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There are 2421 results for: content related to: Association Between In Vivo Alcohol Metabolism and Genetic Variation in Pathways that Metabolize the Carbon Skeleton of Ethanol and NADH Reoxidation in the Alcohol Challenge Twin Study

  1. Association between genetic variants in SLC25A12 and risk of autism spectrum disorders: An integrated meta-analysis

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 4, June 2015, Pages: 236–246, Jun Liu, Aiping Yang, Qunwei Zhang, Guohui Yang, Wenjun Yang, Heyue Lei, Jianjun Quan, Fei Qu, Min Wang, Zengyu Zhang and Ke Yu

    Version of Record online : 29 APR 2015, DOI: 10.1002/ajmg.b.32304

  2. An analysis of candidate autism loci on chromosome 2q24–q33: Evidence for association to the STK39 gene

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 7, 5 October 2008, Pages: 1152–1158, Nicolas Ramoz, Guiqing Cai, Jennifer G. Reichert, Jeremy M. Silverman and Joseph D. Buxbaum

    Version of Record online : 17 MAR 2008, DOI: 10.1002/ajmg.b.30739

  3. SLC25A19 mutation as a cause of neuropathy and bilateral striatal necrosis

    Annals of Neurology

    Volume 66, Issue 3, September 2009, Pages: 419–424, Ronen Spiegel, Avraham Shaag, Simon Edvardson, Hanna Mandel, Polina Stepensky, Stavit A. Shalev, Yoseph Horovitz, Ophry Pines and Orly Elpeleg

    Version of Record online : 22 JUN 2009, DOI: 10.1002/ana.21752

  4. You have free access to this content
    A novel long noncoding RNA Lnc-HC binds hnRNPA2B1 to regulate expressions of Cyp7a1 and Abca1 in hepatocytic cholesterol metabolism


    Volume 64, Issue 1, July 2016, Pages: 58–72, Xi Lan, Jidong Yan, Juan Ren, Bo Zhong, Jing Li, Yue Li, Li Liu, Jing Yi, Qingzhu Sun, Xudong Yang, Jian Sun, Liesu Meng, Wenhua Zhu, Rikard Holmdahl, Dongmin Li and Shemin Lu

    Version of Record online : 22 JAN 2016, DOI: 10.1002/hep.28391

  5. Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism

    Autism Research

    Volume 1, Issue 3, June 2008, Pages: 189–192, Joni A. Turunen, Karola Rehnström, Helena Kilpinen, Mikko Kuokkanen, Elli Kempas and Tero Ylisaukko-oja

    Version of Record online : 18 JUL 2008, DOI: 10.1002/aur.25

  6. Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts

    Clinical Genetics

    Volume 76, Issue 2, August 2009, Pages: 188–194, F Molinari, A Kaminska, G Fiermonte, N Boddaert, A Raas-Rothschild, P Plouin, L Palmieri, F Brunelle, F Palmieri, O Dulac, A Munnich and L Colleaux

    Version of Record online : 24 SEP 2009, DOI: 10.1111/j.1399-0004.2009.01236.x

  7. Amish microcephaly: Long-term survival and biochemical characterization

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 7, July 2010, Pages: 1747–1751, Victoria Mok Siu, Suzanne Ratko, Asuri N. Prasad, Chitra Prasad and C. Anthony Rupar

    Version of Record online : 25 JUN 2010, DOI: 10.1002/ajmg.a.33373

  8. You have full text access to this OnlineOpen article
    The Concise Guide to PHARMACOLOGY 2013/14: Transporters

    British Journal of Pharmacology

    Volume 170, Issue 8, December 2013, Pages: 1706–1796, Stephen P.H. Alexander, Helen E. Benson, Elena Faccenda, Adam J. Pawson, Joanna L. Sharman, Michael Spedding, John A. Peters, Anthony J. Harmar and CGTP Collaborators

    Version of Record online : 17 DEC 2013, DOI: 10.1111/bph.12450

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    British Journal of Pharmacology

    Volume 164, Issue s1, November 2011, Pages: S213–S278, SPH Alexander, A Mathie and JA Peters

    Version of Record online : 1 NOV 2011, DOI: 10.1111/j.1476-5381.2011.01649_8.x

  10. You have full text access to this OnlineOpen article
    The Concise Guide to PHARMACOLOGY 2015/16: Transporters

    British Journal of Pharmacology

    Volume 172, Issue 24, December 2015, Pages: 6110–6202, Stephen PH Alexander, Eamonn Kelly, Neil Marrion, John A Peters, Helen E Benson, Elena Faccenda, Adam J Pawson, Joanna L Sharman, Christopher Southan, Jamie A Davies and CGTP Collaborators

