Regulation of cell-surface major histocompatibility complex class I expression by the endopeptidase EC3.4.24.15 (thimet oligopeptidase).

Por Kim, Sandra I, Pabon, Amanda, Swanson, Todd A, Glucksman, Marc J
Publicado em 2003

Signaling pathway adaptations and novel protein kinase A substrates related to behavioral sensitization to cocaine

Por Boudreau, Amy C., Ferrario, Carrie R., Glucksman, Marc J., Wolf, Marina E.
Publicado em 2009

Identification and characterization of Aβ peptide interactors in Alzheimer’s disease by structural approaches

Por Philibert, Keith D., Marr, Robert A., Norstrom, Eric M., Glucksman, Marc J.
Publicado em 2014

A novel matrix metalloproteinase 2 (MMP2) terminal hemopexin domain mutation in a family with multicentric osteolysis with nodulosis and arthritis with cardiac defects

Por Tuysuz, Beyhan, Mosig, Rebecca, Altun, Gürkan, Sancak, Selim, Glucksman, Marc J, Martignetti, John A
Publicado em 2009

Metallopeptidase inhibition potentiates bradykinin-induced hyperalgesia

Por Gomez, Ruben, Por, Elaine D., Berg, Kelly A., Clarke, William P., Glucksman, Marc J., Jeske, Nathaniel A.
Publicado em 2011

EP24.15 as a Potential Regulator of Kisspeptin Within the Neuroendocrine Hypothalamus

Por Woitowich, Nicole C., Philibert, Keith D., Leitermann, Randy J., Wungjiranirun, Manida, Urban, Janice H., Glucksman, Marc J.
Publicado no Endocrinology (2016)

Flexibility in substrate recognition by thimet oligopeptidase as revealed by denaturation studies

Por Sigman, Jeffrey A., Patwa, Tasneem H., Tablante, Ana V., Joseph, Calleen D., Glucksman, Marc J., Wolfson, Adele J.
Publicado em 2005

Human membrane metallo-endopeptidase-like protein (MMEL) degrades both Aβ(42) and Aβ(40)

Por Huang, Jeffrey Y., Bruno, Angela M., Patel, Chetak A., Huynh, Alexis M., Philibert, Keith D., Glucksman, Marc J., Marr, Robert A.
Publicado em 2008

Mutation of Membrane Type-1 Metalloproteinase, MT1-MMP, Causes the Multicentric Osteolysis and Arthritis Disease Winchester Syndrome

Por Evans, Brad R., Mosig, Rebecca A., Lobl, Mollie, Martignetti, Chiara R., Camacho, Catalina, Grum-Tokars, Valerie, Glucksman, Marc J., Martignetti, John A.
Publicado em 2012

A-Kinase Anchoring Protein 79/150 Scaffolds Transient Receptor Potential A 1 Phosphorylation and Sensitization by Metabotropic Glutamate Receptor Activation

Por Brackley, Allison Doyle, Gomez, Ruben, Guerrero, Kristi A., Akopian, Armen N., Glucksman, Marc J., Du, Junhui, Carlton, Susan M., Jeske, Nathaniel A.
Publicado no Sci Rep (2017)

Hydrogen bond residue positioning in the 599-611 loop of thimet oligopeptidase is required for substrate selection

Por Bruce, Lisa A., Sigman, Jeffrey A., Randall, Danica, Rodriguez, Scott, Song, Michelle M., Dai, Yi, Elmore, Donald E., Pabon, Amanda, Glucksman, Marc J., Wolfson, Adele J.
Publicado em 2008

Characterization of Prefibrillar Tau Oligomers in Vitro and in Alzheimer Disease

Por Patterson, Kristina R., Remmers, Christine, Fu, Yifan, Brooker, Sarah, Kanaan, Nicholas M., Vana, Laurel, Ward, Sarah, Reyes, Juan F., Philibert, Keith, Glucksman, Marc J., Binder, Lester I.
Publicado em 2011

Interaction with calmodulin is important for the secretion of thimet oligopeptidase following stimulation

Por Russo, Lilian C., Goñi, Camila N., Castro, Leandro M., Asega, Amanda F., Camargo, Antonio C. M., Trujillo, Cleber A., Ulrich, Henning, Glucksman, Marc J., Scavone, Cristoforo, Ferro, Emer S.
Publicado em 2009

Age-dependent Effects of 17β-estradiol on the Dynamics of Estrogen Receptor β (ERβ) Protein–Protein Interactions in the Ventral Hippocampus

Por Mott, Natasha N., Pinceti, Elena, Rao, Yathindar S., Przybycien-Szymanska, Magdalena M., Prins, Sarah A., Shults, Cody L., Yang, Xinli, Glucksman, Marc J., Roberts, James L., Pak, Toni R.
Publicado em 2014

Mutations in Capillary Morphogenesis Gene-2 Result in the Allelic Disorders Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis

Por Dowling, Oonagh, Difeo, Analisa, Ramirez, Maria C., Tukel, Turgut, Narla, Goutham, Bonafe, Luisa, Kayserili, Hulya, Yuksel-Apak, Memnune, Paller, Amy S., Norton, Karen, Teebi, Ahmad S., Grum-Tokars, Valerie, Martin, Gail S., Davis, George E., Glucksman, Marc J., Martignetti, John A.
Publicado em 2003

Nonmuscle Myosin Heavy Chain IIA Mutations Define a Spectrum of Autosomal Dominant Macrothrombocytopenias: May-Hegglin Anomaly and Fechtner, Sebastian, Epstein, and Alport-Like Syn...

Por Heath, Karen E., Campos-Barros, Angel, Toren, Amos, Rozenfeld-Granot, Galit, Carlsson, Lena E., Savige, Judy, Denison, Joyce C., Gregory, Martin C., White, James G., Barker, David F, Greinacher, Andreas, Epstein, Charles J., Glucksman, Marc J., Martignetti, John A.
Publicado em 2001

Primate Genome Gain and Loss: A Bone Dysplasia, Muscular Dystrophy, and Bone Cancer Syndrome Resulting from Mutated Retroviral-Derived MTAP Transcripts

Por Camacho-Vanegas, Olga, Camacho, Sandra Catalina, Till, Jacob, Miranda-Lorenzo, Irene, Terzo, Esteban, Ramirez, Maria Celeste, Schramm, Vern, Cordovano, Grace, Watts, Giles, Mehta, Sarju, Kimonis, Virginia, Hoch, Benjamin, Philibert, Keith D., Raabe, Carsten A., Bishop, David F., Glucksman, Marc J., Martignetti, John A.
Publicado em 2012

Morbid Obesity Resulting from Inactivation of the Ciliary Protein CEP19 in Humans and Mice

Por Shalata, Adel, Ramirez, Maria C., Desnick, Robert J., Priedigkeit, Nolan, Buettner, Christoph, Lindtner, Claudia, Mahroum, Mohammed, Abdul-Ghani, Muhammad, Dong, Feng, Arar, Nazik, Camacho-Vanegas, Olga, Zhang, Rui, Camacho, Sandra C., Chen, Ying, Ibdah, Mwafaq, DeFronzo, Ralph, Gillespie, Virginia, Kelley, Kevin, Dynlacht, Brian D., Kim, Sehyun, Glucksman, Marc J., Borochowitz, Zvi U., Martignetti, John A.
Publicado em 2013