Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Publikationen
Suchbegriffe: INTRONS - , . Treffer: 11
2016
Ibrahim-Verbaas, CA; Bressler, J; Debette, S; Schuur, M; Smith, AV; Bis, JC; Davies, G; Trompet, S; Smith, JA; Wolf, C; Chibnik, LB; Liu, Y; Vitart, V; Kirin, M; Petrovic, K; Polasek, O; Zgaga, L; Fawns-Ritchie, C; Hoffmann, P; Karjalainen, J; Lahti, J; Llewellyn, DJ; Schmidt, CO; Mather, KA; Chouraki, V; Sun, Q; Resnick, SM; Rose, LM; Oldmeadow, C; Stewart, M; Smith, BH; Gudnason, V; Yang, Q; Mirza, SS; Jukema, JW; deJager, PL; Harris, TB; Liewald, DC; Amin, N; Coker, LH; Stegle, O; Lopez, OL; Schmidt, R; Teumer, A; Ford, I; Karbalai, N; Becker, JT; Jonsdottir, MK; Au, R; Fehrmann, R; Herms, S; Nalls, M; Zhao, W; Turner, ST; Yaffe, K; Lohman, K; van Swieten, JC; Kardia, S; Knopman, DS; Meeks, WM; Heiss, G; Holliday, EG; Schofield, PW; Tanaka, T; Stott, DJ; Wang, J; Ridker, P; Gow, AJ; Pattie, A; Starr, JM; Hocking, LJ; Armstrong, NJ; McLachlan, S; Shulman, JM; Pilling, LC; Eiriksdottir, G; Scott, RJ; Kochan, NA; Palotie, A; Hsieh, YC; Eriksson, JG; Penman, A; Gottesman, RF; Oostra, BA; Yu, L; DeStefano, AL; Beiser, A; Garcia, M; Rotter, JI; Nöthen, MM; Hofman, A; Slagboom, PE; Westendorp, R; Buckley, BM; Wolf, PA; Uitterlinden, AG; Psaty, BM; Grabe, HJ; Bandinelli, S; Chasman, DI; Grodstein, F; Räikkönen, K; Lambert, JC; Porteous, DJ; Generation Scotland; Price, JF; Sachdev, PS; Ferrucci, L; Attia, JR; Rudan, I; Hayward, C; Wright, AF; Wilson, JF; Cichon, S; Franke, L; Schmidt, H; Ding, J; de Craen, A; Fornage, M; Bennett, DA; Deary, IJ; Ikram, MA; Launer, LJ; Fitzpatrick, AL; Seshadri, S; van Duijn, CM; Mosley, TH
GWAS for executive function and processing speed suggests involvement of the CADM2 gene.
Mol Psychiatry. 2016; 21(2):189-197
Doi: 10.1038/mp.2015.37
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2013
Kodaganur, SG; Tontanahal, SJ; Sarda, A; Shah, MH; Bhat, V; Kumar, A
Clinical phenotype and the lack of mutations in the CHRNG, CHRND, and CHRNA1 genes in two Indian families with Escobar syndrome.
Clin Dysmorphol. 2013; 22(2): 54-58.
Doi: 10.1097/MCD.0b013e32835f9ac0
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2012
Fiorillo, C; Moro, F; Brisca, G; Astrea, G; Nesti, C; Balint, Z; Olschewski, A; Meschini, MC; Guelly, C; Auer-Grumbach, M; Battini, R; Pedemonte, M; Romano, A; Menchise, V; Biancheri, R; Santorelli, FM; Bruno, C
TRPV4 mutations in children with congenital distal spinal muscular atrophy.
Neurogenetics. 2012; 13(3):195-203
Doi: 10.1007/s10048-012-0328-7
(- Case Report)
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Kraus, JP; Spector, E; Venezia, S; Estes, P; Chiang, PW; Creadon-Swindell, G; Müllerleile, S; de Silva, L; Barth, M; Walter, M; Walter, K; Meissner, T; Lindner, M; Ensenauer, R; Santer, R; Bodamer, OA; Baumgartner, MR; Brunner-Krainz, M; Karall, D; Haase, C; Knerr, I; Marquardt, T; Hennermann, JB; Steinfeld, R; Beblo, S; Koch, HG; Konstantopoulou, V; Scholl-Bürgi, S; van Teeffelen-Heithoff, A; Suormala, T; Ugarte, M; Sperl, W; Superti-Furga, A; Schwab, KO; Grünert, SC; Sass, JO
Mutation analysis in 54 propionic acidemia patients.
J INHERIT METAB DIS. 2012; 35(1): 51-63.
Doi: 10.1007/s10545-011-9399-0
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2006
Bundschu, K; Gattenlohner, S; Knobeloch, KP; Walter, U; Schuh, K
Tissue-specific Spred-2 promoter activity characterized by a gene trap approach.
Gene Expr Patterns. 2006; 6(3):247-255
Doi: 10.1016/j.modgep.2005.08.003
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2005
Stolle, K; Schnoor, M; Fuellen, G; Spitzer, M; Engel, T; Spener, F; Cullen, P; Lorkowski, S
Cloning, cellular localization, genomic organization, and tissue-specific expression of the TGFbeta1-inducible SMAP-5 gene.
Gene. 2005; 351(6-7):119-130
Doi: 10.1016/j.gene.2005.03.012
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2004
Schmidt, HH; Strehl, S; Thaler, D; Strunk, D; Sill, H; Linkesch, W; Jäger, U; Sperr, W; Greinix, HT; König, M; Emberger, W; Haas, OA
RT-PCR and FISH analysis of acute myeloid leukemia with t(8;16)(p11;p13) and chimeric MOZ and CBP transcripts: breakpoint cluster region and clinical implications.
Leukemia. 2004; 18(6):1115-1121
Doi: 10.1038/sj.leu.2403353
(- Case Report)
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2001
Legler, TJ; Maas, JH; Köhler, M; Wagner, T; Daniels, GL; Perco, P; Panzer, S
RHD sequencing: a new tool for decision making on transfusion therapy and provision of Rh prophylaxis.
Transfus Med. 2001; 11(5):383-388
Doi: 10.1046%2Fj.1365-3148.2001.00327.x
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1998
Greinix, HT; Reiter, E; Schulenburg, A; Keil, F; Lechner, K; Fischer, G; Rosenmayr, A; Leitner, G; Kalhs, P
Matched unrelated donor marrow transplantation in patients with advanced acute leukemia.
Bone Marrow Transplant. 1998; 22 Suppl 4(8):S53-S56
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Nagl, UO; Erdel, M; Bergmann, F; Oehl, B; Scandella, E; Musante, L; Galietta, LJ; Gschwentner, M; Fürst, J; Schmarda, A; Hofer, S; Utermann, G; Deetjen, P; Paulmichl, M
Characterization of the human gene coding for the swelling-dependent chloride channel ICln at position 11q13.5-14.1 (CLNS1A) and further characterization of the chromosome 6 (CLNS1B) localization.
Gene. 1998; 209(1-2):59-63
Doi: 10.1016/S0378-1119(98)00002-X
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1991
Zechner, R; Newman, TC; Steiner, E; Breslow, JL
The structure of the mouse lipoprotein lipase gene: a B1 repetitive element is inserted into the 3' untranslated region of the mRNA.
Genomics. 1991; 11(1):62-76
Doi: 10.1016/0888-7543(91)90102-K
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