    Version of Record online : 9 DEC 2015, DOI: 10.1111/bph.13355

  11. SLC25A22 is a novel gene for migrating partial seizures in infancy

    Annals of Neurology

    Volume 74, Issue 6, December 2013, Pages: 873–882, Annapurna Poduri, Erin L. Heinzen, Vida Chitsazzadeh, Francesco Massimo Lasorsa, P. Christina Elhosary, Christopher M. LaCoursiere, Emilie Martin, Christopher J. Yuskaitis, Robert Sean Hill, Kutay Deniz Atabay, Brenda Barry, Jennifer N. Partlow, Fahad A. Bashiri, Radwan M. Zeidan, Salah A. Elmalik, Mohammad M. U. Kabiraj, Sanjeev Kothare, Tommy Stödberg, Amy McTague, Manju A. Kurian, Ingrid E. Scheffer, A. James Barkovich, Ferdinando Palmieri, Mustafa A. Salih and Christopher A. Walsh

    Version of Record online : 17 OCT 2013, DOI: 10.1002/ana.23998

  12. You have full text access to this OnlineOpen article
    SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome

    EMBO Molecular Medicine

    Alexandre Janer, Julien Prudent, Vincent Paupe, Somayyeh Fahiminiya, Jacek Majewski, Nicolas Sgarioto, Christine Des Rosiers, Anik Forest, Zhen-Yuan Lin, Anne-Claude Gingras, Grant Mitchell, Heidi M McBride and Eric A Shoubridge

    Version of Record online : 7 JUL 2016, DOI: 10.15252/emmm.201506159

  13. Novel pathogenic SLC25A46 splice-site mutation causes an optic atrophy spectrum disorder

    Clinical Genetics

    M. Nguyen, I. Boesten, D. M. E. I. Hellebrekers, N. M. Mulder-den Hartog, I. F. M. de Coo, H. J. M. Smeets and M. Gerards

    Version of Record online : 8 APR 2016, DOI: 10.1111/cge.12774

  14. Mitochondrial Carriers

    Standard Article


    Araceli Arco and Jorgina Satrústegui

    Published Online : 15 MAR 2013, DOI: 10.1002/9780470015902.a0024196

  15. Polymorphism of SLC25A32, the folate transporter gene, is associated with plasma folate levels and bone fractures in Japanese postmenopausal women

    Geriatrics & Gerontology International

    Volume 14, Issue 4, October 2014, Pages: 942–946, Tomohiko Urano, Masataka Shiraki, Mitsuru Saito, Noriko Sasaki, Yasuyoshi Ouchi and Satoshi Inoue

    Version of Record online : 5 DEC 2013, DOI: 10.1111/ggi.12201

  16. Hypermethioninemias of genetic and non-genetic origin: A review

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 157, Issue 1, 15 February 2011, Pages: 3–32, S. Harvey Mudd

    Version of Record online : 9 FEB 2011, DOI: 10.1002/ajmg.c.30293

  17. Transcriptome analysis of muscle in horses suffering from recurrent exertional rhabdomyolysis revealed energetic pathway alterations and disruption in the cytosolic calcium regulation

    Animal Genetics

    Volume 43, Issue 3, June 2012, Pages: 271–281, E. Barrey, L. Jayr, E. Mucher, S. Gospodnetic, F. Joly, P. Benech, O. Alibert, X. Gidrol, X. Mata, A. Vaiman and G. Guérin

    Version of Record online : 27 SEP 2011, DOI: 10.1111/j.1365-2052.2011.02246.x

  18. Low levels of citrin (SLC25A13) expression in adult mouse brain restricted to neuronal clusters

    Journal of Neuroscience Research

    Volume 88, Issue 5, April 2010, Pages: 1009–1016, Laura Contreras, Almudena Urbieta, Keiko Kobayashi, Takeyori Saheki and Jorgina Satrústegui

    Version of Record online : 11 NOV 2009, DOI: 10.1002/jnr.22283

  19. Gene expression analysis by oligonucleotide microarray in oral leukoplakia

    Journal of Oral Pathology & Medicine

    Volume 38, Issue 4, April 2009, Pages: 356–361, Yuri Kuribayashi, Kei-ichi Morita, Hirofumi Tomioka, Masaru Uekusa, Daisuke Ito and Ken Omura

    Version of Record online : 9 FEB 2009, DOI: 10.1111/j.1600-0714.2008.00731.x

  20. Idiopathic eruptive macular pigmentation in a child with citrin deficiency

    Pediatrics International

    Chu-Li Fu, Yun-Feng Hu and Yuan-Zong Song

    Version of Record online : 7 JUL 2016, DOI: 10.1111/ped.13007