PubMed for id: 6712

Year	Number of Results
1993	1
1994	1
1997	1
1998	4
2000	1
2001	2
2002	3
2003	1
2004	3
2006	2
2007	3
2008	2
2009	1
2010	3
2011	3
2012	7
2013	4
2014	5
2015	3
2016	7
2017	9
2018	10
2019	8
2020	3
2021	12
2022	12
2023	11
2024	2

1

Increased Actin Binding Is a Shared Molecular Consequence of Numerous SCA5 Mutations in β-III-Spectrin.

Atang AE, Keller AR, Denha SA, Avery AW. Atang AE, et al. Cells. 2023 Aug 19;12(16):2100. doi: 10.3390/cells12162100. Cells. 2023. PMID: 37626910 Free PMC article.

2

SPTBN2 Promotes the Progression of Thyroid Cancer by Accelerating G1/S Transition and Inhibiting Apoptosis.

Zhou X, Lin L, Qi Y, Xu M, Xu Q, Wang Y, Qu J. Zhou X, et al. Dis Markers. 2022 Aug 3;2022:2562595. doi: 10.1155/2022/2562595. eCollection 2022. Dis Markers. 2022. PMID: 35968508 Free PMC article.

3

Expanding the β-III Spectrin-Associated Phenotypes toward Non-Progressive Congenital Ataxias with Neurodegeneration.

Sancho P, Andrés-Bordería A, Gorría-Redondo N, Llano K, Martínez-Rubio D, Yoldi-Petri ME, Blumkin L, Rodríguez de la Fuente P, Gil-Ortiz F, Fernández-Murga L, Sánchez-Monteagudo A, Lupo V, Pérez-Dueñas B, Espinós C, Aguilera-Albesa S. Sancho P, et al. Int J Mol Sci. 2021 Mar 2;22(5):2505. doi: 10.3390/ijms22052505. Int J Mol Sci. 2021. PMID: 33801522 Free PMC article.

4

Two novel missense variants in SPTBN2 likely associated with spinocerebellar ataxia type 5.

Bian X, Wang S, Jin S, Xu S, Zhang H, Wang D, Shang W, Wang P. Bian X, et al. Neurol Sci. 2021 Dec;42(12):5195-5203. doi: 10.1007/s10072-021-05204-3. Epub 2021 Apr 2. Neurol Sci. 2021. PMID: 33797620 Free PMC article.

5

β-III-spectrin immunohistochemistry as a potential diagnostic tool with high sensitivity for malignant peripheral nerve sheath tumors.

Hirbe AC, Zhang X, Dahiya S, Godec A, Chrisinger J, Tao Y, Luo J, Gutmann DH. Hirbe AC, et al. Neuro Oncol. 2018 May 18;20(6):858-860. doi: 10.1093/neuonc/noy038. Neuro Oncol. 2018. PMID: 29596596 Free PMC article. No abstract available.

6

A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature.

Al-Muhaizea MA, AlMutairi F, Almass R, AlHarthi S, Aldosary MS, Alsagob M, AlOdaib A, Colak D, Kaya N. Al-Muhaizea MA, et al. Cerebellum. 2018 Jun;17(3):276-285. doi: 10.1007/s12311-017-0893-2. Cerebellum. 2018. PMID: 29196973 Review.

7

Structural basis for high-affinity actin binding revealed by a β-III-spectrin SCA5 missense mutation.

Avery AW, Fealey ME, Wang F, Orlova A, Thompson AR, Thomas DD, Hays TS, Egelman EH. Avery AW, et al. Nat Commun. 2017 Nov 7;8(1):1350. doi: 10.1038/s41467-017-01367-w. Nat Commun. 2017. PMID: 29116080 Free PMC article.

8

Progressive SCAR14 with unclear speech, developmental delay, tremor, and behavioral problems caused by a homozygous deletion of the SPTBN2 pleckstrin homology domain.

Yıldız Bölükbaşı E, Afzal M, Mumtaz S, Ahmad N, Malik S, Tolun A. Yıldız Bölükbaşı E, et al. Am J Med Genet A. 2017 Sep;173(9):2494-2499. doi: 10.1002/ajmg.a.38332. Epub 2017 Jun 21. Am J Med Genet A. 2017. PMID: 28636205

9

A Novel Missense Mutation in the Spectrin Beta Nonerythrocytic 2 Gene Likely Associated with Spinocerebellar Ataxia Type 5.

Liu LZ, Ren M, Li M, Ren YT, Sun B, Sun XS, Chen SY, Li SY, Huang XS. Liu LZ, et al. Chin Med J (Engl). 2016 Oct 20;129(20):2516-2517. doi: 10.4103/0366-6999.191834. Chin Med J (Engl). 2016. PMID: 27748352 Free PMC article. No abstract available.

10

Dysfunction of the β2-spectrin-based pathway in human heart failure.

Smith SA, Hughes LD, Kline CF, Kempton AN, Dorn LE, Curran J, Makara M, Webb TR, Wright P, Voigt N, Binkley PF, Janssen PM, Kilic A, Carnes CA, Dobrev D, Rasband MN, Hund TJ, Mohler PJ. Smith SA, et al. Am J Physiol Heart Circ Physiol. 2016 Jun 1;310(11):H1583-91. doi: 10.1152/ajpheart.00875.2015. Epub 2016 Apr 22. Am J Physiol Heart Circ Physiol. 2016. PMID: 27106045 Free PMC article.

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