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Items: 1 to 20 of 113

1.

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients.

Jacquet H, Raux G, Thibaut F, Hecketsweiler B, Houy E, Demilly C, Haouzir S, Allio G, Fouldrin G, Drouin V, Bou J, Petit M, Campion D, Frébourg T.

Hum Mol Genet. 2002 Sep 15;11(19):2243-9.

2.

Functional consequences of PRODH missense mutations.

Bender HU, Almashanu S, Steel G, Hu CA, Lin WW, Willis A, Pulver A, Valle D.

Am J Hum Genet. 2005 Mar;76(3):409-20. Epub 2005 Jan 20.

3.

Hyperprolinemia is a risk factor for schizoaffective disorder.

Jacquet H, Demily C, Houy E, Hecketsweiler B, Bou J, Raux G, Lerond J, Allio G, Haouzir S, Tillaux A, Bellegou C, Fouldrin G, Delamillieure P, Ménard JF, Dollfus S, D'Amato T, Petit M, Thibaut F, Frébourg T, Campion D.

Mol Psychiatry. 2005 May;10(5):479-85.

PMID:
15494707
4.

Early neurological phenotype in 4 children with biallelic PRODH mutations.

Afenjar A, Moutard ML, Doummar D, Guët A, Rabier D, Vermersch AI, Mignot C, Burglen L, Heron D, Thioulouse E, de Villemeur TB, Campion D, Rodriguez D.

Brain Dev. 2007 Oct;29(9):547-52. Epub 2007 Apr 6.

PMID:
17412540
5.

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.

Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, Fantini C, Brévière GM, Di Rosa G, Pustorino G, Vogels A, Swillen A, Legallic S, Bou J, Opolczynski G, Drouin-Garraud V, Lemarchand M, Philip N, Gérard-Desplanches A, Carlier M, Philippe A, Nolen MC, Heron D, Sarda P, Lacombe D, Coizet C, Alembik Y, Layet V, Afenjar A, Hannequin D, Demily C, Petit M, Thibaut F, Frebourg T, Campion D.

Hum Mol Genet. 2007 Jan 1;16(1):83-91. Epub 2006 Nov 29.

6.

Hyperprolinemia is not associated with childhood onset schizophrenia.

Jacquet H, Rapoport JL, Hecketsweiler B, Bobb A, Thibaut F, Frébourg T, Campion D.

Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5;141B(2):192.

PMID:
16389584
7.

Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia.

Williams HJ, Williams N, Spurlock G, Norton N, Zammit S, Kirov G, Owen MJ, O'Donovan MC.

Am J Med Genet B Neuropsychiatr Genet. 2003 Jul 1;120B(1):42-6.

PMID:
12815738
8.

Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population.

Li T, Ma X, Sham PC, Sun X, Hu X, Wang Q, Meng H, Deng W, Liu X, Murray RM, Collier DA.

Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):13-5.

PMID:
15274030
9.

Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia.

Zinkstok J, Schmitz N, van Amelsvoort T, Moeton M, Baas F, Linszen D.

Genes Brain Behav. 2008 Feb;7(1):61-9. Epub 2007 May 14.

10.

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
11.

Type I hyperprolinemia and proline dehydrogenase (PRODH) mutations in four Italian children with epilepsy and mental retardation.

Di Rosa G, Pustorino G, Spano M, Campion D, Calabrò M, Aguennouz M, Caccamo D, Legallic S, Sgro DL, Bonsignore M, Tortorella G.

Psychiatr Genet. 2008 Feb;18(1):40-2. doi: 10.1097/YPG.0b013e3282f08a3d.

PMID:
18197084
12.

Identification of PRODH mutations in Korean neonates with type I hyperprolinemia.

Jang MA, Kim BC, Ki CS, Lee SY, Kim JW, Choi TY, Lee DH, Song J, Lee YW, Park HD.

Ann Clin Lab Sci. 2013 Winter;43(1):31-6.

PMID:
23462603
13.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
15.

PRODH gene is associated with executive function in schizophrenic families.

Li T, Ma X, Hu X, Wang Y, Yan C, Meng H, Liu X, Toulopoulou T, Murray RM, Collier DA.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 5;147B(5):654-7. doi: 10.1002/ajmg.b.30648.

PMID:
18163391
16.

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.

Prasad SE, Howley S, Murphy KC.

Dev Disabil Res Rev. 2008;14(1):26-34. doi: 10.1002/ddrr.5. Review.

PMID:
18636634
17.

Vitamin D insufficiency and schizophrenia risk: evaluation of hyperprolinemia as a mediator of association.

Clelland JD, Read LL, Drouet V, Kaon A, Kelly A, Duff KE, Nadrich RH, Rajparia A, Clelland CL.

Schizophr Res. 2014 Jun;156(1):15-22. doi: 10.1016/j.schres.2014.03.017. Epub 2014 Apr 29.

18.

A family-based association study of T1945C polymorphism in the proline dehydrogenase gene and schizophrenia in the Chinese population.

Fan JB, Ma J, Zhang CS, Tang JX, Gu NF, Feng GY, St Clair D, He L.

Neurosci Lett. 2003 Mar 6;338(3):252-4.

PMID:
12581843
19.

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice.

Gogos JA, Santha M, Takacs Z, Beck KD, Luine V, Lucas LR, Nadler JV, Karayiorgou M.

Nat Genet. 1999 Apr;21(4):434-9.

PMID:
10192398
20.

[In search of susceptibility genes for schizophrenia].

Schosser A, Aschauer HN.

Wien Klin Wochenschr. 2004 Dec 30;116(24):827-33. Review. German.

PMID:
15690966
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