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    Results: 1 to 20 of 22

    1.

    Reprogramming of proline and glutamine metabolism contributes to the proliferative and metabolic responses regulated by oncogenic transcription factor c-MYC.

    Liu W, Le A, Hancock C, Lane AN, Dang CV, Fan TW, Phang JM.

    Proc Natl Acad Sci U S A. 2012 Jun 5;109(23):8983-8. doi: 10.1073/pnas.1203244109. Epub 2012 May 21.

    PMID:
    22615405
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    2.

    Expression in Escherichia coli of the catalytic domain of human proline oxidase.

    Tallarita E, Pollegioni L, Servi S, Molla G.

    Protein Expr Purif. 2012 Apr;82(2):345-51. doi: 10.1016/j.pep.2012.01.021. Epub 2012 Feb 8.

    PMID:
    22333530
    [PubMed - indexed for MEDLINE]
    3.

    Proline metabolism and cancer.

    Phang JM, Liu W.

    Front Biosci. 2012 Jan 1;17:1835-45. Review.

    PMID:
    22201839
    [PubMed - indexed for MEDLINE]
    4.

    Proline dehydrogenase: a key enzyme in controlling cellular homeostasis.

    Servet C, Ghelis T, Richard L, Zilberstein A, Savoure A.

    Front Biosci. 2012 Jan 1;17:607-20. Review.

    PMID:
    22201764
    [PubMed - indexed for MEDLINE]
    5.

    Proline dehydrogenase is a positive regulator of cell death in different kingdoms.

    Cecchini NM, Monteoliva MI, Alvarez ME.

    Plant Signal Behav. 2011 Aug;6(8):1195-7. doi: 10.4161/psb.6.8.15791. Epub 2011 Aug 1.

    PMID:
    21757996
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    6.

    DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.

    Alkelai A, Lupoli S, Greenbaum L, Kohn Y, Kanyas-Sarner K, Ben-Asher E, Lancet D, Macciardi F, Lerer B.

    Int J Neuropsychopharmacol. 2012 May;15(4):459-69. doi: 10.1017/S1461145711000903. Epub 2011 Jun 20. Erratum in: Int J Neuropsychopharmacol. 2012 May;15(4):541.

    PMID:
    21682944
    [PubMed - indexed for MEDLINE]
    7.

    Reduced transcript expression of genes affected by inherited and de novo CNVs in autism.

    Nord AS, Roeb W, Dickel DE, Walsh T, Kusenda M, O'Connor KL, Malhotra D, McCarthy SE, Stray SM, Taylor SM, Sebat J; STAART Psychopharmacology Network, King B, King MC, McClellan JM.

    Eur J Hum Genet. 2011 Jun;19(6):727-31. doi: 10.1038/ejhg.2011.24. Epub 2011 Mar 30.

    PMID:
    21448237
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    8.

    Polymorphisms in inflammatory pathway genes and their association with colorectal cancer risk.

    Frank B, Hoffmeister M, Klopp N, Illig T, Chang-Claude J, Brenner H.

    Int J Cancer. 2010 Dec 15;127(12):2822-30. doi: 10.1002/ijc.25299.

    PMID:
    21351261
    [PubMed - indexed for MEDLINE]
    9.

    Type I hyperprolinemia: genotype/phenotype correlations.

    Guilmatre A, Legallic S, Steel G, Willis A, Di Rosa G, Goldenberg A, Drouin-Garraud V, Guet A, Mignot C, Des Portes V, Valayannopoulos V, Van Maldergem L, Hoffman JD, Izzi C, Espil-Taris C, Orcesi S, Bonafé L, Le Galloudec E, Maurey H, Ioos C, Afenjar A, Blanchet P, Echenne B, Roubertie A, Frebourg T, Valle D, Campion D.

    Hum Mutat. 2010 Aug;31(8):961-5. doi: 10.1002/humu.21296.

    PMID:
    20524212
    [PubMed - indexed for MEDLINE]
    10.

    Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome.

    Meechan DW, Tucker ES, Maynard TM, LaMantia AS.

    Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16434-45. doi: 10.1073/pnas.0905696106. Epub 2009 Sep 10.

    PMID:
    19805316
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    11.

    Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.

