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High-resolution melting analysis for rapid screening of BRCA1 and BRCA2 Spanish mutations

Breast cancer research and treatment, 2009-05, Vol.115 (2), p.405-414

2009

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The potential effect of gender in combination with common genetic polymorphisms of drug-metabolizing enzymes on the risk of developing acute leukemia

Haematologica (Roma), 2007-03, Vol.92 (3), p.308-314

2007

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Standardized quantitative assessment of BCR-ABL1 transcripts on an international scale

Clinical chemistry (Baltimore, Md.), 2013-06, Vol.59 (6), p.874-875

Bolufer, Pascual

2013

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Treatment With All-Trans Retinoic Acid and Anthracycline Monochemotherapy for Children With Acute Promyelocytic Leukemia: A Multicenter Study by the PETHEMA Group

Journal of clinical oncology, 2005-10, Vol.23 (30), p.7632-7640

2005

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MicroRNA signatures in hereditary breast cancer

Breast cancer research and treatment, 2013-11, Vol.142 (1), p.19-30

2013

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The t(4;22)(q12;q11) in atypical chronic myeloid leukaemia fuses BCR to PDGFRA

Human molecular genetics, 2002-06, Vol.11 (12), p.1391-1397

2002

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Fragment length analysis screening for detection of CEBPA mutations in intermediate-risk karyotype acute myeloid leukemia

Annals of hematology, 2012-01, Vol.91 (1), p.1-7

2012

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Analysis of SNP rs16754 of WT1 gene in a series of de novo acute myeloid leukemia patients

Annals of hematology, 2012-12, Vol.91 (12), p.1845-1853

2012

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Advantage of high-resolution melting curve analysis over conformation-sensitive gel electrophoresis for mutational screening of BRCA1 and BRCA2 genes

Clinica chimica acta, 2011-03, Vol.412 (7), p.578-582

2011

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CASP8 D302H polymorphism delays the age of onset of breast cancer in BRCA1 and BRCA2 carriers

Breast cancer research and treatment, 2010, Vol.119 (1), p.87-93

2010

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Broad BRCA1 and BRCA2 mutational spectrum and high incidence of recurrent and novel mutations in the eastern Spain population

Breast cancer research and treatment, 2010-05, Vol.121 (1), p.257-260

2010

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Advantages of the high resolution melting in the detection of BRCA1 or BRCA2 mutation carriers

Clinical biochemistry, 2009-10, Vol.42 (15), p.1572-1576

2009

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Complex Variant t(9;22) Chromosome Translocations in Five Cases of Chronic Myeloid Leukemia

Advances in Hematology, 2009, Vol.2009, p.187125-4

2009

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Science and technology in the 20th century as seen through the journal Ibérica (1914-2003)

Contributions to science (Barcelona, Spain), 2012

Bolufer, Pascual

2012

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Quantitative assessment of PML-RARa and BCR-ABL by two real-time PCR instruments: Multiinstitutional laboratory trial

Clinical chemistry (Baltimore, Md.), 2004-06, Vol.50 (6), p.1088-1092

2004

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Incidence and prognostic value of FLT3 internal tandem duplication and D835 mutations in acute myeloid leukemia

Haematologica (Roma), 2003-01, Vol.88 (1), p.19

2003

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Adverse prognostic value of MYBL2 overexpression and association with microRNA-30 family in acute myeloid leukemia patients

Leukemia research, 2013-12, Vol.37 (12), p.1690-1696

2013

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Prognostic implications of Wilms' tumor gene (WT1) expression in patients with de novo acute myeloid leukemia

Haematologica (Roma), 2004-08, Vol.89 (8), p.926

2004

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Influence of genetic polymorphisms on the risk of developing leukemia and on disease progression

Leukemia research, 2006-12, Vol.30 (12), p.1471-1491

2006

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Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence

Familial cancer, 2010-09, Vol.9 (3), p.291-295

2010

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Variants in DNA double-strand break repair genes and breast cancer susceptibility

Human molecular genetics, 2002-06, Vol.11 (12), p.1399-1407

2002

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CÉLULA DE COMBUSTIBLE SIN PLATINO Pasos para la búsqueda de una solución

DYNA ENERGIA Y SOSTENIBILIDAD, 2017, Vol.6 (1), p.3 p.-3 p.

BOLUFER MAYANS, PASCUAL

2017

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High-resolution melting analysis for rapid screening of BRCA1 and BRCA2 Spanish mutations

The potential effect of gender in combination with common genetic polymorphisms of drug-metabolizing enzymes on the risk of developing acute leukemia

Standardized quantitative assessment of BCR-ABL1 transcripts on an international scale

Treatment With All-Trans Retinoic Acid and Anthracycline Monochemotherapy for Children With Acute Promyelocytic Leukemia: A Multicenter Study by the PETHEMA Group

MicroRNA signatures in hereditary breast cancer

The t(4;22)(q12;q11) in atypical chronic myeloid leukaemia fuses BCR to PDGFRA

Fragment length analysis screening for detection of CEBPA mutations in intermediate-risk karyotype acute myeloid leukemia

Analysis of SNP rs16754 of WT1 gene in a series of de novo acute myeloid leukemia patients

Advantage of high-resolution melting curve analysis over conformation-sensitive gel electrophoresis for mutational screening of BRCA1 and BRCA2 genes

CASP8 D302H polymorphism delays the age of onset of breast cancer in BRCA1 and BRCA2 carriers

Broad BRCA1 and BRCA2 mutational spectrum and high incidence of recurrent and novel mutations in the eastern Spain population

Advantages of the high resolution melting in the detection of BRCA1 or BRCA2 mutation carriers

Complex Variant t(9;22) Chromosome Translocations in Five Cases of Chronic Myeloid Leukemia

Science and technology in the 20th century as seen through the journal Ibérica (1914-2003)

Risk-adapted treatment of acute promyelocytic leukemia with all-trans-retinoic acid and anthracycline monochemotherapy: a multicenter study by the PETHEMA group

Risk-adapted treatment of acute promyelocytic leukemia with all-trans retinoic acid and anthracycline monochemotherapy: long-term outcome of the LPA 99 multicenter study by the PETHEMA Group

Quantitative assessment of PML-RARa and BCR-ABL by two real-time PCR instruments: Multiinstitutional laboratory trial

Definition of relapse risk and role of nonanthracycline drugs for consolidation in patients with acute promyelocytic leukemia: a joint study of the PETHEMA and GIMEMA cooperative groups

Incidence and prognostic value of FLT3 internal tandem duplication and D835 mutations in acute myeloid leukemia

Adverse prognostic value of MYBL2 overexpression and association with microRNA-30 family in acute myeloid leukemia patients

Prognostic implications of Wilms' tumor gene (WT1) expression in patients with de novo acute myeloid leukemia

Influence of genetic polymorphisms on the risk of developing leukemia and on disease progression

Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence

Variants in DNA double-strand break repair genes and breast cancer susceptibility

CÉLULA DE COMBUSTIBLE SIN PLATINO Pasos para la búsqueda de una solución

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