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	121.	Elucidating the genetic basis of an oligogenic birth defect using whole genome sequence data in a non-model organism, Bubalus bubalis. [electronic resource] by Whitacre, Lynsey K Hoff, Jesse L Schnabel, Robert D Albarella, Sara Ciotola, Francesca Peretti, Vincenzo Strozzi, Francesco Ferrandi, Chiara Ramunno, Luigi Sonstegard, Tad S Williams, John L Taylor, Jeremy F Decker, Jared E Producer: 20181024 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	122.	Association of modifiers and other genetic factors explain Marfan syndrome clinical variability. [electronic resource] by Aubart, Melodie Gazal, Steven Arnaud, Pauline Benarroch, Louise Gross, Marie-Sylvie Buratti, Julien Boland, Anne Meyer, Vincent Zouali, Habib Hanna, Nadine Milleron, Olivier Stheneur, Chantal Bourgeron, Thomas Desguerre, Isabelle Jacob, Marie-Paule Gouya, Laurent Génin, Emmanuelle Deleuze, Jean-François Jondeau, Guillaume Boileau, Catherine Producer: 20190328 In: European journal of human genetics : EJHG vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	123.	PRTFDC1 is a genetic modifier of HPRT-deficiency in the mouse. [electronic resource] by Keebaugh, Alaine C Mitchell, Heather A Gaval-Cruz, Meriem Freeman, Kimberly G Edwards, Gaylen L Weinshenker, David Thomas, James W Producer: 20111206 In: PloS one vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	124.	Mutations in epigenetic modifiers in the pathogenesis and therapy of acute myeloid leukemia. [electronic resource] by Abdel-Wahab, Omar Levine, Ross L Producer: 20130704 In: Blood vol. 121 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	125.	A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene. [electronic resource] by Kemaladewi, Dwi U Bassi, Prabhpreet S Erwood, Steven Al-Basha, Dhekra Gawlik, Kinga I Lindsay, Kyle Hyatt, Elzbieta Kember, Rebekah Place, Kara M Marks, Ryan M Durbeej, Madeleine Prescott, Steven A Ivakine, Evgueni A Cohn, Ronald D Producer: 20191126 In: Nature vol. 572 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	Transcript levels of plastin 3 and neuritin 1 modifier genes in spinal muscular atrophy siblings. [electronic resource] by Yener, İnci Hande Topaloglu, Haluk Erdem-Özdamar, Sevim Dayangac-Erden, Didem Producer: 20170510 In: Pediatrics international : official journal of the Japan Pediatric Society vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	127.	In silico search for modifier genes associated with pancreatic and liver disease in Cystic Fibrosis. [electronic resource] by Trouvé, Pascal Génin, Emmanuelle Férec, Claude Producer: 20170825 In: PloS one vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	128.	FAM13A is a modifier gene of cystic fibrosis lung phenotype regulating rhoa activity, actin cytoskeleton dynamics and epithelial-mesenchymal transition. [electronic resource] by Corvol, Harriet Rousselet, Nathalie Thompson, Kristin E Berdah, Laura Cottin, Guillaume Foussigniere, Tobias Longchampt, Elisabeth Fiette, Laurence Sage, Edouard Prunier, Céline Drumm, Mitchell Hodges, Craig A Boëlle, Pierre-Yves Guillot, Loic Producer: 20191112 In: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	129.	Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing. [electronic resource] by Lanktree, Matthew B Haghighi, Amirreza Guiard, Elsa Iliuta, Ioan-Andrei Song, Xuewen Harris, Peter C Paterson, Andrew D Pei, York Producer: 20190916 In: Journal of the American Society of Nephrology : JASN vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	130.	A modifier in the 129S2/SvPasCrl genome is responsible for the viability of Notch1[12f/12f] mice. [electronic resource] by Varshney, Shweta Wei, Hua-Xing Batista, Frank Nauman, Mohd Sundaram, Subha Siminovitch, Katherine Tanwar, Ankit Stanley, Pamela Producer: 20200716 In: BMC developmental biology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	131.	Genome-wide screen for modifiers of Na (+) /K (+) ATPase alleles identifies critical genetic loci. [electronic resource] by Talsma, Aaron D Chaves, John F LaMonaca, Alexandra Wieczorek, Emily D Palladino, Michael J Producer: 20151110 In: Molecular brain vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	132.	Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient mice. [electronic resource] by Alcaraz, Wendy A Chen, Edward Valdes, Phoebe Kim, Eunnie Lo, Yuan Hung Vo, Jennifer Hamilton, Bruce A Producer: 20120120 In: Human molecular genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	133.	Dopamine β Hydroxylase (DBH) is a potential modifier gene associated with Parkinson's disease in Eastern India. [electronic resource] by Ghosh, Arunibha Sadhukhan, Tamal Giri, Subhajit Biswas, Arindam Das, Shyamal Kumar Ray, Kunal Ray, Jharna Producer: 20191227 In: Neuroscience letters vol. 706 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	134.	Causes and consequences of genetic background effects illuminated by integrative genomic analysis. [electronic resource] by Chandler, Christopher H Chari, Sudarshan Tack, David Dworkin, Ian Producer: 20150204 In: Genetics vol. 196 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	135.	Benign infantile convulsions (IC) and subsequent paroxysmal kinesigenic dyskinesia (PKD) in a patient with 16p11.2 microdeletion syndrome. [electronic resource] by Weber, Axel Köhler, Angelika Hahn, Andreas Neubauer, Bernd Müller, Ulrich Producer: 20140623 In: Neurogenetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	136.	A Novel Frizzled-Based Screening Tool Identifies Genetic Modifiers of Planar Cell Polarity in Drosophila Wings. [electronic resource] by Carvajal-Gonzalez, Jose Maria Mulero-Navarro, Sonia Smith, Michael Mlodzik, Marek Producer: 20171109 In: G3 (Bethesda, Md.) vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	137.	A novel pathogenic germline mutation in the adenomatous polyposis coli gene in a Tunisian family with FAP. [electronic resource] by Miladi-Abdennadher, Imen Amouri, Ali Ayadi, Lobna Khabir, Abdelmajid Ellouze, Sameh Tahri, Nabil Frikha, Mounir Sellami-Boudawara, Tahia Mokdad-Gargouri, Raja Producer: 20120110 In: Familial cancer vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	138.	Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes. [electronic resource] by Delplancq, Geoffroy Tarris, Georges Vitobello, Antonio Nambot, Sophie Sorlin, Arthur Philippe, Christophe Carmignac, Virginie Duffourd, Yannis Denis, Charlotte Eicher, Jean Christophe Chevarin, Martin Millat, Gilles Khallouk, Bouchra Rousseau, Thierry Falcon-Eicher, Sylvie Vasiljevic, Alexandre Harizay, Fara T Thauvin-Robinet, Christel Faivre, Laurence Kuentz, Paul Producer: 20210106 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 184 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	139.	Initial interrogation, confirmation and fine mapping of modifying genes: STAT3, IL1B and IFNGR1 determine cystic fibrosis disease manifestation. [electronic resource] by Labenski, Heike Hedtfeld, Silke Becker, Tim Tümmler, Burkhard Stanke, Frauke Producer: 20120423 In: European journal of human genetics : EJHG vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	140.	K-rasG12V mediated lung tumor models identified three new quantitative trait loci modifying events post-K-ras mutation. [electronic resource] by Saito, Hiromitsu Suzuki, Noboru Producer: 20141201 In: Biochemical and biophysical research communications vol. 452 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 262 results.