These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 9811926)

  • 1. Functional analysis of Gscl in the pathogenesis of the DiGeorge and velocardiofacial syndromes.
    Wakamiya M; Lindsay EA; Rivera-Pérez JA; Baldini A; Behringer RR
    Hum Mol Genet; 1998 Nov; 7(12):1835-40. PubMed ID: 9811926
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Goosecoid-like (Gscl), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse development.
    Saint-Jore B; Puech A; Heyer J; Lin Q; Raine C; Kucherlapati R; Skoultchi AI
    Hum Mol Genet; 1998 Nov; 7(12):1841-9. PubMed ID: 9811927
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11.
    Funke B; Saint-Jore B; Puech A; Sirotkin H; Edelmann L; Carlson C; Raft S; Pandita RK; Kucherlapati R; Skoultchi A; Morrow BE
    Genomics; 1997 Dec; 46(3):364-72. PubMed ID: 9441739
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Goosecoid-like, a gene deleted in DiGeorge and velocardiofacial syndromes, recognizes DNA with a bicoid-like specificity and is expressed in the developing mouse brain.
    Gottlieb S; Hanes SD; Golden JA; Oakey RJ; Budarf ML
    Hum Mol Genet; 1998 Sep; 7(9):1497-505. PubMed ID: 9700206
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Gscl, a gene within the minimal DiGeorge critical region, is expressed in primordial germ cells and the developing pons.
    Galili N; Epstein JA; Leconte I; Nayak S; Buck CA
    Dev Dyn; 1998 May; 212(1):86-93. PubMed ID: 9603426
    [TBL] [Abstract][Full Text] [Related]  

  • 6. ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene.
    Lindsay EA; Harvey EL; Scambler PJ; Baldini A
    Hum Mol Genet; 1998 Apr; 7(4):629-35. PubMed ID: 9499415
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development.
    Gottlieb S; Emanuel BS; Driscoll DA; Sellinger B; Wang Z; Roe B; Budarf ML
    Am J Hum Genet; 1997 May; 60(5):1194-201. PubMed ID: 9150167
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome.
    Long JM; LaPorte P; Merscher S; Funke B; Saint-Jore B; Puech A; Kucherlapati R; Morrow BE; Skoultchi AI; Wynshaw-Boris A
    Neurogenetics; 2006 Nov; 7(4):247-57. PubMed ID: 16900388
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region.
    Galili N; Baldwin HS; Lund J; Reeves R; Gong W; Wang Z; Roe BA; Emanuel BS; Nayak S; Mickanin C; Budarf ML; Buck CA
    Genome Res; 1997 Jan; 7(1):17-26. PubMed ID: 9037598
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.
    Kimber WL; Hsieh P; Hirotsune S; Yuva-Paylor L; Sutherland HF; Chen A; Ruiz-Lozano P; Hoogstraten-Miller SL; Chien KR; Paylor R; Scambler PJ; Wynshaw-Boris A
    Hum Mol Genet; 1999 Nov; 8(12):2229-37. PubMed ID: 10545603
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit.
    Berti L; Mittler G; Przemeck GK; Stelzer G; Günzler B; Amati F; Conti E; Dallapiccola B; Hrabé de Angelis M; Novelli G; Meisterernst M
    Genomics; 2001 Jun; 74(3):320-32. PubMed ID: 11414760
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects.
    Funke B; Epstein JA; Kochilas LK; Lu MM; Pandita RK; Liao J; Bauerndistel R; Schüler T; Schorle H; Brown MC; Adams J; Morrow BE
    Hum Mol Genet; 2001 Oct; 10(22):2549-56. PubMed ID: 11709542
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Craniofacial Phenotypes and Genetics of DiGeorge Syndrome.
    Funato N
    J Dev Biol; 2022 May; 10(2):. PubMed ID: 35645294
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Loss of Goosecoid-like and DiGeorge syndrome critical region 14 in interpeduncular nucleus results in altered regulation of rapid eye movement sleep.
    Funato H; Sato M; Sinton CM; Gautron L; Williams SC; Skach A; Elmquist JK; Skoultchi AI; Yanagisawa M
    Proc Natl Acad Sci U S A; 2010 Oct; 107(42):18155-60. PubMed ID: 20921407
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rnf4, a RING protein expressed in the developing nervous and reproductive systems, interacts with Gscl, a gene within the DiGeorge critical region.
    Galili N; Nayak S; Epstein JA; Buck CA
    Dev Dyn; 2000 May; 218(1):102-11. PubMed ID: 10822263
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Altered replication timing of the HIRA/Tuple1 locus in the DiGeorge and Velocardiofacial syndromes.
    D'Antoni S; Mattina T; Di Mare P; Federico C; Motta S; Saccone S
    Gene; 2004 May; 333():111-9. PubMed ID: 15177686
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.
    Guris DL; Fantes J; Tara D; Druker BJ; Imamoto A
    Nat Genet; 2001 Mar; 27(3):293-8. PubMed ID: 11242111
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
    Driscoll DA; Salvin J; Sellinger B; Budarf ML; McDonald-McGinn DM; Zackai EH; Emanuel BS
    J Med Genet; 1993 Oct; 30(10):813-7. PubMed ID: 8230155
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.
    Stalmans I
    Verh K Acad Geneeskd Belg; 2005; 67(4):229-76. PubMed ID: 16334858
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation.
    Holmes SE; Riazi MA; Gong W; McDermid HE; Sellinger BT; Hua A; Chen F; Wang Z; Zhang G; Roe B; Gonzalez I; McDonald-McGinn DM; Zackai E; Emanuel BS; Budarf ML
    Hum Mol Genet; 1997 Mar; 6(3):357-67. PubMed ID: 9147638
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.