Impaired glucose homeostasis, neutrophil trafficking and function in mice lacking the glucose-6-phosphate transporter (English)
- New search for: Chen, Li-Yuan
- New search for: Shieh, Jeng-Jer
- New search for: Lin, Baochuan
- New search for: Pan, Chi-Jiunn
- New search for: Gao, Ji-Liang
- New search for: Murphy, Philip M.
- New search for: Roe, Thomas F.
- New search for: Moses, Shimon
- New search for: Ward, Jerrold M.
- New search for: Lee, Eric J.
- New search for: Westphal, Heiner
- New search for: Mansfield, Brian C.
- New search for: Chou, Janice Yang
- New search for: Chen, Li-Yuan
- New search for: Shieh, Jeng-Jer
- New search for: Lin, Baochuan
- New search for: Pan, Chi-Jiunn
- New search for: Gao, Ji-Liang
- New search for: Murphy, Philip M.
- New search for: Roe, Thomas F.
- New search for: Moses, Shimon
- New search for: Ward, Jerrold M.
- New search for: Lee, Eric J.
- New search for: Westphal, Heiner
- New search for: Mansfield, Brian C.
- New search for: Chou, Janice Yang
In:
Human molecular genetics
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12
, 19
;
2547-
;
2003
- Article (Journal) / Electronic Resource
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Title:Impaired glucose homeostasis, neutrophil trafficking and function in mice lacking the glucose-6-phosphate transporter
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Contributors:Chen, Li-Yuan ( author ) / Shieh, Jeng-Jer ( author ) / Lin, Baochuan ( author ) / Pan, Chi-Jiunn ( author ) / Gao, Ji-Liang ( author ) / Murphy, Philip M. ( author ) / Roe, Thomas F. ( author ) / Moses, Shimon ( author ) / Ward, Jerrold M. ( author ) / Lee, Eric J. ( author )
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Published in:Human molecular genetics ; 12, 19 ; 2547-
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Publisher:
- New search for: Oxford University Press
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Publication date:2003-10-01
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 12, Issue 19
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.
- 2411
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A unification of mosaic structures in the human genomeLercher, Martin J. / Urrutia, Araxi O. / Pavlícek, Adam / Hurst, Laurence D. et al. | 2003
- 2417
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LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndromeBitoun, Emmanuelle / Micheloni, Alessia / Lamant, Laurence / Bonnart, Chrystelle / Tartaglia-Polcini, Alessandro / Cobbold, Christian / Al Saati, Talal / Mariotti, Feliciana / Mazereeuw-Hautier, Juliette / Boralevi, Franck et al. | 2003
- 2431
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Complexin II is essential for normal neurological function in miceGlynn, Dervila / Bortnick, Rachel A. / Morton, A. Jennifer et al. | 2003
- 2449
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Lowe syndrome protein OCRL1 interacts with Rac GTPase in the trans-Golgi networkFaucherre, Adèle / Desbois, Pierrette / Satre, Véronique / Lunardi, Joël / Dorseuil, Olivier / Gacon, Gérard et al. | 2003
- 2457
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Gene expression changes presage neurodegeneration in a Drosophila model of Parkinson's diseaseScherzer, Clemens R. / Jensen, Roderick V. / Gullans, Steven R. / Feany, Mel B. et al. | 2003
- 2467
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Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased {alpha}7 integrin, utrophin and associated glycoproteinsMoghadaszadeh, Behzad / Albrechtsen, Reidar / Guo, Ling T. / Zaik, Michaela / Kawaguchi, Nobuko / Borup, Rehannah H. / Kronqvist, Pauliina / Schröder, Henrik D. / Davies, Kay E. / Voit, Thomas et al. | 2003
- 2481
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Valproic acid increases the SMN2 protein level: a well-known drug as a potential therapy for spinal muscular atrophyBrichta, L. / Hofmann, Y. / Hahnen, E. / Siebzehnrubl, F. A. / Raschke, H. / Blumcke, I. / Eyupoglu, I. Y. / Wirth, B. et al. | 2003
- 2491
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Identification of SATB2 as the cleft palate gene on 2q32-q33FitzPatrick, David R. / Carr, Ian M. / McLaren, Lorna / Leek, Jack P. / Wightman, Patrick / Williamson, Kathy / Gautier, Philippe / McGill, Niolette / Hayward, Caroline / Firth, Helen et al. | 2003
- 2503
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Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1Hussain, Shobbir / Witt, Emily / Huber, Pia A.J. / Medhurst, Annette L. / Ashworth, Alan / Mathew, Christopher G. et al. | 2003
- 2511
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Significant linkage to migraine with aura on chromosome 11q24Cader, Zameel M. / Noble-Topham, Sandra / Dyment, David A. / Cherny, Stacey S. / Brown, John D. / Rice, George P.A. / Ebers, George C. et al. | 2003
- 2519
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Increased expression of the glial glutamate transporter EAAT2 modulates excitotoxicity and delays the onset but not the outcome of ALS in miceGuo, Hong / Lai, Liching / Butchbach, Matthew E.R. / Stockinger, Michael P. / Shan, Xiu / Bishop, Georgia A. / Lin, Chien-liang Glenn et al. | 2003
- 2533
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A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemiaKao, Jau-Tsuen / Wen, Hui-Chin / Chien, Kuo-Liong / Hsu, Hey-Chi / Lin, Shu-Wha et al. | 2003
- 2541
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Association of TNF-{alpha} promoter polymorphisms with the clearance of hepatitis B virus infectionKim, Yoon Jun / Lee, Hyo-Suk / Yoon, Jung-Hwan / Kim, Chung Yong / Park, Myoung Hee / Kim, Lyoung Hyo / Park, Byung Lae / Shin, Hyoung Doo et al. | 2003
- 2547
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Impaired glucose homeostasis, neutrophil trafficking and function in mice lacking the glucose-6-phosphate transporterChen, Li-Yuan / Shieh, Jeng-Jer / Lin, Baochuan / Pan, Chi-Jiunn / Gao, Ji-Liang / Murphy, Philip M. / Roe, Thomas F. / Moses, Shimon / Ward, Jerrold M. / Lee, Eric J. et al. | 2003
- 2559
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X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesisHansen, R. Scott et al. | 2003