Robinson MB - Search Results

1

Adenovirus-mediated in vivo gene transfer rapidly protects ornithine transcarbamylase-deficient mice from an ammonium challenge.

Ye X, Robinson MB, Pabin C, Quinn T, Jawad A, Wilson JM, Batshaw ML. Ye X, et al. Among authors: robinson mb. Pediatr Res. 1997 Apr;41(4 Pt 1):527-34. doi: 10.1203/00006450-199704000-00012. Pediatr Res. 1997. PMID: 9098855

2

Quinolinate in brain and cerebrospinal fluid in rat models of congenital hyperammonemia.

Robinson MB, Heyes MP, Anegawa NJ, Gorry E, Djali S, Mellits ED, Batshaw ML. Robinson MB, et al. Pediatr Res. 1992 Oct;32(4):483-8. doi: 10.1203/00006450-199210000-00021. Pediatr Res. 1992. PMID: 1279510

3

Brain serotonin2 and serotonin1A receptors are altered in the congenitally hyperammonemic sparse fur mouse.

Robinson MB, Anegawa NJ, Gorry E, Qureshi IA, Coyle JT, Lucki I, Batshaw ML. Robinson MB, et al. J Neurochem. 1992 Mar;58(3):1016-22. doi: 10.1111/j.1471-4159.1992.tb09356.x. J Neurochem. 1992. PMID: 1531355

4

Effect of sodium benzoate and sodium phenylacetate on brain serotonin turnover in the ornithine transcarbamylase-deficient sparse-fur mouse.

Batshaw ML, Hyman SL, Coyle JT, Robinson MB, Qureshi IA, Mellits ED, Quaskey S. Batshaw ML, et al. Among authors: robinson mb. Pediatr Res. 1988 Apr;23(4):368-74. doi: 10.1203/00006450-198804000-00006. Pediatr Res. 1988. PMID: 3374991

5

Quinolinic acid in children with congenital hyperammonemia.

Batshaw ML, Robinson MB, Hyland K, Djali S, Heyes MP. Batshaw ML, et al. Among authors: robinson mb. Ann Neurol. 1993 Nov;34(5):676-81. doi: 10.1002/ana.410340509. Ann Neurol. 1993. PMID: 7694541

6

Prolonged metabolic correction in adult ornithine transcarbamylase-deficient mice with adenoviral vectors.

Ye X, Robinson MB, Batshaw ML, Furth EE, Smith I, Wilson JM. Ye X, et al. Among authors: robinson mb. J Biol Chem. 1996 Feb 16;271(7):3639-46. doi: 10.1074/jbc.271.7.3639. J Biol Chem. 1996. PMID: 8631974 Free article.

7

The sparse fur mouse as a model for gene therapy in ornithine carbamoyltransferase deficiency.

Batshaw ML, Yudkoff M, McLaughlin BA, Gorry E, Anegawa NJ, Smith IA, Hyman SL, Robinson MB. Batshaw ML, et al. Among authors: robinson mb. Gene Ther. 1995 Dec;2(10):743-9. Gene Ther. 1995. PMID: 8750014

8

Evidence of excitotoxicity in the brain of the ornithine carbamoyltransferase deficient sparse fur mouse.

Robinson MB, Hopkins K, Batshaw ML, McLaughlin BA, Heyes MP, Oster-Granite ML. Robinson MB, et al. Brain Res Dev Brain Res. 1995 Dec 21;90(1-2):35-44. doi: 10.1016/0165-3806(96)83484-5. Brain Res Dev Brain Res. 1995. PMID: 8777776 Free article.

9

Developing adenoviral-mediated in vivo gene therapy for ornithine transcarbamylase deficiency.

Raper SE, Wilson JM, Yudkoff M, Robinson MB, Ye X, Batshaw ML. Raper SE, et al. Among authors: robinson mb. J Inherit Metab Dis. 1998;21 Suppl 1:119-37. doi: 10.1023/a:1005369926784. J Inherit Metab Dis. 1998. PMID: 9686350

10

Efficient mitochondrial import of newly synthesized ornithine transcarbamylase (OTC) and correction of secondary metabolic alterations in spf(ash) mice following gene therapy of OTC deficiency.

Zimmer KP, Bendiks M, Mori M, Kominami E, Robinson MB, Ye X, Wilson JM. Zimmer KP, et al. Among authors: robinson mb. Mol Med. 1999 Apr;5(4):244-53. Mol Med. 1999. PMID: 10448647 Free PMC article.

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