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Evolutionary implications of bacterial polyketide synthases

Molecular biology and evolution, 2005-10, Vol.22 (10), p.2027-2039

2005

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Optimized linker sequences for the expression of monomeric and dimeric bispecific single-chain diabodies

Protein engineering, 2001-10, Vol.14 (10), p.815-823

2001

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In vitro and in vivo characterization of the actin polymerizing compound chondramide as an angiogenic inhibitor

Cardiovascular research, 2014-11, Vol.104 (2), p.303-314

2014

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Novel RGD lipopeptides for the targeting of liposomes to integrin-expressing endothelial and melanoma cells

Protein engineering, design and selection, 2004-05, Vol.17 (5), p.433-441

2004

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Comparative genomic analysis of fruiting body formation in Myxococcales

Molecular biology and evolution, 2011-02, Vol.28 (2), p.1083-1097

2011

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Isolation from phage display libraries of lysine‐deficient human epidermal growth factor variants for directional conjugation as targeting ligands

Protein engineering, 2003-12, Vol.16 (12), p.1107-1113

2003

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Increased serum concentration of carbohydrate-deficient transferrin in patients with combined pancreas and kidney transplantation

Clinical chemistry (Baltimore, Md.), 1997-02, Vol.43 (2), p.344-351

1997

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Similar rate of O 6 -ethylguanine elimination from DNA in normal human fibroblast and xeroderma pigmentosum cell strains not transformed by SV40

Carcinogenesis (New York), 1983, Vol.4 (8), p.1075-1077

1983

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Efficacy of Temozolomide Therapy in Patients With Aggressive Pituitary Adenomas and Carcinomas—A German Survey

The journal of clinical endocrinology and metabolism, 2020-03, Vol.105 (3), p.e660-e675

2020

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Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases

Brain (London, England : 1878), 2010-10, Vol.133 (10), p.2920-2941

2010

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A 3'-UTR mutation creates a microRNA target site in the GFPT1 gene of patients with congenital myasthenic syndrome

Human molecular genetics, 2015-06, Vol.24 (12), p.3418-3426

2015

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Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies

Brain (London, England : 1878), 2023-12, Vol.146 (12), p.4880-4890

2023

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Incidence and management of complications after neoadjuvant chemotherapy followed by extrapleural pneumonectomy for malignant pleural mesothelioma

European journal of cardio-thoracic surgery, 2006-04, Vol.29 (4), p.579-584

2006

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Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts

Human molecular genetics, 2001-12, Vol.10 (26), p.3025-3035

2001

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High Prevalence of Peripheral Arterial Disease in HIV-Infected Persons

Clinical infectious diseases, 2008-03, Vol.46 (5), p.761-767

2008

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Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients

Brain (London, England : 1878), 2007-12, Vol.130 (12), p.3250-3264

2007

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Effect of Gastric Bypass and Gastric Banding on Proneurotensin Levels in Morbidly Obese Patients

The journal of clinical endocrinology and metabolism, 2006-09, Vol.91 (9), p.3544-3547

2006

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Anticoagulant-free Genius® haemodialysis using low molecular weight heparin-coated circuits

Nephrology, dialysis, transplantation, 2006-04, Vol.21 (4), p.1013-1018

2006

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Long-term treatment with valganciclovir improves lentiviral suicide gene therapy of glioblastoma

Neuro-oncology (Charlottesville, Va.), 2019-07, Vol.21 (7), p.890-900

2019

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Disturbed Glutathione Metabolism and Decreased Antioxidant Levels in Human Immunodeficiency Virus-Infected Patients during Highly Active Antiretroviral Therapy—Potential Immunomodulatory Effects of Antioxidants

The Journal of infectious diseases, 2003-07, Vol.188 (2), p.232-238

2003

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Comprehensive Allelotype and Genetic Analysis of 466 Human Nervous System Tumors

Journal of neuropathology and experimental neurology, 2000-06, Vol.59 (6), p.544-558

2000

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Early or deferred cardiovascular magnetic resonance after ST-segment-elevation myocardial infarction for effective risk stratification

European heart journal cardiovascular imaging, 2020-06, Vol.21 (6), p.632-639

2020

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Variant of the CHEK2 gene as a prognostic marker in glioblastoma multiforme

Neurosurgery, 2006-11, Vol.59 (5), p.1078-85; discussion 1085

2006

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A newly identified chromosomal microdeletion and an N-box mutation of the AChRε gene cause a congenital myasthenic syndrome

Brain (London, England : 1878), 2002-05, Vol.125 (Pt 5), p.1005-1013

2002

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Evolutionary implications of bacterial polyketide synthases

Optimized linker sequences for the expression of monomeric and dimeric bispecific single-chain diabodies

In vitro and in vivo characterization of the actin polymerizing compound chondramide as an angiogenic inhibitor

Novel RGD lipopeptides for the targeting of liposomes to integrin-expressing endothelial and melanoma cells

Comparative genomic analysis of fruiting body formation in Myxococcales

Isolation from phage display libraries of lysine‐deficient human epidermal growth factor variants for directional conjugation as targeting ligands

Increased serum concentration of carbohydrate-deficient transferrin in patients with combined pancreas and kidney transplantation

Similar rate of O 6 -ethylguanine elimination from DNA in normal human fibroblast and xeroderma pigmentosum cell strains not transformed by SV40

Efficacy of Temozolomide Therapy in Patients With Aggressive Pituitary Adenomas and Carcinomas—A German Survey

Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases

A 3'-UTR mutation creates a microRNA target site in the GFPT1 gene of patients with congenital myasthenic syndrome

Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies

Incidence and management of complications after neoadjuvant chemotherapy followed by extrapleural pneumonectomy for malignant pleural mesothelioma

Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts

High Prevalence of Peripheral Arterial Disease in HIV-Infected Persons

Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients

Effect of Gastric Bypass and Gastric Banding on Proneurotensin Levels in Morbidly Obese Patients

Anticoagulant-free Genius® haemodialysis using low molecular weight heparin-coated circuits

Long-term treatment with valganciclovir improves lentiviral suicide gene therapy of glioblastoma

Disturbed Glutathione Metabolism and Decreased Antioxidant Levels in Human Immunodeficiency Virus-Infected Patients during Highly Active Antiretroviral Therapy—Potential Immunomodulatory Effects of Antioxidants

Low-frequency drug-resistant HIV-1 and risk of virological failure to first-line NNRTI-based ART: a multicohort European case-control study using centralized ultrasensitive 454 pyrosequencing

Comprehensive Allelotype and Genetic Analysis of 466 Human Nervous System Tumors

Early or deferred cardiovascular magnetic resonance after ST-segment-elevation myocardial infarction for effective risk stratification

Variant of the CHEK2 gene as a prognostic marker in glioblastoma multiforme

A newly identified chromosomal microdeletion and an N-box mutation of the AChRε gene cause a congenital myasthenic syndrome

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