Morrow BE - Search Results

1

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. Long JM, et al. Among authors: morrow be. Neurogenetics. 2006 Nov;7(4):247-57. doi: 10.1007/s10048-006-0054-0. Epub 2006 Aug 10. Neurogenetics. 2006. PMID: 16900388

2

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.

Merscher S, Funke B, Epstein JA, Heyer J, Puech A, Lu MM, Xavier RJ, Demay MB, Russell RG, Factor S, Tokooya K, Jore BS, Lopez M, Pandita RK, Lia M, Carrion D, Xu H, Schorle H, Kobler JB, Scambler P, Wynshaw-Boris A, Skoultchi AI, Morrow BE, Kucherlapati R. Merscher S, et al. Among authors: morrow be. Cell. 2001 Feb 23;104(4):619-29. doi: 10.1016/s0092-8674(01)00247-1. Cell. 2001. PMID: 11239417 Free article.

3

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. Funke B, et al. Among authors: morrow be. Genomics. 2001 May 1;73(3):264-71. doi: 10.1006/geno.2000.6506. Genomics. 2001. PMID: 11350118

4

Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome.

Sirotkin H, O'Donnell H, DasGupta R, Halford S, St Jore B, Puech A, Parimoo S, Morrow B, Skoultchi A, Weissman SM, Scambler P, Kucherlapati R. Sirotkin H, et al. Genomics. 1997 Apr 1;41(1):75-83. doi: 10.1006/geno.1997.4627. Genomics. 1997. PMID: 9126485 Free article.

5

Identification, characterization, and precise mapping of a human gene encoding a novel membrane-spanning protein from the 22q11 region deleted in velo-cardio-facial syndrome.

Sirotkin H, Morrow B, Saint-Jore B, Puech A, Das Gupta R, Patanjali SR, Skoultchi A, Weissman SM, Kucherlapati R. Sirotkin H, et al. Genomics. 1997 Jun 1;42(2):245-51. doi: 10.1006/geno.1997.4734. Genomics. 1997. PMID: 9192844 Free article.

6

A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice.

Hiroi N, Zhu H, Lee M, Funke B, Arai M, Itokawa M, Kucherlapati R, Morrow B, Sawamura T, Agatsuma S. Hiroi N, et al. Proc Natl Acad Sci U S A. 2005 Dec 27;102(52):19132-7. doi: 10.1073/pnas.0509635102. Epub 2005 Dec 19. Proc Natl Acad Sci U S A. 2005. PMID: 16365290 Free PMC article.

7

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. Funke B, et al. Among authors: morrow be. Genomics. 1997 Dec 15;46(3):364-72. doi: 10.1006/geno.1997.5046. Genomics. 1997. PMID: 9441739

8

Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization.

Puech A, Saint-Jore B, Funke B, Gilbert DJ, Sirotkin H, Copeland NG, Jenkins NA, Kucherlapati R, Morrow B, Skoultchi AI. Puech A, et al. Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14608-13. doi: 10.1073/pnas.94.26.14608. Proc Natl Acad Sci U S A. 1997. PMID: 9405660 Free PMC article.

9

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. Funke B, et al. Genomics. 1998 Oct 15;53(2):146-54. doi: 10.1006/geno.1998.5488. Genomics. 1998. PMID: 9790763

10

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. Funke B, et al. Among authors: morrow be. Am J Hum Genet. 1999 Mar;64(3):747-58. doi: 10.1086/302284. Am J Hum Genet. 1999. PMID: 10053009 Free PMC article.

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