Majores M - Search Results

1

Allelic association between the D10S1423 marker and Alzheimer's disease in a German population.

Majores M, Bagli M, Papassotiropoulos A, Schwab SG, Jessen F, Rao ML, Maier W, Heun R. Majores M, et al. Neurosci Lett. 2000 Aug 11;289(3):224-6. doi: 10.1016/s0304-3940(00)01283-0. Neurosci Lett. 2000. PMID: 10961670

2

The insulin gene VNTR polymorphism in Alzheimer's disease: results of a pilot study.

Majores M, Kölsch H, Bagli M, Ptok U, Kockler M, Becker K, Rao ML, Maier W, Heun R. Majores M, et al. J Neural Transm (Vienna). 2002 Jul;109(7-8):1029-34. doi: 10.1007/s007020200086. J Neural Transm (Vienna). 2002. PMID: 12111440

3

Polymorphism in the peroxisome proliferator-activated receptor alpha gene influences the risk for Alzheimer's disease.

Brune S, Kölsch H, Ptok U, Majores M, Schulz A, Schlosser R, Rao ML, Maier W, Heun R. Brune S, et al. Among authors: majores m. J Neural Transm (Vienna). 2003 Sep;110(9):1041-50. doi: 10.1007/s00702-003-0018-6. J Neural Transm (Vienna). 2003. PMID: 12938026

4

Putative association of polymorphism in the mannose 6-phosphate receptor gene with major depression and Alzheimer's disease.

Kölsch H, Ptok U, Majores M, Schmitz S, Rao ML, Maier W, Heun R. Kölsch H, et al. Among authors: majores m. Psychiatr Genet. 2004 Jun;14(2):97-100. doi: 10.1097/01.ypg.0000129204.58574.c2. Psychiatr Genet. 2004. PMID: 15167696

5

Distinct allelic variants of TSC1 and TSC2 in epilepsy-associated cortical malformations without balloon cells.

Majores M, Blümcke I, Urbach H, Meroni A, Hans V, Holthausen H, Elger CE, Schramm J, Galli C, Spreafico R, Wiestler OD, Becker AJ. Majores M, et al. J Neuropathol Exp Neurol. 2005 Jul;64(7):629-37. doi: 10.1097/01.jnen.0000171651.32460.19. J Neuropathol Exp Neurol. 2005. PMID: 16042315

6

Mutational and expression analysis of CDK1, cyclinA2 and cyclinB1 in epilepsy-associated glioneuronal lesions.

Schick V, Majores M, Fassunke J, Engels G, Simon M, Elger CE, Becker AJ. Schick V, et al. Among authors: majores m. Neuropathol Appl Neurobiol. 2007 Apr;33(2):152-62. doi: 10.1111/j.1365-2990.2006.00788.x. Neuropathol Appl Neurobiol. 2007. PMID: 17359356

7

Increased frequency of distinct TSC2 allelic variants in focal cortical dysplasias with balloon cells and mineralization.

Schönberger A, Niehusmann P, Urbach H, Majores M, Grote A, Holthausen H, Blümcke I, Deckert M, Becker AJ. Schönberger A, et al. Among authors: majores m. Neuropathology. 2009 Oct;29(5):559-65. doi: 10.1111/j.1440-1789.2009.01018.x. Epub 2009 Apr 21. Neuropathology. 2009. PMID: 19422538

8

Activation of Akt independent of PTEN and CTMP tumor-suppressor gene mutations in epilepsy-associated Taylor-type focal cortical dysplasias.

Schick V, Majores M, Engels G, Spitoni S, Koch A, Elger CE, Simon M, Knobbe C, Blümcke I, Becker AJ. Schick V, et al. Among authors: majores m. Acta Neuropathol. 2006 Dec;112(6):715-25. doi: 10.1007/s00401-006-0128-y. Epub 2006 Sep 30. Acta Neuropathol. 2006. PMID: 17013611

9

Genetic alterations of protein-o-mannosyltransferase-1 in glioneuronal and glial brain tumors with subarachnoid spread.

Snoei J, Urbach H, Engels G, Fassunke J, von Lehe M, Becker AJ, Majores M. Snoei J, et al. Among authors: majores m. Neuropathology. 2009 Apr;29(2):116-24. doi: 10.1111/j.1440-1789.2008.00954.x. Epub 2008 Jul 20. Neuropathology. 2009. PMID: 18647264

10

Molecular profiling of temporal lobe epilepsy: comparison of data from human tissue samples and animal models.

Majores M, Eils J, Wiestler OD, Becker AJ. Majores M, et al. Epilepsy Res. 2004 Jul-Aug;60(2-3):173-8. doi: 10.1016/j.eplepsyres.2004.07.002. Epilepsy Res. 2004. PMID: 15380561 Review.

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