Allelic expression imbalance of the human CYP3A4 gene and individual phenotypic status (English)
- New search for: Hirota, T.
- New search for: Ieiri, I.
- New search for: Takane, H.
- New search for: Maegawa, S.
- New search for: Hosokawa, M.
- New search for: Kobayashi, K.
- New search for: Chiba, K.
- New search for: Nanba, E.
- New search for: Oshimura, M.
- New search for: Sato, T.
- New search for: Hirota, T.
- New search for: Ieiri, I.
- New search for: Takane, H.
- New search for: Maegawa, S.
- New search for: Hosokawa, M.
- New search for: Kobayashi, K.
- New search for: Chiba, K.
- New search for: Nanba, E.
- New search for: Oshimura, M.
- New search for: Sato, T.
In:
HUMAN MOLECULAR GENETICS
;
13
, 23
;
2959-2969
;
2004
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ISSN:
- Article (Journal) / Print
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Title:Allelic expression imbalance of the human CYP3A4 gene and individual phenotypic status
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Contributors:Hirota, T. ( author ) / Ieiri, I. ( author ) / Takane, H. ( author ) / Maegawa, S. ( author ) / Hosokawa, M. ( author ) / Kobayashi, K. ( author ) / Chiba, K. ( author ) / Nanba, E. ( author ) / Oshimura, M. ( author ) / Sato, T. ( author )
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Published in:HUMAN MOLECULAR GENETICS ; 13, 23 ; 2959-2969
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Publisher:
- New search for: Oxford University Press
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Publication date:2004-01-01
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Size:11 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 572.8
- Further information on Dewey Decimal Classification
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Classification:
DDC: 572.8 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 13, Issue 23
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 2893
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A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early agingKopra, Outi / Vesa, Jouni / von Schantz, Carina / Manninen, Tuula / Minye, Helena / Fabritius, Anna-Liisa / Rapola, Juhani / Diggelen, Otto P. van / Saarela, Janna / Jalanko, Anu et al. | 2004
- 2907
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CD72 polymorphisms associated with alternative splicing modify susceptibility to human systemic lupus erythematosus through epistatic interaction with FCGR2BHitomi, Yuki / Tsuchiya, Naoyuki / Kawasaki, Aya / Ohashi, Jun / Suzuki, Takeshi / Kyogoku, Chieko / Fukazawa, Toru / Bejrachandra, Sasitorn / Siriboonrit, Usanee / Chandanayingyong, Dasnayanee et al. | 2004
- 2919
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The co-inheritance of type 1 diabetes and multiple sclerosis in Sardinia cannot be explained by genotype variation in the HLA region aloneMarrosu, Maria Giovanna / Motzo, Costantino / Murru, Raffaele / Lampis, Rosanna / Costa, Gianna / Zavattari, Patrizia / Contu, Daniela / Fadda, Elisabetta / Cocco, Eleonora / Cucca, Francesco et al. | 2004
- 2925
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Disruption of a novel ectodermal neural cortex 1 antisense gene, ENC-1AS and identification of ENC-1 overexpression in hairy cell leukemiaHammarsund, Marianne / Lerner, Mikael / Zhu, Chaoyong / Merup, Mats / Jansson, Monika / Gahrton, Gösta / Kluin-Nelemans, Hanneke / Einhorn, Stefan / Grandér, Dan / Sangfelt, Olle et al. | 2004
- 2937
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ATM is required for the cellular response to thymidine induced replication fork stressBolderson, Emma / Scorah, Jennifer / Helleday, Thomas / Smythe, Carl / Meuth, Mark et al. | 2004
- 2947
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A mouse model of AChR deficiency syndrome with a phenotype reflecting the human conditionCossins, Judy / Webster, Richard / Maxwell, Susan / Burke, Georgina / Vincent, Angela / Beeson, David et al. | 2004
- 2959
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Allelic expression imbalance of the human CYP3A4 gene and individual phenotypic statusHirota, Takeshi / Ieiri, Ichiro / Takane, Hiroshi / Maegawa, Shinji / Hosokawa, Masakiyo / Kobayashi, Kaoru / Chiba, Kan / Nanba, Eiji / Oshimura, Mitsuo / Sato, Tetsuo et al. | 2004
- 2971
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Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion miceChamberlain, Stormy J. / Johnstone, Karen A. / DuBose, Amanda J. / Simon, Thomas A. / Bartolomei, Marisa S. / Resnick, James L. / Brannan, Camilynn I. et al. | 2004
- 2979
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Genome-wide demethylation destabilizes CTGCAG trinucleotide repeats in mammalian cellsGorbunova, V. / Seluanov, A. / Mittelman, D. / Wilson, J. H. et al. | 2004
- 2979
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Genome-wide demethylation destabilizes CTG{middle dot}CAG trinucleotide repeats in mammalian cellsGorbunova, Vera / Seluanov, Andrei / Mittelman, David / Wilson, John H. et al. | 2004
- 2991
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Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8Chen, Wu-Yan / Shi, Yong-Yong / Zheng, Yong-Lan / Zhao, Xin-Zhi / Zhang, Guang-Ji / Chen, Sheng-Qi / Yang, Pei-Di / He, Lin et al. | 2004
- 2997
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Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophyPujol, Aurora / Ferrer, Isidre / Camps, Carme / Metzger, Elisabeth / Hindelang, Colette / Callizot, Noëlle / Ruiz, Montse / Pàmpols, Teresa / Giròs, Marisa / Mandel, Jean Louis et al. | 2004
- 3007
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Iron-sulfur protein maturation in human cells: evidence for a function of frataxinStehling, Oliver / Elsässer, Hans-Peter / Brückel, Bernd / Mühlenhoff, Ulrich / Lill, Roland et al. | 2004
- 3017
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Interconnections of CLN3, Hook1 and Rab proteins link Batten disease to defects in the endocytic pathwayLuiro, Kaisu / Yliannala, Kristiina / Ahtiainen, Laura / Maunu, Heidi / Järvelä, Irma / Kyttälä, Aija / Jalanko, Anu et al. | 2004