Filtros de búsqueda

Lista de obras de Jordi Surrallés

A DIGE-based approach to study interacting proteins

artículo científico publicado en 2007

A collaborative study on the improvement of the micronucleus test in cultured human lymphocytes

artículo científico publicado en 1992

A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain

artículo científico publicado en 2004

A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network

artículo científico publicado en 2006

Activation of the Fanconi anemia/BRCA pathway at low doses of ionization radiation

artículo científico publicado en 2015

Analysis of loss of inactive X chromosomes in interphase cells.

artículo científico publicado en 1996

Anemias raras y fallos medulares hereditarios

Aneugenic activity in human cultured lymphocytes. An overall study with colchicine using the micronucleus assay and fluorescence in situ hybridization techniques

artículo científico publicado en 1997

Basal and induced micronucleus frequencies in human lymphocytes with different GST and NAT2 genetic backgrounds

artículo científico publicado en 2006

Bcr/Abl interferes with the Fanconi anemia/BRCA pathway: implications in the chromosomal instability of chronic myeloid leukemia cells

artículo científico publicado en 2010

Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia

artículo científico publicado en 2017

Breaks at telomeres and TRF2-independent end fusions in Fanconi anemia

scientific article published on 01 February 2002

CRISPR Screens in Synthetic Lethality and Combinatorial Therapies for Cancer

artículo científico publicado en 2021

Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact

artículo científico publicado en 2011

Chromosomes with high gene density are preferentially repaired in human cells ⬇️

artículo científico publicado el 1 de noviembre de 1997

Clinical and molecular characteristics of squamous cell carcinomas from Fanconi anemia patients

artículo científico publicado en 2008

Clinical consequences of BRCA2 hypomorphism

publication published on 09 September 2021

Clusters of transcription-coupled repair in the human genome

artículo científico publicado en 2002

Constitutive activation of caspase-3 and Poly ADP ribose polymerase cleavage in fanconi anemia cells.

artículo científico publicado en 2010

Coordinated action of the Fanconi anemia and ataxia telangiectasia pathways in response to oxidative damage

artículo científico publicado en 2011

Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells.

artículo científico publicado en 2009

Disruption of the Fanconi anemia/BRCA pathway in sporadic cancer

artículo científico publicado en 2005

Dysfunctional telomeres in primary cells from Fanconi anemia FANCD2 patients

artículo científico publicado en 2012

Dyslipidemia and chronic inflammation markers are correlated with telomere length shortening in Cushing's syndrome.

artículo científico publicado en 2015

Engraftment and in vivo proliferation advantage of gene corrected mobilized CD34(+) cells from Fanconi anemia patients.

artículo científico

Epidemiology of rare anaemias in Europe

artículo científico publicado en 2010

Epigenetic Alterations in Fanconi Anaemia: Role in Pathophysiology and Therapeutic Potential.

artículo científico publicado en 2015

Equal induction and persistence of chromosome aberrations involving chromosomes 1, 4 and 10 in thyroid cancer patients treated with radioactive iodine.

artículo científico

Equal induction and persistence of chromosome aberrations involving chromosomes with heterogeneous lengths and gene densities.

artículo científico

Evaluation of micronucleus induction in a Chilean population environmentally exposed to arsenic.

artículo científico publicado en 2004

Evaluation of rare variants in the new fanconi anemia gene ERCC4 (FANCQ) as familial breast/ovarian cancer susceptibility alleles.

artículo científico publicado en 2013

Exploring the link between MORF4L1 and risk of breast cancer

artículo científico publicado en 2011

FANCD2 depletion sensitizes cancer cells repopulation ability in vitro

artículo científico publicado en 2007

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

artículo científico publicado en 2015

FISH analysis of 1cen1q12 breakage, chromosome 1 numerical abnormalities and centromeric content of micronuclei in buccal cells from thyroid cancer and hyperthyroidism patients treated with radioactive iodine

artículo científico publicado en 1999

Fanconi anemia protein FANCD2 inhibits TRF1 polyADP-ribosylation through tankyrase1-dependent manner

artículo científico publicado en 2011

Fanconi anemia: a model disease for studies on human genetics and advanced therapeutics

artículo científico

Functional Comparison of XPF Missense Mutations Associated to Multiple DNA Repair Disorders

article

Genotoxic evaluation of the herbicide paraquat in cultured human lymphocytes

artículo científico publicado en 1997

Genotoxicity of the herbicides alachlor and maleic hydrazide in cultured human lymphocytes

scientific article published on 01 May 1996

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair.

artículo científico publicado en 2015

Glutathione S-transferase polymorphisms in thyroid cancer patients

artículo científico publicado en 2003

Hematopoietic dysfunction in a mouse model for Fanconi anemia group D1

scientific journal article

Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability

scientific journal article

Human lymphocytes micronucleus assay in Europe. An international survey.

artículo científico publicado en 1997

Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype

artículo científico publicado en 2007

In vivo cytogenetic damage revealed by FISH analysis of micronuclei in uncultured human T lymphocytes

article

In vivo proliferation advantage of genetically corrected hematopoietic stem cells in a mouse model of Fanconi anemia FA-D1.

