Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Kaly A Mueller"'
Autor:
Tiziana Petrozziello, Amanda M Dios, Kaly A Mueller, Christine A Vaine, William T Hendriks, Kelly E Glajch, Alexandra N Mills, Kotchaphorn Mangkalaphiban, Ellen B Penney, Naoto Ito, Cara Fernandez-Cerado, Gierold Paul A Legarda, M Salvie Velasco-Andrada, Patrick J Acuña, Mark A Ang, Edwin L Muñoz, Cid Czarina E Diesta, Regina Macalintal-Canlas, Geraldine Acuña, Nutan Sharma, Laurie J Ozelius, D Cristopher Bragg, Ghazaleh Sadri-Vakili
Publikováno v:
PLoS ONE, Vol 15, Iss 12, p e0243655 (2020)
X-linked Dystonia-Parkinsonism (XDP) is a neurodegenerative disease linked to an insertion of a SINE-VNTR-Alu (SVA)-type retrotransposon within an intron of TAF1. This SVA insertion induces aberrant TAF1 splicing and partial intron retention, thereby
Externí odkaz:
https://doaj.org/article/589a61b80bba4eb7bc6d53099ba584bd
Autor:
Kelly E Glajch, Laura Ferraiuolo, Kaly A Mueller, Matthew J Stopford, Varsha Prabhkar, Achille Gravanis, Pamela J Shaw, Ghazaleh Sadri-Vakili
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0164103 (2016)
Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease caused by loss of motor neurons. ALS patients experience rapid deterioration in muscle function with an average lifespan of 3-5 years after diagnosis. Currently, the most effective th
Externí odkaz:
https://doaj.org/article/ba52bc4531a84a88a18f6278fedb2d1b
Autor:
James D. Berry, Kaly A. Mueller, Kelly E. Glajch, Alexandra N. Mills, Sheena Chew, Sali M.K. Farhan, Eric J. Granucci, Ghazaleh Sadri-Vakili, Tiziana Petrozziello, James Chan
Publikováno v:
Muscle & Nerve. 62:272-283
Background The exact mechanisms underlying neuroinflammation and how they contribute to amyotrophic lateral sclerosis (ALS) pathogenesis remain unclear. One possibility is the secretion of neurotoxic factors, such as lipocalin-2 (LCN2), that lead to
Autor:
Eric J. Granucci, David R. Elmaleh, Merit Cudkowicz, Alexandra N. Mills, James D. Berry, Ghazaleh Sadri-Vakili, Danielle McGinty, Sabrina Paganoni, Hoang Le, Ana Griciuc, Amanda M. Dios, Rudolph E. Tanzi, João D. Pereira, Kaly A. Mueller
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-17 (2019)
Accumulating evidence suggests that neuroinflammatory processes are implicated in the initiation and progression of amyotrophic lateral sclerosis (ALS). Previous reports have demonstrated an increase in microgliosis and astrogliosis in the lumbar spi
Autor:
Kaly A. Mueller, Michael A. Schwarzschild, Rachit Bakshi, Eric J. Granucci, Yuehang Xu, Ghazaleh Sadri-Vakili, Sabrina Paganoni, Xiqun Chen
Publikováno v:
Molecular and Cellular Neuroscience. 92:12-16
Dominant mutations in an antioxidant enzyme superoxide dismutase-1 (SOD1) cause amyotrophic lateral sclerosis (ALS), an adult-onset neurodegenerative disease characterized by loss of motor neurons. Oxidative stress has also been linked to many of the
Autor:
Michael J. LaQuaglia, Marian DiFiglia, Remi A. Wilson, Kaly A. Mueller, Maria Iuliano, Khashayar Vakili, Adelaide Tousley, Kelly E. Glajch, Megan N. Huizenga, Eric J. Granucci, Kimberly B. Kegel-Gleason, Ghazaleh Sadri-Vakili, Elizabeth Weisman, Amanda M. Dios
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-13 (2018)
Scientific Reports
Scientific Reports
The Hippo signaling pathway is involved in organ size regulation and tumor suppression. Although inhibition of Hippo leads to tumorigenesis, activation of Hippo may play a role in neurodegeneration. Specifically, activation of the upstream regulator,
Autor:
Kaly A. Mueller, Jonathan D. Glass, Paul Cernasov, Jacob M. Hooker, Alexandra N. Mills, Mohamad J. Alshikho, James D. Berry, Amanda M. Dios, Nicole R. Zürcher, Ghazaleh Sadri-Vakili, Tonya M. Gilbert, Eric J. Granucci, Suma Babu, Nazem Atassi
Publikováno v:
MusclenerveREFERENCES. 60(4)
Introduction There is an unmet need for mechanism-based biomarkers and effective disease modifying treatments in amyotrophic lateral sclerosis (ALS). Previous findings have provided evidence that histone deacetylases (HDAC) are altered in ALS, provid
Autor:
Laurie J. Ozelius, Kelly E. Glajch, D. Cristopher Bragg, Geraldine Acuña, Edwin L. Muñoz, Regina Macalintal-Canlas, Christine A. Vaine, Naoto Ito, Nutan Sharma, Gierold Paul A. Legarda, Tiziana Petrozziello, Mark A. Ang, M. Salvie Velasco-Andrada, Ghazaleh Sadri-Vakili, Patrick J. Acuña, Cara Fernandez-Cerado, Alexandra N. Mills, Cid Czarina E. Diesta, William T. Hendriks, Kaly A. Mueller, Ellen B. Penney, Amanda M. Dios, Kotchaphorn Mangkalaphiban
Publikováno v:
PLoS ONE, Vol 15, Iss 12, p e0243655 (2020)
PLoS ONE
PLoS ONE
X-linked Dystonia-Parkinsonism (XDP) is a neurodegenerative disease linked to an insertion of a SINE-VNTR-Alu (SVA)-type retrotransposon within an intron of TAF1. This SVA insertion induces aberrant TAF1 splicing and partial intron retention, thereby
Autor:
Debra Ann Fadool, Pradeep G. Bhide, Megan N. Huizenga, Kaly A. Mueller, Deirdre M. McCarthy, Elisa N. Cannon, Genevieve A. Bell, Ghazaleh Sadri-Vakili
Publikováno v:
Developmental Neuroscience. 38:354-364
Prenatal cocaine exposure remains a major public health concern because of its adverse impact on cognitive function in children and adults. We report that prenatal cocaine exposure produces significant deficits in reversal learning, a key component o
Autor:
Rachit, Bakshi, Yuehang, Xu, Kaly A, Mueller, Xiqun, Chen, Eric, Granucci, Sabrina, Paganoni, Ghazaleh, Sadri-Vakili, Michael A, Schwarzschild
Publikováno v:
Molecular and cellular neurosciences. 92
Dominant mutations in an antioxidant enzyme superoxide dismutase-1 (SOD1) cause amyotrophic lateral sclerosis (ALS), an adult-onset neurodegenerative disease characterized by loss of motor neurons. Oxidative stress has also been linked to many of the