Funke B - Search Results

1

Gene expression profile of trisomy 21 placentas: a potential approach for designing noninvasive techniques of prenatal diagnosis.

Gross SJ, Ferreira JC, Morrow B, Dar P, Funke B, Khabele D, Merkatz I. Gross SJ, et al. Among authors: funke b. Am J Obstet Gynecol. 2002 Aug;187(2):457-62. doi: 10.1067/mob.2002.123542. Am J Obstet Gynecol. 2002. PMID: 12193943

2

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. Genomics. 2001 May 1;73(3):264-71. doi: 10.1006/geno.2000.6506. Genomics. 2001. PMID: 11350118

3

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. Am J Hum Genet. 1999 Mar;64(3):747-58. doi: 10.1086/302284. Am J Hum Genet. 1999. PMID: 10053009 Free PMC article.

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

5

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: funke b. 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.

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

7

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. Edelmann L, et al. Among authors: funke b. Hum Mol Genet. 1999 Jul;8(7):1157-67. doi: 10.1093/hmg/8.7.1157. Hum Mol Genet. 1999. PMID: 10369860

8

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. Funke B, et al. Hum Mol Genet. 2001 Oct 15;10(22):2549-56. doi: 10.1093/hmg/10.22.2549. Hum Mol Genet. 2001. PMID: 11709542

9

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. Among authors: funke b. 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.

10

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: funke b. 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.

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