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Year | Number of Results |
---|---|
1991 | 1 |
1992 | 1 |
1998 | 2 |
2024 | 0 |
PubMed (OMIM) for id: 861164
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Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndrome.
Am J Med Genet. 1998 Sep 23;79(3):161-7. doi: 10.1002/(sici)1096-8628(19980923)79:3<161::aid-ajmg2>3.0.co;2-q.
Am J Med Genet. 1998.
PMID: 9788554
An oncogenic fusion product of the phosphatidylinositol 3-kinase p85beta subunit and HUMORF8, a putative deubiquitinating enzyme.
Janssen JW, Schleithoff L, Bartram CR, Schulz AS.
Janssen JW, et al.
Oncogene. 1998 Apr 2;16(13):1767-72. doi: 10.1038/sj.onc.1201695.
Oncogene. 1998.
PMID: 9582025
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Characterization of two 85 kd proteins that associate with receptor tyrosine kinases, middle-T/pp60c-src complexes, and PI3-kinase.
Otsu M, Hiles I, Gout I, Fry MJ, Ruiz-Larrea F, Panayotou G, Thompson A, Dhand R, Hsuan J, Totty N, et al.
Otsu M, et al.
Cell. 1991 Apr 5;65(1):91-104. doi: 10.1016/0092-8674(91)90411-q.
Cell. 1991.
PMID: 1707345
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Chromosomal localization of human p85 alpha, a subunit of phosphatidylinositol 3-kinase, and its homologue p85 beta.
Volinia S, Patracchini P, Otsu M, Hiles I, Gout I, Calzolari E, Bernardi F, Rooke L, Waterfield MD.
Volinia S, et al.
Oncogene. 1992 Apr;7(4):789-93.
Oncogene. 1992.
PMID: 1314371
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