Dietrich P - Search Results

1

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

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

Conditional mutagenesis in mice with heat shock promoter-driven cre transgenes.

Dietrich P, Dragatsis I, Xuan S, Zeitlin S, Efstratiadis A. Dietrich P, et al. Mamm Genome. 2000 Mar;11(3):196-205. doi: 10.1007/s003350010037. Mamm Genome. 2000. PMID: 10723724

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

Neuronal deletion of Lepr elicits diabesity in mice without affecting cold tolerance or fertility.

McMinn JE, Liu SM, Liu H, Dragatsis I, Dietrich P, Ludwig T, Boozer CN, Chua SC Jr. McMinn JE, et al. Among authors: dietrich p. Am J Physiol Endocrinol Metab. 2005 Sep;289(3):E403-11. doi: 10.1152/ajpendo.00535.2004. Epub 2005 May 3. Am J Physiol Endocrinol Metab. 2005. PMID: 15870101 Free article.

6

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.

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

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.

9

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.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

589 results

Search Page

Filters