Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Tana S. Pottorf"'
Autor:
Travis M. Rotterman, Zoë Haley-Johnson, Tana S. Pottorf, Tavishi Chopra, Ethan Chang, Shannon Zhang, William M. McCallum, Sarah Fisher, Haley Franklin, Myriam Alvarez, Timothy C. Cope, Francisco J. Alvarez
Publikováno v:
Cell Reports, Vol 43, Iss 2, Pp 113776- (2024)
Summary: Microglia-mediated synaptic plasticity after CNS injury varies depending on injury severity, but the mechanisms that adjust synaptic plasticity according to injury differences are largely unknown. This study investigates differential actions
Externí odkaz:
https://doaj.org/article/0e92a46fa7a146cca2bafeead0696db0
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Gait dysfunction and fall risk have been well documented in people with Alzheimer's Disease (AD) and individuals with mild cognitive impairment (MCI). Normal locomotor adaptation may be an important prerequisite for normal and safe community walking
Externí odkaz:
https://doaj.org/article/c41f7a1a3e0b47daa20ce406e4c0571a
Autor:
Tana S. Pottorf, Travis M. Rotterman, William M. McCallum, Zoë A. Haley-Johnson, Francisco J. Alvarez
Publikováno v:
Cells, Vol 11, Iss 13, p 2083 (2022)
Peripheral nerve injuries induce a pronounced immune reaction within the spinal cord, largely governed by microglia activation in both the dorsal and ventral horns. The mechanisms of activation and response of microglia are diverse depending on the l
Externí odkaz:
https://doaj.org/article/e10900e911bb4768a82bce08db661df1
Autor:
Wei Wang, Luciane M. Silva, Henry H. Wang, Matthew A. Kavanaugh, Tana S. Pottorf, Bailey A. Allard, Damon T. Jacobs, Ruochen Dong, Joseph T. Cornelius, Aakriti Chaturvedi, Katherine I. Swenson-Fields, Timothy A. Fields, Michele T. Pritchard, Madhulika Sharma, Chad Slawson, Darren P. Wallace, James P. Calvet, Pamela V. Tran
Publikováno v:
Kidney International. 102:577-591
Primary cilia are sensory organelles built and maintained by intraflagellar transport (IFT) multiprotein complexes. Deletion of several IFT-B genes attenuates polycystic kidney disease (PKD) severity in juvenile and adult autosomal dominant polycysti
Autor:
Luciane M. Silva, Brittany Jack, Wei Wang, Pamela V. Tran, Erin E. Bumann, Jinxi Wang, Tana S Pottorf, Hammad Mumtaz, Bailey A. Allard, Henry H. Wang, Damon T. Jacobs
Publikováno v:
Cell Mol Life Sci
Mutations in the intraflagellar transport-A (IFT-A) gene, THM1, have been identified in skeletal ciliopathies. Here, we report a genetic interaction between Thm1, and its paralog, Thm2, in postnatal skeletogenesis. THM2 localizes to primary cilia, bu
Autor:
Wei Wang, Luciane M. Silva, Henry H. Wang, Matthew A. Kavanaugh, Tana S. Pottorf, Bailey A. Allard, Damon T. Jacobs, Ruochen Dong, Joseph T. Cornelius, Aakriti Chaturvedi, Katherine I. Swenson-Fields, Timothy A. Fields, Michele T. Pritchard, Madhulika Sharma, Chad Slawson, Darren P. Wallace, James P. Calvet, Pamela V. Tran
Publikováno v:
Kidney International. 103:429
Autor:
Henry H. Wang, Ruochen Dong, Wei Wang, Joseph T Cornelius, Tana S Pottorf, Matthew A. Kavanaugh, Udayan Apte, Madhulika Sharma, Michele T. Pritchard, Katie Dennis, Pamela V. Tran
Publikováno v:
J Pathol
Polycystic liver disease (PLD) is characterized by the growth of numerous biliary cysts and presents in patients with autosomal dominant polycystic kidney disease (ADPKD), causing significant morbidity. Interestingly, deletion of intraflagellar trans
Publikováno v:
Neurochemistry International. 121:86-97
Golgi fragmentation and loss of Nicotinamide Mononucleotide Adenylyltransferase 2 (NMNAT2) are the early key features of many neurodegenerative disorders. We investigated the link between NMNAT2 loss, Golgi fragmentation and axon degeneration. Golgi
Autor:
Udayan Apte, Madhulika Sharma, Michele T. Pritchard, Ruochen Dong, Matthew A. Kavanaugh, Joseph T Cornelius, Tana S Pottorf, Wei Wang, Pamela V. Tran, Henry H. Wang
Polycystic liver disease (PLD) is characterized by the growth of numerous biliary cysts and presents in patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD), causing significant morbidity. Interestingly, deletion of intraflagellar trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c752634e1b6b739720771b417b682f87
https://doi.org/10.1101/2020.09.10.289645
https://doi.org/10.1101/2020.09.10.289645
Autor:
Luciane M. Silva, Wei Wang, Joseph T Cornelius, Michele T. Pritchard, Madhulika Sharma, Tana S Pottorf, Chad Slawson, Darren P. Wallace, Pamela V. Tran, James P. Calvet, Damon T. Jacobs, Matthew A. Kavanaugh, Bailey A. Allard, Henry H. Wang, Aakriti Chaturvedi, Rouchen Dong
Primary cilia are sensory organelles built and maintained by intraflagellar transport (IFT) multi-protein complexes. Deletion of different IFT-B genes attenuates polycystic kidney disease (PKD) severity in juvenile and adult Autosomal Dominant (AD) P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d829244e0221180846518e818ef4a1d3
https://doi.org/10.1101/2020.04.26.061796
https://doi.org/10.1101/2020.04.26.061796