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

Molecular cloning: A laboratory manual

1990 • 85,659 citations

A simple method for displaying the hydropathic character of a protein

1982 • 22,471 citations

Fusion of a Kinase Gene, ALK , to a Nucleolar Protein Gene, NPM , in Non-Hodgkin's Lymphoma

1994 • 2,375 citations

Analysis of membrane and surface protein sequences with the hydrophobic moment plot

1984 • 2,234 citations

Chromosomal translocations in human cancer

1994 • 1,551 citations

Two interdependent basic domains in nucleoplasmin nuclear targeting sequence: Identification of a class of bipartite nuclear targeting sequence

1991 • 1,501 citations

Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation

1994 • 1,211 citations

Structures of the Tyrosine Kinase Domain of Fibroblast Growth Factor Receptor in Complex with Inhibitors

1997 • 1,098 citations

Interpreting cDNA sequences: Some insights from studies on translation

1996 • 785 citations

Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3

1997 • 657 citations

Cloning and expression of two distinct high-affinity receptors cross-reacting with acidic and basic fibroblast growth factors.

1990 • 635 citations

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

1994 • 617 citations

Protein motifs 5. Zinc fingers.

1995 • 544 citations

Zinc fingers

1995 • 501 citations

The human fibroblast growth factor receptor genes: a common structural arrangement underlies the mechanisms for generating receptor forms that differ in their third immunoglobulin domain.

1991 • 406 citations

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

1998 • 332 citations

Fibroblast-growth-factor receptor mutations in human skeletal disorders

1995 • 300 citations

Functions of fibroblast growth factors and their receptors

1995 • 254 citations

Fibroblast Growth Factor Receptors from Liver Vary in Three Structural Domains

1991 • 227 citations

Sequence and Analysis of the Human ABL Gene, the BCR Gene, and Regions Involved in the Philadelphia Chromosomal Translocation

1995 • 215 citations

Fibroblast growth factor receptors have different signaling and mitogenic potentials

1994 • 214 citations

Functions of fibroblast growth factors in vertebrate development

1996 • 208 citations

Ligand-induced transphosphorylation between different FGF receptors.

1991 • 189 citations

A syndrome of lymphoblastic lymphoma, eosinophilia, and myeloid hyperplasia/malignancy associated with t(8;13)(p11;q11): description of a distinctive clinicopathologic entity [see comments]

1995 • 144 citations

A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: a review.

1995 • 143 citations

Hyping up the letdown gene

1995 • 125 citations

The Human Fibroblast Growth Factor Receptor Genes: a Common Structural Arrangement Underlies the Mechanisms for Generating Receptor Forms That Differ in Their Third Immunoglobulin Domain

1991 • 123 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

Chronic myelomonocytic leukemia: Tel-a-kinase what Ets all about

1994 • 97 citations

Ret in human development and oncogenesis

1997 • 79 citations

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

1996 • 74 citations

t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12

1998 • 63 citations

Expression of basic fibroblast growth factor (bFGF) and FGF-receptors in human leukemic cells.

1995 • 53 citations

Expression of fibroblast growth factor receptors in human leukemia cells.

1992 • 49 citations

FRAG1, a gene that potently activates fibroblast growth factor receptor by C-terminal fusion through chromosomal rearrangement.

1996 • 44 citations

Simultaneous occurrence of a T-cell lymphoma and a chronic myelogenous leukemia with an unusual karyotype

1984 • 42 citations

Translocation (8;13) and T-cell lymphoma

1993 • 41 citations

t(8;13) (p11;q12) translocation in a myeloproliferative disorder associated with a T‐cell non‐Hodgkin lymphoma

1994 • 36 citations

Novel reciprocal translocation between chromosomes 8 and 9 found in a patient with myeloproliferative disorder

1983 • 36 citations

Philadelphia chromosome-negative chronic myelogenous leukemia in a child with t(8;9)(p11 or 12;q34).

1983 • 34 citations

Fusion and amplification of two originally non‐syntenic chromosomal regions in a mammary carcinoma cell line

1992 • 33 citations

Chronic myelomonocytic leukaemia with t(8;9)(p11;q34) in childhood: an example of the 8p11 myeloproliferative disorder?

1996 • 33 citations

Amino acid residues which distinguish the mitogenic potentials of two FGF receptors

1997 • 32 citations

About the t(8;13)(p11;q12) clinico-pathologic entity [letter]

1996 • 28 citations

t(8;9)(p11;q32) IN ATYPICAL CHRONIC MYELOID LEUKAEMIA: A NEW CYTOGENETTC‐CLINICOPATHOLOGIC ASSOCIATION?

1992 • 27 citations

Localization of the 8;13 translocation breakpoint associated with myeloproliferative disease to a 1.5 mbp region of chromosome 13

1995 • 27 citations

Reciprocal translocation between chromosomes 8 and 9 in atypical chronic myeloid leukaemia.

1985 • 26 citations

Translocation t(8;13)(p11;q11‐12) in stem cell leukemia/lymphoma of t‐cell and myeloid lineages

1995 • 24 citations

Developments in cytogenetics and oncogenes in acute leukemia

1997 • 23 citations

A young child with acquired t(8;9)(p11;q34): additional proof that 8p11 is involved in mixed myeloid/T lymphoid malignancies.

1996 • 23 citations

Identification of a YAC spanning the translocation breakpoint t(8;22) associated with acute monocytic leukemia

1996 • 21 citations

Myeloproliferative disorder associated with 8p11 translocations [letter; comment]

1995 • 14 citations

A 3.1-Mb YAC contig within the Werner syndrome region, on the short arm of human chromosome 8

1996 • 14 citations

Translocation t(8;13) in a patient with T cell lymphoma and features of a myeloproliferative syndrome.

1995 • 12 citations