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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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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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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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Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens

The New England journal of medicine, 1995-06, Vol.332 (22), p.1475-1480

1995

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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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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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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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Testicular CFTR Splice Variants in Patients with Congenital Absence of the Vas Deferens

Human molecular genetics, 1998-10, Vol.7 (11), p.1739-1744

1998

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Multimutational analysis of eleven cystic fibrosis mutations common in the mediterranean areas

Clinical chemistry (Baltimore, Md.), 2004-11, Vol.50 (11), p.2155-2157

2004

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Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers

Human molecular genetics, 1993-07, Vol.2 (7), p.1015-1022

1993

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Low incidence of PRSS1 and SPINK1 mutations in patients with chronic pancreatitis in Spain

Gastroenterology (New York, N.Y. 1943), 2003-04, Vol.124 (4), p.A584-A584

2003

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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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Identification of a 31-bp insertion (3860ins31) in exon 20 of the cysticfibrosis (CFTR) gene

Human molecular genetics, 1993-08, Vol.2 (8), p.1317-1318

1993

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Novel alleles, hemizygosity and deletions at an Alu-repeat within the neurofibromatosis type 1 (NF1) gene

Human molecular genetics, 1993-06, Vol.2 (6), p.725-730

1993

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Identification of a new missense mutation (P205S) in the first transmembrane domain of the CFTR gene associated with a mild cystic fibrosis phenotype

Human molecular genetics, 1993-10, Vol.2 (10), p.1741-1742

1993

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Haplotype analysis to determine the position of a mutation among closely linked DNA markers

Human molecular genetics, 1993-07, Vol.2 (7), p.1007-1014

1993

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Temporal effects of prescribed burning on terpene production in Mediterranean pines

Tree physiology, 2017-12, Vol.37 (12), p.1622-1636

2017

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Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases

Journal of allergy and clinical immunology, 2019-01, Vol.143 (1), p.359-368

2019

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Novel Inhibitors of Fatty Acid Synthase with Anticancer Activity

Clinical cancer research, 2009-12, Vol.15 (24), p.7608-7615

2009

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542: Influence of vaginal microbiota on the pathophysiology of intra-amniotic infection and sterile-inflammation in preterm labor

American journal of obstetrics and gynecology, 2019-01, Vol.220 (1), p.S361-S363

2019

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Extreme selective sweeps independently targeted the X chromosomes of the great apes

Proceedings of the National Academy of Sciences - PNAS, 2015-05, Vol.112 (20), p.6413-6418

2015

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Performance of the preliminary classification criteria for cryoglobulinaemic vasculitis and clinical manifestations in hepatitis C virus-unrelated cryoglobulinaemic vasculitis

Clinical and experimental rheumatology, 2012-01, Vol.30 (1 Suppl 70), p.S48

2012

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Etiopathogenic role of surfactant protein d in the clinical and immunological expression of primary Sjögren syndrome

Journal of rheumatology, 2015-01, Vol.42 (1), p.111-118

2015

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

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

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

Mutations in the Cystic Fibrosis Gene in Patients with Congenital 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

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

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

Testicular CFTR Splice Variants in Patients with Congenital Absence of the Vas Deferens

Multimutational analysis of eleven cystic fibrosis mutations common in the mediterranean areas

Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers

Low incidence of PRSS1 and SPINK1 mutations in patients with chronic pancreatitis in Spain

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

Identification of a 31-bp insertion (3860ins31) in exon 20 of the cysticfibrosis (CFTR) gene

Novel alleles, hemizygosity and deletions at an Alu-repeat within the neurofibromatosis type 1 (NF1) gene

Identification of a new missense mutation (P205S) in the first transmembrane domain of the CFTR gene associated with a mild cystic fibrosis phenotype

Haplotype analysis to determine the position of a mutation among closely linked DNA markers

Temporal effects of prescribed burning on terpene production in Mediterranean pines

Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases

Novel Inhibitors of Fatty Acid Synthase with Anticancer Activity

542: Influence of vaginal microbiota on the pathophysiology of intra-amniotic infection and sterile-inflammation in preterm labor

Extreme selective sweeps independently targeted the X chromosomes of the great apes

Performance of the preliminary classification criteria for cryoglobulinaemic vasculitis and clinical manifestations in hepatitis C virus-unrelated cryoglobulinaemic vasculitis

Etiopathogenic role of surfactant protein d in the clinical and immunological expression of primary Sjögren syndrome

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