Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ritesh Ravi"'
Autor:
Annie Arguello, René Meisner, Elliot R. Thomsen, Hoang N. Nguyen, Ritesh Ravi, Jeffrey Simms, Iris Lo, Jessica Speckart, Julia Holtzman, Thomas M. Gill, Darren Chan, Yuhsiang Cheng, Chi-Lu Chiu, Jason C. Dugas, Meng Fang, Isabel A. Lopez, Hilda Solanoy, Buyankhishig Tsogtbaatar, Yuda Zhu, Akhil Bhalla, Kirk R. Henne, Anastasia G. Henry, Anthony Delucchi, Simona Costanzo, Jeffrey M. Harris, Dolores Diaz, Kimberly Scearce-Levie, Pascal E. Sanchez
Publikováno v:
JCI Insight, Vol 6, Iss 19 (2021)
Mucopolysaccharidosis type II (MPS II) is a lysosomal storage disorder caused by deficiency of the iduronate-2-sulfatase (IDS) enzyme, resulting in cellular accumulation of glycosaminoglycans (GAGs) throughout the body. Treatment of MPS II remains a
Externí odkaz:
https://doaj.org/article/7257efca6a4647a28c441e395328432c
Autor:
Akhil Bhalla, Khishig Tsogtbaatar, Ritesh Ravi, Meng Fang, Sonnet S. Davis, Imanol Zubizarreta, Ajith Karunakara, Yuda Zhu, Elizabeth Sinclair, Dominique Jacquemet-Engelhart, Shyeilla V. Dhuria, Tony Hung, Matthew Troyer, Peter Chin, Jeff M. Harris, Anna Bakardjiev
Publikováno v:
Molecular Genetics and Metabolism. 138:107031
Autor:
Ryan J. Watts, Kathryn M. Monroe, Junhua Wang, Melina Lenser, Jennifer Hsiao-Nakamoto, Hoang Nguyen, Todd P. Logan, Do Jin Kim, Fen Huang, Ritesh Ravi, Gilbert Di Paolo, Anil Rana, Kannan Gunasekaran, Yaneth Robles-Colmenares, Gerald M. Cherf, Buyankhishig Tsogtbaatar, Ceyda Llapashtica, Kirk R. Henne, Hilda Solanoy, Pascal E. Sanchez, Yashas Rajendra, Mihalis Kariolis, Ray Lieh Yoon Low, Roni Chau, Laralynne Przybyla, Michelle E. Pizzo, Chi-Lu Chiu, Meng Fang, Anastasia G. Henry, Giuseppe Astarita, Mark S. Dennis, Adam L. Boxer, Sarah L. DeVos, Sonnet S. Davis, Hilary W. Heuer, René Meisner, Joseph W. Lewcock, Devendra B. Srivastava, Bradley F. Boeve, Meredith E. K. Calvert, Katrina W. Lexa, Rachel Prorok, Lukas L. Skuja, Dolores Diaz, Akhil Bhalla, Matthew Simon, Jung H. Suh, Ankita Srivastava, Timothy K. Earr, Howard J. Rosen, Joseph Duque, Bettina Van Lengerich, Elizabeth W. Sun
Publikováno v:
Cell
Cell, vol 184, iss 18
Cell, vol 184, iss 18
GRN mutations cause frontotemporal dementia (GRN-FTD) due to deficiency in progranulin (PGRN), a lysosomal and secreted protein with unclear function. Here, we found that Grn(−/−) mice exhibit a global deficiency in bis(monoacylglycero)phosphate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6e8760616b55660b5a69ea73b7ad6da
https://europepmc.org/articles/PMC8489356/
https://europepmc.org/articles/PMC8489356/
Autor:
Ritesh Ravi, Annie Arguello, Sonnet S. Davis, Chi-Lu Chiu, Yuda Zhu, Junhua Wang, Dolores Diaz, Hoang N. Nguyen, Jeffrey M. Harris, Meng Fang, Jessica R. Blumenfeld, Damian Fiore, Timothy K. Earr, Matthew D. Troyer, Heather Cahan, Akhil Bhalla, Maria L. Escolar, Kimberly Scearce-Levie, Giuseppe Astarita
