Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Rian de Laat"'
Autor:
Scholz Matthew Rein, Rian de Laat, Monika Swietlicka, Xu Mei, R. Scott McIvor, Erik R. Olson, Kole D. Meeker
Publikováno v:
Molecular Genetics and Metabolism. 129:S108
Autor:
Thomas J. Montine, Rian de Laat, Jesse C. Wiley, Mark Bothwell, Mark P. Hudson, James S. Meabon
Publikováno v:
Pathobiology of Aging & Age-related Diseases, Vol 5, Iss 0, Pp 1-11 (2015)
Pathobiology of Aging & Age Related Diseases
Pathobiology of Aging & Age-related Diseases; Vol 5 (2015) incl Supplements
Pathobiology of Aging & Age Related Diseases
Pathobiology of Aging & Age-related Diseases; Vol 5 (2015) incl Supplements
Sequential proteolytic cleavages of amyloid-β protein precursor (AβPP) by β-secretase and γ-secretase generate amyloid β (Aβ) peptides, which are thought to contribute to Alzheimer’s disease (AD). Much of this processing occurs in endosomes f
Publikováno v:
NeuroToxicology. 43:3-9
Paraoxonase 2 (PON2) is a member of a gene family which also includes the more studied PON1, as well as PON3. PON2 is unique among the three PONs, as it is expressed in brain tissue. PON2 is a lactonase and displays anti-oxidant and anti-inflammatory
Autor:
Mark Bothwell, Randy J. Kulesza, Yuan Wang, Hitomi Sakano, Karisa Beebe, Maile R. Brown, Edwin W. Rubel, Rian de Laat
Publikováno v:
Journal of Comparative Neurology. 522:2107-2128
Neuronal dendrites are structurally and functionally dynamic in response to changes in afferent activity. The fragile X mental retardation protein (FMRP) is an mRNA binding protein that regulates activity-dependent protein synthesis and morphological
Autor:
Lucio G. Costa, Leah J. Tait, Khoi Dao, Claudia Pellacani, Gennaro Giordano, Clement E. Furlong, Toby B. Cole, Rian de Laat
Publikováno v:
Neurochemical Research. 38:1809-1818
Quercetin is a common flavonoid polyphenol which has been shown to exert neuroprotective actions in vitro and in vivo. Though quercetin has antioxidant properties, it has been suggested that neuroprotection may be ascribed to its ability of inducing
Autor:
Judit Marsillach, Clement E. Furlong, Rian de Laat, John D. Elsworth, Khoi Dao, Toby B. Cole, Lucio G. Costa, Jacqueline M. Garrick
Publikováno v:
Chemico-biological interactions. 259
Paraoxonase 2 (PON2) is a member of the paraoxonase gene family also comprising PON1 and PON3. PON2 functions as a lactonase and exhibits anti-bacterial as well as antioxidant properties. At the cellular level, PON2 localizes to the mitochondrial and
Autor:
B. Russel Huber, Rian de Laat, Jesse C. Wiley, Dmitry Serbzhinsky, James S. Meabon, Katsuaki Ieguchi, Mark P. Hudson, Mark Bothwell
Publikováno v:
Molecular and cellular neurosciences. 70
Neurotrophins, essential regulators of many aspects of neuronal differentiation and function, signal via four receptors, p75, TrkA, TrkB and TrkC. The three Trk paralogs are members of the LIG superfamily of membrane proteins, which share extracellul
LINGO-1 Protein Interacts with the p75 Neurotrophin Receptor in Intracellular Membrane Compartments*
Autor:
Rian de Laat, Mark P. Hudson, James S. Meabon, Jesse C. Wiley, Mark Bothwell, Katsuaki Ieguchi
Background: LINGO-1·p75NTR·NgR complexes at the cell surface are believed to mediate responses to myelin inhibitors of axon growth. Results: LINGO-1 is intracellular and competes with NgR for binding to p75NTR. Conclusion: The existence of cell-sur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::449c35ee1a21a82255a461d90069d9db
https://europepmc.org/articles/PMC4392256/
https://europepmc.org/articles/PMC4392256/
Polybrominated diphenyl ethers (PBDEs), extensively used in the past few decades as flame retardants in a variety of consumer products, have become world-wide persistent environmental pollutants. Levels in North America are usually higher than those
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8fa9f8f4140c9cdc07ae6bb39355888
https://europepmc.org/articles/PMC4028440/
https://europepmc.org/articles/PMC4028440/
Autor:
Kendra A. Hyland, R. Scott McIvor, Rian de Laat, Mei Xu, Erik R. Olson, Scholz Matthew Rein, Herbig Eric J
Publikováno v:
Molecular Therapy. 23:S151
Hemophilia A and hemophilia B are X-linked, genetic disorders that are caused by defective or deficient coagulation factor VIII and IX, respectively, resulting in the inability to form blood clots and sustained bleeding after trauma or injury. Recomb