Puech A - Search Results

1

Variation in IL-1beta gene expression is a major determinant of genetic differences in arthritis aggressivity in mice.

Ohmura K, Johnsen A, Ortiz-Lopez A, Desany P, Roy M, Besse W, Rogus J, Bogue M, Puech A, Lathrop M, Mathis D, Benoist C. Ohmura K, et al. Among authors: puech a. Proc Natl Acad Sci U S A. 2005 Aug 30;102(35):12489-94. doi: 10.1073/pnas.0504325102. Epub 2005 Aug 19. Proc Natl Acad Sci U S A. 2005. PMID: 16113081 Free PMC article.

2

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.

3

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia.

Chumakov I, Blumenfeld M, Guerassimenko O, Cavarec L, Palicio M, Abderrahim H, Bougueleret L, Barry C, Tanaka H, La Rosa P, Puech A, Tahri N, Cohen-Akenine A, Delabrosse S, Lissarrague S, Picard FP, Maurice K, Essioux L, Millasseau P, Grel P, Debailleul V, Simon AM, Caterina D, Dufaure I, Malekzadeh K, Belova M, Luan JJ, Bouillot M, Sambucy JL, Primas G, Saumier M, Boubkiri N, Martin-Saumier S, Nasroune M, Peixoto H, Delaye A, Pinchot V, Bastucci M, Guillou S, Chevillon M, Sainz-Fuertes R, Meguenni S, Aurich-Costa J, Cherif D, Gimalac A, Van Duijn C, Gauvreau D, Ouellette G, Fortier I, Raelson J, Sherbatich T, Riazanskaia N, Rogaev E, Raeymaekers P, Aerssens J, Konings F, Luyten W, Macciardi F, Sham PC, Straub RE, Weinberger DR, Cohen N, Cohen D. Chumakov I, et al. Among authors: puech a. Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13675-80. doi: 10.1073/pnas.182412499. Epub 2002 Oct 3. Proc Natl Acad Sci U S A. 2002. PMID: 12364586 Free PMC article.

4

Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region.

Puech A, Saint-Jore B, Merscher S, Russell RG, Cherif D, Sirotkin H, Xu H, Factor S, Kucherlapati R, Skoultchi AI. Puech A, et al. Proc Natl Acad Sci U S A. 2000 Aug 29;97(18):10090-5. doi: 10.1073/pnas.97.18.10090. Proc Natl Acad Sci U S A. 2000. PMID: 10963672 Free PMC 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. Among authors: puech a. Genomics. 1997 Jun 1;42(2):245-51. doi: 10.1006/geno.1997.4734. Genomics. 1997. PMID: 9192844 Free 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: puech a. Genomics. 1997 Dec 15;46(3):364-72. doi: 10.1006/geno.1997.5046. Genomics. 1997. PMID: 9441739

7

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. Among authors: puech a. Genomics. 1998 Oct 15;53(2):146-54. doi: 10.1006/geno.1998.5488. Genomics. 1998. PMID: 9790763

8

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: puech a. Genomics. 1997 Apr 1;41(1):75-83. doi: 10.1006/geno.1997.4627. Genomics. 1997. PMID: 9126485 Free article.

9

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. Saint-Jore B, et al. Among authors: puech a. Hum Mol Genet. 1998 Nov;7(12):1841-9. doi: 10.1093/hmg/7.12.1841. Hum Mol Genet. 1998. PMID: 9811927

10

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

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