Dragatsis I - Search Results

1

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. Among authors: dragatsis i. 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.

2

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. 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

3

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. Among authors: dragatsis i. 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.

4

Familial Dysautonomia: Mechanisms and Models.

Dietrich P, Dragatsis I. Dietrich P, et al. Among authors: dragatsis i. Genet Mol Biol. 2016 Oct-Dec;39(4):497-514. doi: 10.1590/1678-4685-GMB-2015-0335. Epub 2016 Aug 4. Genet Mol Biol. 2016. PMID: 27561110 Free PMC article.

5

Genetics and neuropathology of Huntington's disease.

Reiner A, Dragatsis I, Dietrich P. Reiner A, et al. Among authors: dragatsis i. 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.

6

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. Among authors: dragatsis i. PLoS One. 2011;6(10):e27015. doi: 10.1371/journal.pone.0027015. Epub 2011 Oct 28. PLoS One. 2011. PMID: 22046433 Free PMC article.

7

Sensory and autonomic deficits in a new humanized mouse model of familial dysautonomia.

Morini E, Dietrich P, Salani M, Downs HM, Wojtkiewicz GR, Alli S, Brenner A, Nilbratt M, LeClair JW, Oaklander AL, Slaugenhaupt SA, Dragatsis I. Morini E, et al. Among authors: dragatsis i. Hum Mol Genet. 2016 Mar 15;25(6):1116-28. doi: 10.1093/hmg/ddv634. Epub 2016 Jan 13. Hum Mol Genet. 2016. PMID: 26769677 Free PMC article.

8

Elimination of huntingtin in the adult mouse leads to progressive behavioral deficits, bilateral thalamic calcification, and altered brain iron homeostasis.

Dietrich P, Johnson IM, Alli S, Dragatsis I. Dietrich P, et al. Among authors: dragatsis i. PLoS Genet. 2017 Jul 17;13(7):e1006846. doi: 10.1371/journal.pgen.1006846. eCollection 2017 Jul. PLoS Genet. 2017. PMID: 28715425 Free PMC article.

9

ELP1 Splicing Correction Reverses Proprioceptive Sensory Loss in Familial Dysautonomia.

Morini E, Gao D, Montgomery CM, Salani M, Mazzasette C, Krussig TA, Swain B, Dietrich P, Narasimhan J, Gabbeta V, Dakka A, Hedrick J, Zhao X, Weetall M, Naryshkin NA, Wojtkiewicz GG, Ko CP, Talkowski ME, Dragatsis I, Slaugenhaupt SA. Morini E, et al. Among authors: dragatsis i. Am J Hum Genet. 2019 Apr 4;104(4):638-650. doi: 10.1016/j.ajhg.2019.02.009. Epub 2019 Mar 21. Am J Hum Genet. 2019. PMID: 30905397 Free PMC article.

10

Selective retinal ganglion cell loss and optic neuropathy in a humanized mouse model of familial dysautonomia.

Chekuri A, Logan EM, Krauson AJ, Salani M, Ackerman S, Kirchner EG, Bolduc JM, Wang X, Dietrich P, Dragatsis I, Vandenberghe LH, Slaugenhaupt SA, Morini E. Chekuri A, et al. Among authors: dragatsis i. Hum Mol Genet. 2022 Jun 4;31(11):1776-1787. doi: 10.1093/hmg/ddab359. Hum Mol Genet. 2022. PMID: 34908112 Free PMC article.

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