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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 2
1988 3
1989 6
1990 2
1991 3
1992 4
1994 1
1995 1
1996 1
1999 1
2020 0
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24 results
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Page 1
Molecular genetics of the monoamine oxidases.
Hsu YP, Powell JF, Sims KB, Breakefield XO. Hsu YP, et al. J Neurochem. 1989 Jul;53(1):12-8. doi: 10.1111/j.1471-4159.1989.tb07289.x. J Neurochem. 1989. PMID: 2656914 Review. No abstract available.
Biochemistry and genetics of monoamine oxidase.
Weyler W, Hsu YP, Breakefield XO. Weyler W, et al. Pharmacol Ther. 1990;47(3):391-417. doi: 10.1016/0163-7258(90)90064-9. Pharmacol Ther. 1990. PMID: 2290855 Review.
Mutations in the Norrie disease gene.
Schuback DE, Chen ZY, Craig IW, Breakefield XO, Sims KB. Schuback DE, et al. Hum Mutat. 1995;5(4):285-92. doi: 10.1002/humu.1380050403. Hum Mutat. 1995. PMID: 7627181
Structure of the human gene for monoamine oxidase type A.
Chen ZY, Hotamisligil GS, Huang JK, Wen L, Ezzeddine D, Aydin-Muderrisoglu N, Powell JF, Huang RH, Breakefield XO, Craig I, et al. Chen ZY, et al. Nucleic Acids Res. 1991 Aug 25;19(16):4537-41. doi: 10.1093/nar/19.16.4537. Nucleic Acids Res. 1991. PMID: 1886775 Free PMC article.
Monoamine oxidase deficiency in males with an X chromosome deletion.
Sims KB, de la Chapelle A, Norio R, Sankila EM, Hsu YP, Rinehart WB, Corey TJ, Ozelius L, Powell JF, Bruns G, et al. Sims KB, et al. Neuron. 1989 Jan;2(1):1069-76. doi: 10.1016/0896-6273(89)90231-6. Neuron. 1989. PMID: 2483108
Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: implications for Norrie disease.
Levy ER, Powell JF, Buckle VJ, Hsu YP, Breakefield XO, Craig IW. Levy ER, et al. Genomics. 1989 Aug;5(2):368-70. doi: 10.1016/0888-7543(89)90072-4. Genomics. 1989. PMID: 2793188
Human monoamine oxidase A gene determines levels of enzyme activity.
Hotamisligil GS, Breakefield XO. Hotamisligil GS, et al. Am J Hum Genet. 1991 Aug;49(2):383-92. Am J Hum Genet. 1991. PMID: 1678250 Free PMC article.
Norrie disease gene is distinct from the monoamine oxidase genes.
Sims KB, Ozelius L, Corey T, Rinehart WB, Liberfarb R, Haines J, Chen WJ, Norio R, Sankila E, de la Chapelle A, et al. Sims KB, et al. Am J Hum Genet. 1989 Sep;45(3):424-34. Am J Hum Genet. 1989. PMID: 2773935 Free PMC article.
Molecular genetic insights into neurologic diseases.
Breakefield XO, Cambi F. Breakefield XO, et al. Annu Rev Neurosci. 1987;10:535-94. doi: 10.1146/ Annu Rev Neurosci. 1987. PMID: 3551764 Review. No abstract available.
Highly polymorphic (GT)n repeat sequence in intron II of the human MAOB gene.
Konradi C, Ozelius L, Breakefield XO. Konradi C, et al. Genomics. 1992 Jan;12(1):176-7. doi: 10.1016/0888-7543(92)90426-s. Genomics. 1992. PMID: 1733859 No abstract available.
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