PubMed for id: 6389

Year	Number of Results
1993	2
1994	3
1995	1
1999	1
2000	2
2002	1
2003	3
2004	3
2005	4
2006	4
2007	4
2008	3
2009	5
2010	8
2011	9
2012	15
2013	16
2014	7
2015	16
2016	20
2017	14
2018	19
2019	18
2020	24
2021	18
2022	32
2023	10
2024	3

1

SDHA Germline Mutations in SDH-Deficient GISTs: A Current Update.

Schipani A, Nannini M, Astolfi A, Pantaleo MA. Schipani A, et al. Genes (Basel). 2023 Mar 4;14(3):646. doi: 10.3390/genes14030646. Genes (Basel). 2023. PMID: 36980917 Free PMC article. Review.

2

PIKE-A Modulates Mitochondrial Metabolism through Increasing SDHA Expression Mediated by STAT3/FTO Axis.

Sun M, Yan Q, Qiao Y, Zhao H, Wang Y, Shan C, Zhang S. Sun M, et al. Int J Mol Sci. 2022 Sep 25;23(19):11304. doi: 10.3390/ijms231911304. Int J Mol Sci. 2022. PMID: 36232604 Free PMC article.

3

Single nucleotide variants of succinate dehydrogenase A gene in renal cell carcinoma.

Kamai T, Higashi S, Murakami S, Arai K, Namatame T, Kijima T, Abe H, Jamiyan T, Ishida K, Shirataki H, Yoshida KI. Kamai T, et al. Cancer Sci. 2021 Aug;112(8):3375-3387. doi: 10.1111/cas.14977. Epub 2021 Jun 17. Cancer Sci. 2021. PMID: 34014604 Free PMC article.

4

Upregulation of SDHA inhibited proliferation, migration, and invasion of clear cell renal cell carcinoma cells via inactivation of the Wnt/β-catenin pathway.

Xu X, Zhang N, Gao R, Wang J, Dai Z, Bi J. Xu X, et al. J Recept Signal Transduct Res. 2022 Apr;42(2):180-188. doi: 10.1080/10799893.2021.1883060. Epub 2021 Feb 18. J Recept Signal Transduct Res. 2022. PMID: 33602019

5

A novel de novo heterozygous pathogenic variant in the SDHA gene results in childhood onset bilateral optic atrophy and cognitive impairment.

Zehavi Y, Saada A, Jabaly-Habib H, Dessau M, Shaag A, Elpeleg O, Spiegel R. Zehavi Y, et al. Metab Brain Dis. 2021 Apr;36(4):581-588. doi: 10.1007/s11011-021-00671-1. Epub 2021 Jan 20. Metab Brain Dis. 2021. PMID: 33471299 Review.

6

Somatic SDHA mutations in paragangliomas in siblings: Case report of 2 cases.

Huang YC, Chang HH, Chen MH, Huang KH, Li AF, Lin CH, Shyr YM, Fang WL. Huang YC, et al. Medicine (Baltimore). 2020 Oct 9;99(41):e22497. doi: 10.1097/MD.0000000000022497. Medicine (Baltimore). 2020. PMID: 33031286 Free PMC article.

7

Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study.

van der Tuin K, Mensenkamp AR, Tops CMJ, Corssmit EPM, Dinjens WN, van de Horst-Schrivers ANA, Jansen JC, de Jong MM, Kunst HPM, Kusters B, Leter EM, Morreau H, van Nesselrooij BMP, Oldenburg RA, Spruijt L, Hes FJ, Timmers HJLM. van der Tuin K, et al. J Clin Endocrinol Metab. 2018 Feb 1;103(2):438-445. doi: 10.1210/jc.2017-01762. J Clin Endocrinol Metab. 2018. PMID: 29177515

8

SDHA mutated paragangliomas may be at high risk of metastasis.

Tufton N, Ghelani R, Srirangalingam U, Kumar AV, Drake WM, Iacovazzo D, Skordilis K, Berney D, Al-Mrayat M, Khoo B, Akker SA. Tufton N, et al. Endocr Relat Cancer. 2017 Jul;24(7):L43-L49. doi: 10.1530/ERC-17-0030. Epub 2017 May 12. Endocr Relat Cancer. 2017. PMID: 28500238 No abstract available.

9

SDHA mutation with dominant transmission results in complex II deficiency with ocular, cardiac, and neurologic involvement.

Courage C, Jackson CB, Hahn D, Euro L, Nuoffer JM, Gallati S, Schaller A. Courage C, et al. Am J Med Genet A. 2017 Jan;173(1):225-230. doi: 10.1002/ajmg.a.37986. Epub 2016 Sep 28. Am J Med Genet A. 2017. PMID: 27683074

10

Good survival outcome of metastatic SDH-deficient gastrointestinal stromal tumors harboring SDHA mutations.

Pantaleo MA, Lolli C, Nannini M, Astolfi A, Indio V, Saponara M, Urbini M, La Rovere S, Gill A, Goldstein D, Ceccarelli C, Santini D, Rossi G, Fiorentino M, Di Scioscio V, Fusaroli P, Mandrioli A, Gatto L, Catena F, Basso U, Ercolani G, Pinna AD, Biasco G. Pantaleo MA, et al. Genet Med. 2015 May;17(5):391-5. doi: 10.1038/gim.2014.115. Epub 2014 Sep 4. Genet Med. 2015. PMID: 25188872 Free article.

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