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There are 13317 results for: content related to: Solute carrier family 2 member 1 is involved in the development of nonalcoholic fatty liver disease

  1. Ovarian Steroids Influence Cerebral Glucose Transporter Expression in a Region- and Isoform-Specific Pattern

    Journal of Neuroendocrinology

    Volume 26, Issue 4, April 2014, Pages: 217–225, C. S. Harrell, J. Burgado, S. D. Kelly and G. N. Neigh

    Version of Record online : 3 APR 2014, DOI: 10.1111/jne.12139

  2. Favourable response to ketogenic dietary therapies: undiagnosed glucose 1 transporter deficiency syndrome is only one factor

    Developmental Medicine & Child Neurology

    Volume 57, Issue 10, October 2015, Pages: 969–976, Natasha E Schoeler, Judith Helen Cross, Suzanne Drury, Nicholas Lench, Jacinta M McMahon, Mark T MacKay, Ingrid E Scheffer, Josemir W Sander and Sanjay M Sisodiya

    Version of Record online : 23 APR 2015, DOI: 10.1111/dmcn.12781

  3. Glucose transporter 1 deficiency in the idiopathic generalized epilepsies

    Annals of Neurology

    Volume 72, Issue 5, November 2012, Pages: 807–815, Todor Arsov, Saul A. Mullen, Sue Rogers, A. Marie Phillips, Kate M. Lawrence, John A. Damiano, Hadassa Goldberg-Stern, Zaid Afawi, Sara Kivity, Chantal Trager, Steven Petrou, Samuel F. Berkovic and Ingrid E. Scheffer

    Version of Record online : 27 DEC 2012, DOI: 10.1002/ana.23702

  4. The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome

    Epilepsia

    Volume 56, Issue 12, December 2015, Pages: e203–e208, Jan Larsen, Katrine Marie Johannesen, Jakob Ek, Shan Tang, Carla Marini, Susanne Blichfeldt, Maria Kibæk, Sarah von Spiczak, Sarah Weckhuysen, Mimoza Frangu, Bernd Axel Neubauer, Peter Uldall, Pasquale Striano, Federico Zara, MAE working group of the EuroEPINOMICS RES Consortium, Rebecca Kleiss, Michael Simpson, Hiltrud Muhle, Marina Nikanorova, Birgit Jepsen, Niels Tommerup, Ulrich Stephani, Renzo Guerrini, Morten Duno, Helle Hjalgrim, Deb Pal, Ingo Helbig and Rikke Steensbjerre Møller

    Version of Record online : 5 NOV 2015, DOI: 10.1111/epi.13222

  5. Paroxysmal dyskinesias revisited: A review of 500 genetically proven cases and a new classification

    Movement Disorders

    Volume 29, Issue 9, August 2014, Pages: 1108–1116, Roberto Erro, Una-Marie Sheerin and Kailash P. Bhatia

    Version of Record online : 25 JUN 2014, DOI: 10.1002/mds.25933

  6. You have full text access to this Open Access content
    Tumor-suppressive microRNA-1291 directly regulates glucose transporter 1 in renal cell carcinoma

    Cancer Science

    Volume 104, Issue 11, November 2013, Pages: 1411–1419, Takeshi Yamasaki, Naohiko Seki, Hirofumi Yoshino, Toshihiko Itesako, Yasutoshi Yamada, Shuichi Tatarano, Hideo Hidaka, Tomokazu Yonezawa, Masayuki Nakagawa and Hideki Enokida

    Version of Record online : 22 AUG 2013, DOI: 10.1111/cas.12240

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    Corticosterone alters materno-fetal glucose partitioning and insulin signalling in pregnant mice

    The Journal of Physiology

    Volume 593, Issue 5, 1 March 2015, Pages: 1307–1321, O. R. Vaughan, H. M. Fisher, K. N. Dionelis, E. C. Jefferies, J. S. Higgins, B. Musial, A. N. Sferruzzi-Perri and A. L. Fowden

    Version of Record online : 29 JAN 2015, DOI: 10.1113/jphysiol.2014.287177

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    Set7/9 Impacts COL2A1 Expression Through Binding and Repression of SirT1 Histone Deacetylation

    Journal of Bone and Mineral Research

    Volume 29, Issue 2, February 2014, Pages: 348–360, Hanna Oppenheimer, Ashok Kumar, Hadar Meir, Israel Schwartz, Avi Zini, Amir Haze, Leonid Kandel, Yoav Mattan, Meir Liebergall and Mona Dvir-Ginzberg

    Version of Record online : 17 JAN 2014, DOI: 10.1002/jbmr.2052

  9. Post-hatching development of in vitro bovine embryos from day 7 to 14 in vivo versus in vitro

    Molecular Reproduction and Development

    Volume 80, Issue 11, November 2013, Pages: 936–947, G.M. Machado, A.R. Ferreira, I. Pivato, A. Fidelis, J.F. Spricigo, F. Paulini, C.M. Lucci, M.M. Franco and M.A. Dode

    Version of Record online : 10 SEP 2013, DOI: 10.1002/mrd.22230

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    A new long form of Sox5 (L-Sox5), Sox6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II collagen gene

    The EMBO Journal

    Volume 17, Issue 19, October 1, 1998, Pages: 5718–5733, Véronique Lefebvre, Ping Li and Benoit de Crombrugghe

    Version of Record online : 1 OCT 1998, DOI: 10.1093/emboj/17.19.5718

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    Adaptations in placental phenotype support fetal growth during undernutrition of pregnant mice

    The Journal of Physiology

    Volume 588, Issue 3, February 2010, Pages: 527–538, P. M. Coan, O. R. Vaughan, Y. Sekita, S. L. Finn, G. J. Burton, M. Constancia and A. L. Fowden

