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In:
HUMAN MOLECULAR GENETICS
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18
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NP-NP
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2009
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- Aufsatz (Zeitschrift) / Print
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Titel:Subscription Page
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Erschienen in:HUMAN MOLECULAR GENETICS ; 18, 20 ; NP-NP
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Verlag:
- Neue Suche nach: Oxford University Press
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Erscheinungsdatum:01.01.2009
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Format / Umfang:NP-NP
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ISSN:
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Medientyp:Aufsatz (Zeitschrift)
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Format:Print
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Sprache:Englisch
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Inhaltsverzeichnis – Band 18, Ausgabe 20
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Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
- 3769
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DNA methylation and gene expression differences in children conceived in vitro or in vivoKatari, S. / Turan, N. / Bibikova, M. / Erinle, O. / Chalian, R. / Foster, M. / Gaughan, J. P. / Coutifaris, C. / Sapienza, C. et al. | 2009
- 3779
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Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expressionDaoud, F. / Angeard, N. / Demerre, B. / Martie, I. / Benyaou, R. / Leturcq, F. / Cossee, M. / Deburgrave, N. / Saillour, Y. / Tuffery, S. et al. | 2009
- 3795
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Tissue-specific alternative splicing of TCF7L2Prokunina-Olsson, L. / Welch, C. / Hansson, O. / Adhikari, N. / Scott, L. J. / Usher, N. / Tong, M. / Sprau, A. / Swift, A. / Bonnycastle, L. L. et al. | 2009
- 3805
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The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signallingTsang, H. T. / Edwards, T. L. / Wang, X. / Connell, J. W. / Davies, R. J. / Durrington, H. J. / OKane, C. J. / Luzio, J. P. / Reid, E. et al. | 2009
- 3822
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Pathogenic human L1-CAM mutations reduce the adhesion-dependent activation of EGFRNagaraj, K. / Kristiansen, L. V. / Skrzynski, A. / Castiella, C. / Garcia-Alonso, L. / Hortsch, M. et al. | 2009
- 3832
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Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repairRothfuss, O. / Fischer, H. / Hasegawa, T. / Maisel, M. / Leitner, P. / Miesel, F. / Sharma, M. / Bornemann, A. / Berg, D. / Gasser, T. et al. | 2009
- 3851
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Dysbindin-1 in dorsolateral prefrontal cortex of schizophrenia cases is reduced in an isoform-specific manner unrelated to dysbindin-1 mRNA expressionTang, J. / LeGros, R. P. / Louneva, N. / Yeh, L. / Cohen, J. W. / Hahn, C. G. / Blake, D. J. / Arnold, S. E. / Talbot, K. et al. | 2009
- 3864
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Expression differences by continent of origin point to the immortalization processDavis, A. R. / Kohane, I. S. et al. | 2009
- 3876
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Neutralization of granulocyte macrophage colony-stimulating factor decreases amyloid beta 1-42 and suppresses microglial activity in a transgenic mouse model of Alzheimers diseaseManczak, M. / Mao, P. / Nakamura, K. / Bebbington, C. / Park, B. / Reddy, P. H. et al. | 2009
- 3894
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Analyses of mental dysfunction-related ACSl4 in Drosophila reveal its requirement for Dpp/BMP production and visual wiring in the brainZhang, Y. / Chen, D. / Wang, Z. et al. | 2009
- 3906
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Delivery of a read-through inducing compound, TC007, lessens the severity of a spinal muscular atrophy animal modelMattis, V. B. / Ebert, A. D. / Fosso, M. Y. / Chang, C. W. / Lorson, C. L. et al. | 2009
- 3914
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Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in miceSuzuki, G. / Harper, K. M. / Hiramoto, T. / Funke, B. / Lee, M. / Kang, G. / Buell, M. / Geyer, M. A. / Kucherlapati, R. / Morrow, B. et al. | 2009
- 3926
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Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle traffickingHsiao, Y. C. / Tong, Z. J. / Westfall, J. E. / Ault, J. G. / Page-McCaw, P. S. / Ferland, R. J. et al. | 2009
- 3942
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Mutant huntingtin interacts with b-tubulin and disrupts vesicular transport and insulin secretionSmith, R. / Bacos, K. / Fedele, V. / Soulet, D. / Walz, H. A. / Obermuller, S. / Lindqvist, A. / Bjorkqvist, M. / Klein, P. / Onnerfjord, P. et al. | 2009
- 3955
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Mutations in the LRRK2 Roc-COR tandem domain link Parkinsons disease to Wnt signalling pathwaysSancho, R. M. / Law, B. M. / Harvey, K. et al. | 2009
- 3969
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Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucomaNarooie-Nejad, M. / Paylakhi, S. H. / Shojaee, S. / Fazlali, Z. / Rezaei Kanavi, M. / Nilforushan, N. / Yazdani, S. / Babrzadeh, F. / Suri, F. / Ronaghi, M. et al. | 2009
- 3978
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Targeted disruption of the Wnk4 gene decreases phosphorylation of Na-Cl cotransporter, increases Na excretion and lowers blood pressureOhta, A. / Rai, T. / Yui, N. / Chiga, M. / Yang, S. S. / Lin, S. H. / Sohara, E. / Sasaki, S. / Uchida, S. et al. | 2009
- 3987
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Potential late-onset Alzheimers disease-associated mutations in the ADAM10 gene attenuate a-secretase activityKim, M. / Suh, J. / Romano, D. / Truong, M. H. / Mullin, K. / Hooli, B. / Norton, D. / Tesco, G. / Elliott, K. / Wagner, S. L. et al. | 2009
- 3997
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Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosisSabatelli, M. / Eusebi, F. / Al-Chalabi, A. / Conte, A. / Madia, F. / Luigetti, M. / Mancuso, I. / Limatola, C. / Trettel, F. / Sobrero, F. et al. | 2009
- 4007
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Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15Keskitalo, K. / Broms, U. / Heliovaara, M. / Ripatti, S. / Surakka, I. / Perola, M. / Pitkaniemi, J. / Peltonen, L. / Aromaa, A. / Kaprio, J. et al. | 2009
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