F. Bullrich

发表

MicroRNA profiling reveals distinct signatures in B cell chronic lymphocytic leukemias.

C. Croce, M. Ferracin, Chang-gong Liu, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Frequent deletions and down-regulation of micro- RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia

C. Croce, G. Calin, M. Negrini, 2002, Proceedings of the National Academy of Sciences of the United States of America.

An oligonucleotide microchip for genome-wide microRNA profiling in human and mouse tissues.

C. Croce, M. Ferracin, Chang-gong Liu, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers.

C. Croce, G. Calin, M. Negrini, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Cytogenetic and interphase cytogenetic characterization of atypical chronic lymphocytic leukemia carrying BCL1 translocation.

M. Negrini, F. Bullrich, A. Cuneo, 1997, Cancer research.

leukemia Minimal region of loss at 13 q 14 in B-cell chronic lymphocytic

C. Croce, F. Bullrich, Reed, 2002 .

Isolation of human and mouse genes based on homology to REC2, a recombinational repair gene from the fungus Ustilago maydis.

F. Bullrich, M. Rice, E. Kmiec, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Akt phosphorylates and regulates the orphan nuclear receptor Nur77

Y. Pekarsky, C. Hallas, C. Croce, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Characterization of the 13 q 14 Tumor Suppressor Locus in CLL : Identification of ALT 1 , an Alternative Splice Variant of the LEU 2 Gene 1

Y. Pekarsky, C. Croce, G. Calin, 2001 .

Cutaneous vasculitis in non Hodgkin's lymphoma

M. Negrini, F. Bullrich, A. Cuneo, 1994 .

Advances in Brief Cloning and Characterization of CLLD 6 , CLLD 7 , and CLLD 8 , Novel Candidate Genes for Leukemogenesis at Chromosome 13 q 14 , a Region Commonly Deleted in B-Cell Chronic Lymphocytic Leukemia 1

C. Croce, G. Calin, M. Negrini, 2001 .

In vitro activation of CPP 32 and Mch 3 by Mch 4 , a novel human apoptotic cysteine protease containing two FADD-like domains ( granzyme B / Mch 2 / protease cascade / FAS / APO-I-receptor )

E. Alnemri, F. Bullrich, T. Fernandes-Alnemri, 2005 .

The human transaldolase gene (TALDO1) is located on chromosome 11 at p15.4-p15.5.

R. Eddy, T. Shows, C. Croce, 1997, Genomics.

Identification and characterization of the ARP1 gene, a target for the human acute leukemia ALL1 gene.

C. Croce, M. Shimizu, F. Bullrich, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Chromosome aberrations in atypical chronic lymphocytic leukemia: a cytogenetic and interphase cytogenetic study

M. Negrini, F. Bullrich, A. Cuneo, 1997, Leukemia.

FLT4 Receptor Tyrosine Kinase Gene Mapping to Chromosome Band 5q35 in Relation to the t(2;5), t(5;6), and t(3;5) Translocations

K. Huebner, K. Alitalo, J. Wasmuth, 1993, Genes, chromosomes & cancer.

huASH1 protein, a putative transcription factor encoded by a human homologue of the Drosophila ash1 gene, localizes to both nuclei and cell-cell tight junctions.

C. Croce, B. Geiger, F. Bullrich, 2000, Proceedings of the National Academy of Sciences of the United States of America.

ATM mutations in B-cell chronic lymphocytic leukemia.

C. Croce, T. Kipps, John Calvin Reed, 1999, Cancer research.

in myeloid leukemia in BXH-2 mice. Meis1, a PBX1-related homeobox gene involved

K. Huebner, J. Moskow, F. Bullrich, 2013 .

Meis1, a PBX1-related homeobox gene involved in myeloid leukemia in BXH-2 mice

K. Huebner, J. Moskow, F. Bullrich, 1995, Molecular and cellular biology.

Definition and refinement of chromosome 8p regions of loss of heterozygosity in gastric cancer.

C. Croce, H. Ishii, R. Baffa, 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.

Oncogenes and Mammary Carcinogenesis

C. Croce, F. Bullrich, M. L. Veronese, 1999 .

Characterization of the 13q14 tumor suppressor locus in CLL: identification of ALT1, an alternative splice variant of the LEU2 gene.

Y. Pekarsky, C. Croce, G. Calin, 2001, Cancer research.

FLAME-1, a Novel FADD-like Anti-apoptotic Molecule That Regulates Fas/TNFR1-induced Apoptosis*

S. Srinivasula, E. Alnemri, C. Croce, 1997, The Journal of Biological Chemistry.

Chromosomal mapping of members of the cdc2 family of protein kinases, cdk3, cdk6, PISSLRE, and PITALRE, and a cdk inhibitor, p27Kip1, to regions involved in human cancer.

C. Croce, N. Chiorazzi, F. Bullrich, 1995, Cancer research.

Structure and expression pattern of human ALR, a novel gene with strong homology to ALL-1 involved in acute leukemia and to Drosophila trithorax

C. Croce, K. Huebner, H. Alder, 1997, Oncogene.

Expression of apoptosis-regulating proteins in chronic lymphocytic leukemia: correlations with In vitro and In vivo chemoresponses.

C. Croce, John Calvin Reed, S. Krajewski, 1998, Blood.

Chromosomal mapping of the genes GPRK5 and GPRK6 encoding G protein-coupled receptor kinases GRK5 and GRK6.

K. Huebner, F. Bullrich, K. Gripp, 1995, Cytogenetics and cell genetics.

Minimal region of loss at 13q14 in B-cell chronic lymphocytic leukemia.

M. Caligiuri, C. Croce, John Calvin Reed, 1996, Blood.

Cloning and characterization of CLLD6, CLLD7, and CLLD8, novel candidate genes for leukemogenesis at chromosome 13q14, a region commonly deleted in B-cell chronic lymphocytic leukemia.

C. Croce, G. Calin, M. Negrini, 2001, Cancer research.

In vitro activation of CPP32 and Mch3 by Mch4, a novel human apoptotic cysteine protease containing two FADD-like domains.

S. Srinivasula, E. Alnemri, J. Trapani, 1996, Proceedings of the National Academy of Sciences of the United States of America.

The t(6;16)(p21;q22) chromosome translocation in the LNCaP prostate carcinoma cell line results in a tpc/hpr fusion gene.

C. Croce, M. Negrini, F. Bullrich, 1996, Cancer research.

Nucleophosmin (NPM) gene rearrangements in Ki-1-positive lymphomas.

S. Pileri, H. Stein, C. Croce, 1994, Cancer research.

Cytogenetic profile of lymphoma of follicle mantle lineage: correlation with clinicobiologic features.

F. Birg, H. Döhner, A. Hagemeijer, 1999, Blood.

Familial cancer associated with a polymorphism in ARLTS1.

D. Neuberg, G. Russo, C. Croce, 2005, The New England journal of medicine.

Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosa.

J. Uitto, F. Bullrich, L. Weiss, 1997, American journal of human genetics.

Tumor suppressor functions of ARLTS1 in lung cancers.

George A Calin, Massimo Negrini, Masayoshi Shimizu, 2007, Cancer research.

Chromosomal mapping of cell death proteases CPP32, MCH2, and MCH3.

E. Alnemri, C. Croce, F. Bullrich, 1996, Genomics.

Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization.

E. Lane, R. Ray, S. DeArmond, 1996, Genes & development.