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Mouse model implicates GNB3 duplication in a childhood obesity syndrome.

Goldlust IS, Hermetz KE, Catalano LM, Barfield RT, Cozad R, Wynn G, Ozdemir AC, Conneely KN, Mulle JG, Dharamrup S, Hegde MR, Kim KH, Angle B, Colley A, Webb AE, Thorland EC, Ellison JW, Rosenfeld JA, Ballif BC, Shaffer LG, Demmer LA; Unique Rare Chromosome Disorder Support Group, Rudd MK.

Proc Natl Acad Sci U S A. 2013 Sep 10;110(37):14990-4. doi: 10.1073/pnas.1305999110. Epub 2013 Aug 26.


Ablation of the GNB3 gene in mice does not affect body weight, metabolism or blood pressure, but causes bradycardia.

Ye Y, Sun Z, Guo A, Song LS, Grobe JL, Chen S.

Cell Signal. 2014 Nov;26(11):2514-20. doi: 10.1016/j.cellsig.2014.07.030. Epub 2014 Aug 2.


A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men.

Lacaria M, Saha P, Potocki L, Bi W, Yan J, Girirajan S, Burns B, Elsea S, Walz K, Chan L, Lupski JR, Gu W.

PLoS Genet. 2012;8(5):e1002713. doi: 10.1371/journal.pgen.1002713. Epub 2012 May 24.


[Genetic diagnosis and analysis of related genes for a pedigree with 2p25 and 12p13 cryptic rearrangements].

Tu X, Zeng J, Cong X, Yan A, Lin Y, Zhang X, Qiu L, Zhou Y, Lan F.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Aug;31(4):444-8. doi: 10.3760/cma.j.issn.1003-9406.2014.04.007. Chinese.


Studies of the association of the GNB3 825C>T polymorphism with components of the metabolic syndrome in white Danes.

Andersen G, Overgaard J, Albrechtsen A, Glümer C, Borch-Johnsen K, Jørgensen T, Hansen T, Pedersen O.

Diabetologia. 2006 Jan;49(1):75-82. Epub 2005 Nov 12.


G-protein beta3 subunit (GNB3) gene polymorphisms and cardiovascular disease: the Ludwigshafen Risk and Cardiovascular Health (LURIC) study.

Renner W, Hoffmann MM, Grünbacher G, Winkelmann BR, Boehm BO, März W.

Atherosclerosis. 2007 May;192(1):108-12. Epub 2006 Aug 14.


Effects of the C825T polymorphism of the GNB3 gene on body adiposity and blood pressure in fertile and menopausal women: a population-based study.

Casiglia E, Tikhonoff V, Caffi S, Martini B, Guidotti F, Bolzon M, Bascelli A, D'Este D, Mazza A, Pessina AC.

J Hypertens. 2008 Feb;26(2):238-43. doi: 10.1097/HJH.0b013e3282f2b90c.


Identification and ethnic distribution of major haplotypes in the gene GNB3 encoding the G-protein beta3 subunit.

Rosskopf D, Manthey I, Siffert W.

Pharmacogenetics. 2002 Apr;12(3):209-20.


Gene-environment interaction and the GNB3 gene in the Atherosclerosis Risk in Communities study.

Grove ML, Morrison A, Folsom AR, Boerwinkle E, Hoelscher DM, Bray MS.

Int J Obes (Lond). 2007 Jun;31(6):919-26. Epub 2007 Feb 13.


Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.

Blumenthal I, Ragavendran A, Erdin S, Klei L, Sugathan A, Guide JR, Manavalan P, Zhou JQ, Wheeler VC, Levin JZ, Ernst C, Roeder K, Devlin B, Gusella JF, Talkowski ME.

Am J Hum Genet. 2014 Jun 5;94(6):870-83. doi: 10.1016/j.ajhg.2014.05.004.


Multivariate meta-analysis of the association of G-protein beta 3 gene (GNB3) haplotypes with cardiovascular phenotypes.

Pereira TV, Kimura L, Suwazono Y, Nakagawa H, Daimon M, Oizumi T, Kayama T, Kato T, Li L, Chen S, Gu D, Renner W, März W, Yamada Y, Bagos PG, Mingroni-Netto RC.

Mol Biol Rep. 2014 May;41(5):3113-25. doi: 10.1007/s11033-014-3171-0. Epub 2014 Jan 30.


The -308G/A of Tumor Necrosis Factor (TNF)-α and 825C/T of Guanidine Nucleotide Binding Protein 3 (GNB3) are associated with the onset of acute myocardial infarction and obesity in Taiwan.

Chang WT, Wang YC, Chen CC, Zhang SK, Liu CH, Chang FH, Hsu LS.

Int J Mol Sci. 2012;13(2):1846-57. doi: 10.3390/ijms13021846. Epub 2012 Feb 9.


Two New Cases of 1p21.3 Deletions and an Unbalanced Translocation t(8;12) among Individuals with Syndromic Obesity.

D'Angelo CS, Moller Dos Santos MF, Alonso LG, Koiffmann CP.

Mol Syndromol. 2015 Jul;6(2):63-70. doi: 10.1159/000371600. Epub 2015 Jan 28.


Intellectual disability secondary to a 16p13 duplication in a 1;16 translocation. Extended phenotype in a four-generation family.

Mohamed AM, Kamel A, Mahmoud W, Abdelraouf E, Meguid N.

Am J Med Genet A. 2015 Jan;167A(1):128-36. doi: 10.1002/ajmg.a.36834. Epub 2014 Nov 25.


A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections.

Xu X, Xu Q, Zhang Y, Zhang X, Cheng T, Wu B, Ding Y, Lu P, Zheng J, Zhang M, Qiu Z, Yu X.

BMC Med Genet. 2012 Aug 21;13:75. doi: 10.1186/1471-2350-13-75.


Obesity reveals an association between blood pressure and the G-protein beta3-subunit gene: a study of female dizygotic twins.

Dong Y, Zhu H, Wang X, Dalageorgou C, Carter N, Spector TD, Snieder H.

Pharmacogenetics. 2004 Jul;14(7):419-27.


Chromosomal rearrangements in patients with clinical features of Silver-Russell syndrome.

Fokstuen S, Kotzot D.

Am J Med Genet A. 2014 Jun;164A(6):1595-605. doi: 10.1002/ajmg.a.36464. Epub 2014 Mar 24.

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