Search Results - "van de Wetering, C."
-
1
Lymphoma development in Bax transgenic mice is inhibited by Bcl-2 and associated with chromosomal instability
Published in Cell death and differentiation (01-06-2003)“…Bax is a Bcl-2 family member that promotes apoptosis but has paradoxical effects on lymphoma development in p53-deficient mice. To better understand the…”
Get full text
Journal Article -
2
Seagrass spatial data synthesis from north‐east Australia, Torres Strait and Gulf of Carpentaria, 1983 to 2022
Published in Limnology and oceanography letters (01-02-2024)“…The Gulf of Carpentaria and Torres Strait in north‐eastern Australia support globally significant seagrass ecosystems that underpin fishing and cultural…”
Get full text
Journal Article -
3
Exposure to acrolein disrupts the molecular regulation of mitochondrial metabolism in epithelial cells of the human airways
Published in Toxicology letters (01-09-2021)Get full text
Journal Article -
4
Glutathione-S-transferase P promotes glycolysis in asthma in association with oxidation of pyruvate kinase M2
Published in Redox biology (01-11-2021)“…Interleukin-1-dependent increases in glycolysis promote allergic airways disease in mice and disruption of pyruvate kinase M2 (PKM2) activity is critical…”
Get full text
Journal Article Web Resource -
5
Widespread Dispersal of Cholera Toxin Subunit b to Brain and Spinal Cord Neurons Following Systemic Delivery
Published in Experimental neurology (01-11-2002)“…We have discovered novel transport properties of cholera toxin subunit b beyond well-known anterograde and retrograde axonal transport. Injection of 1500 μg of…”
Get full text
Journal Article -
6
Assignment of the human gene for receptor-type protein tyrosine phosphatase IA-2 (PTPRN) to chromosome region 2q35 --> q36.1 and identification of an intragenic genetic marker
Published in Cytogenetics and cell genetics (01-01-1996)“…Using a mouse protein tyrosine phosphatase cDNA fragment as a probe, cosmid clones containing segments of the human IA-2 PTPase gene (PTPRN) were isolated. The…”
Get more information
Journal Article -
7
Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene
Published in Neuromuscular disorders : NMD (01-10-2002)“…Hereditary neuropathy with liability to pressure palsies is associated with a deficiency in the Peripheral Myelin Protein 22 (PMP22). Most hereditary…”
Get full text
Journal Article