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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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Detecting human melanoma cell re-differentiation following BRAF or heat shock protein 90 inhibition using photoacoustic and magnetic resonance imaging

Scientific reports, 2017-08, Vol.7 (1), p.8215-9, Article 8215

2017

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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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Abstract 444: Monocarboxylate transporter 1 inhibition with AZD3965 increases cancer cell dependence on bioenergetic metabolism predicating combination therapy with mitochondrial inhibitors

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.444-444

2017

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

European journal of human genetics : EJHG, 2008-08, Vol.17 (1), p.51-65

2008

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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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Abstract 4108: Longitudinal diffusion-weighted MRI assessment of NRAS mutant melanoma response to dual RAF-MEK inhibition reveals differences associated with collagen deposition

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.4108-4108

2018

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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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MCT1 inhibitor AZD3965 increases mitochondrial metabolism, facilitating combination therapy and non-invasive magnetic resonance spectroscopy

Cancer research (Chicago, Ill.), 2017-09, Vol.77 (21), p.5913-5924

2017

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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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Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutations

Journal of cystic fibrosis, 2005-12, Vol.4 (4), p.233-237

2005

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Prevalencia de las enfermedades: estimación y relevancia

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

Casals-Senent, Teresa

2005

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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

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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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

Detecting human melanoma cell re-differentiation following BRAF or heat shock protein 90 inhibition using photoacoustic and magnetic resonance imaging

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

Abstract 444: Monocarboxylate transporter 1 inhibition with AZD3965 increases cancer cell dependence on bioenergetic metabolism predicating combination therapy with mitochondrial inhibitors

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

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

Abstract 4108: Longitudinal diffusion-weighted MRI assessment of NRAS mutant melanoma response to dual RAF-MEK inhibition reveals differences associated with collagen deposition

Optimizing strategies for CFTR molecular testing

MCT1 inhibitor AZD3965 increases mitochondrial metabolism, facilitating combination therapy and non-invasive magnetic resonance spectroscopy

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

Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutations

Prevalencia de las enfermedades: estimación y relevancia

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

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