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24篇 您的检索式：作者名="Marynen"

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	题名	作者	年代	出处	被引量
1	A deletion polymorphism in the human alph a-2-m acroglobulin(A2M)gene显示文摘	Matthijs G Marynen P	1991	Nucleic Acids Res1991，19，18：	1
2	Interaction partners for human ZNF384/ CIZ/NMP4--zyxin as a mediator for p130c~s signaling? 显示文摘	Janssen H Marynen P	2006	Exp Cell Res2006，312，7：	1
3	A deletion polymorphism in the human alpha-2-macroglobulin (A2M)gene显示文摘	Matthijs G Marynen P	1991	Nucleic Acids Res1991，19，18：	1
4	ALK-AT- IC fusion in urinary bladder inflammatory myofihroblastic tumor 显示文摘	Debiec--Rychter M Marynen P Hagemeijer A	2003	Genes Chromosomes Cancer2003，38，2：	1
5	Identi cation of a novel conserved human gene,TEGT显示文摘	Walter L Marynen P Szpirer J	1995	Genomics1995，28，2：	1
6	The Product of the t(11;18), an API2 - MLT Fusion, Marks Nearly Half of Gastric MALT Type Lymphomas without Large Cell Proliferation显示文摘	Mathijs Baens Brigitte Maes Anja Steyls Karel Geboes Peter Marynen Christiane De Wolf-Peeters	2000	The American Journal of Pathology2000，，4：	1
7	X-linked mental retardation :vanishing boundaries between non-specific (MRX)and syndromic (MRXS) forms显示文摘	Frints SGM Froyen G Marynen P	2002	Clin Genet2002，64，2：	1
8	A human homologue(BICD1) of the Drosophila bicaudal–D gene显示文摘	Baens M Marynen P	1997	Genomics1997，45，：	1
9	Inv(2)(p23q35) in anaplastic large-cell lymphoma induces constitutive anaplastic lymphoma kinase (ALK) tyrosine kinase activation by fusion to ATIC, an enzyme involved in purine nucleotide biosynthesis 显示文摘	Ma Z Cools J Marynen P	2000	Blood2000，95，6：	1
10	X-linked mental retardation:vanishing boundaries between non-specific(MRX) and syndromic(MRXS) forms显示文摘	Frints SGM Froyen G Marynen P	2002	Clin Genet2002，，62：	1
11	TEL gene is involved in myelodysplastic syndromes with either the typical t (5;12) (q33;p13) translocation or its variant t (10;12) (q24;p13) 显示文摘	Wlodarska I Mecucci C Marynen P	1995	Blood1995，85，10：	1
12	Identification of a no- vel conserved human gene, TEGT显示文摘	Walter L Marynen P Szpirer J	1995	Genomics1995，28，：	1
13	X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromie (MRXS) forms显示文摘	Frints SG Froyen G Marynen P	2002	Clin Genet2002，62，6：	1
14	X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms显示文摘	Frints SG Froyen G Marynen P	2002	Clin Genet2002，62，6：	1
15	Genetic insights in the pathogenesis of T-cell acute lymphoblastic leukemia 显示文摘	De Keersmaecker K Marynen P Cools J	2005	Haematologica2005，90，8：	1
16	TEL gene is involved in myelodysplastic syndromes with either the typical t (5;12) (q33;p13) translocation or its variant t(10;12) (q24;p13) 显示文摘	Wlodarska I Mecucci C Marynen P	1995	Blood1995，85，10：	1
17	Identification of a novel conserved human gene,TEGT显示文摘	Walter L Marynen P Szpirer J	1995	Genomics1995，28，2：	1
18	Resistance to tyrosine ki-nase inhibitors : Calling on extra forces显示文摘	Cools J Maertens C Marynen P	2005	Drug Resis-tance Updates2005，8，3：	1
19	Evidence for the existence of a pristanoyl-CoA oxidase gene in man显示文摘	Vanhooren J C Marynen P Mannaerts G P	1997	Biochem J1997，325，3：	1
20	Identification of a novel conserved human gene, TEGT 显示文摘	Walter L Marynen P Szpirer J	1995	Genomies1995，28，：	1

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