Glycosylation of the OCTN2 carnitine transporter: Study of natural mutations identified in patients with primary carnitine deficiency (English)
- New search for: Filippo, C. A.
- New search for: Ardon, O.
- New search for: Longo, N.
- New search for: Filippo, C. A.
- New search for: Ardon, O.
- New search for: Longo, N.
In:
BIOCHIMICA ET BIOPHYSICA ACTA
;
1812
, 3
;
312-320
;
2011
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ISSN:
- Article (Journal) / Print
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Title:Glycosylation of the OCTN2 carnitine transporter: Study of natural mutations identified in patients with primary carnitine deficiency
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Contributors:
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Published in:BIOCHIMICA ET BIOPHYSICA ACTA ; 1812, 3 ; 312-320
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Publisher:
- New search for: Elsevier Science B.V., Amsterdam.
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Publication date:2011-01-01
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Size:9 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: 571 / 572
- Further information on Dewey Decimal Classification
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Classification:
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Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 1812, Issue 3
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.
- 283
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The role of CDX2 in intestinal homeostasis and inflammationCoskun, Mehmet et al. | 2011
- 290
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Essential role of neutrophil mobilization in concanavalin A-induced hepatitis is based on classic IL-6 signaling but not on IL-6 trans-signalingMalchow, Sven et al. | 2011
- 302
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Truncated forms of BNIP3 act as dominant negatives inhibiting hypoxia-induced cell deathBristow, Nicolle et al. | 2011
- 312
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Glycosylation of the OCTN2 carnitine transporter: Study of natural mutations identified in patients with primary carnitine deficiencyFilippo, Cristina Amat di San et al. | 2011
- 321
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POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblastsStewart, Joanna D. et al. | 2011
- 326
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Molecular characterization of tissue-nonspecific alkaline phosphatase with an Ala to Thr substitution at position 116 associated with dominantly inherited hypophosphatasiaIshida, Yoko et al. | 2011
- 333
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Preface: Zebrafish Models of NeurologyAllison, W. Ted et al. | 2011
- 335
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Zebrafish models for the functional genomics of neurogenetic disordersKabashi, Edor et al. | 2011
- 346
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Zebrafish as a tool in Alzheimer's disease researchNewman, Morgan et al. | 2011
- 353
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Zebrafish models of TauopathyBai, Qing et al. | 2011
- 364
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Investigating regeneration and functional integration of CNS neurons: Lessons from zebrafish genetics and other fish speciesFleisch, Valerie C. et al. | 2011
- 381
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Behavioural assessments of neurotoxic effects and neurodegeneration in zebrafishTierney, Keith B. et al. | 2011
- 390
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Aberrant forebrain signaling during early development underlies the generation of holoprosencephaly and colobomaGongal, Patricia A. et al. | 2011
- 402
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Fish models in prion biology: Underwater issuesMálaga-Trillo, Edward et al. | 2011
- 415
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Microdomain-forming proteins and the role of the reggies/flotillins during axon regeneration in zebrafishStuermer, Claudia A.O. et al. | 2011
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Editorial Board| 2011