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A dual apolipoprotein C-II mimetic–apolipoprotein C-III antagonist peptide lowers plasma triglycerides.
Published in:
Science Translational Medicine, 2020, v. 12, n. 528, p. 1, doi. 10.1126/scitranslmed.aaw7905
By:
- Wolska, Anna;
- Lo, Larry;
- Sviridov, Denis O.;
- Pourmousa, Mohsen;
- Pryor, Milton;
- Ghosh, Soumitra S.;
- Kakkar, Rahul;
- Davidson, Michael;
- Wilson, Sierra;
- Pastor, Richard W.;
- Goldberg, Ira J.;
- Basu, Debapriya;
- Drake, Steven K.;
- Cougnoux, Antony;
- Wu, Ming Jing;
- Neher, Saskia B.;
- Freeman, Lita A.;
- Tang, Jingrong;
- Amar, Marcelo;
- Devalaraja, Matt
Publication type:
Article
Gastrointestinal Tract Pathology in a BALB/c Niemann-Pick Disease Type C1 Null Mouse Model.
Published in:
2018
By:
- Cougnoux, Antony;
- Movassaghi, Miyad;
- Picache, Jaqueline A;
- Iben, James R;
- Navid, Fatemeh;
- Salman, Alexander;
- Martin, Kyle;
- Farhat, Nicole Y;
- Cluzeau, Celine;
- Tseng, Wei-Chia;
- Burkert, Kathryn;
- Sojka, Caitlin;
- Wassif, Christopher A;
- Cawley, Niamh X;
- Bonnet, Richard;
- Porter, Forbes D
Publication type:
journal article
FTY720/fingolimod increases NPC1 and NPC2 expression and reduces cholesterol and sphingolipid accumulation in Niemann-Pick type C mutant fibroblasts.
Published in:
FASEB Journal, 2017, v. 31, n. 4, p. 1719, doi. 10.1096/fj.201601041R
By:
- Newton, Jason;
- Hait, Nitai C.;
- Maceyka, Michael;
- Colaco, Alexandria;
- Maczis, Melissa;
- Wassif, Christopher A.;
- Cougnoux, Antony;
- Porter, Forbes D.;
- Milstien, Sheldon;
- Platt, Nicholas;
- Platt, Frances M.;
- Spiegel, Sarah
Publication type:
Article
Differential Proteomics Reveals miR-155 as a Novel Indicator of Liver and Spleen Pathology in the Symptomatic Niemann-Pick Disease, Type C1 Mouse Model.
Published in:
Molecules, 2019, v. 24, n. 5, p. 994, doi. 10.3390/molecules24050994
By:
- Pergande, Melissa R.;
- Cougnoux, Antony;
- Rathnayake, Rathnayake A. C.;
- Porter, Forbes D.;
- Cologna, Stephanie M.;
- Zhang, Zhenbin
Publication type:
Article
Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice.
Published in:
2015
By:
- Xekouki, Paraskevi;
- Szarek, Eva;
- Bullova, Petra;
- Giubellino, Alessio;
- Quezado, Martha;
- Mastroyannis, Spyridon A;
- Mastorakos, Panagiotis;
- Wassif, Christopher A;
- Raygada, Margarita;
- Rentia, Nadia;
- Dye, Louis;
- Cougnoux, Antony;
- Koziol, Deloris;
- Sierra, Maria de La Luz;
- Lyssikatos, Charalampos;
- Belyavskaya, Elena;
- Malchoff, Carl;
- Moline, Jessica;
- Eng, Charis;
- Maher 3rd, Louis James
Publication type:
journal article
Correction: LYST deficiency impairs autophagic lysosome reformation in neurons and alters lysosome number and size.
Published in:
2023
By:
- Serra-Vinardell, Jenny;
- Sandler, Maxwell B.;
- De Pace, Raffaella;
- Manzella-Lapeira, Javier;
- Cougnoux, Antony;
- Keyvanfar, Keyvan;
- Introne, Wendy J.;
- Brzostowski, Joseph A.;
- Ward, Michael E.;
- Gahl, William A.;
- Sharma, Prashant;
- Malicdan, May Christine V.
Publication type:
Correction Notice
LYST deficiency impairs autophagic lysosome reformation in neurons and alters lysosome number and size.
Published in:
Cellular & Molecular Life Sciences, 2023, v. 80, n. 2, p. 1, doi. 10.1007/s00018-023-04695-x
By:
- Serra-Vinardell, Jenny;
- Sandler, Maxwell B.;
- De Pace, Raffaella;
- Manzella-Lapeira, Javier;
- Cougnoux, Antony;
- Keyvanfar, Keyvan;
- Introne, Wendy J.;
- Brzostowski, Joseph A.;
- Ward, Michael E.;
- Gahl, William A.;
- Sharma, Prashant;
- Malicdan, May Christine C.
Publication type:
Article
Unique molecular signature in mucolipidosis type IV microglia.