    Version of Record online : 29 JAN 2010, DOI: 10.1113/jphysiol.2009.181214

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    Adaptations in placental nutrient transfer capacity to meet fetal growth demands depend on placental size in mice

    The Journal of Physiology

    Volume 586, Issue 18, September 2008, Pages: 4567–4576, P. M. Coan, E. Angiolini, I. Sandovici, G. J. Burton, M. Constância and A. L. Fowden

    Version of Record online : 15 SEP 2008, DOI: 10.1113/jphysiol.2008.156133

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    Sox genes regulate type 2 collagen expression in avian neural crest cells

    Development, Growth & Differentiation

    Volume 48, Issue 8, October 2006, Pages: 477–486, Takashi Suzuki, Daisuke Sakai, Noriko Osumi, Hiroshi Wada and Yoshio Wakamatsu

    Version of Record online : 9 OCT 2006, DOI: 10.1111/j.1440-169X.2006.00886.x

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    Clinical dissection of early onset absence epilepsy in children and prognostic implications

    Epilepsia

    Volume 54, Issue 10, October 2013, Pages: 1761–1770, Sergio Agostinelli, Patrizia Accorsi, Francesca Beccaria, Vincenzo Belcastro, Maria Paola Canevini, Giuseppe Capovilla, Silvia Cappanera, Bernardo Dalla Bernardina, Francesca Darra, Luigi Del Gaudio, Maurizio Elia, Raffaele Falsaperla, Lucio Giordano, Giuseppe Gobbi, Carlo Minetti, Francesco Nicita, Pasquale Parisi, Piero Pavone, Marianna Pezzella, Michela Sesta, Alberto Spalice, Salvatore Striano, Elisabetta Tozzi, Monica Traverso, Stella Vari, Aglaia Vignoli, Nelia Zamponi, Federico Zara, Pasquale Striano, Alberto Verrotti and on behalf of the SINP (Società Italiana Neurologia Pediatrica) Collaborative Working Group

    Version of Record online : 27 AUG 2013, DOI: 10.1111/epi.12341

  15. Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution

    European Journal of Neurology

    Volume 20, Issue 5, May 2013, Pages: 856–859, S. Agostinelli, M. Traverso, P. Accorsi, F. Beccaria, V. Belcastro, G. Capovilla, S. Cappanera, A. Coppola, B. Dalla Bernardina, F. Darra, M. Ferretti, M. Elia, D. Galeone, L. Giordano, G. Gobbi, F. Nicita, P. Parisi, M. Pezzella, A. Spalice, S. Striano, E. Tozzi, A. Vignoli, C. Minetti, F. Zara, P. Striano and A. Verrotti, on behalf of the collaborative group of Società Italiana di Neurologia Pediatrica (SINP)

    Version of Record online : 30 SEP 2012, DOI: 10.1111/j.1468-1331.2012.03871.x

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    Emerging roles of metal solute carriers in cancer mechanisms and treatment

    Biopharmaceutics & Drug Disposition

    Volume 35, Issue 8, November 2014, Pages: 450–462, Nancy N. Jong and Mark J. McKeage

    Version of Record online : 5 SEP 2014, DOI: 10.1002/bdd.1903

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    A common novel splice variant of SLC22A1 (OCT1) is associated with impaired responses to imatinib in patients with chronic myeloid leukaemia

    British Journal of Haematology

    Volume 163, Issue 5, December 2013, Pages: 631–639, Jacob Grinfeld, Gareth Gerrard, Mary Alikian, Juan Alonso-Dominguez, Sakuntala Ale, Mikel Valgañon, Georgios Nteliopoulos, Deborah White, David Marin, Corinne Hedgley, Stephen O'Brien, Richard Clark, John M. Goldman, Dragana Milojkovic, Jane F. Apperley and Letizia Foroni

    Version of Record online : 10 OCT 2013, DOI: 10.1111/bjh.12591

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    Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency

    Epilepsia

    Volume 53, Issue 12, December 2012, Pages: e204–e207, Todor Arsov, Saul A. Mullen, John A. Damiano, Kate M. Lawrence, Linda L. Huh, Melinda Nolan, Helen Young, Anaïs Thouin, Hans-Henrik M. Dahl, Samuel F. Berkovic, Douglas E. Crompton, Lynette G. Sadleir and Ingrid E. Scheffer

    Version of Record online : 25 OCT 2012, DOI: 10.1111/epi.12007

  19. Association of a polymorphism of BTN2A1 with Type 2 diabetes mellitus in Japanese individuals

    Diabetic Medicine

    Volume 28, Issue 11, November 2011, Pages: 1381–1387, M. Hiramatsu, M. Oguri, K. Kato, T. Yoshida, T. Fujimaki, H. Horibe, K. Yokoi, S. Watanabe, K. Satoh, Y. Aoyagi, M. Tanaka, H. Yoshida, S. Shinkai, Y. Nozawa, T. Murohara and Y. Yamada

    Version of Record online : 17 OCT 2011, DOI: 10.1111/j.1464-5491.2011.03358.x

  20. Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1

    Annals of Neurology

    Volume 66, Issue 3, September 2009, Pages: 415–419, Arvid Suls, Saul A. Mullen, Yvonne G. Weber, Kristien Verhaert, Berten Ceulemans, Renzo Guerrini, Thomas V. Wuttke, Alberto Salvo-Vargas, Liesbet Deprez, Lieve R. F. Claes, Albena Jordanova, Samuel F. Berkovic, Holger Lerche, Peter De Jonghe and Ingrid E. Scheffer

    Version of Record online : 13 APR 2009, DOI: 10.1002/ana.21724