-6906, 12 p.Article

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