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SDF-1 involvement in endothelial phenotype and ischemia-induced recruitment of bone marrow progenitor cells

Blood, 2004-12, Vol.104 (12), p.3472-3482

2004

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Myoendothelial Differentiation of Human Umbilical Cord Blood–Derived Stem Cells in Ischemic Limb Tissues

Circulation research, 2003-09, Vol.93 (5), p.e51-e62

2003

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The novel atypical retinoid ST1926 is active in ATRA resistant neuroblastoma cells acting by a different mechanism

Biochemical pharmacology, 2007-03, Vol.73 (5), p.643-655

2007

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Altered SDF‐1‐mediated differentiation of bone marrow‐derived endothelial progenitor cells in diabetes mellitus

Journal of cellular and molecular medicine, 2009-09, Vol.13 (9b), p.3405-3414

2009

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Preclinical evaluation of the novel 7-substituted camptothecin Namitecan (ST1968) in paediatric tumour models

Cancer chemotherapy and pharmacology, 2012-12, Vol.70 (6), p.811-822

2012

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Abstract C205: Persistent cell cycle perturbations and apoptosis mediate the antitumor activity of ST1968 in pediatric models

Molecular cancer therapeutics, 2011-11, Vol.10 (11_Supplement), p.C205-C205

2011

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Altered SDF-1-mediated differentiation of bone marrow-derived endothelial progenitor cells in diabetes mellitus

Journal of cellular and molecular medicine, 2009-09, Vol.13 (9B), p.3405-3414

2009

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SDF-1 AND A G1 CHECKPOINT DRIVE ENDOTHELIAL COMMITMENT OF BONE MARROW ENDOTHELIAL PROGENITOR CELLS

Cardiovascular pathology, 2004-05, Vol.13 (3), p.169-169

2004

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MYO/ENDOTHELIAL DIFFERENTIATION OF HUMAN UMBILICAL CORD BLOOD-DERIVED STEM CELLS IN ISCHEMIC LIMB TISSUES

Cardiovascular pathology, 2004-05, Vol.13 (3), p.11-11

2004

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Myoendothelial Differentiation of Human Umbilical Cord Blood–Derived Stem Cells in Ischemic Limb Tissues

Circulation research, 2003-09, Vol.93 (5), p.479-479

2003

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Therapeutic homology-independent targeted integration in retina and liver

Nature communications, 2022-04, Vol.13 (1), p.1963-1963, Article 1963

2022

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Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

European journal of human genetics : EJHG, 2021-09, Vol.29 (9), p.1325-1331

2021

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Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

European journal of human genetics : EJHG, 2021-09, Vol.29 (9), p.1337-1347

2021

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Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes

European journal of human genetics : EJHG, 2024-08, Vol.32 (8), p.998-1004

2024

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Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1)

European journal of human genetics : EJHG, 2021-09, Vol.29 (9), p.1348-1353

2021

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Solving unsolved rare neurological diseases-a Solve-RD viewpoint

European journal of human genetics : EJHG, 2021-09, Vol.29 (9), p.1332-1336

2021

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A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis

European journal of human genetics : EJHG, 2021-09, Vol.29 (9), p.1359-1368

2021

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Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis

European journal of human genetics : EJHG, 2021-09, Vol.29 (9), p.1470-1471

2021

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Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

European journal of human genetics : EJHG, 2021-09, Vol.29 (9), p.1470-1471

2021

Volltextzugriff (PDF)

Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant

European journal of medical genetics, 2022-01, Vol.65 (1), p.104402-104402, Article 104402

2022

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Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

HGG advances, 2023-04, Vol.4 (2), p.100186-100186, Article 100186

2023

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Telecare Provides comparable efficacy to conventional self-monitored blood glucose in patients with type 2 diabetes titrating one injection of insulin glulisine-the ELEONOR study

Diabetes technology & therapeutics, 2012-02, Vol.14 (2), p.175

2012

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Optimizing Insulin Glargine Plus One Injection of Insulin Glulisine in Type 2 Diabetes in the ELEONOR Study: Similar effects of telecare and conventional self-monitoring of blood glucose on patient functional health status and treatment satisfaction

Diabetes care, 2011-12, Vol.34 (12), p.2524-2526

2011

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SDF-1 involvement in endothelial phenotype and ischemia-induced recruitment of bone marrow progenitor cells

Myoendothelial Differentiation of Human Umbilical Cord Blood–Derived Stem Cells in Ischemic Limb Tissues

The novel atypical retinoid ST1926 is active in ATRA resistant neuroblastoma cells acting by a different mechanism

Altered SDF‐1‐mediated differentiation of bone marrow‐derived endothelial progenitor cells in diabetes mellitus

Preclinical evaluation of the novel 7-substituted camptothecin Namitecan (ST1968) in paediatric tumour models

Abstract C205: Persistent cell cycle perturbations and apoptosis mediate the antitumor activity of ST1968 in pediatric models

Altered SDF-1-mediated differentiation of bone marrow-derived endothelial progenitor cells in diabetes mellitus

SDF-1 AND A G1 CHECKPOINT DRIVE ENDOTHELIAL COMMITMENT OF BONE MARROW ENDOTHELIAL PROGENITOR CELLS

MYO/ENDOTHELIAL DIFFERENTIATION OF HUMAN UMBILICAL CORD BLOOD-DERIVED STEM CELLS IN ISCHEMIC LIMB TISSUES

Myoendothelial Differentiation of Human Umbilical Cord Blood–Derived Stem Cells in Ischemic Limb Tissues

Therapeutic homology-independent targeted integration in retina and liver

Genotype-phenotype correlations in recessive titinopathies

Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study

Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes

Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1)

Solving unsolved rare neurological diseases-a Solve-RD viewpoint

A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis

Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis

Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant

Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

Telecare Provides comparable efficacy to conventional self-monitored blood glucose in patients with type 2 diabetes titrating one injection of insulin glulisine-the ELEONOR study

Optimizing Insulin Glargine Plus One Injection of Insulin Glulisine in Type 2 Diabetes in the ELEONOR Study: Similar effects of telecare and conventional self-monitoring of blood glucose on patient functional health status and treatment satisfaction

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