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Results for
""Chromosomes, Human, Pair 3""[mesh_terms]

24 Results

Searching titles within these results

Meta-analysis of 4 coronary heart disease genome-wide linkage studies confirms a susceptibility locus on chromosome 3q.

Benedetta D Chiodini, Cathryn M Lewis

Arteriosclerosis, thrombosis, and vascular biology 2004;23(10):1863-8

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Abstract

Mutations in BTD causing biotinidase deficiency.

J Hymes, C M Stanley, B Wolf

Human mutation 2002;18(5):375-81

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Hailey-Hailey disease exacerbated by multiple pregnancies: case report and review of the literature.

Shakuntala H Mauzo, Daryl J Sulit

Dermatology online journal 2015;20(10):13030/qt9zj522bb

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Alterations of the FHIT gene in human hepatocellular carcinoma.

B Z Yuan, C Keck-Waggoner, D B Zimonjic, S S Thorgeirsson, N C Popescu

Cancer research 2000;60(4):1049-53

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Familial benign hypocalciuric hypercalcemia.

Ghada El-Hajj Fuleihan

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2003;17 Suppl 2():N51-6

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Chromosome 3p and breast cancer.

Qifeng Yang, Goro Yoshimura, Ichiro Mori, Takeo Sakurai, Kennichi Kakudo

Journal of human genetics 2002;47(9):453-9

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Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20.

Aurélien Juven, Sophie Nambot, Amélie Piton, Nolwenn Jean-Marçais, Alice Masurel, Patrick Callier, Nathalie Marle, Anne-Laure Mosca-Boidron, Paul Kuentz, Christophe Philippe, Martin Chevarin, Yannis Duffourd, Elodie Gautier, Arnold Munnich, Marlène Rio, Sophie Rondeau, Salima El Chehadeh, Élise Schaefer, Bénédicte Gérard, Sonia Bouquillon, Catherine Vincent Delorme, Christine Francannet, Fanny Laffargue, Laetitia Gouas, Bertrand Isidor, Marie Vincent, Sophie Blesson, Fabienne Giuliano, Olivier Pichon, Cédric Le Caignec, Hubert Journel, Laurence Perrin-Sabourin, Jennifer Fabre-Teste, Dominique Martin, Gaelle Vieville, Klaus Dieterich, Didier Lacombe, Anne-Sophie Denommé-Pichon, Christel Thauvin-Robinet, Laurence Faivre

European journal of human genetics : EJHG 2021;28(8):1044-1055

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Cytogenetics and molecular genetics of lung cancer.

Yasuhiro Mitsuuchi, Joseph R Testa

American journal of medical genetics 2003;115(3):183-8

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Genetics of primary intraocular tumors.

Nisha Nagarkatti-Gude, Yujuan Wang, Mohammad Javed Ali, Santosh G Honavar, Martine J Jager, Chi-Chao Chan

Ocular immunology and inflammation 2013;20(4):244-54

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Genetic factors in diabetic nephropathy.

Barry I Freedman, Meredith Bostrom, Pirouz Daeihagh, Donald W Bowden

Clinical journal of the American Society of Nephrology : CJASN 2007;2(6):1306-16

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Rs710521[A] on chromosome 3q28 close to TP63 is associated with increased urinary bladder cancer risk.

Marie-Louise Lehmann, Silvia Selinski, Meinolf Blaszkewicz, Michael Orlich, Daniel Ovsiannikov, Oliver Moormann, Christoph Guballa, Alexander Kress, Michael C Truss, Holger Gerullis, Thomas Otto, Dimitri Barski, Günter Niegisch, Peter Albers, Sebastian Frees, Walburgis Brenner, Joachim W Thüroff, Miriam Angeli-Greaves, Thilo Seidel, Gerhard Roth, Holger Dietrich, Rainer Ebbinghaus, Hans M Prager, Hermann M Bolt, Michael Falkenstein, Anna Zimmermann, Torsten Klein, Thomas Reckwitz, Hermann C Roemer, Dietrich Löhlein, Wobbeke Weistenhöfer, Wolfgang Schöps, Anwer E Beg, Muhammad Aslam, Gergely Bánfi, Imre Romics, Katja Ickstadt, Holger Schwender, Andreas Winterpacht, Jan G Hengstler, Klaus Golka

Archives of toxicology 2011;84(12):967-78

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Genetic association of the CCR5 region with lipid levels in at-risk cardiovascular patients.