Published in:
2019
By:
- Cougnoux, Antony;
- Drummond, Rebecca A.;
- Fellmeth, Mason;
- Navid, Fatemeh;
- Collar, Amanda L.;
- Iben, James;
- Kulkarni, Ashok B.;
- Pickel, James;
- Schiffmann, Raphael;
- Wassif, Christopher A.;
- Cawley, Niamh X.;
- Lionakis, Michail S.;
- Porter, Forbes D.
Publication type:
journal article
Chromosome-mediated OXA-48 carbapenemase in highly virulent Escherichia coli.
Published in:
2013
By:
- Beyrouthy, Racha;
- Robin, Frédéric;
- Cougnoux, Antony;
- Dalmasso, Guillaume;
- Darfeuille-Michaud, Arlette;
- Mallat, Hassan;
- Dabboussi, Fouad;
- Hamzé, Monzer;
- Bonnet, Richard
Publication type:
Journal Article
Chromosome-mediated OXA-48 carbapenemase in highly virulent Escherichia coli.
Published in:
Journal of Antimicrobial Chemotherapy (JAC), 2013, v. 68, n. 7, p. 1558, doi. 10.1093/jac/dkt051
By:
- Beyrouthy, Racha;
- Robin, Frédéric;
- Cougnoux, Antony;
- Dalmasso, Guillaume;
- Darfeuille-Michaud, Arlette;
- Mallat, Hassan;
- Dabboussi, Fouad;
- Hamzé, Monzer;
- Bonnet, Richard
Publication type:
Article
Abnormal LAMP1 glycosylation may play a role in Niemann-Pick disease, type C pathology.
Published in:
PLoS ONE, 2020, v. 15, n. 1, p. 1, doi. 10.1371/journal.pone.0227829
By:
- Cawley, Niamh X.;
- Sojka, Caitlin;
- Cougnoux, Antony;
- Lyons, Anna T.;
- Nicoli, Elena‐Raluca;
- Wassif, Christopher A.;
- Porter, Forbes D.
Publication type:
Article
The Role of Autophagy in the Degradation of Misfolded HLA–B27 Heavy Chains.
Published in:
Arthritis & Rheumatology, 2018, v. 70, n. 5, p. 746, doi. 10.1002/art.40414
By:
- Navid, Fatemeh;
- Layh‐Schmitt, Gerlinde;
- Sikora, Keith A.;
- Cougnoux, Antony;
- Colbert, Robert A.
Publication type:
Article
Association of NPC1 variant p.P237S with a pathogenic splice variant in two Niemann-Pick disease type C1 patients.
Published in:
American Journal of Medical Genetics. Part A, 2017, v. 173, n. 4, p. 1038, doi. 10.1002/ajmg.a.38104
By:
- Salman, Alexander;
- Cougnoux, Antony;
- Farhat, Nicole;
- Wassif, Christopher A.;
- Porter, Forbes D.
Publication type:
Article
Altered cerebrospinal fluid proteins in Smith-Lemli-Opitz syndrome patients.
Published in:
American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 8, p. 2060, doi. 10.1002/ajmg.a.37720
By:
- Cologna, Stephanie M.;
- Shieh, Christine;
- Toth, Cynthia L.;
- Cougnoux, Antony;
- Burkert, Kathryn R.;
- Bianconi, Simona E.;
- Wassif, Christopher A.;
- Porter, Forbes D.
Publication type:
Article
Single Cell Transcriptome Analysis of Niemann–Pick Disease, Type C1 Cerebella.
Published in:
International Journal of Molecular Sciences, 2020, v. 21, n. 15, p. 5368, doi. 10.3390/ijms21155368
By:
- Cougnoux, Antony;
- Yerger, Julia C.;
- Fellmeth, Mason;
- Serra-Vinardell, Jenny;
- Martin, Kyle;
- Navid, Fatemeh;
- Iben, James;
- Wassif, Christopher A.;
- Cawley, Niamh X.;
- Porter, Forbes D.
Publication type:
Article
Identification of Novel Pathways Associated with Patterned Cerebellar Purkinje Neuron Degeneration in Niemann-Pick Disease, Type C1.
Published in:
International Journal of Molecular Sciences, 2020, v. 21, n. 1, p. 292, doi. 10.3390/ijms21010292
By:
- Martin, Kyle B.;
- Williams, Ian M.;
- Cluzeau, Celine V.;
- Cougnoux, Antony;
- Dale, Ryan K.;
- Iben, James R.;
- Cawley, Niamh X.;
- Wassif, Christopher A.;
- Porter, Forbes D.
Publication type:
Article
Microglia activation in Niemann-Pick disease, type C1 is amendable to therapeutic intervention.
Published in:
Human Molecular Genetics, 2018, v. 27, n. 12, p. 2076, doi. 10.1093/hmg/ddy112
By:
- Cougnoux, Antony;
- Drummond, Rebecca A.;
- Collar, Amanda L.;
- Iben, James R.;
- Salman, Alexander;
- Westgarth, Harrison;
- Wassif, Christopher A.;
- Cawley, Niamh X.;
- Farhat, Nicole Y.;
- Ozato, Keiko;
- Lionakis, Michail S.;
- Porter, Forbes D.
Publication type:
Article

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