| 1 | SMS,UBB
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| Genotype-phenotype correlation of 30 Smith-Magenis Syndrome patients using CGH-array: cleft palate in SMS is associated with larger deletions.
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| Andrieux J, Villenet C, Quief S, Lignon S, Geffroy S, Roumier C, de Leersnyder H, de Blois MC, Manouvrier S, Delobel B, Benzacken B, Bitoun P, Attie-Bitach T, Thomas S, Lyonnet S, Vekemans M, Kerckaert JP.
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| J Med Genet [Epub ahead of print] 2007
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| 2 | CD4, HLA-A, MARCHF1, MARCHF2, MARCHF3, MARCHF4, MARCHF5, MARCHF6, MARCHF7, MARCHF8, MARCHF9, UBB, UBE2H
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| Downregulation of major histocompatibility complex class I by human ubiquitin ligases related to viral immune evasion proteins.
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| Bartee E, Mansouri M, Hovey Nerenberg BT, Gouveia K, Fruh K.
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| J Virol 78(3):1109-20. 2004
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| 3 | UBB
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| Frameshift mutants of beta amyloid precursor protein and ubiquitin-B in Alzheimer's and Down patients.
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| van Leeuwen FW, de Kleijn DP, van den Hurk HH, Neubauer A, Sonnemans MA, Sluijs JA, Koycu S, Ramdjielal RD, Salehi A, Martens GJ, Grosveld FG, Peter J, Burbach H, Hol EM.
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| Science 279(5348):242-7. 1998
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| 4 | CHRNB1, UBB
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| Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p.
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| Guzzetta V, Franco B, Trask BJ, Zhang H, Saucedo-Cardenas O, Montes de Oca-Luna R, Greenberg F, Chinault AC, Lupski JR, Patel PI.
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| Genomics 13(3):551-9. 1992
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| 5 | UBB
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| The human ubiquitin-52 amino acid fusion protein gene shares several structural features with mammalian ribosomal protein genes.
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| Baker RT, Board PG.
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| Nucleic Acids Res 19(5):1035-40.
1991
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| 6 | UBB, UBBP1
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| Localization of the human UbB polyubiquitin gene to chromosome band 17p11.1-17p12.
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| Webb GC, et al.
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| Am J Hum Genet 46 : 308-315. 1990
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