Citations for
1ACTG2, MMIH2
Diagnosis of Chronic Intestinal Pseudo-obstruction & Megacystis by Sequencing the ACTG2 Gene.
Milunsky A, Baldwin C, Zhang X, Primack D, Curnow A, Milunsky J.
J Pediatr Gastroenterol Nutr Pediatr Gastroenterol Nutr. 2017 Apr 18. doi: 10.1097/MPG.0000000000001608. [Epub ahead of print] 2017
2ACTG2
Identification of ACTG2 functions as a promoter gene in hepatocellular carcinoma cells migration and tumor metastasis.
Wu Y, Liu ZG, Shi MQ, Yu HZ, Jiang XY, Yang AH, Fu XS, Xu Y, Yang S, Ni H, Shen SJ, Li WD.
Biochem Biophys Res Commun 491(2):537-544. doi: 10.1016/j.bbrc.2017.04.007. Epub 2017 Apr 4. 2017
3ACTG2, MMIH2
ACTG2 variants impair actin polymerization in sporadic Megacystis Microcolon Intestinal Hypoperistalsis Syndrome.
Halim D, Hofstra RM, Signorile L, Verdijk RM, van der Werf CS, Sribudiani Y, Brouwer RW, van IJcken WF, Dahl N, Verheij JB, Baumann C, Kerner J, van Bever Y, Galjart N, Wijnen RM, Tibboel D, Burns AJ, Muller F, Brooks AS, Alves MM.
Hum Mol Genet 25(3):571-83. doi: 10.1093/hmg/ddv497. Epub 2015 Dec 8. 2016
4ACTG2, MMIH2
Mutation in Actin γ-2 Responsible for Megacystis Microcolon Intestinal Hypoperistalsis Syndrome in 4 Chinese Patients.
Lu W, Xiao Y, Huang J, Tao Y, Yan W, Lu L, Cao Y, Cai W.
J Pediatr Gastroenterol Nutr 63(6):624-626. 2016
5ACTG2, MMIH2
Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstruction.
Matera I, Rusmini M, Guo Y, Lerone M, Li J, Zhang J, Di Duca M, Nozza P, Mosconi M, Pini Prato A, Martucciello G, Barabino A, Morandi F, De Giorgio R, Stanghellini V, Ravazzolo R, Devoto M, Hakonarson H, Ceccherini I.
Eur J Hum Genet 24(8):1211-5. doi: 10.1038/ejhg.2015.275. Epub 2016 Jan 27. 2016
6ACTG2, MMIH2
Phenotypic expansion of visceral myopathy associated with ACTG2 tandem base substitution.
Klar J, Raykova D, Gustafson E, Tóthová I, Ameur A, Wanders A, Dahl N.
Eur J Hum Genet 23(12):1679-83. doi: 10.1038/ejhg.2015.49. Epub 2015 Mar 18. 2015
7ACTG2
Gamma-smooth muscle actin expression is associated with epithelial-mesenchymal transition and stem-like properties in hepatocellular carcinoma.
Benzoubir N, Mussini C, Lejamtel C, Dos Santos A, Guillaume C, Desterke C, Samuel D, Bréchot C, Bourgeade MF, Guettier C.
PLoS One 10(6):e0130559. doi: 10.1371/journal.pone.0130559. eCollection 2015. 2015
8ACTG2, MMIH2
Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndrome.
Wangler MF, Gonzaga-Jauregui C, Gambin T, Penney S, Moss T, Chopra A, Probst FJ, Xia F, Yang Y, Werlin S, Eglite I, Kornejeva L, Bacino CA, Baldridge D, Neul J, Lehman EL, Larson A, Beuten J, Muzny DM, Jhangiani S; Baylor-Hopkins Center for Mendelian Genomics, Gibbs RA, Lupski JR, Beaudet A.
PLoS Genet 10(3):e1004258. doi: 10.1371/journal.pgen.1004258. eCollection 2014 Mar. 2014
9ACTG2, MMIH2
De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis.
Thorson W, Diaz-Horta O, Foster J 2nd, Spiliopoulos M, Quintero R, Farooq A, Blanton S, Tekin M.
Hum Genet 133(6):737-42. doi: 10.1007/s00439-013-1406-0. Epub 2013 Dec 13. 2014
10ACTG2, MMIH2
De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis.
Thorson W, Diaz-Horta O, Foster J 2nd, Spiliopoulos M, Quintero R, Farooq A, Blanton S, Tekin M.
Hum Genet 133(6):737-42. doi: 10.1007/s00439-013-1406-0. Epub 2013 Dec 13. 2014
11ACTG2, MMIH2
Segregation of a missense variant in enteric smooth muscle actin γ-2 with autosomal dominant familial visceral myopathy.
Lehtonen HJ, Sipponen T, Tojkander S, Karikoski R, Järvinen H, Laing NG, Lappalainen P, Aaltonen LA, Tuupanen S.
Gastroenterology 143(6):1482-1491.e3. doi: 10.1053/j.gastro.2012.08.045. Epub 2012 Sep 6. 2012
12NKX3-1, ACTG2
The smooth muscle gamma-actin gene is androgen responsive in prostate epithelia.
Filmore RA, Dean DA, Zimmer WE.
Gene Expr 10(5-6):201-11. 2002
13ACTG2
Chromosomal mapping of the human smooth muscle actin gene (enteric type,ACTA3) to 2p13.1 and molecular nature of the hindIII polymorphism.
Ueyama H, et al.
Genomics 25 : 720-723. 1995
14ACTG2
Structure, chromosome location, and expression of the human smooth muscle (enteric type) gamma-actin gene : evolution of six human actin genes.
Miwa T, et al.
Mol Cell Biol 11 : 3296-3306. 1991
15ACTG2
A HindIII DNA polymorphism in the human enteric type smooth muscle actin gene (ACTSG).
Ueyama H.
Nucleic Acids Res 19 : 411. 1991
16ACTA1, ACTG2, ACTL4
The actin gene family in man : assignment of the gene for skeletal muscle alpha-actin to chromosome 1, and presence of actin sequences on autosomes 2 and 3, and on the X and Y chromosomes.
Hanauer A, et al.
(HGM7) Cytogenet Cell Genet 37 : 487-488. 1984