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MCT1 Inhibitor AZD3965 Increases Mitochondrial Metabolism, Facilitating Combination Therapy and Noninvasive Magnetic Resonance Spectroscopy

Cancer research (Chicago, Ill.), 2017-11, Vol.77 (21), p.5913-5924

2017

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Monocarboxylate transporter 1 blockade with AZD3965 inhibits lipid biosynthesis and increases tumour immune cell infiltration

British journal of cancer, 2020-03, Vol.122 (6), p.895-903

2020

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Increased inflammatory lipid metabolism and anaplerotic mitochondrial activation follow acquired resistance to vemurafenib in BRAF-mutant melanoma cells

British journal of cancer, 2020-01, Vol.122 (1), p.72-81

2020

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Targeting DNA Repair Defects for Precision Medicine in Prostate Cancer

Current oncology reports, 2019-05, Vol.21 (5), p.42-10, Article 42

2019

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Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens

Fertility and sterility, 2010-11, Vol.94 (6), p.2122-2127

2010

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Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders - updated European recommendations

European journal of human genetics : EJHG, 2009-01, Vol.17 (1), p.51-65

2009

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Assessing the residual CFTR gene expression in human nasal epithelium cells bearing CFTR splicing mutations causing cystic fibrosis

European journal of human genetics : EJHG, 2014-06, Vol.22 (6), p.784-791

2014

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GUSB and ATP2B4 are suitable reference genes for CFTR gene expression data normalization in nasal epithelium cells

Journal of cystic fibrosis, 2012-09, Vol.11 (5), p.398-404

2012

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Optimizing strategies for CFTR molecular testing

Journal of cystic fibrosis, 2011-03, Vol.10 (2), p.143-144

2011

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Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13

Nature genetics, 1999-06, Vol.22 (2), p.128-129

1999

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Can a Place of Origin of the Main Cystic Fibrosis Mutations Be Identified?

American journal of human genetics, 2002-01, Vol.70 (1), p.257-264

2002

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Common mutations in cuban cystic fibrosis patients

Journal of cystic fibrosis, 2009-01, Vol.8 (1), p.47-49

2009

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The p.Arg258Gly mutation in intracellular loop 2 of CFTR is associated with CFTR-related disorders

Genetic testing and molecular biomarkers, 2009-12, Vol.13 (6), p.765-768

2009

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Mutational spectrum of cystic fibrosis patients from Córdoba province and its zone of influence: Implications of molecular diagnosis in Argentina

Molecular genetics and metabolism, 2006-04, Vol.87 (4), p.370-375

2006

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High heterogeneity for cystic fibrosis in Spanish families : 75 mutations account for 90% of chromosomes

Human genetics, 1997-12, Vol.101 (3), p.365-370

1997

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A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals

Human genetics, 2000-02, Vol.106 (2), p.172-178

2000

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Prevalence of diseases: estimation and relevance

Medicina clínica, 2005-10, Vol.125 (13), p.496-497

Casals-Senent, Teresa

2005

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CA/GT microsatellite alleles within the cystic fibrosis transmembrane conductance regulator (CFTR) gene are not generated by unequal crossingover

Genomics (San Diego, Calif.), 1991-07, Vol.10 (3), p.692-698

1991

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CFTR and asthma in the French EGEA study

European journal of human genetics : EJHG, 2001-01, Vol.9 (1), p.67-69

2001

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Independent origins of cystic fibrosis mutations R334W, R347P, R1162X, and 3849 + 10kbC-->T provide evidence of mutation recurrence in the CFTR gene

American journal of human genetics, 1994-11, Vol.55 (5), p.890-898

1994

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Recurrence of a nonsense mutation in the NF1 gene causing classical neurofibromatosis type 1

Human genetics, 1991-12, Vol.88 (2), p.185-188

1991

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Cystic fibrosis in Spain : high frequency of mutation G542X in the Mediterranean coastal area

Human genetics, 1993-03, Vol.91 (1), p.66-70

1993

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Allele Frequencies in a Worldwide Survey of a CA Repeat in the First Intron of the CFTR Gene

Human heredity, 1999-01, Vol.49 (1), p.15-20

1999

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Drought-induced dieback of riparian black alder as revealed by tree rings and oxygen isotopes

Forest ecology and management, 2020-12, Vol.478, p.118500, Article 118500

2020

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MCT1 Inhibitor AZD3965 Increases Mitochondrial Metabolism, Facilitating Combination Therapy and Noninvasive Magnetic Resonance Spectroscopy

Monocarboxylate transporter 1 blockade with AZD3965 inhibits lipid biosynthesis and increases tumour immune cell infiltration

Increased inflammatory lipid metabolism and anaplerotic mitochondrial activation follow acquired resistance to vemurafenib in BRAF-mutant melanoma cells

Targeting DNA Repair Defects for Precision Medicine in Prostate Cancer

Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens

Advanced Prostate Cancer with ATM Loss: PARP and ATR Inhibitors

Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders - updated European recommendations

Assessing the residual CFTR gene expression in human nasal epithelium cells bearing CFTR splicing mutations causing cystic fibrosis

GUSB and ATP2B4 are suitable reference genes for CFTR gene expression data normalization in nasal epithelium cells

Optimizing strategies for CFTR molecular testing

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13

Can a Place of Origin of the Main Cystic Fibrosis Mutations Be Identified?

Common mutations in cuban cystic fibrosis patients

The p.Arg258Gly mutation in intracellular loop 2 of CFTR is associated with CFTR-related disorders

Mutational spectrum of cystic fibrosis patients from Córdoba province and its zone of influence: Implications of molecular diagnosis in Argentina

High heterogeneity for cystic fibrosis in Spanish families : 75 mutations account for 90% of chromosomes

A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals

Prevalence of diseases: estimation and relevance

CA/GT microsatellite alleles within the cystic fibrosis transmembrane conductance regulator (CFTR) gene are not generated by unequal crossingover

CFTR and asthma in the French EGEA study

Independent origins of cystic fibrosis mutations R334W, R347P, R1162X, and 3849 + 10kbC-->T provide evidence of mutation recurrence in the CFTR gene

Recurrence of a nonsense mutation in the NF1 gene causing classical neurofibromatosis type 1

Cystic fibrosis in Spain : high frequency of mutation G542X in the Mediterranean coastal area

Allele Frequencies in a Worldwide Survey of a CA Repeat in the First Intron of the CFTR Gene

Drought-induced dieback of riparian black alder as revealed by tree rings and oxygen isotopes

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