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Cloning and Mapping of Members of the MYM Family

Data up to Jan 2025

Published1999
Citations28
References18

Total Citations Per Year

Abstract

References (18)

Dimerization of cell surface receptors in signal transduction

1995 • 1,631 citations

Does this have a familiar RING?

1996 • 632 citations

Zinc fingers are sticking together

1998 • 464 citations

Role of the Nucleophosmin (NPM) Portion of the Non-Hodgkin’s Lymphoma-Associated NPM-Anaplastic Lymphoma Kinase Fusion Protein in Oncogenesis

1997 • 371 citations

FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome

1998 • 332 citations

The TEL/platelet-derived growth factor β receptor (PDGFβR) fusion in chronic myelomonocytic leukemia is a transforming protein that self-associates and activates PDGFβR kinase-dependent signaling pathways

1996 • 285 citations

A domain of TEL conserved in a subset of ETS proteins defines a specific oligomerization interface essential to the mitogenic properties of the TEL-PDGFRbeta oncoprotein

1997 • 220 citations

Cytogenetics and molecular genetics of carcinomas arising from thyroid epithelial follicular cells

1996 • 166 citations

Does this have a familiar RING?

1996 • 165 citations

Consistent Fusion of ZNF198 to the Fibroblast Growth Factor Receptor-1 in the t(8;13)(p11;q12) Myeloproliferative Syndrome

1998 • 164 citations

Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)(p12;q12)

1998 • 154 citations

Assignment of the Muscle-Eye-Brain Disease Gene to 1p32-p34 by Linkage Analysis and Homozygosity Mapping

1999 • 137 citations

The t(8;13)(p11;q11-12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP

1998 • 112 citations

Deletion mapping of two potential chromosome 14 tumor suppressor gene loci in ovarian carcinoma.

1997 • 95 citations

Identification of a consistent region of allelic loss on 1p32 in meningiomas: correlation with increased morbidity.

1998 • 78 citations

Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1

1996 • 74 citations

Expression of Mutated Glucocerebrosidase Alleles in Human Cells

1997 • 34 citations

Characterization of a t(8;13)(p11;q11-12) in an atypical myeloproliferative disorder

1998 • 17 citations

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Cloning and Mapping of Members of the MYM Family (1999) – Genomics | Metascience Observatory Explorer