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Novel antisense therapy targeting microRNA-132 in patients with heart failure

European heart journal, 2021-10, Vol.42 (Supplement_1)

2021

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Quantification of lipoprotein(a): comparison of an automated latex-enhanced nephelometric assay with an immunoenzymometric method

European journal of clinical chemistry and clinical biochemistry, 1996-02, Vol.34 (2), p.119

1996

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Quantification of Lipoprotein(a): Comparison of an Automated Latex-Enhanced Nephelometric Assay with an Immunoenzymometric Method

Clinical chemistry and laboratory medicine, 1996, Vol.34 (2), p.119-124

1996

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BLM-DNA2-RPA-MRN and EXO1-BLM-RPA-MRN constitute two DNA end resection machineries for human DNA break repair

Genes & development, 2011-02, Vol.25 (4), p.350-362

2011

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Human exonuclease 1 and BLM helicase interact to resect DNA and initiate DNA repair

Proceedings of the National Academy of Sciences - PNAS, 2008-11, Vol.105 (44), p.16906-16911

2008

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Genetic basis for increased intestinal permeability in families with Crohn’s disease: role of CARD15 3020insC mutation?

Gut, 2006-03, Vol.55 (3), p.342-347

2006

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Einfache und sichere Diagnostik der primären Laktoseintoleranz durch Bestimmung der DNA Variante C/C-13910

Zeitschrift für Gastroenterologie, 2015, Vol.41 (8)

2015

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Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperation

Alimentary pharmacology & therapeutics, 2004-05, Vol.19 (10), p.1073-1078

2004

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Interaction of E. coli Single-Stranded DNA Binding Protein (SSB) with Exonuclease I. The Carboxy-Terminus of SSB Is the Recognition Site for the Nuclease

Biological chemistry, 2000-03, Vol.381 (3), p.183-192

2000

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In vitro and in vivo function of the C-terminus of Escherichia coli single-stranded DNA binding protein

Nucleic acids research, 1996-07, Vol.24 (14), p.2706-2711

1996

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Robustness of central carbohydrate metabolism in developing maize kernels

Phytochemistry (Oxford), 2006-07, Vol.67 (14), p.1460-1475

2006

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Changes in flux pattern of the central carbohydrate metabolism during kernel development in maize

Phytochemistry (Oxford), 2005-11, Vol.66 (22), p.2632-2642

2005

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DLG5 variants in inflammatory bowel disease

The American journal of gastroenterology, 2006-04, Vol.101 (4), p.786-792

2006

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L'État et l'exercice de l'autorité politique Dénationalisation et administration

Revue française de sociologie, 2011-07, Vol.52 (3), p.509-535

2011

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final step of pantothenate biosynthesis in higher plants: cloning and characterization of pantothenate synthetase from Lotus japonicus and Oryza sativum (rice)

Biochemical journal, 1999-08, Vol.341 (3), p.669-678

1999

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The C/C_₁₃₉₁₀ and G/G_₂₂₀₁₈ Genotypes for Adult-type Hypolactasia are not Associated with Inflammatory Bowel Disease

Scandinavian journal of gastroenterology, 2003, Vol.38 (5), p.538-542

2003

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FH clinical phenotype in Greek patients with LDL-R defective vs. negative mutations

European journal of clinical investigation, 2004-06, Vol.34 (6), p.402-409

2004

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A common core for binding single-stranded DNA: structural comparison of the single-stranded DNA-binding proteins (SSB) from E. coli and human mitochondria

FEBS letters, 1997-07, Vol.411 (2), p.313-316

1997

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Escherichia coli L-aspartate-alpha-decarboxylase: preprotein processing and observation of reaction intermediates by electrospray mass spectrometry

Biochemical journal, 1997-05, Vol.323 ( Pt 3) (3), p.661-669

1997

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Molecular characterization of familial hypercholesterolemia in German and Greek patients

Human mutation, 2004-03, Vol.23 (3), p.285-286

2004

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Introducing Genetic Testing for Adult-Type Hypolactasia

Digestion, 2005-01, Vol.71 (4), p.245-250

2005

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A homozygous HFE gene splice site mutation (IVS5+1 G/A) in a hereditary hemochromatosis patient of Vietnamese origin

Gastroenterology (New York, N.Y. 1943), 2002-03, Vol.122 (3), p.789-795

2002

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A new LMNA mutation causing limb girdle muscular dystrophy 1B

Journal of neurology, 2005-05, Vol.252 (5), p.621-623

2005

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Dyslipemia in Familial Partial Lipodystrophy Caused by an R482W Mutation in the LMNA Gene

The journal of clinical endocrinology and metabolism, 2001-05, Vol.86 (5), p.2289-2295

2001

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Einfluss von Polymorphismen des MDR1-Gens auf Ausbruch und Verlauf chronisch entzündlicher Darmerkrankungen

Zeitschrift für Gastroenterologie, 2006, Vol.43 (5)

2006

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Novel antisense therapy targeting microRNA-132 in patients with heart failure

Quantification of lipoprotein(a): comparison of an automated latex-enhanced nephelometric assay with an immunoenzymometric method

Quantification of Lipoprotein(a): Comparison of an Automated Latex-Enhanced Nephelometric Assay with an Immunoenzymometric Method

BLM-DNA2-RPA-MRN and EXO1-BLM-RPA-MRN constitute two DNA end resection machineries for human DNA break repair

Human exonuclease 1 and BLM helicase interact to resect DNA and initiate DNA repair

Genetic basis for increased intestinal permeability in families with Crohn’s disease: role of CARD15 3020insC mutation?

Einfache und sichere Diagnostik der primären Laktoseintoleranz durch Bestimmung der DNA Variante C/C-13910

Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperation

Interaction of E. coli Single-Stranded DNA Binding Protein (SSB) with Exonuclease I. The Carboxy-Terminus of SSB Is the Recognition Site for the Nuclease

In vitro and in vivo function of the C-terminus of Escherichia coli single-stranded DNA binding protein

Robustness of central carbohydrate metabolism in developing maize kernels

Changes in flux pattern of the central carbohydrate metabolism during kernel development in maize

DLG5 variants in inflammatory bowel disease

L'État et l'exercice de l'autorité politique Dénationalisation et administration

final step of pantothenate biosynthesis in higher plants: cloning and characterization of pantothenate synthetase from Lotus japonicus and Oryza sativum (rice)

The C/C_₁₃₉₁₀ and G/G_₂₂₀₁₈ Genotypes for Adult-type Hypolactasia are not Associated with Inflammatory Bowel Disease

FH clinical phenotype in Greek patients with LDL-R defective vs. negative mutations

A common core for binding single-stranded DNA: structural comparison of the single-stranded DNA-binding proteins (SSB) from E. coli and human mitochondria

Escherichia coli L-aspartate-alpha-decarboxylase: preprotein processing and observation of reaction intermediates by electrospray mass spectrometry

Molecular characterization of familial hypercholesterolemia in German and Greek patients

Introducing Genetic Testing for Adult-Type Hypolactasia

A homozygous HFE gene splice site mutation (IVS5+1 G/A) in a hereditary hemochromatosis patient of Vietnamese origin

A new LMNA mutation causing limb girdle muscular dystrophy 1B

Dyslipemia in Familial Partial Lipodystrophy Caused by an R482W Mutation in the LMNA Gene

Einfluss von Polymorphismen des MDR1-Gens auf Ausbruch und Verlauf chronisch entzündlicher Darmerkrankungen

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