M. Muleris

发表

Azathioprine induction of tumors with microsatellite instability: Risk evaluation using a mouse model

V. Penard-Lacronique, N. Brousse, A. Duval, 2015, Oncotarget.

Noninvolvement of a constitutional heritable fragile site at 10q24.2 in rearranged chromosomes from rectal carcinoma cells.

B. Dutrillaux, M. Lombard, M. Muleris, 1987, Cancer genetics and cytogenetics.

Identification, nuclear localization, and binding activities of OZF, a human protein solely composed of zinc-finger motifs.

A. Vincent-Salomon, C. Le Chalony, G. Goubin, 1996, European journal of biochemistry.

Relationships between UMPK and PGD activities and deletions of chromosome 1p in colorectal cancers.

B. Dutrillaux, A. Bravard, M. Muleris, 1991, Cancer genetics and cytogenetics.

CGH analysis of radon-induced rat lung tumors indicates similarities with human lung cancers.

B. Dutrillaux, A. El‐Naggar, S. Chevillard, 2000 .

CGH analysis of radon‐induced rat lung tumors indicates similarities with human lung cancers

B. Dutrillaux, A. El‐Naggar, S. Chevillard, 2000, Genes, chromosomes & cancer.

GAC1, a new member of the leucine-rich repeat superfamily on chromosome band 1q32.1, is amplified and overexpressed in malignant gliomas

S. Hanash, B. Dutrillaux, B. Malfoy, 1998, Oncogene.

Characterization of human Rab20 overexpressed in exocrine pancreatic carcinoma.

F. Real, T. Gress, C. Antony, 2006, Human pathology.

Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D)

A. Duval, K. Wimmer, Y. Goldberg, 2014, Journal of Medical Genetics.

Chromosomal phylogeny of forty-two species or subspecies of cercopithecoids (Primates Catarrhini).

M. Lombard, M. Muleris, J. Couturier, 1982, Annales de genetique.

Distinct chromosomal alterations associated with TP53 status of LoVo cells under PALA selective pressure: a parallel with cytogenetic pathways of colorectal cancers

B. Dutrillaux, M. Poupon, M. Muleris, 1999, Oncogene.

Adaptation to 5‐fluorouracil of the heterogeneous human colon tumor cell line ht‐29 results in the selection of cells committed to differentiation

B. Dutrillaux, A. Barbat, T. Lesuffleur, 1991, International journal of cancer.

Preservation of chromosome and DNA characteristics of human colorectal adenocarcinomas after passage in nude mice

G. Thomas, O. Delattre, B. Dutrillaux, 1989, International journal of cancer.

Comprehensive RNA and protein functional assessments contribute to the clinical interpretation of MSH2 variants causing in-frame splicing alterations

T. Frebourg, F. Coulet, P. Gaildrat, 2022, Journal of Medical Genetics.

Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy

L. Messiaen, K. Wimmer, E. Legius, 2018, Journal of Medical Genetics.

[Clinical and molecular consequences of microsatellite instability in human cancers].

H. Zouali, A. Duval, R. Hamelin, 2008, Bulletin du cancer.

Report of the fifth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Leiden, The Netherlands, July 6th 2019

M. Kloor, K. Wimmer, Y. Goldberg, 2020, Familial Cancer.

Cytogenetic and molecular approaches of polyploidization in colorectal adenocarcinomas.

G. Thomas, O. Delattre, B. Dutrillaux, 1990, Cancer genetics and cytogenetics.

Cytogenetic characterization of a colon adenocarcinoma from a familial polyposis coli patient.

B. Dutrillaux, B. Nordlinger, M. Muleris, 1989, Cancer genetics and cytogenetics.

Characteristic chromosomal imbalances in 18 near-diploid colorectal tumors.

B. Dutrillaux, P. Vielh, B. Zafrani, 1987, Cancer genetics and cytogenetics.

Amplification and over‐expression of OZF, a gene encoding a zinc finger protein, in human pancreatic carcinomas

S. Hanash, B. Dutrillaux, B. Terris, 1999, International journal of cancer.

Characterization of chromosome changes in two human prostatic carcinoma cell lines (PC-3 and DU145) using chromosome painting and comparative genomic hybridization.

B. Dutrillaux, C. Bourgeois, B. Malfoy, 1997, Cancer genetics and cytogenetics.

Induction of increased salvage pathways of nucleotide synthesis by dosage effect due to chromosome imbalances may be fundamental in carcinogenesis: the example of colorectal carcinoma.

B. Dutrillaux, M. Muleris, 1986, Annales de Genetique.

Oncogene amplification in human gliomas: a molecular cytogenetic analysis.

