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Transactivating mutation of the MYOD1 gene is a frequent event in adult spindle cell rhabdomyosarcoma

The Journal of pathology, 2014-02, Vol.232 (3), p.300-307

2014

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Defining practice variation and exploring influencing factors on needs assessment in home care nursing: A Delphi study

Journal of advanced nursing, 2023-09, Vol.79 (9), p.3426-3439

2023

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Osteosarcoma originates from mesenchymal stem cells in consequence of aneuploidization and genomic loss of Cdkn2

The Journal of pathology, 2009-11, Vol.219 (3), p.294-305

2009

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Synthetic Phenolic Glycolipids for Application in Diagnostic Tests for Leprosy

Chembiochem : a European journal of chemical biology, 2021-04, Vol.22 (8), p.1487-1493

2021

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Investigation into the cellular origins of posterior regeneration in the annelid Capitella teleta

Regeneration, 2018-03, Vol.5 (1), p.61-77

2018

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Fusion events lead to truncation of FOS in epithelioid hemangioma of bone

Genes chromosomes & cancer, 2015-09, Vol.54 (9), p.565-574

2015

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Ca2+-BK channel clusters in olfactory receptor neurons and their role in odour coding

The European journal of neuroscience, 2015-12, Vol.42 (11), p.2985-2995

2015

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Intronic deletion and duplication proximal of the EXT1 gene: A novel causative mechanism for multiple osteochondromas

Genes chromosomes & cancer, 2013-04, Vol.52 (4), p.431-436

2013

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To what extent do home care nurses feel free to assess the care that is needed for their patients? A nationwide survey in the Netherlands

Health science reports, 2021-12, Vol.4 (4), p.e420-n/a

2021

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Cerebrospinal fluid analysis differentiates multiple system atrophy from Parkinson's disease

Movement disorders, 2004-05, Vol.19 (5), p.571-579

2004

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Genetic characterization of mesenchymal, clear cell, and dedifferentiated chondrosarcoma

Genes chromosomes & cancer, 2012-10, Vol.51 (10), p.899-909

2012

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Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome

Epilepsia open, 2023-12, Vol.8 (4), p.1300-1313

2023

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Generation of induced pluripotent stem cells from human foetal fibroblasts using the Sleeping Beauty transposon gene delivery system

Differentiation (London), 2013-07, Vol.86 (1-2), p.30-37

2013

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DNA-binding characteristics of cnidarian Pax-C and Pax-B proteins in vivo and in vitro: No simple relationship with the Pax-6 and Pax-2/5/8 classes

Journal of experimental zoology. Part B, Molecular and developmental evolution, 2003-10, Vol.299B (1), p.26-35

2003

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Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization are complementary techniques to detect cytogenetic abnormalities in multiple myeloma

Genes chromosomes & cancer, 2013-09, Vol.52 (9), p.785-793

2013

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Array CGH analysis identifies two distinct subgroups of primary angiosarcoma of bone

Genes chromosomes & cancer, 2015-02, Vol.54 (2), p.72-81

2015

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Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients

Human mutation, 2011-02, Vol.32 (2), p.E2036-E2049

2011

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Ca(2+)-BK channel clusters in olfactory receptor neurons and their role in odour coding

The European journal of neuroscience, 2015-12, Vol.42 (11), p.2985-2995

2015

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Ca 2+ –BK channel clusters in olfactory receptor neurons and their role in odour coding

The European journal of neuroscience, 2015-12, Vol.42 (11), p.2985-2995

2015

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Cerebrospinal fluid Aβ42 levels in multiple system atrophy

Movement disorders, 2004-02, Vol.19 (2), p.238-240

2004

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P2-145: Cerebrospinal fluid neurofilament concentrations in dementia syndromes

Alzheimer's & dementia, 2006-07, Vol.2 (3), p.S276-S276

2006

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Transactivating mutation of the MYOD1 gene is a frequent event in adult spindle cell rhabdomyosarcoma: MYOD1 mutation in adult spindle cell rhabdomyosarcoma

The Journal of pathology, 2014-02, Vol.232 (3), p.300-307

2014

Volltextzugriff (PDF)

Cerebrospinal fluid Aβ 42 levels in multiple system atrophy

Movement disorders, 2004-02, Vol.19 (2), p.238-240

2004

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Cerebrospinal fluid Abeta42 levels in multiple system atrophy

Movement disorders, 2004-02, Vol.19 (2), p.238-40; author reply 240-1

2004

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Cerebrospinal fluid Ab42 levels in multiple system atrophy

Movement disorders, 2004-02, Vol.19 (2), p.238-240

2004

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Transactivating mutation of the MYOD1 gene is a frequent event in adult spindle cell rhabdomyosarcoma

Defining practice variation and exploring influencing factors on needs assessment in home care nursing: A Delphi study

Osteosarcoma originates from mesenchymal stem cells in consequence of aneuploidization and genomic loss of Cdkn2

Synthetic Phenolic Glycolipids for Application in Diagnostic Tests for Leprosy

Investigation into the cellular origins of posterior regeneration in the annelid Capitella teleta

Fusion events lead to truncation of FOS in epithelioid hemangioma of bone

Ca2+-BK channel clusters in olfactory receptor neurons and their role in odour coding

Intronic deletion and duplication proximal of the EXT1 gene: A novel causative mechanism for multiple osteochondromas

To what extent do home care nurses feel free to assess the care that is needed for their patients? A nationwide survey in the Netherlands

Cerebrospinal fluid analysis differentiates multiple system atrophy from Parkinson's disease

Genetic characterization of mesenchymal, clear cell, and dedifferentiated chondrosarcoma

Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome

Generation of induced pluripotent stem cells from human foetal fibroblasts using the Sleeping Beauty transposon gene delivery system

DNA-binding characteristics of cnidarian Pax-C and Pax-B proteins in vivo and in vitro: No simple relationship with the Pax-6 and Pax-2/5/8 classes

Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization are complementary techniques to detect cytogenetic abnormalities in multiple myeloma

Array CGH analysis identifies two distinct subgroups of primary angiosarcoma of bone

Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients

Ca(2+)-BK channel clusters in olfactory receptor neurons and their role in odour coding

Ca 2+ –BK channel clusters in olfactory receptor neurons and their role in odour coding

Cerebrospinal fluid Aβ42 levels in multiple system atrophy

P2-145: Cerebrospinal fluid neurofilament concentrations in dementia syndromes

Transactivating mutation of the MYOD1 gene is a frequent event in adult spindle cell rhabdomyosarcoma: MYOD1 mutation in adult spindle cell rhabdomyosarcoma

Cerebrospinal fluid Aβ 42 levels in multiple system atrophy

Cerebrospinal fluid Abeta42 levels in multiple system atrophy

Cerebrospinal fluid Ab42 levels in multiple system atrophy

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