| 1 | GOLGA8B, MYH11
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| Non-coding variants in MYH11, FZD3, and SORCS3 are associated with dementia in women
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| Blue EE, Thornton TA, Kooperberg C, Liu S, Wactawski-Wende J, Manson J, Kuller L, Hayden K, Reiner AP.
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| Alzheimers Dement. Feb;17(2):215-225. doi: 10.1002/alz.12181. Epub 2020 Sep 23. 2021
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| 2 | MYH11, MYLK, PKD1, SOD3, TAGLN
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| Comparison of gene expression profiles in aortic dissection and normal human aortic tissues.
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| Zhang L, Yu C, Chang Q, Luo X, Qiu J, Liu S.
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| Biomed Rep 5(4):421-427. Epub 2016 Aug 9.
2016
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| 3 | MYH11, TAAD1
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| Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections.
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| Kuang SQ, Guo DC, Prakash SK, McDonald ML, Johnson RJ, Wang M, Regalado ES, Russell L, Cao JM, Kwartler C, Fraivillig K, Coselli JS, Safi HJ, Estrera AL, Leal SM, Lemaire SA, Belmont JW, Milewicz DM; GenTAC Investigators.
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| PLoS Genet 7(6):e1002118. Epub 2011 Jun 16.
2011
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| 4 | MYH11
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| Prognostic value of minimal residual disease by real-time quantitative PCR in acute myeloid leukemia with CBFB-MYH11 rearrangement: the French experience.
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| Guièze R, Renneville A, Cayuela JM, Abdelali RB, Boissel N, de Botton S, Rubio MT, Mazingue F, Macintyre EA, Cheok M, Sigaux F, Fenaux P, Dombret H, Preudhomme C.
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| Leukemia 24(7):1386-8. Epub 2010 May 27. No abstract available.
2010
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| 5 | MYH11
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| Unregulated smooth-muscle myosin in human intestinal neoplasia.
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| Alhopuro P, Phichith D, Tuupanen S, Sammalkorpi H, Nybondas M, Saharinen J, Robinson JP, Yang Z, Chen LQ, Orntoft T, Mecklin JP, JŠrvinen H, Eng C, Moeslein G, Shibata D, Houlston RS, Lucassen A, Tomlinson IP, Launonen V, RistimŠki A, Arango D, Karhu A, Sweeney HL, Aaltonen LA.
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| Proc Natl Acad Sci U S A 105(14):5513-8. Epub 2008 Apr 7. 2008
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| 6 | ACTA2, ACTC1, ASD3, ASD5, CMD1R, CMD1S, CMH1, CMH6, CMHNE, MYBPC3, MYH11, MYH6, MYH7, TAAD1, TAAD4
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| Mutations in sarcomeric protein genes not only lead to cardiomyopathy but also to congenital cardiovascular malformations.
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| Wessels MW, Willems PJ.
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| Clin Genet 74(1):16-9. Epub 2008 Apr 8. 2008
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| 7 | MYH11
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| Mutation analysis of MYH11 in acute myeloid leukemia.
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| Sammalkorpi H, Alhopuro P, Niittymäki I, Orntoft TF, Hokland P, Karhu A, Aaltonen LA.
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| Leuk Lymphoma 49(9):1829-31. No abstract available.
2008
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| 8 | MYH11
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| Comparative analysis of genes regulated in acute myelomonocytic leukemia with and without inv(16)(p13q22) using microarray techniques, real-time PCR, immunohistochemistry, and flow cytometry immunophenotyping.
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| Sun X, Zhang W, Ramdas L, Stivers DN, Jones DM, Kantarjian HM, Estey EH, Vadhan-Raj S, Medeiros LJ, Bueso-Ramos CE.
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| Mod Pathol 20(8):811-20. Epub 2007 Jun 15. 2007
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| 9 | MYH11, TAAD1
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| MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II.
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| Pannu H, Tran-Fadulu V, Papke CL, Scherer S, Liu Y, Presley C, Guo D, Estrera AL, Safi HJ, Brasier AR, Vick GW, Marian AJ, Raman CS, Buja LM, Milewicz DM.
