PubMed for id: 2643756730

Year	Number of Results
2004	1
2006	1
2009	1
2010	2
2011	2
2021	1
2022	1
2023	2
2024	2

1

Functional genetic variants of the disulfidptosis-related INF2 gene predict survival of hepatitis B virus-related hepatocellular carcinoma.

Wei J, Wen Q, Zhan S, Cao J, Jiang Y, Lian J, Mai Y, Qiu M, Liu Y, Chen P, Lin Q, Wei X, Wei Y, Huang Q, Zhang R, He S, Yuan G, Wei Q, Zhou Z, Yu H. Wei J, et al. Carcinogenesis. 2024 Apr 12;45(4):199-209. doi: 10.1093/carcin/bgae003. Carcinogenesis. 2024. PMID: 38270181

2

Phosphorylation of INF2 by AMPK promotes mitochondrial fission and oncogenic function in endometrial cancer.

Ding Y, Lv Z, Cao W, Shi W, He Q, Gao K. Ding Y, et al. Cell Death Dis. 2024 Jan 17;15(1):65. doi: 10.1038/s41419-024-06431-0. Cell Death Dis. 2024. PMID: 38233384 Free PMC article.

3

FBXO7, a tumor suppressor in endometrial carcinoma, suppresses INF2-associated mitochondrial division.

Zhang H, Zhao Y, Wang J, Li J, Xia J, Lin Y, Zhong Y, Cao X, Jin J, Li X, Yang W, Ye M, Jin X. Zhang H, et al. Cell Death Dis. 2023 Jun 21;14(6):368. doi: 10.1038/s41419-023-05891-0. Cell Death Dis. 2023. PMID: 37344480 Free PMC article.

4

INF2 mutations in patients with a broad phenotypic spectrum of Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.

Park JH, Kwon HM, Nam DE, Kim HJ, Nam SH, Kim SB, Choi BO, Chung KW. Park JH, et al. J Peripher Nerv Syst. 2023 Mar;28(1):108-118. doi: 10.1111/jns.12530. Epub 2023 Jan 20. J Peripher Nerv Syst. 2023. PMID: 36637069

5

Role of formin INF2 in human diseases.

Zhao Y, Zhang H, Wang H, Ye M, Jin X. Zhao Y, et al. Mol Biol Rep. 2022 Jan;49(1):735-746. doi: 10.1007/s11033-021-06869-x. Epub 2021 Oct 26. Mol Biol Rep. 2022. PMID: 34698992 Review.

6

Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis.

Boyer O, Benoit G, Gribouval O, Nevo F, Tête MJ, Dantal J, Gilbert-Dussardier B, Touchard G, Karras A, Presne C, Grunfeld JP, Legendre C, Joly D, Rieu P, Mohsin N, Hannedouche T, Moal V, Gubler MC, Broutin I, Mollet G, Antignac C. Boyer O, et al. J Am Soc Nephrol. 2011 Feb;22(2):239-45. doi: 10.1681/ASN.2010050518. Epub 2011 Jan 21. J Am Soc Nephrol. 2011. PMID: 21258034 Free PMC article.

7

Variable renal phenotype in a family with an INF2 mutation.

Lee HK, Han KH, Jung YH, Kang HG, Moon KC, Ha IS, Choi Y, Cheong HI. Lee HK, et al. Pediatr Nephrol. 2011 Jan;26(1):73-6. doi: 10.1007/s00467-010-1644-5. Epub 2010 Aug 28. Pediatr Nephrol. 2011. PMID: 20803156

8

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.

Brown EJ, Schlöndorff JS, Becker DJ, Tsukaguchi H, Tonna SJ, Uscinski AL, Higgs HN, Henderson JM, Pollak MR. Brown EJ, et al. Nat Genet. 2010 Jan;42(1):72-6. doi: 10.1038/ng.505. Epub 2009 Dec 20. Nat Genet. 2010. PMID: 20023659 Free PMC article.

9

INF2 Is a WASP homology 2 motif-containing formin that severs actin filaments and accelerates both polymerization and depolymerization.

Chhabra ES, Higgs HN. Chhabra ES, et al. J Biol Chem. 2006 Sep 8;281(36):26754-67. doi: 10.1074/jbc.M604666200. Epub 2006 Jul 3. J Biol Chem. 2006. PMID: 16818491 Free article.

10

Formin' new ideas about actin filament generation.

Bindschadler M, McGrath JL. Bindschadler M, et al. Proc Natl Acad Sci U S A. 2004 Oct 12;101(41):14685-6. doi: 10.1073/pnas.0406317101. Epub 2004 Oct 4. Proc Natl Acad Sci U S A. 2004. PMID: 15466701 Free PMC article. No abstract available.

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