PubMed (OMIM) for id: 2767

Year	Number of Results
1981	1
1991	2
1992	2
1996	1
1998	1
2004	1
2006	1
2007	2
2008	1
2010	1
2013	2
2014	1
2016	2
2024	0

1

Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma.

Ayturk UM, Couto JA, Hann S, Mulliken JB, Williams KL, Huang AY, Fishman SJ, Boyd TK, Kozakewich HP, Bischoff J, Greene AK, Warman ML. Ayturk UM, et al. Am J Hum Genet. 2016 Apr 7;98(4):789-95. doi: 10.1016/j.ajhg.2016.03.009. Am J Hum Genet. 2016. PMID: 27058448 Free PMC article.

2

A G-protein Subunit-α11 Loss-of-Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2).

Gorvin CM, Cranston T, Hannan FM, Rust N, Qureshi A, Nesbit MA, Thakker RV. Gorvin CM, et al. J Bone Miner Res. 2016 Jun;31(6):1200-6. doi: 10.1002/jbmr.2778. Epub 2016 Feb 6. J Bone Miner Res. 2016. PMID: 26729423 Free PMC article.

3

Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization.

Li D, Opas EE, Tuluc F, Metzger DL, Hou C, Hakonarson H, Levine MA. Li D, et al. J Clin Endocrinol Metab. 2014 Sep;99(9):E1774-83. doi: 10.1210/jc.2014-1029. Epub 2014 May 13. J Clin Endocrinol Metab. 2014. PMID: 24823460 Free PMC article.

4

Germline mutations affecting Gα11 in hypoparathyroidism.

Mannstadt M, Harris M, Bravenboer B, Chitturi S, Dreijerink KM, Lambright DG, Lim ET, Daly MJ, Gabriel S, Jüppner H. Mannstadt M, et al. N Engl J Med. 2013 Jun 27;368(26):2532-4. doi: 10.1056/NEJMc1300278. N Engl J Med. 2013. PMID: 23802536 Free PMC article. No abstract available.

5

Mutations affecting G-protein subunit α11 in hypercalcemia and hypocalcemia.

Nesbit MA, Hannan FM, Howles SA, Babinsky VN, Head RA, Cranston T, Rust N, Hobbs MR, Heath H 3rd, Thakker RV. Nesbit MA, et al. N Engl J Med. 2013 Jun 27;368(26):2476-2486. doi: 10.1056/NEJMoa1300253. N Engl J Med. 2013. PMID: 23802516 Free PMC article.

6

Mutations in GNA11 in uveal melanoma.

Van Raamsdonk CD, Griewank KG, Crosby MB, Garrido MC, Vemula S, Wiesner T, Obenauf AC, Wackernagel W, Green G, Bouvier N, Sozen MM, Baimukanova G, Roy R, Heguy A, Dolgalev I, Khanin R, Busam K, Speicher MR, O'Brien J, Bastian BC. Van Raamsdonk CD, et al. N Engl J Med. 2010 Dec 2;363(23):2191-9. doi: 10.1056/NEJMoa1000584. Epub 2010 Nov 17. N Engl J Med. 2010. PMID: 21083380 Free PMC article.

7

G12-G13-LARG-mediated signaling in vascular smooth muscle is required for salt-induced hypertension.

Wirth A, Benyó Z, Lukasova M, Leutgeb B, Wettschureck N, Gorbey S, Orsy P, Horváth B, Maser-Gluth C, Greiner E, Lemmer B, Schütz G, Gutkind JS, Offermanns S. Wirth A, et al. Nat Med. 2008 Jan;14(1):64-8. doi: 10.1038/nm1666. Epub 2007 Dec 16. Nat Med. 2008. PMID: 18084302

8

Thyrocyte-specific Gq/G11 deficiency impairs thyroid function and prevents goiter development.

Kero J, Ahmed K, Wettschureck N, Tunaru S, Wintermantel T, Greiner E, Schütz G, Offermanns S. Kero J, et al. J Clin Invest. 2007 Sep;117(9):2399-407. doi: 10.1172/JCI30380. J Clin Invest. 2007. PMID: 17694176 Free PMC article.

9

Forebrain-specific inactivation of Gq/G11 family G proteins results in age-dependent epilepsy and impaired endocannabinoid formation.

Wettschureck N, van der Stelt M, Tsubokawa H, Krestel H, Moers A, Petrosino S, Schütz G, Di Marzo V, Offermanns S. Wettschureck N, et al. Mol Cell Biol. 2006 Aug;26(15):5888-94. doi: 10.1128/MCB.00397-06. Mol Cell Biol. 2006. PMID: 16847339 Free PMC article.

10

Effects of G-protein mutations on skin color.

Van Raamsdonk CD, Fitch KR, Fuchs H, de Angelis MH, Barsh GS. Van Raamsdonk CD, et al. Nat Genet. 2004 Sep;36(9):961-8. doi: 10.1038/ng1412. Epub 2004 Aug 22. Nat Genet. 2004. PMID: 15322542 Free PMC article.

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