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| Hum Mol Genet 16(20):3453-62. Epub 2007 Jul 31. 2007
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| 10 | TAAD1, MYH11
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| Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus.
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| Zhu L, Vranckx R, Van Kien PK, Lalande A, Boisset N, Mathieu F, Wegman M, Glancy L, Gasc JM, Brunotte F, Bruneval P, Wolf JE, Michel JB, Jeunemaitre X.
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| Nat Genet 38(3):343-9. Epub 2006 Jan 29. 2006
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| 11 | CBFB, MYH11, RUNX2
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| Identification of genes that synergize with Cbfb-MYH11 in the pathogenesis of acute myeloid leukemia.
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| Castilla LH, Perrat P, Martinez NJ, Landrette SF, Keys R, Oikemus S, Flanegan J, Heilman S, Garrett L, Dutra A, Anderson S, Pihan GA, Wolff L, Liu PP.
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| Proc Natl Acad Sci U S A 101(14):4924-9. Epub 2004 Mar 24. 2004
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| 12 | CBFB, MYH11
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| Molecular analysis of a new variant of the CBF beta-MYH11 gene fusion.
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| Stulberg J, Kamel-Reid S, Chun K, Tokunaga J, Wells RA.
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| Leuk Lymphoma 43(10):2021-6. 2002
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| 13 | CBFB, MYH11
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| The PEBP2betaMYH11 fusion created by Inv(16)(p13;q22) in myeloid leukemia impairs neutrophil maturation and contributes to granulocytic dysplasia.
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| Kogan SC, et al.
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| Proc Natl Acad Sci U S A 95 : 11863-11868. 1998
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| 14 | CBFB, MYH11
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| Detection of CBFbeta/MYH11 fusion transcripts in acute myeloid leukemia: heterogeneity of cytological and molecular characteristics.
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| Costello R, Sainty D, Lecine P, Cusenier A, Mozziconacci MJ, Arnoulet C, Maraninchi D, Gastaut JA, Imbert J, Lafage-Pochitaloff M, Gabert J.
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| Leukemia 11(5):644-50. 1997
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| 15 | CBFB, MYH11
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| Identification of the chimeric protein product of the CBFB-MYHII fusion gene in inv(16) leukemia cells.
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| Liu PP, et al.
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| Genes Chromosomes Cancer 16 : 77-87. 1996
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| 16 | CBFB, MYH11
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| Detection of the chromosome 16 CBF beta-MYH11 fusion transcript in myelomonocytic leukemias.
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| Poirel H, et al.
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| Blood 85 : 1313-1322. 1995
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| 17 | MYH11
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| A gene for a myosin peptide is disrupted by the inv(16)(p13q22) in acute nonlymphocytic leukemia M4Eo.
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| Van der Reijden BA, et al.
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| Blood 82 : 2948-2952. 1993
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| 18 | MYH11
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| Human smooth muscle myosin heavy chain gene mapped to chromosomal region 16q12.
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| Matsuoka R, et al.
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| Am J Med Genet 46 : 61-67. 1993
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| 19 | CBFB, MYH11, AMLM4EO
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| Fusion between transcription factor CBFbeta/PEBP2beta and a myosin heavy chain in acute myeloid leukemia.
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| Liu P, et al.
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| Science 261 : 1041-1044. 1993
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| 20 | AMLM4EO, MYH11, CBFB
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| Cloning the breakpoint cluster region of the inv(16) in acute nonlymphocytic leukemia M4 Eo.
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| Dauwerse JG, et al.
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| Hum Mol Genet 2 : 1527-1534. 1993
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| 21 | MYH11
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| Smooth muscle myosin heavy chain locus (MYH11) maps to 16p13.13-p13.12 and establishes a new region of conserved synteny between human 16p and mouse 16.
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| Deng Z, et al.
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| Genomics 18 : 156-159. 1993
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| 22 | MYH11
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| Human smooth muscle myosin heavy-chain gene mapped to chromosomal region 16q12.1-q12.2.
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| Matsuoka R, et al.
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| (HGM11) Cytogenet Cell Genet 58 : 2000-2001. 1991
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