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Coactivator-Associated Arginine Methyltransferase 1 (CARM1) Is a Positive Regulator of the Cyclin E1 Gene
Messaoudi, Selma El, Fabbrizio, Eric, Rodriguez, Carmen, Chuchana, Paul, Fauquier, Lucas, Cheng, Donghang, Theillet, Charles, Vandel, Laurence, Bedford, Mark T., Sardet, Claude
Published in Proceedings of the National Academy of Sciences - PNAS (05.09.2006)
Published in Proceedings of the National Academy of Sciences - PNAS (05.09.2006)
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Journal Article
m 6 A enhances the phase separation potential of mRNA
Ries, Ryan J, Zaccara, Sara, Klein, Pierre, Olarerin-George, Anthony, Namkoong, Sim, Pickering, Brian F, Patil, Deepak P, Kwak, Hojoong, Lee, Jun Hee, Jaffrey, Samie R
Published in Nature (London) (01.07.2019)
Published in Nature (London) (01.07.2019)
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Journal Article
A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a japanese family
Takano, Kyoko, Nakagawa, Eiji, Inoue, Ken, Kamada, Fumiaki, Kure, Shigeo, Goto, Yu-ichi
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.06.2008)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.06.2008)
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Journal Article
Ethnic Variation of Thiopurine S -Methyltransferase Activity: A Large, Prospective Population Study
Cooper, Sheldon C, Ford, Loretta T, Berg, Jonathan D, Lewis, Matthew JV
Published in Pharmacogenomics (01.03.2008)
Published in Pharmacogenomics (01.03.2008)
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Journal Article
Stochastic imprinting in the progeny of Dnmt3L−/− females
Arnaud, Philippe, Hata, Kenichiro, Kaneda, Masahiro, Li, En, Sasaki, Hiroyuki, Feil, Robert, Kelsey, Gavin
Published in Human molecular genetics (15.02.2006)
Published in Human molecular genetics (15.02.2006)
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Journal Article
Glycine N‐methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia
Mudd, S. H., Cerone, R., Schiaffino, M. C., Fantasia, A. R., Minniti, G., Caruso, U., Lorini, R., Watkins, D., Matiaszuk, N., Rosenblatt, D. S., Schwahn, B., Rozen, R., LeGros, L., Kotb, M., Capdevila, A., Luka, Z., Finkelstein, J. D., Tangerman, A., Stabler, S. P., Allen, R. H., Wagner, C.
Published in Journal of inherited metabolic disease (01.07.2001)
Published in Journal of inherited metabolic disease (01.07.2001)
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Journal Article
Deficiency of a Protein-Repair Enzyme Results in the Accumulation of Altered Proteins, Retardation of Growth, and Fatal Seizures in Mice
Kim, Edward, Lowenson, Jonathan D., MacLaren, Duncan C., Clarke, Steven, Young, Stephen G.
Published in Proceedings of the National Academy of Sciences - PNAS (10.06.1997)
Published in Proceedings of the National Academy of Sciences - PNAS (10.06.1997)
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Journal Article
Thiopurine S-methyltransferase deficiency : Two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians
HUNG-LIANG TAI, KRYNETSKI, E. Y, YATES, C. R, LOENNECHEN, T, FESSING, M. Y, KRYNETSKAIA, N. F, EVANS, W. E
Published in American journal of human genetics (01.04.1996)
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Published in American journal of human genetics (01.04.1996)
Journal Article
Rapid genotyping of common deficient thiopurine S-methyltransferase alleles using the DNA-microchip technique
Nasedkina, Tatyana V, Fedorova, Olga E, Glotov, Andrei S, Chupova, Natalia V, Samochatova, Elena V, Maiorova, Olga A, Zemlyakova, Valeria V, Roudneva, Anastasia E, Chudinov, Alexander V, Yurasov, Roman A, Kozhekbaeva, Janna M, Barsky, Victor E, Krynetskiy, Eugene Y, Krynetskaia, Natalia F, Cheng, Cheng, Ribeiro, Raul C, Evans, William E, Roumyantsev, Alexander G, Zasedatelev, Alexander S
Published in European journal of human genetics : EJHG (01.09.2006)
Published in European journal of human genetics : EJHG (01.09.2006)
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Journal Article
Human thiopurine S-methyltransferase activity in uremia and after renal transplantation
Weyer, N., Kröplin, T., Fricke, L., Iven, H.
Published in European journal of clinical pharmacology (01.05.2001)
Published in European journal of clinical pharmacology (01.05.2001)
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Journal Article
Pharmacogenetics of human erythrocyte thiopurine methyltransferase activity in a French population
Tinel, M, Berson, A, Pessayre, D, Letteron, P, Cattoni, MP, Horsmans, Y, Larrey, D
Published in British journal of clinical pharmacology (01.12.1991)
Published in British journal of clinical pharmacology (01.12.1991)
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Journal Article
COMT Genetic Reduction Produces Sexually Divergent Effects on Cortical Anatomy and Working Memory in Mice and Humans
Sannino, Sara, Gozzi, Alessandro, Cerasa, Antonio, Piras, Fabrizio, Scheggia, Diego, Managò, Francesca, Damiano, Mario, Galbusera, Alberto, Erickson, Lucy C., De Pietri Tonelli, Davide, Bifone, Angelo, Tsaftaris, Sotirios A., Caltagirone, Carlo, Weinberger, Daniel R., Spalletta, Gianfranco, Papaleo, Francesco
Published in Cerebral cortex (New York, N.Y. 1991) (01.09.2015)
Published in Cerebral cortex (New York, N.Y. 1991) (01.09.2015)
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Journal Article
Simultaneous determination of creatine and guanidinoacetate in plasma by liquid chromatography–tandem mass spectrometry (LC–MS/MS)
Boenzi, Sara, Rizzo, Cristiano, Di Ciommo, Vincenzo Maria, Martinelli, Diego, Goffredo, Bianca Maria, la Marca, Giancarlo, Dionisi-Vici, Carlo
Published in Journal of pharmaceutical and biomedical analysis (05.12.2011)
Published in Journal of pharmaceutical and biomedical analysis (05.12.2011)
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Journal Article
Inborn Errors of Sulfur-Containing Amino Acid Metabolism
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Journal Article
Conference Proceeding
Creatine uptake in mouse hearts with genetically altered creatine levels
Hove, Michiel ten, Makinen, Kimmo, Sebag-Montefiore, Liam, Hunyor, Imre, Fischer, Alexandra, Wallis, Julie, Isbrandt, Dirk, Lygate, Craig, Neubauer, Stefan
Published in Journal of molecular and cellular cardiology (01.09.2008)
Published in Journal of molecular and cellular cardiology (01.09.2008)
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Journal Article