Shehadeh J - Search Results

1

Levels of mutant huntingtin influence the phenotypic severity of Huntington disease in YAC128 mouse models.

Graham RK, Slow EJ, Deng Y, Bissada N, Lu G, Pearson J, Shehadeh J, Leavitt BR, Raymond LA, Hayden MR. Graham RK, et al. Among authors: shehadeh j. Neurobiol Dis. 2006 Feb;21(2):444-55. doi: 10.1016/j.nbd.2005.08.007. Epub 2005 Oct 17. Neurobiol Dis. 2006. PMID: 16230019

2

Potentiation of NMDA receptor-mediated excitotoxicity linked with intrinsic apoptotic pathway in YAC transgenic mouse model of Huntington's disease.

Zeron MM, Fernandes HB, Krebs C, Shehadeh J, Wellington CL, Leavitt BR, Baimbridge KG, Hayden MR, Raymond LA. Zeron MM, et al. Among authors: shehadeh j. Mol Cell Neurosci. 2004 Mar;25(3):469-79. doi: 10.1016/j.mcn.2003.11.014. Mol Cell Neurosci. 2004. PMID: 15033175

3

Striatal neuronal apoptosis is preferentially enhanced by NMDA receptor activation in YAC transgenic mouse model of Huntington disease.

Shehadeh J, Fernandes HB, Zeron Mullins MM, Graham RK, Leavitt BR, Hayden MR, Raymond LA. Shehadeh J, et al. Neurobiol Dis. 2006 Feb;21(2):392-403. doi: 10.1016/j.nbd.2005.08.001. Epub 2005 Sep 13. Neurobiol Dis. 2006. PMID: 16165367

4

Wild-type huntingtin protects neurons from excitotoxicity.

Leavitt BR, van Raamsdonk JM, Shehadeh J, Fernandes H, Murphy Z, Graham RK, Wellington CL, Raymond LA, Hayden MR. Leavitt BR, et al. Among authors: shehadeh j. J Neurochem. 2006 Feb;96(4):1121-9. doi: 10.1111/j.1471-4159.2005.03605.x. Epub 2006 Jan 17. J Neurochem. 2006. PMID: 16417581 Free article.

5

Cleavage at the caspase-6 site is required for neuronal dysfunction and degeneration due to mutant huntingtin.

Graham RK, Deng Y, Slow EJ, Haigh B, Bissada N, Lu G, Pearson J, Shehadeh J, Bertram L, Murphy Z, Warby SC, Doty CN, Roy S, Wellington CL, Leavitt BR, Raymond LA, Nicholson DW, Hayden MR. Graham RK, et al. Among authors: shehadeh j. Cell. 2006 Jun 16;125(6):1179-91. doi: 10.1016/j.cell.2006.04.026. Cell. 2006. PMID: 16777606 Free article.

6

Polyglutamine-modulated striatal calpain activity in YAC transgenic huntington disease mouse model: impact on NMDA receptor function and toxicity.

Cowan CM, Fan MM, Fan J, Shehadeh J, Zhang LY, Graham RK, Hayden MR, Raymond LA. Cowan CM, et al. Among authors: shehadeh j. J Neurosci. 2008 Nov 26;28(48):12725-35. doi: 10.1523/JNEUROSCI.4619-08.2008. J Neurosci. 2008. PMID: 19036965 Free PMC article.

7

Expression of tyrosine hydroxylase isoforms and phosphorylation at serine 40 in the human nigrostriatal system in Parkinson's disease.

Shehadeh J, Double KL, Murphy KE, Bobrovskaya L, Reyes S, Dunkley PR, Halliday GM, Dickson PW. Shehadeh J, et al. Neurobiol Dis. 2019 Oct;130:104524. doi: 10.1016/j.nbd.2019.104524. Epub 2019 Jul 2. Neurobiol Dis. 2019. PMID: 31276794

8

The low affinity dopamine binding site on tyrosine hydroxylase: the role of the N-terminus and in situ regulation of enzyme activity.

Gordon SL, Webb JK, Shehadeh J, Dunkley PR, Dickson PW. Gordon SL, et al. Among authors: shehadeh j. Neurochem Res. 2009 Oct;34(10):1830-7. doi: 10.1007/s11064-009-9989-5. Epub 2009 May 16. Neurochem Res. 2009. PMID: 19448984

9

The emotional and social concerns of mothers of children with cleft palate: A cross-sectional study.

El-Hneiti M, Shehadeh JH, Qatamin BA, Shaheen A. El-Hneiti M, et al. Among authors: shehadeh jh. J Pediatr Nurs. 2024 May-Jun;76:e140-e148. doi: 10.1016/j.pedn.2024.02.024. Epub 2024 Apr 3. J Pediatr Nurs. 2024. PMID: 38570228

10

The Intersection of Atrial Fibrillation and Coronary Artery Disease in Middle Eastern Patients. Analysis from the Jordan Atrial Fibrillation Study.

Hammoudeh A, Badaineh Y, Tabbalat R, Ahmad A, Bahhour M, Ja'ara D, Shehadeh J, Jum'ah MA, Migdad A, Hani M, Alhaddad IA. Hammoudeh A, et al. Among authors: shehadeh j. Glob Heart. 2024 Mar 12;19(1):29. doi: 10.5334/gh.1312. eCollection 2024. Glob Heart. 2024. PMID: 38505303 Free PMC article.

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