Craig L Hyde, Alan Macinnes, Frances A Sanders, John F Thompson, Richard A Mazzarella, Ole Faergeman, Diederik F van Wijk, Linda Wood, Maruja Lira, Sara A Paciga

Circulation. Cardiovascular genetics 2010;3(2):162-8

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Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load.

Paul J McLaren, Cedric Coulonges, István Bartha, Tobias L Lenz, Aaron J Deutsch, Arman Bashirova, Susan Buchbinder, Mary N Carrington, Andrea Cossarizza, Judith Dalmau, Andrea De Luca, James J Goedert, Deepti Gurdasani, David W Haas, Joshua T Herbeck, Eric O Johnson, Gregory D Kirk, Olivier Lambotte, Ma Luo, Simon Mallal, Daniëlle van Manen, Javier Martinez-Picado, Laurence Meyer, José M Miro, James I Mullins, Niels Obel, Guido Poli, Manjinder S Sandhu, Hanneke Schuitemaker, Patrick R Shea, Ioannis Theodorou, Bruce D Walker, Amy C Weintrob, Cheryl A Winkler, Steven M Wolinsky, Soumya Raychaudhuri, David B Goldstein, Amalio Telenti, Paul I W de Bakker, Jean-François Zagury, Jacques Fellay

Proceedings of the National Academy of Sciences of the United States of America 2016;112(47):14658-63

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Genome-wide linkage and positional candidate gene study of blood pressure response to dietary potassium intervention: the genetic epidemiology network of salt sensitivity study.

Tanika N Kelly, James E Hixson, Dabeeru C Rao, Hao Mei, Treva K Rice, Cashell E Jaquish, Lawrence C Shimmin, Karen Schwander, Chung-Shuian Chen, Depei Liu, Jichun Chen, Concetta Bormans, Pramila Shukla, Naveed Farhana, Colin Stuart, Paul K Whelton, Jiang He, Dongfeng Gu

Circulation. Cardiovascular genetics 2011;3(6):539-47

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Evidence for defective retinoid transport and function in late onset Alzheimer's disease.

Ann B Goodman, Arthur B Pardee

Proceedings of the National Academy of Sciences of the United States of America 2003;100(5):2901-5

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Results: 1 – 15 / 24

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Results for ""Chromosomes, Human, Pair 3""[mesh_terms]

Meta-analysis of 4 coronary heart disease genome-wide linkage studies confirms a susceptibility locus on chromosome 3q.

Mutations in BTD causing biotinidase deficiency.

Hailey-Hailey disease exacerbated by multiple pregnancies: case report and review of the literature.

Alterations of the FHIT gene in human hepatocellular carcinoma.

Familial benign hypocalciuric hypercalcemia.

Chromosome 3p and breast cancer.

Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20.

Cytogenetics and molecular genetics of lung cancer.

Genetics of primary intraocular tumors.

Genetic factors in diabetic nephropathy.

Rs710521[A] on chromosome 3q28 close to TP63 is associated with increased urinary bladder cancer risk.

Genetic association of the CCR5 region with lipid levels in at-risk cardiovascular patients.

Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load.

Genome-wide linkage and positional candidate gene study of blood pressure response to dietary potassium intervention: the genetic epidemiology network of salt sensitivity study.

Evidence for defective retinoid transport and function in late onset Alzheimer's disease.

Results for
""Chromosomes, Human, Pair 3""[mesh_terms]