J. Delattre, B. Dutrillaux, B. Malfoy, 1994, Oncogene.

Azathioprine May Not be Associated With Development of Colorectal Tumors With Microsatellite Instability in Patients With Inflammatory Bowel Disease

A. Duval, P. Seksik, L. Beaugerie, 2016, The American Journal of Gastroenterology.

Diagrammatic representation for chromosomal mutagenesis studies. III. Radiation-induced rearrangements in Pan troglodytes (chimpanzee).

B. Dutrillaux, M. Prieur, M. Muleris, 1985, Mutation research.

Extensive characterization of sphere models established from colorectal cancer cell lines

A. Reyniès, A. Duval, A. Faussat, 2013, Cellular and Molecular Life Sciences.

Recurrent deletions of chromosomes 11q and 3p in anal canal carcinoma

B. Dutrillaux, B. Zafrani, M. Muleris, 1987, International journal of cancer.

Report of the fifth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Leiden, The Netherlands, July 6th 2019

K. Wimmer, Y. Goldberg, E. Bleiker, 2020, Familial Cancer.

Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort

G. Leverger, F. Andreiuolo, L. Guerrini-Rousseau, 2015, Journal of Medical Genetics.

Gene dosage and expression, and enzyme activity of thymidine kinase and thymidylate synthase in xenografted colorectal adenocarcinomas

B. Dutrillaux, L. Sabatier, M. Muleris, 1994, International journal of cancer.

Cytogenetics of colorectal adenocarcinomas.

B. Dutrillaux, M. Muleris, R. Salmon, 1990, Cancer genetics and cytogenetics.

Activity of thymidylate synthetase, thymidine kinase and galactokinase in primary and xenografted human colorectal cancers in relation to their chromosomal patterns

B. Dutrillaux, M. Muleris, V Bardot, 1991, International journal of cancer.

Chromosomal and enzymatic patterns provide evidence for two types of human colon cancers with abnormal nucleotide metabolism.

B. Dutrillaux, L. Sabatier, M. Muleris, 1988, Mutation research.

Imbalance of sex chromosomes, with gain of early‐replicating X, in human solid tumors

B. Dutrillaux, M. Muleris, M. G. Seureau, 1986, International journal of cancer.

Existence of two distinct processes of chromosomal evolution in near-diploid colorectal tumors.

B. Dutrillaux, M. Muleris, R. Salmon, 1988, Cancer genetics and cytogenetics.

Chromosomal study demonstrating the clonal evolution and metastatic origin of a metachronous colorectal carcinoma

B. Dutrillaux, M. Muleris, R. Salmon, 1986, International journal of cancer.

Ductal Breast Carcinomas with Whole Chromosome Gains as a Particular Subset of Near-Diploid Tumors with Different Metastasis Free Survival

B. Dutrillaux, B. Asselain, C. Elie, 2005, Breast Cancer Research and Treatment.

Ductal breast carcinoma develops through different patterns of chromosomal evolution

B. Dutrillaux, X. Sastre-Garau, M. Muleris, 2005, Genes, chromosomes & cancer.

Characterization of a new cytogenetic subtype of ductal breast carcinomas

B. Dutrillaux, M. Muleris, Y. Remvikos, 2004, Oncogene.

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘Care for CMMRD’ (C4CMMRD)

A. Duval, K. Wimmer, Y. Goldberg, 2014, Journal of Medical Genetics.

Consistent deficiencies of chromosome 18 and of the short arm of chromosome 17 in eleven cases of human large bowel cancer: a possible recessive determinism.

B. Dutrillaux, B. Zafrani, M. Muleris, 1985, Annales de genetique.

Survival and acquired genetic alterations in colorectal cancer.

O. Delattre, P. Laurent-Puig, P. Validire, 1992, Gastroenterology.

Predominance of normal karyotype in colorectal tumors from hereditary non‐polyposis colorectal cancer patients

B. Dutrillaux, S. Olschwang, M. Muleris, 1995, Genes, chromosomes & cancer.

Colorectal carcinogenesis: from chromosomal evolution pathways to molecular pathogenesis.

B. Dutrillaux, M. Muleris, R. Salmon, 1997, Cancer genetics and cytogenetics.

MLL2, the second human homolog of the Drosophila trithorax gene, maps to 19q13.1 and is amplified in solid tumor cell lines

S. Chin, C. Caldas, S. Aparicio, 1999, Oncogene.

Detection of DNA amplification in 17 primary breast carcinomas with homogeneously staining regions by a modified comparative genomic hybridization technique

B. Dutrillaux, B. Malfoy, M. Muleris, 1994, Genes, chromosomes & cancer.

Cloning of the mRNA of overexpression in colon carcinoma-1: a sequence overexpressed in a subset of colon carcinomas.

