Kucherlapati R - Search Results

1

The role of neural crest during cardiac development in a mouse model of DiGeorge syndrome.

Kochilas L, Merscher-Gomez S, Lu MM, Potluri V, Liao J, Kucherlapati R, Morrow B, Epstein JA. Kochilas L, et al. Among authors: kucherlapati r. Dev Biol. 2002 Nov 1;251(1):157-66. doi: 10.1006/dbio.2002.0819. Dev Biol. 2002. PMID: 12413905 Free article.

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: kucherlapati r. Cell. 2001 Feb 23;104(4):619-29. doi: 10.1016/s0092-8674(01)00247-1. Cell. 2001. PMID: 11239417 Free article.

3

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: kucherlapati r. Neurogenetics. 2006 Nov;7(4):247-57. doi: 10.1007/s10048-006-0054-0. Epub 2006 Aug 10. Neurogenetics. 2006. PMID: 16900388

4

Gene targeting in mammalian cells by homologous recombination.

Morrow B, Kucherlapati R. Morrow B, et al. Among authors: kucherlapati r. Curr Opin Biotechnol. 1993 Oct;4(5):577-82. doi: 10.1016/0958-1669(93)90080-g. Curr Opin Biotechnol. 1993. PMID: 7764209 Review.

5

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. Among authors: kucherlapati r. 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.

6

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: kucherlapati r. Genomics. 1997 Dec 15;46(3):364-72. doi: 10.1006/geno.1997.5046. Genomics. 1997. PMID: 9441739

7

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. Among authors: kucherlapati r. Genomics. 1997 Apr 1;41(1):75-83. doi: 10.1006/geno.1997.4627. Genomics. 1997. PMID: 9126485 Free article.

8

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. Among authors: kucherlapati r. Genomics. 1997 Jun 1;42(2):245-51. doi: 10.1006/geno.1997.4734. Genomics. 1997. PMID: 9192844 Free article.

9

A novel, single nucleotide polymorphism-based assay to detect 22q11 deletions.

Funke BH, Brown AC, Ramoni MF, Regan ME, Baglieri C, Finn CT, Babcock M, Shprintzen RJ, Morrow BE, Kucherlapati R. Funke BH, et al. Among authors: kucherlapati r. Genet Test. 2007 Spring;11(1):91-100. doi: 10.1089/gte.2006.0507. Genet Test. 2007. PMID: 17394398

10

Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice.

Suzuki G, Harper KM, Hiramoto T, Funke B, Lee M, Kang G, Buell M, Geyer MA, Kucherlapati R, Morrow B, Männistö PT, Agatsuma S, Hiroi N. Suzuki G, et al. Among authors: kucherlapati r. Hum Mol Genet. 2009 Oct 15;18(20):3914-25. doi: 10.1093/hmg/ddp334. Epub 2009 Jul 19. Hum Mol Genet. 2009. PMID: 19617637 Free PMC article.

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