These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

785 related items for PubMed ID: 17893705

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Molecular genetic studies of the arginine vasopressin 1a receptor (AVPR1a) and the oxytocin receptor (OXTR) in human behaviour: from autism to altruism with some notes in between.
    Israel S, Lerer E, Shalev I, Uzefovsky F, Reibold M, Bachner-Melman R, Granot R, Bornstein G, Knafo A, Yirmiya N, Ebstein RP.
    Prog Brain Res; 2008; 170():435-49. PubMed ID: 18655900
    [Abstract] [Full Text] [Related]

  • 5. Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean.
    Yoo HJ, Lee SK, Park M, Cho IH, Hyun SH, Lee JC, Yang SY, Kim SA.
    Neurosci Res; 2009 Mar; 63(3):172-6. PubMed ID: 19100789
    [Abstract] [Full Text] [Related]

  • 6. Association between the oxytocin receptor gene and amygdalar volume in healthy adults.
    Inoue H, Yamasue H, Tochigi M, Abe O, Liu X, Kawamura Y, Takei K, Suga M, Yamada H, Rogers MA, Aoki S, Sasaki T, Kasai K.
    Biol Psychiatry; 2010 Dec 01; 68(11):1066-72. PubMed ID: 20832055
    [Abstract] [Full Text] [Related]

  • 7. Two genetic variants of CD38 in subjects with autism spectrum disorder and controls.
    Munesue T, Yokoyama S, Nakamura K, Anitha A, Yamada K, Hayashi K, Asaka T, Liu HX, Jin D, Koizumi K, Islam MS, Huang JJ, Ma WJ, Kim UH, Kim SJ, Park K, Kim D, Kikuchi M, Ono Y, Nakatani H, Suda S, Miyachi T, Hirai H, Salmina A, Pichugina YA, Soumarokov AA, Takei N, Mori N, Tsujii M, Sugiyama T, Yagi K, Yamagishi M, Sasaki T, Yamasue H, Kato N, Hashimoto R, Taniike M, Hayashi Y, Hamada J, Suzuki S, Ooi A, Noda M, Kamiyama Y, Kido MA, Lopatina O, Hashii M, Amina S, Malavasi F, Huang EJ, Zhang J, Shimizu N, Yoshikawa T, Matsushima A, Minabe Y, Higashida H.
    Neurosci Res; 2010 Jun 01; 67(2):181-91. PubMed ID: 20435366
    [Abstract] [Full Text] [Related]

  • 8. Family-based association study between GRIK2 polymorphisms and autism spectrum disorders in the Korean trios.
    Kim SA, Kim JH, Park M, Cho IH, Yoo HJ.
    Neurosci Res; 2007 Jul 01; 58(3):332-5. PubMed ID: 17428563
    [Abstract] [Full Text] [Related]

  • 9. Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.
    Dutta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Usha R.
    Neurosci Lett; 2008 Aug 15; 441(1):56-60. PubMed ID: 18597938
    [Abstract] [Full Text] [Related]

  • 10. Analysis of serotonin receptor 2A gene (HTR2A): association study with autism spectrum disorder in the Indian population and investigation of the gene expression in peripheral blood leukocytes.
    Guhathakurta S, Singh AS, Sinha S, Chatterjee A, Ahmed S, Ghosh S, Usha R.
    Neurochem Int; 2009 Dec 15; 55(8):754-9. PubMed ID: 19647026
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Association of GABRB3 polymorphisms with autism spectrum disorders in Korean trios.
    Kim SA, Kim JH, Park M, Cho IH, Yoo HJ.
    Neuropsychobiology; 2006 Dec 15; 54(3):160-5. PubMed ID: 17230033
    [Abstract] [Full Text] [Related]

  • 14. Low CD38 expression in lymphoblastoid cells and haplotypes are both associated with autism in a family-based study.
    Lerer E, Levi S, Israel S, Yaari M, Nemanov L, Mankuta D, Nurit Y, Ebstein RP.
    Autism Res; 2010 Dec 15; 3(6):293-302. PubMed ID: 21182206
    [Abstract] [Full Text] [Related]

  • 15. Modeling clinical outcome of children with autistic spectrum disorders.
    Coplan J, Jawad AF.
    Pediatrics; 2005 Jul 15; 116(1):117-22. PubMed ID: 15995041
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. No association between the neuronal pentraxin II gene polymorphism and autism.
    Marui T, Koishi S, Funatogawa I, Yamamoto K, Matsumoto H, Hashimoto O, Ishijima M, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Kato N, Sasaki T.
    Prog Neuropsychopharmacol Biol Psychiatry; 2007 May 09; 31(4):940-3. PubMed ID: 17408830
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 40.