Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Samuel Eaton"'
Autor:
Zhamshid Okhunov, Benjamin Lee, Athanasios Papatsoris, R. John Honey, Kemal Sarica, Demetrius Bagley, Ben Chew, Amy Krambeck, Bodo Knudsen, Thomas Tailly, Roger Low, Ahmed El-Nahas, Hyuk Jin Cho, Christopher Netsch, Madhu Agrawal, Sero Andonian, Mantu Gupta, Samuel Eaton, Dean Assimos, David Lee, Brian Matlaga, John Davis, Thomas Knoll, Christopher Ho
Publikováno v:
Journal of Endourology. 30:484-488
Ronney Abaza Mehran Abolbashari Ahmad Abolyosr Ashraf Abou-Elela Omar Aboumarzouk Jose Benito Abraham Peter Acher Alex Acosta-Miranda Samiran Adhikary Ramez Adrawis Anshuman Agarwal Mayank Agarwal Madhu Agrawal Sachin Agrawal Rajesh Ahlawat Tom Ahler
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3e11704de222bb387866d2f068134a3
https://doi.org/10.1089/end.2016.29014.ack
https://doi.org/10.1089/end.2016.29014.ack
Autor:
Athanasios Papatsoris, Thomas Knoll, Dean Assimos, Samuel Eaton, Zhamshid Okhunov, Jeffrey Cadeddu, Benjamin Lee, Ahmed EL-Nahas, Thomas Tailly, Pilar Laguna
Publikováno v:
Journal of Endourology. 29:490-494
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c13d4e87ed1a7607ba1342bc2210ffbd
https://doi.org/10.1089/end.2015.1512
https://doi.org/10.1089/end.2015.1512
Autor:
Daniel A. Kirschner, Constance M. Moore, Thomas N. Seyfried, Elif M. Sikoglu, Huapeng Li, Reuben Matalon, Jun Xie, Sylvia Szucs, Terence R. Flotte, Ana A. Liso Navarro, Andrew R. Denninger, Guangping Gao, Hongwei Zhang, Samuel Eaton, Seemin Seher Ahmed, Chunyan Cao, Qin Su
Publikováno v:
Molecular Therapy. 21:2136-2147
Canavan's disease (CD) is a fatal pediatric leukodystrophy caused by mutations in aspartoacylase (AspA) gene. Currently, there is no effective treatment for CD; however, gene therapy is an attractive approach to ameliorate the disease. Here, we studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::909841e3b2242fd785a839a676201b74
https://doi.org/10.1038/mt.2013.138
https://doi.org/10.1038/mt.2013.138
Autor:
Aime K. Johnson, Hannah E. Rockwell, Ashley N. Randle, Miguel Sena-Esteves, Judith A. Hudson, Douglas R. Martin, Heather L. Gray-Edwards, Victoria J. McCurdy, Allison M. Bradbury, Samuel Eaton, Henry J. Baker, Nancy R. Cox, Diane U. Wilson, Thomas N. Seyfried
Publikováno v:
ASN NEURO
ASN Neuro, Vol 7 (2015)
ASN Neuro, Vol 7 (2015)
Sandhoff disease (SD) is an autosomal recessive neurodegenerative disease caused by a mutation in the gene for the β-subunit of β-N-acetylhexosaminidase (Hex), resulting in the inability to catabolize ganglioside GM2 within the lysosomes. SD presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00cada2388a7fa1d37bd90a5ed34804e
http://europepmc.org/articles/PMC4720176
http://europepmc.org/articles/PMC4720176
Autor:
Rebecca M. Ducore, Amy S. Tidwell, Rajanikarath Maganti, Robert Causey, Betty Wang, Joseph Alroy, John H. Keating, Ildiko Erdelyi, Rolf Pfannl, Philip March, Mark A. Pokras, Bai Jin Zeng, Samuel Eaton, Rita L. Seger, Paola Torres, Nicole T. Waliszewski, Florina S. Tseng, Bain J. Perry, Thomas N. Seyfried, Edwin H. Kolodny, Sureshkumar Muthupalani
Publikováno v:
Molecular genetics and metabolism. 111(4)
G(M1)-gangliosidosis is a rare progressive neurodegenerative disorder due to an autosomal recessively inherited deficiency of lysosomal β-galactosidase. We have identified seven American black bears (Ursus americanus) found in the Northeast United S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::184c07cb2816f02edef8f7e7a8e3a369
https://pubmed.ncbi.nlm.nih.gov/24581871
https://pubmed.ncbi.nlm.nih.gov/24581871