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

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

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

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

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

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

Predicting metabolic engineering knockout strategies for chemical production: accounting for competing pathwaysTEPPER, Naama; SHLOMI, Tomer.Bioinformatics (Oxford. Print). 2010, Vol 26, Num 4, pp 536-543, issn 1367-4803, 8 p.Article

Rbpj conditional knockout reveals distinct functions of Notch4/Int3 in mammary gland development and tumorigenesisRAAFAT, A; LAWSON, S; BARGO, S et al.Oncogene (Basingstoke). 2009, Vol 28, Num 2, pp 219-230, issn 0950-9232, 12 p.Article

Progress and prospects : genetic engineering in xenotransplantationLE BAS-BERNARDET, S; ANEGON, I; BLANCHO, G et al.Gene therapy (Basingstoke). 2008, Vol 15, Num 18, pp 1247-1256, issn 0969-7128, 10 p.Article

Increased longevity and refractoriness to Ca²⁺-dependent neurodegeneration in Surf1 knockout miceDELL'AGNELLO, Carlotta; LEO, Sara; AGOSTINO, Alessandro et al.Human molecular genetics (Print). 2007, Vol 16, Num 4, pp 431-444, issn 0964-6906, 14 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

Novel role of NADPH oxidase in ischemic myocardium: a study with Nox2 knockout miceTHIRUNAVUKKARASU, Mahesh; ADLURI, Ram Sudheer; JUHASZ, Bela et al.Functional & integrative genomics (Print). 2012, Vol 12, Num 3, pp 501-514, issn 1438-793X, 14 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

Conditional Mutagenesis in DrosophilaCHING MAN CHOI; VILAIN, Sven; LANGEN, Marion et al.Science (Washington, D.C.). 2009, Vol 324, Num 5923, pp 54-54, issn 0036-8075, 1 p.Article

Null Mutations in LTBP2 Cause Primary Congenital GlaucomaALI, Manir; MCKIBBIN, Martin; GILMOUR, David F et al.American journal of human genetics. 2009, Vol 84, Num 5, pp 664-671, issn 0002-9297, 8 p.Article

Altered gene expression profiles and higher frequency of spontaneous DNA strand breaks in APEX2-null thymusDAN, Yukihiko; OHTA, Yutaka; TSUCHIMOTO, Daisuke et al.DNA repair. 2008, Vol 7, Num 9, pp 1437-1454, issn 1568-7864, 18 p.Article