Laurence Pibouin, G. Goubin, M. Muleris, 2002, Cancer genetics and cytogenetics.

Chromosome study of Presbytis cristatus: presence of a complex Y-autosome rearrangement in the male.

B. Dutrillaux, J. Couturier, M. Muleris, 1984, Annales de genetique.

The mechanisms underlying MMR deficiency in immunodeficiency‐related non‐Hodgkin lymphomas are different from those in other sporadic microsatellite instable neoplasms

P. Gaulard, A. Duval, R. Hamelin, 2009, International journal of cancer.

Detection of 1q polysomy in interphase nuclei of human solid tumors with a biotinylated probe

B. Dutrillaux, E. Viégas-Péquignot, M. Muleris, 1989, Human Genetics.

Cytogenetic study of 30 colorectal adenomas.

B. Dutrillaux, P. Validire, B. Zafrani, 1994, Cancer genetics and cytogenetics.

Cytogenetic aspects of Primate evolution.

B. Dutrillaux, J. Couturier, E. Viégas-Péquignot, 1982, Progress in clinical and biological research.

Identification of amplified DNA sequences in breast cancer and their organization within homogeneously staining regions

B. Dutrillaux, B. Malfoy, M. Muleris, 1995, Genes, chromosomes & cancer.

Acquired chromosome rearrangements in human lymphocytes: effect of aging

B. Dutrillaux, A. Aurias, M. Ricoul, 1988, Human Genetics.

The rate of chromosome breakage is age dependent in lymphocytes of adult controls

B. Dutrillaux, A. Aurias, L. Sabatier, 1986, Human Genetics.

Virtual genome scan: a tool for restriction landmark-based scanning of the human genome.

R. Kuick, J. Rouillard, A. E. Erson, 2001, Genome research.

12 – Specific Sites of Chromosomal Radiation-induced Rearrangements

B. Dutrillaux, L. Sabatier, M. Prieur, 1989 .

Premature condensation induces breaks at the interface of early and late replicating chromosome bands bearing common fragile sites.

B. Dutrillaux, M. Debatisse, M. Muleris, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients

G. Thomas, P. Laurent-Puig, S. Olschwang, 1993, Cell.

TP53 status and gene amplification in human colorectal carcinomas.

B. Dutrillaux, B. Asselain, R. Hamelin, 1999, Cancer genetics and cytogenetics.

Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group

W. Foulkes, Y. Goldberg, U. Tabori, 2021, Journal of Medical Genetics.

Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.

H. Blanché, A. Duval, R. Hamelin, 2015, Gastroenterology.

Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-to-CMMRD Phenotypic Continuum

Á. Carracedo, K. Wimmer, J. Cameselle-Teijeiro, 2019, Cancers.

Diagnostic challenges in a child with early onset desmoplastic medulloblastoma and homozygous variants in MSH2 and MSH6

C. Fauth, A. Borkhardt, M. Kuhlen, 2018, European Journal of Human Genetics.

Detection of methylcytosine-rich heterochromatin on banded chromosomes. Application to cells with various status of DNA methylation.

A. Niveleau, A. Gibaud, C. Montpellier, 1994, Cancer genetics and cytogenetics.

Azathioprine-induced carcinogenesis in mice according to Msh2 genotype.

V. Penard-Lacronique, A. Duval, N. Antoine, 2010, Journal of the National Cancer Institute.

Isoacentric and isocentric chromosomes originating after deletions of human chromosomes

B. Dutrillaux, A. Aurias, M. Ricoul, 1987, Human Genetics.

Diagrammatic representation for chromosomal mutagenesis studies. II. Radiation-induced rearrangements in Macaca fascicularis.

B. Dutrillaux, M. Muleris, M. Paravatou-Petsota, 1984, Mutation research.

Inversion (14)(q12qter) or (q11.2q32.3): The most frequently acquired rearrangement in lymphocytes

B. Dutrillaux, A. Aurias, J. Couturier, 2004, Human Genetics.

A rapid and simple method to isolate and characterize highly polymorphic markers from the centromeric regions of the human chromosomes.

A. Laurent, B. Marçais, G. Roizes, 1994, Nucleic acids research.

Diagrammatic representation for chromosomal mutagenesis studies. I. Karyotypes most similar to that of man.

B. Dutrillaux, M. Muleris, M. Paravatou-Petsota, 1984, Mutation research.

Chromosome instability in lymphocytes from patients affected by or genetically predisposed to colorectal cancer.