artículo científico publicado en 2008

Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility

artículo científico

Induction of instability of normal length trinucleotide repeats within human disease genes.

artículo científico publicado en 2004

Induction of mitotic micronuclei by the pyrethroid insecticide fenvalerate in cultured human lymphocytes.

artículo científico publicado en 1990

Induction, processing and persistence of radiation-induced chromosomal aberrations involving hamster euchromatin and heterochromatin

artículo científico publicado en 2000

Intra- and inter-laboratory variation in the scoring of micronuclei and nucleoplasmic bridges in binucleated human lymphocytes. Results of an international slide-scoring exercise by the HUMN project

artículo científico publicado en 2003

Lack of genotoxicity of the herbicide atrazine in cultured human lymphocytes

artículo científico publicado en 1998

Links between chromatin structure, DNA repair and chromosome fragility

artículo científico publicado en 1998

Low level of DNA repair in human chromosome 1 heterochromatin

artículo científico publicado en 1997

Micronuclei assessment in buccal cells of people environmentally exposed to arsenic in northern Chile.

artículo científico publicado en 2005

Micronuclei induced by alachlor, mitomycin-C and vinblastine in human lymphocytes: presence of centromeres and kinetochores and influence of staining technique.

artículo científico publicado en 1995

Modelling Fanconi anemia pathogenesis and therapeutics using integration-free patient-derived iPSCs

artículo científico publicado en 2014

Molecular cloning of the Drosophila Fanconi anaemia gene FANCD2 cDNA.

artículo científico publicado en 2003

Molecular cross-talk among chromosome fragility syndromes

artículo científico publicado en 2004

Molecular cytogenetic analysis of buccal cells and lymphocytes from benzene-exposed workers.

artículo científico publicado en 1997

Molecular mechanisms of micronucleus, nucleoplasmic bridge and nuclear bud formation in mammalian and human cells

artículo científico publicado en 2011

Multicolour FISH detection of radioactive iodine-induced 17cen-p53 chromosomal breakage in buccal cells from therapeutically exposed patients

artículo científico publicado en 2000

Mutagenic stress modulates the dynamics of CTG repeat instability associated with myotonic dystrophy type 1.

artículo científico publicado en 2003

Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia

artículo científico publicado en 2013

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder

artículo científico publicado en 2018

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder

artículo científico publicado en 2018

New roads to FA/BRCA pathway: H2AX

artículo científico publicado en 2007

Novel Somatic Genetic Variants as Predictors of Resistance to EGFR-Targeted Therapies in Metastatic Colorectal Cancer Patients

artículo científico publicado en 2020

On the role of FAN1 in Fanconi anemia

artículo científico publicado en 2012

Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations

artículo científico publicado en 2011

Position effect of translocations involving the inactive X chromosome: physical linkage to XIC/XIST does not lead to long-range de novo inactivation in human differentiated cells.

artículo científico publicado en 1998

Quantitative PCR analysis reveals a high incidence of large intragenic deletions in the FANCA gene in Spanish Fanconi anemia patients.

artículo científico publicado en 2004

Quick two-dimensional differential in gel electrophoresis-based method to determine length and secondary structures of telomeric DNA

artículo científico publicado en 2008

Radiosensitivity and repair of the inactive X-chromosome. Insights from FISH and immunocytogenetics ⬇️

artículo científico publicado el 11 de mayo de 1998

Relationship between chromosome fragility, aneuploidy and severity of the haematological disease in Fanconi anaemia

artículo científico publicado en 2002

Report from the In Vitro Micronucleus Assay Working Group

artículo científico publicado en 2000

Report from the in vitro micronucleus assay working group

artículo científico publicado en 2003

Role of the Met(287)Thr polymorphism in the AS3MT gene on the metabolic arsenic profile

artículo científico publicado en 2007

Savior siblings and Fanconi anemia: analysis of success rates from the family's perspective

artículo científico publicado en 2015

Segregation of sex chromosomes in human lymphocytes

artículo científico publicado en 2000

Spontaneous and induced genetic damage in T lymphocyte subsets evaluated by the Comet assay

artículo científico publicado en 2002

Targeted gene therapy and cell reprogramming in Fanconi anemia

artículo científico publicado en 2014

Telomere dysfunction in genome instability syndromes.

artículo científico publicado en 2004

Telomere length analysis in Cushing's syndrome

article

Telomere length modulates human radiation sensitivity in vitro

Telomeres and endocrine dysfunction of the adrenal and GH/IGF-1 axes

artículo científico publicado en 2013

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

scientific article published on 01 November 2019

The Fanconi anaemia genome stability and tumour suppressor network.

artículo científico publicado en 2002

The effect of cytochalasin-B concentration on the frequency of micronuclei induced by four standard mutagens. Results from two laboratories

article

The origin of micronuclei induced by cytosine arabinoside and its synergistic interaction with hydroxyurea in human lymphocytes

artículo científico publicado en 1994

The suitability of the micronucleus assay in human lymphocytes as a new biomarker of excision repair

scientific article published on 01 March 1995

Therapeutic research in the crystal chromosome disease Fanconi anemia

article published in 2018

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda