Dietrich P - Search Results

1

IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formation.

Cheishvili D, Dietrich P, Maayan C, Even A, Weil M, Dragatsis I, Razin A. Cheishvili D, et al. Among authors: dietrich p. PLoS One. 2014 Apr 23;9(4):e94612. doi: 10.1371/journal.pone.0094612. eCollection 2014. PLoS One. 2014. PMID: 24760006 Free PMC article.

2

Expression of the Huntingtin-associated protein 1 gene in the developing and adult mouse.

Dragatsis I, Dietrich P, Zeitlin S. Dragatsis I, et al. Among authors: dietrich p. Neurosci Lett. 2000 Mar 17;282(1-2):37-40. doi: 10.1016/s0304-3940(00)00872-7. Neurosci Lett. 2000. PMID: 10713390 Free article.

3

An allelic series for the leptin receptor gene generated by CRE and FLP recombinase.

McMinn JE, Liu SM, Dragatsis I, Dietrich P, Ludwig T, Eiden S, Chua SC Jr. McMinn JE, et al. Among authors: dietrich p. Mamm Genome. 2004 Sep;15(9):677-85. doi: 10.1007/s00335-004-2340-1. Mamm Genome. 2004. PMID: 15389315

4

Huntingtin-associated protein 1 (Hap1) mutant mice bypassing the early postnatal lethality are neuroanatomically normal and fertile but display growth retardation.

Dragatsis I, Zeitlin S, Dietrich P. Dragatsis I, et al. Among authors: dietrich p. Hum Mol Genet. 2004 Dec 15;13(24):3115-25. doi: 10.1093/hmg/ddh328. Epub 2004 Oct 20. Hum Mol Genet. 2004. PMID: 15496430

5

Congenital hydrocephalus associated with abnormal subcommissural organ in mice lacking huntingtin in Wnt1 cell lineages.

Dietrich P, Shanmugasundaram R, Shuyu E, Dragatsis I. Dietrich P, et al. Hum Mol Genet. 2009 Jan 1;18(1):142-50. doi: 10.1093/hmg/ddn324. Epub 2008 Oct 6. Hum Mol Genet. 2009. PMID: 18838463 Free PMC article.

6

CAG repeat lengths > or =335 attenuate the phenotype in the R6/2 Huntington's disease transgenic mouse.

Dragatsis I, Goldowitz D, Del Mar N, Deng YP, Meade CA, Liu L, Sun Z, Dietrich P, Yue J, Reiner A. Dragatsis I, et al. Among authors: dietrich p. Neurobiol Dis. 2009 Mar;33(3):315-30. doi: 10.1016/j.nbd.2008.10.009. Epub 2008 Nov 6. Neurobiol Dis. 2009. PMID: 19027857 Free PMC article.

7

Genetics and neuropathology of Huntington's disease.

Reiner A, Dragatsis I, Dietrich P. Reiner A, et al. Among authors: dietrich p. Int Rev Neurobiol. 2011;98:325-72. doi: 10.1016/B978-0-12-381328-2.00014-6. Int Rev Neurobiol. 2011. PMID: 21907094 Free PMC article. Review.

8

Ciliogenesis is regulated by a huntingtin-HAP1-PCM1 pathway and is altered in Huntington disease.

Keryer G, Pineda JR, Liot G, Kim J, Dietrich P, Benstaali C, Smith K, Cordelières FP, Spassky N, Ferrante RJ, Dragatsis I, Saudou F. Keryer G, et al. Among authors: dietrich p. J Clin Invest. 2011 Nov;121(11):4372-82. doi: 10.1172/JCI57552. Epub 2011 Oct 10. J Clin Invest. 2011. PMID: 21985783 Free PMC article.

9

Deletion of exon 20 of the Familial Dysautonomia gene Ikbkap in mice causes developmental delay, cardiovascular defects, and early embryonic lethality.

Dietrich P, Yue J, E S, Dragatsis I. Dietrich P, et al. PLoS One. 2011;6(10):e27015. doi: 10.1371/journal.pone.0027015. Epub 2011 Oct 28. PLoS One. 2011. PMID: 22046433 Free PMC article.

10

IKAP expression levels modulate disease severity in a mouse model of familial dysautonomia.

Dietrich P, Alli S, Shanmugasundaram R, Dragatsis I. Dietrich P, et al. Hum Mol Genet. 2012 Dec 1;21(23):5078-90. doi: 10.1093/hmg/dds354. Epub 2012 Aug 24. Hum Mol Genet. 2012. PMID: 22922231 Free PMC article.

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