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 *

353 related articles for article (PubMed ID: 11350118)

  • 1. Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11.
    Funke B; Pandita RK; Morrow BE
    Genomics; 2001 May; 73(3):264-71. PubMed ID: 11350118
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 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. Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11.
    Funke B; Puech A; Saint-Jore B; Pandita R; Skoultchi A; Morrow B
    Genomics; 1998 Oct; 53(2):146-54. PubMed ID: 9790763
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11.
    Funke B; Edelmann L; McCain N; Pandita RK; Ferreira J; Merscher S; Zohouri M; Cannizzaro L; Shanske A; Morrow BE
    Am J Hum Genet; 1999 Mar; 64(3):747-58. PubMed ID: 10053009
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.
    Kelly D; Goldberg R; Wilson D; Lindsay E; Carey A; Goodship J; Burn J; Cross I; Shprintzen RJ; Scambler PJ
    Am J Med Genet; 1993 Feb; 45(3):308-12. PubMed ID: 8434616
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Chromosome 22q11 and schizophrenia].
    Agatsuma S; Hiroi N
    Nihon Shinkei Seishin Yakurigaku Zasshi; 2005 Apr; 25(2):79-84. PubMed ID: 16220657
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24.
    Ianakiev P; Kilpatrick MW; Dealy C; Kosher R; Korenberg JR; Chen XN; Tsipouras P
    Biochem Biophys Res Commun; 1999 Jul; 261(1):64-70. PubMed ID: 10405324
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart.
    Lindsay EA; Rizzu P; Antonacci R; Jurecic V; Delmas-Mata J; Lee CC; Kim UJ; Scambler PJ; Baldini A
    Genomics; 1996 Feb; 32(1):104-12. PubMed ID: 8786095
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).
    McQuade L; Christodoulou J; Budarf M; Sachdev R; Wilson M; Emanuel B; Colley A
    Am J Med Genet; 1999 Sep; 86(1):27-33. PubMed ID: 10440825
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A common molecular basis for rearrangement disorders on chromosome 22q11.
    Edelmann L; Pandita RK; Spiteri E; Funke B; Goldberg R; Palanisamy N; Chaganti RS; Magenis E; Shprintzen RJ; Morrow BE
    Hum Mol Genet; 1999 Jul; 8(7):1157-67. PubMed ID: 10369860
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Microsatellite DNA markers detects 95% of chromosome 22q11 deletions.
    Bonnet D; Cormier-Daire V; Kachaner J; Szezepanski I; Souillard P; Sidi D; Munnich A; Lyonnet S
    Am J Med Genet; 1997 Jan; 68(2):182-4. PubMed ID: 9028455
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.
    Driscoll DA; Spinner NB; Budarf ML; McDonald-McGinn DM; Zackai EH; Goldberg RB; Shprintzen RJ; Saal HM; Zonana J; Jones MC
    Am J Med Genet; 1992 Sep; 44(2):261-8. PubMed ID: 1360769
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Isolation, characterization, and mapping of the mouse and human WDR8 genes, members of a novel WD-repeat gene family.
    Koshizuka Y; Ikegawa S; Sano M; Nakamura K; Nakamura Y
    Genomics; 2001 Mar; 72(3):252-9. PubMed ID: 11401440
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Computational analysis and refinement of sequence structure on chromosome 22q11.2 region: application to the development of quantitative real-time PCR assay for clinical diagnosis.
    Chen YF; Kou PL; Tsai SJ; Chen KF; Chan HH; Chen CM; Sun HS
    Genomics; 2006 Feb; 87(2):290-7. PubMed ID: 16307865
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene.
    Budarf ML; Collins J; Gong W; Roe B; Wang Z; Bailey LC; Sellinger B; Michaud D; Driscoll DA; Emanuel BS
    Nat Genet; 1995 Jul; 10(3):269-78. PubMed ID: 7670464
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular cloning, expression and chromosomal localization of a novel human REG family gene, REG III.
    Nata K; Liu Y; Xu L; Ikeda T; Akiyama T; Noguchi N; Kawaguchi S; Yamauchi A; Takahashi I; Shervani NJ; Onogawa T; Takasawa S; Okamoto H
    Gene; 2004 Sep; 340(1):161-70. PubMed ID: 15556304
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.