KIS: Synaptic Plasticity's Missing Molecular Link?

di Brudvig, Jon, Cain, Jacob
Pubblicato in J Neurosci (2015)

Germs within Worms: Localization of Neorickettsia sp. within Life Cycle Stages of the Digenean Plagiorchis elegans

di Greiman, Stephen E., Rikihisa, Yasuko, Cain, Jacob, Vaughan, Jefferson A., Tkach, Vasyl V.
Pubblicato in Appl Environ Microbiol (2016)

Therapeutic landscape for Batten disease: current treatments and future prospects

di Johnson, Tyler B., Cain, Jacob T., White, Katherine A., Ramirez-Montealegre, Denia, Pearce, David A., Weimer, Jill M.
Pubblicato in Nat Rev Neurol (2019)

Modulation of CRMP2 via (S)-Lacosamide shows therapeutic promise but is ultimately ineffective in a mouse model of CLN6-Batten disease

di White, Katherine A., Cain, Jacob T., Magee, Helen, Yeon, Seul Ki, Park, Ki Duk, Khanna, Rajesh, Weimer, Jill M.
Pubblicato in Neuronal Signal (2019)

Shifts in the Vascular endothelial growth factor (Vegf) isoforms result in transcriptome changes correlated with early neural stem cell proliferation and differentiation in mouse f...

di Cain, Jacob T., Berosik, Matthew A., Snyder, Stephanie D., Crawford, Natalie F., Nour, Shirin I., Schaubhut, Geoffrey J., Darland, Diane C.
Pubblicazione 2013

A tailored mouse model of CLN2 disease: A nonsense mutant for testing personalized therapies

di Geraets, Ryan D., Langin, Logan M., Cain, Jacob T., Parker, Camille M., Beraldi, Rosanna, Kovacs, Attila D., Weimer, Jill M., Pearce, David A.
Pubblicato in PLoS One (2017)

Tracking sex-dependent differences in a mouse model of CLN6-Batten disease

di Poppens, McKayla J., Cain, Jacob T., Johnson, Tyler B., White, Katherine A., Davis, Samantha S., Laufmann, Rachel, Kloth, Alexander D., Weimer, Jill M.
Pubblicato in Orphanet J Rare Dis (2019)

Searching for novel biomarkers using a mouse model of CLN3-Batten disease

di Timm, Derek, Cain, Jacob T., Geraets, Ryan D., White, Katherine A., Koh, Seung yon, Kielian, Tammy, Pearce, David A., Hastings, Michelle L., Weimer, Jill M.
Pubblicato in PLoS One (2018)

Vascular endothelial growth factor (VEGF) isoform regulation of early forebrain development

di Darland, Diane C., Cain, Jacob T., Berosik, Matthew A., Saint-Geniez, Magali, Odens, Patrick W., Schaubhut, Geoffrey J., Frisch, Sarah, Stemmer-Rachamimov, Anat, Darland, Tristan, D’Amore, Patricia A.
Pubblicazione 2011

Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1

di Johnson, Tyler B., Mechels, Keegan, Anderson, Ruth Ellen, Cain, Jacob T., Sturdevant, David A., Braddock, Stephen, Pinz, Hailey, Wilson, Mark A., Landsverk, Megan, Roux, Kyle J., Weimer, Jill M.
Pubblicato in Sci Rep (2018)

Author Correction: Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1

di Johnson, Tyler B., Mechels, Keegan, Anderson, Ruthellen H., Cain, Jacob T., Sturdevant, David A., Braddock, Stephen, Pinz, Hailey, Wilson, Mark A., Landsverk, Megan, Roux, Kyle J., Weimer, Jill M.
Pubblicato in Sci Rep (2020)

Nonsense Pathogenic Variants in Exon One of PHOX2B Lead to Translational Reinitiation in Congenital Central Hypoventilation Syndrome

di Cain, Jacob T., Kim, Dae I., Quast, Megan, Shivega, Winnie G., Patrick, Ryan J., Moser, Chuanpit, Reuter, Suzanne, Perez, Myrza, Myers, Angela, Weimer, Jill M., Roux, Kyle J., Landsverk, Megan
Pubblicato in Am J Med Genet A (2017)

Age and Sex Influence Mitochondria and Cardiac Health in Offspring Exposed to Maternal Glucolipotoxicity

di Louwagie, Eli J., Larsen, Tricia D., Wachal, Angela L., Gandy, Tyler C.T., Eclov, Julie A., Rideout, Todd C., Kern, Katherine A., Cain, Jacob T., Anderson, Ruthellen H., Mdaki, Kennedy S., Baack, Michelle L.
Pubblicato in iScience (2020)

AAV9 Gene Therapy Increases Lifespan and Treats Pathological and Behavioral Abnormalities in a Mouse Model of CLN8-Batten Disease

di Johnson, Tyler B., White, Katherine A., Brudvig, Jon J., Cain, Jacob T., Langin, Logan, Pratt, Melissa A., Booth, Clarissa D., Timm, Derek J., Davis, Samantha S., Meyerink, Brandon, Likhite, Shibi, Meyer, Kathrin, Weimer, Jill M.
Pubblicato in Mol Ther (2021)

Cancer exosomes induce tumor innervation

di Madeo, Marianna, Colbert, Paul L., Vermeer, Daniel W., Lucido, Christopher T., Cain, Jacob T., Vichaya, Elisabeth G., Grossberg, Aaron J., Muirhead, DesiRae, Rickel, Alex P., Hong, Zhongkui, Zhao, Jing, Weimer, Jill M., Spanos, William C., Lee, John H., Dantzer, Robert, Vermeer, Paola D.
Pubblicato in Nat Commun (2018)

Gene Therapy Corrects Brain and Behavioral Pathologies in CLN6-Batten Disease

di Cain, Jacob T., Likhite, Shibi, White, Katherine A., Timm, Derek J., Davis, Samantha S., Johnson, Tyler B., Dennys-Rivers, Cassandra N., Rinaldi, Federica, Motti, Dario, Corcoran, Sarah, Morales, Pablo, Pierson, Christopher, Hughes, Stephanie M., Lee, Stella Y., Kaspar, Brian K., Meyer, Kathrin, Weimer, Jill M.
Pubblicato in Mol Ther (2019)

A porcine model of neurofibromatosis type 1 that mimics the human disease

di White, Katherine A., Swier, Vicki J., Cain, Jacob T., Kohlmeyer, Jordan L., Meyerholz, David K., Tanas, Munir R., Uthoff, Johanna, Hammond, Emily, Li, Hua, Rohret, Frank A., Goeken, Adam, Chan, Chun-Hung, Leidinger, Mariah R., Umesalma, Shaikamjad, Wallace, Margaret R., Dodd, Rebecca D., Panzer, Karin, Tang, Amy H., Darbro, Benjamin W., Moutal, Aubin, Cai, Song, Li, Wennan, Bellampalli, Shreya S., Khanna, Rajesh, Rogers, Christopher S., Sieren, Jessica C., Quelle, Dawn E., Weimer, Jill M.
Pubblicato in JCI Insight (2018)