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 5188, p 5188 (2020)
Volume 21
Issue 15
International Journal of Molecular Sciences, Vol 21, Iss 5188, p 5188 (2020)
Volume 21
Issue 15
Mucopolysaccharidosis type II is a lysosomal storage disorder caused by a deficiency of iduronate-2-sulfatase (IDS) and characterized by the accumulation of the primary storage substrate, glycosaminoglycans (GAGs). Understanding central nervous syste
Autor:
Adam P. Silverman, Kwan Wanda, Junhua Wang, Alicia A. Nugent, Giuseppe Astarita, Ullman Julie, Nicholas Liang, Catherine Bedard, Sonnet S. Davis, Dolores Diaz, Gilbert Di Paolo, Anastasia G. Henry, Jennifer A. Getz, Hai L. Tran, Jason C. Dugas, Kannan Gunasekaran, Ankita Srivastava, Ryan J. Watts, Suresh Poda, Connie W.Y. Ha, Vinay M. Daryani, Sejal S. Hall, Ritesh Ravi, Michael Tuck, Thomas Sandmann, Robert C. Wells, Richard M. Caprioli, Cathal Mahon, Robert G. Thorne, Hilda Solanoy, Michelle L. Reyzer, Akhil Bhalla, Steve Lianoglou, Mihalis Kariolis, Pascal E. Sanchez, Jessica R. Blumenfeld, Timothy K. Earr, Kirk R. Henne, Hoang Nguyen, Jennifer L. Harvey, Joseph Duque, Do Jin Kim, Mark S. Dennis, Zachary Kevin Sweeney, Tina Giese, Annie Arguello
Publikováno v:
Science Translational Medicine. 12
Most lysosomal storage diseases (LSDs) involve progressive central nervous system (CNS) impairment, resulting from deficiency of a lysosomal enzyme. Treatment of neuronopathic LSDs remains a considerable challenge, as approved intravenously administe
Autor:
Ritesh Ravi, Abhijit Ghosh
Publikováno v:
Journal of Rural Development. 40:424
Autor:
Sonnet S. Davis, Jeffrey M. Harris, Heather Cahan, Hoang N. Nguyen, Meng Fang, Junhua Wang, Akhil Bhalla, Annie Arguello, Dolores Diaz, Giuseppe Astarita, Chi-Lu Chiu, Jessica R. Blumenfeld, Timothy K. Earr, Damian Fiore, Maria L. Escolar, Kimberly Scearce-Levie, Matthew D. Troyer, Ritesh Ravi, Yuda Zhu
Publikováno v:
Molecular Genetics and Metabolism. 132:S20
Autor:
Akhil Bhalla, Jessica Speckart, Pascal E. Sanchez, Buyankhishig Tsogtbaatar, Yuda Zhu, Julia Holtzman, Anastasia G. Henry, Elliot R. Thomsen, Dolores Diaz, Kimberly Scearce-Levie, Ritesh Ravi, Yuhsiang Cheng, Meng Fang, Jeffrey M. Harris, Hilda Solanoy, Annie Arguello, Hoang N. Nguyen, Michael Gill, Matthew D. Troyer, Jeffrey Simms, Simona Costanzo, Anthony Delucchi, René Meisner, Chi-Lu Chiu
Publikováno v:
Molecular Genetics and Metabolism. 132:S16
Autor:
Catherine Bedard, Gilbert Di Paolo, Mark S. Dennis, Mihalis Kariolis, Dolores Diaz, Kirk R. Henne, Kannan Gunasekaran, Cathal Mahon, Jennifer A. Getz, Jessica R. Blumenfeld, Ryan J. Watts, Ullman Julie, Robert G. Thorne, Ankita Srivastava, Junhua Wang, Annie Arguello, Akhil Bhalla, Alicia A. Nugent, Zachary Kevin Sweeney, Giuseppe Astarita, Anastasia G. Henry, Ritesh Ravi, Adam P. Silverman, Steve Lianoglou, Tina Giese
Publikováno v:
Molecular Genetics and Metabolism. 129:S72