BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

269 related articles for article (PubMed ID: 22723016)

  • 1. Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1.
    Wat MJ; Beck TF; Hernández-García A; Yu Z; Veenma D; Garcia M; Holder AM; Wat JJ; Chen Y; Mohila CA; Lally KP; Dickinson M; Tibboel D; de Klein A; Lee B; Scott DA
    Hum Mol Genet; 2012 Sep; 21(18):4115-25. PubMed ID: 22723016
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks.
    Longoni M; Lage K; Russell MK; Loscertales M; Abdul-Rahman OA; Baynam G; Bleyl SB; Brady PD; Breckpot J; Chen CP; Devriendt K; Gillessen-Kaesbach G; Grix AW; Rope AF; Shimokawa O; Strauss B; Wieczorek D; Zackai EH; Coletti CM; Maalouf FI; Noonan KM; Park JH; Tracy AA; Lee C; Donahoe PK; Pober BR
    Am J Med Genet A; 2012 Dec; 158A(12):3148-58. PubMed ID: 23165946
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.
    Wat MJ; Shchelochkov OA; Holder AM; Breman AM; Dagli A; Bacino C; Scaglia F; Zori RT; Cheung SW; Scott DA; Kang SH
    Am J Med Genet A; 2009 Aug; 149A(8):1661-77. PubMed ID: 19606479
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects.
    Keitges EA; Pasion R; Burnside RD; Mason C; Gonzalez-Ruiz A; Dunn T; Masiello M; Gebbia JA; Fernandez CO; Risheg H
    Am J Med Genet A; 2013 Jul; 161A(7):1755-8. PubMed ID: 23696316
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects.
    Jay PY; Bielinska M; Erlich JM; Mannisto S; Pu WT; Heikinheimo M; Wilson DB
    Dev Biol; 2007 Jan; 301(2):602-14. PubMed ID: 17069789
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Decreased expression of GATA4 in the diaphragm of nitrofen-induced congenital diaphragmatic hernia.
    Dingemann J; Doi T; Gosemann JH; Ruttenstock EM; Nakazawa N; Puri P
    Birth Defects Res B Dev Reprod Toxicol; 2013 Apr; 98(2):139-43. PubMed ID: 23426975
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia.
    Arrington CB; Bleyl SB; Matsunami N; Bowles NE; Leppert TI; Demarest BL; Osborne K; Yoder BA; Byrne JL; Schiffman JD; Null DM; DiGeronimo R; Rollins M; Faix R; Comstock J; Camp NJ; Leppert MF; Yost HJ; Brunelli L
    Am J Med Genet A; 2012 Dec; 158A(12):3137-47. PubMed ID: 23165927
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gene expression in the developing diaphragm: significance for congenital diaphragmatic hernia.
    Clugston RD; Zhang W; Greer JJ
    Am J Physiol Lung Cell Mol Physiol; 2008 Apr; 294(4):L665-75. PubMed ID: 18263670
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo copy number variants are associated with congenital diaphragmatic hernia.
    Yu L; Wynn J; Ma L; Guha S; Mychaliska GB; Crombleholme TM; Azarow KS; Lim FY; Chung DH; Potoka D; Warner BW; Bucher B; LeDuc CA; Costa K; Stolar C; Aspelund G; Arkovitz MS; Chung WK
    J Med Genet; 2012 Oct; 49(10):650-9. PubMed ID: 23054247
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal retinoic acid up-regulates pulmonary gene expression of COUP-TFII, FOG2, and GATA4 in pulmonary hypoplasia.
    Doi T; Sugimoto K; Puri P
    J Pediatr Surg; 2009 Oct; 44(10):1933-7. PubMed ID: 19853750
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Downregulation of GATA4 and GATA6 in the heart of rats with nitrofen-induced diaphragmatic hernia.
    Takayasu H; Sato H; Sugimoto K; Puri P
    J Pediatr Surg; 2008 Feb; 43(2):362-6. PubMed ID: 18280291
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia.
    Yu L; Wynn J; Cheung YH; Shen Y; Mychaliska GB; Crombleholme TM; Azarow KS; Lim FY; Chung DH; Potoka D; Warner BW; Bucher B; Stolar C; Aspelund G; Arkovitz MS; Chung WK
    Hum Genet; 2013 Mar; 132(3):285-92. PubMed ID: 23138528
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia.
    Wat MJ; Veenma D; Hogue J; Holder AM; Yu Z; Wat JJ; Hanchard N; Shchelochkov OA; Fernandes CJ; Johnson A; Lally KP; Slavotinek A; Danhaive O; Schaible T; Cheung SW; Rauen KA; Tonk VS; Tibboel D; de Klein A; Scott DA
    J Med Genet; 2011 May; 48(5):299-307. PubMed ID: 21525063
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic factors in congenital diaphragmatic hernia.
    Holder AM; Klaassens M; Tibboel D; de Klein A; Lee B; Scott DA
    Am J Hum Genet; 2007 May; 80(5):825-45. PubMed ID: 17436238
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Muscle connective tissue controls development of the diaphragm and is a source of congenital diaphragmatic hernias.
    Merrell AJ; Ellis BJ; Fox ZD; Lawson JA; Weiss JA; Kardon G
    Nat Genet; 2015 May; 47(5):496-504. PubMed ID: 25807280
    [TBL] [Abstract][Full Text] [Related]  

  • 16. GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease.
    Pehlivan T; Pober BR; Brueckner M; Garrett S; Slaugh R; Van Rheeden R; Wilson DB; Watson MS; Hing AV
    Am J Med Genet; 1999 Mar; 83(3):201-6. PubMed ID: 10096597
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Deletion of 8p23.1 with features of Cornelia de Lange syndrome and congenital diaphragmatic hernia and a review of deletions of 8p23.1 to 8pter? A further locus for Cornelia de Lange syndrome.
    Baynam G; Goldblatt J; Walpole I
    Am J Med Genet A; 2008 Jun; 146A(12):1565-70. PubMed ID: 18470924
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Predisposition to atrioventricular septal defects may be caused by SOX7 variants that impair interaction with GATA4.
    Li B; Li Z; Yang J; Hong N; Jin L; Xu Y; Fu Q; Sun K; Yu Y; Lu Y; Chen S
    Mol Genet Genomics; 2022 May; 297(3):671-687. PubMed ID: 35260939
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genome-wide transcriptomics analysis identifies sox7 and sox18 as specifically regulated by gata4 in cardiomyogenesis.
    Afouda BA; Lynch AT; de Paiva Alves E; Hoppler S
    Dev Biol; 2018 Feb; 434(1):108-120. PubMed ID: 29229250
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.
    Beck TF; Veenma D; Shchelochkov OA; Yu Z; Kim BJ; Zaveri HP; van Bever Y; Choi S; Douben H; Bertin TK; Patel PI; Lee B; Tibboel D; de Klein A; Stockton DW; Justice MJ; Scott DA
    Hum Mol Genet; 2013 Mar; 22(5):1026-38. PubMed ID: 23221805
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.