B. Dutrillaux, F. Richard, M. Muleris, 1994, Cancer genetics and cytogenetics.

Characterization of amplified DNA sequences in human cancers

B. Dutrillaux, B. Malfoy, M. Muleris, 1997 .

Resistance to high concentrations of methotrexate and 5‐fluorouracil of differentiated HT‐29 colon‐cancer cells is restricted to cells of enterocytic phenotype

A. Barbat, T. Lesuffleur, A. Zweibaum, 1998, International journal of cancer.

Constitutional microsatellite instability, genotype, and phenotype correlations in Constitutional Mismatch Repair Deficiency.

L. Guerrini-Rousseau, K. Dahan, G. Borthwick, 2022, Gastroenterology.

Amplification of DNA sequences from chromosome 19q13.1 in human pancreatic cell lines.

R. Kuick, S. Hanash, B. Dutrillaux, 1998, Genomics.

[Analysis by flow cytometry of hepatic metastases of colorectal cancer].

M. Muleris, R. Salmon, Y. Remvikos, 1988, Annales de chirurgie.

HSP110 T17 simplifies and improves the microsatellite instability testing in patients with colorectal cancer

H. Blanché, C. Lepage, A. Duval, 2016, Journal of Medical Genetics.

Methylation Tolerance-based Functional Assay to Assess Variants of Unknown Significance in the MLH1 and MSH2 Genes and Identify Patients With Lynch Syndrome.

A. Duval, F. Coulet, C. Colas, 2019, Gastroenterology.

Loss of alleles on chromosome 18 and on the short arm of chromosome 17 in polyploid colorectal carcinomas

G. Thomas, O. Delattre, B. Dutrillaux, 1988, International journal of cancer.

Sex chromosomes in a series of 79 colorectal cancers: Replication pattern, numerical, and structural changes

B. Dutrillaux, M. Muleris, R. Salmon, 1990, Genes, Chromosomes and Cancer.

Chromosomal Instability in Near-Diploid Colorectal Cancer: A Link between Numbers and Structure

B. Dutrillaux, A. Duval, R. Hamelin, 2008, PloS one.

DNA‐repeat instability is associated with colorectal cancers presenting minimal chromosome rearrangements

B. Dutrillaux, B. Malfoy, M. Muleris, 1995, Genes, chromosomes & cancer.

The frequency of micronuclei with X chromosome increases with age in human females.

B. Dutrillaux, F. Richard, M. Muleris, 1994, Mutation research.

Mapping of 18 probes on human chromosome 18 using single- and double-color FISH.

G. Thomas, F. Apiou, B. Dutrillaux, 1994, Cytogenetics and cell genetics.

Karyotypic and phenotypic variations between cell lines established from a primary colorectal tumour and two corresponding metastases from one patient.

J. Douillard, H. Blottière, M. Muleris, 1993, Invasion & metastasis.

The insulin‐like growth factor I receptor gene is the target for the 15q26 amplicon in breast cancer

B. Dutrillaux, B. Malfoy, M. Muleris, 1994, Genes, chromosomes & cancer.

Constitutional balanced translocations in patients with solid tumors.

B. Dutrillaux, J. Couturier, F. Richard, 1992, Cancer genetics and cytogenetics.

Lynch syndrome: influence of additional susceptibility variants on cancer risk

P. Laurent-Puig, A. Duval, F. Coulet, 2023, European Journal of Human Genetics.

Increased FISH efficiency using APC probes generated by direct incorporation of labeled nucleotides by PCR.

B. Dutrillaux, F. Richard, B. Malfoy, 1994, Cytogenetics and cell genetics.

Chromosome 12 alterations and c-Ki-ras mutations in colorectal tumors.

G. Thomas, B. Dutrillaux, P. Laurent-Puig, 1993, Cancer genetics and cytogenetics.

Assignment of v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2 (ERBB2) to human chromosome band 17q21.1 by in situ hybridization.

B. Dutrillaux, B. Malfoy, M. Muleris, 1997, Cytogenetics and cell genetics.

In situ hybridization approach at infragenic level on metaphase chromosomes.

B. Dutrillaux, Raouf Fetni, B. Malfoy, 1994, Cytogenetics and Cell Genetics.

Growth dependency of human colon cancer xenograft on organ environment is related with their original clinical stage.

B. Dutrillaux, R. Hamelin, M. Poupon, 1998, Anticancer Research.

Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus suggestions for testing a child without malignancy

L. Messiaen, K. Wimmer, E. Legius, 2020 .

The accumulation and occurrence of clonal and unstable rearrangements are independent in colorectal cancer cells.

B. Dutrillaux, M. Muleris, 1996, Cancer genetics and cytogenetics.

Constitutional or biallelic? Settling on a name for a recessively inherited cancer susceptibility syndrome

A. Duval, K. Wimmer, C. Kratz, 2015, Journal of Medical Genetics.