    Guilmatre A, Dubourg C, Mosca AL, Legallic S, Goldenberg A, Drouin-Garraud V, Layet V, Rosier A, Briault S, Bonnet-Brilhault F, Laumonnier F, Odent S, Le Vacon G, Joly-Helas G, David V, Bendavid C, Pinoit JM, Henry C, Impallomeni C, Germano E, Tortorella G, Di Rosa G, Barthelemy C, Andres C, Faivre L, Frébourg T, Saugier Veber P, Campion D.

    Arch Gen Psychiatry. 2009 Sep;66(9):947-56. doi: 10.1001/archgenpsychiatry.2009.80. Review.

    PMID:
    19736351
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    12.

    Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH.

    Bittel DC, Yu S, Newkirk H, Kibiryeva N, Holt A 3rd, Butler MG, Cooley LD.

    Cytogenet Genome Res. 2009;124(2):113-20. doi: 10.1159/000207515. Epub 2009 May 5.

    PMID:
    19420922
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    13.

    Two types of human malignant melanoma cell lines revealed by expression patterns of mitochondrial and survival-apoptosis genes: implications for malignant melanoma therapy.

    Su DM, Zhang Q, Wang X, He P, Zhu YJ, Zhao J, Rennert OM, Su YA.

    Mol Cancer Ther. 2009 May;8(5):1292-304. doi: 10.1158/1535-7163.MCT-08-1030. Epub 2009 Apr 21.

    PMID:
    19383853
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    14.

    A risk PRODH haplotype affects sensorimotor gating, memory, schizotypy, and anxiety in healthy male subjects.

    Roussos P, Giakoumaki SG, Bitsios P.

    Biol Psychiatry. 2009 Jun 15;65(12):1063-70. doi: 10.1016/j.biopsych.2009.01.003. Epub 2009 Feb 20.

    PMID:
    19232576
    [PubMed - indexed for MEDLINE]
    15.

    Identification of DNA copy number aberrations by array comparative genomic hybridization in patients with ruptured intracranial aneurysms.

    Choi JS, Kim SR, Jeon YW, Lee KH, Rha HK.

    J Clin Neurosci. 2009 Feb;16(2):295-301. doi: 10.1016/j.jocn.2007.11.015. Epub 2008 Dec 3.

    PMID:
    19056275
    [PubMed - indexed for MEDLINE]
    16.

    Functional polymorphisms in PRODH are associated with risk and protection for schizophrenia and fronto-striatal structure and function.

    Kempf L, Nicodemus KK, Kolachana B, Vakkalanka R, Verchinski BA, Egan MF, Straub RE, Mattay VA, Callicott JH, Weinberger DR, Meyer-Lindenberg A.

    PLoS Genet. 2008 Nov;4(11):e1000252. doi: 10.1371/journal.pgen.1000252. Epub 2008 Nov 7.

    PMID:
    18989458
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    17.

    Inborn errors of proline metabolism.

    Mitsubuchi H, Nakamura K, Matsumoto S, Endo F.

    J Nutr. 2008 Oct;138(10):2016S-2020S.

    PMID:
    18806117
    [PubMed - indexed for MEDLINE]
    Free Article
    18.

    Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes.

    Maynard TM, Meechan DW, Dudevoir ML, Gopalakrishna D, Peters AZ, Heindel CC, Sugimoto TJ, Wu Y, Lieberman JA, Lamantia AS.

    Mol Cell Neurosci. 2008 Nov;39(3):439-51. doi: 10.1016/j.mcn.2008.07.027. Epub 2008 Aug 15.

    PMID:
    18775783
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    19.

    PRODH variants and risk for schizophrenia.

    Willis A, Bender HU, Steel G, Valle D.

    Amino Acids. 2008 Nov;35(4):673-9. doi: 10.1007/s00726-008-0111-0. Epub 2008 Jun 5. Review.

    PMID:
    18528746
    [PubMed - indexed for MEDLINE]
    20.

    Age-related changes in the expression of schizophrenia susceptibility genes in the human prefrontal cortex.

    Colantuoni C, Hyde TM, Mitkus S, Joseph A, Sartorius L, Aguirre C, Creswell J, Johnson E, Deep-Soboslay A, Herman MM, Lipska BK, Weinberger DR, Kleinman JE.

    Brain Struct Funct. 2008 Sep;213(1-2):255-71. doi: 10.1007/s00429-008-0181-5. Epub 2008 May 10. Erratum in: Brain Struct Funct. 2008 Sep;213(1-2):273.

    PMID:
    18470533
    [PubMed - indexed for MEDLINE]

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