M. Escarceller

发表

Involvement ofEscherichia coli DNA Polymerase II inResponse to Oxidative DamageandAdaptive Mutation

G. Gudmundsson, M. Escarceller, G. Trump, 1994 .

Arrest of S-phase progression is impaired in Fanconi anemia cells.

D. Papadopoulo, E. Moustacchi, D. Rouillard, 2000, Experimental cell research.

Molecular spectra of HPRT deletion mutations in circulating T-lymphocytes in Fanconi anemia patients.

D. Papadopoulo, A. Laquerbe, M. Escarceller, 1999, Mutation research.

Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joining.

P. Jeggo, S. Jackson, M. Buchwald, 1998, Journal of molecular biology.

Use of a Base-Labile Protected Derivative of 6-Mercaptohexanol for the Preparation of Oligonucleotides Containing a Thiol Group at the 5′-End

R. Eritja, F. Albericio, B. G. Torre, 1993 .

Detection of hepatitis B virus DNA in human serumsamples: Use of digoxigenin-labeled oligonucleotides as modified primers for the polymerase chain reaction

R. Eritja, F. Rodríguez-Frías, B. Segundo, 1992 .

LRRN6A/LERN1 (leucine‐rich repeat neuronal protein 1), a novel gene with enriched expression in limbic system and neocortex

X. Estivill, L. Sumoy, L. Carim-Todd, 2003, The European journal of neuroscience.

The fidelity of double strand breaks processing is impaired in complementation groups B and D of fanconi anemia, a genetic instability syndrome

D. Papadopoulo, E. Moustacchi, S. Rousset, 1997, Somatic cell and molecular genetics.

Identification and characterization of BTBD1, a novel BTB domain containing gene on human chromosome 15q24.

X. Estivill, L. Sumoy, L. Carim-Todd, 2001, Gene.

HMG20A and HMG20B map to human chromosomes 15q24 and 19p13.3 and constitute a distinct class of HMG-box genes with ubiquitous expression

M. Gratacós, X. Estivill, M. Pujana, 2000, Cytogenetic and Genome Research.

Involvement of Escherichia coli DNA polymerase II in response to oxidative damage and adaptive mutation

K. McEntee, D. Touati, S. Lovett, 1994, Journal of bacteriology.

Characterization of human FSD1, a novel brain specific gene on chromosome 19 with paralogy to 9q31.

X. Estivill, L. Sumoy, L. Carim-Todd, 2001, Biochimica et biophysica acta.

PALML, a novel paralemmin-related gene mapping on human chromosome 1p21.

X. Estivill, K. Devriendt, L. Sumoy, 2001, Gene.

Cloning of the novel gene TM6SF1 reveals conservation of clusters of paralogous genes between human chromosomes 15q24→q26 and 19p13.3→p12

X. Estivill, L. Sumoy, L. Carim-Todd, 2000, Cytogenetic and Genome Research.

Identification and Expression Analysis of C3orf1, a Novel Human Gene Homologous to the Drosophila RP140—Upstream Gene

X. Estivill, L. Sumoy, R. Pluvinet, 2000, DNA sequence : the journal of DNA sequencing and mapping.

Cloning, mapping and expression analysis of VPS33B, the human orthologue of rat Vps33b

X. Estivill, L. Sumoy, M. Escarceller, 2000, Cytogenetic and Genome Research.