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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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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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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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Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci

Human mutation, 2010-04, Vol.31 (4), p.421-428

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, 2008-08, Vol.17 (1), p.51-65

2008

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New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12

Human molecular genetics, 2003-05, Vol.12 (10), p.1111-1120

2003

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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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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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Heterogeneity for mutations in the CFTR gene and clinical correlations in patients with congenital absence of the vas deferens

Human reproduction (Oxford), 2000-07, Vol.15 (7), p.1476-1483

2000

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Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens

Human mutation, 2011-08, Vol.32 (8), p.912-920

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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Bronchiectasis in adult patients: an expression of heterozygosity for CFTR gene mutations?

Clinical genetics, 2004-06, Vol.65 (6), p.490-495

2004

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Uniparental inheritance of microsatellite alleles of the cystic fibrosis gene (CFTR): identification of a 50 kilobase deletion

Human molecular genetics, 1993-06, Vol.2 (6), p.677-681

1993

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Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens

Human mutation, 2012-02, Vol.33 (2), p.456-456

2012

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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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Patients' Perceptions of Health Related Quality of Life in Rheumatoid Arthritis and Chronic Low Back Pain

Quality of life research, 2006-02, Vol.15 (1), p.93-102

2006

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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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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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Missense mutations in the cystic fibrosis gene in adult patients with asthma

Human mutation, 1999-12, Vol.14 (6), p.510-519

1999

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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

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

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

Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci

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

New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12

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

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

Optimizing strategies for CFTR molecular testing

Heterogeneity for mutations in the CFTR gene and clinical correlations in patients with congenital absence of the vas deferens

Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens

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

Bronchiectasis in adult patients: an expression of heterozygosity for CFTR gene mutations?

Uniparental inheritance of microsatellite alleles of the cystic fibrosis gene (CFTR): identification of a 50 kilobase deletion

Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens

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

Patients' Perceptions of Health Related Quality of Life in Rheumatoid Arthritis and Chronic Low Back Pain

Common mutations in cuban cystic fibrosis patients

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

Prevalencia de las enfermedades: estimación y relevancia

Missense mutations in the cystic fibrosis gene in adult patients with asthma

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