Molecular Organization of Sarcoglycan Complex in Mouse Myotubes in Culture

di Chan, Yiu-mo, Bönnemann, Carsten G., Lidov, Hart G.W., Kunkel, Louis M.
Pubblicazione 1998

Aprotinin Protects the Cerebral Microcirculation during Cardiopulmonary Bypass

di Ishibashi, Nobuyuki, Iwata, Yusuke, Zurakowski, David, Lidov, Hart G.W., Jonas, Richard A.
Pubblicazione 2009

Differential Neuronal Vulnerability varies according to Specific Cardiopulmonary Bypass Insult in a Porcine Survival Model

di Ishibashi, Nobuyuki, Iwata, Yusuke, Okamura, Toru, Zurakowski, David, Lidov, Hart G.W., Jonas, Richard A.
Pubblicazione 2010

Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE

di Boyden, Steven E, Duncan, Anna R, Estrella, Elicia A, Lidov, Hart GW, Mahoney, Lane J, Katz, Jonathan S, Kunkel, Louis M, Kang, Peter B
Pubblicazione 2011

Mice Expressing Myc in Neural Precursors Develop Choroid Plexus and Ciliary Body Tumors

di Shannon, Morgan L., Fame, Ryann M., Chau, Kevin F., Dani, Neil, Calicchio, Monica L., Géléoc, Gwenaelle S., Lidov, Hart G.W., Alexandrescu, Sanda, Lehtinen, Maria K.
Pubblicato in Am J Pathol (2018)

Filamin 2 (Fln2): A Muscle-Specific Sarcoglycan Interacting Protein

di Thompson, Terri G., Chan, Yiu-Mo, Hack, Andrew A., Brosius, Melissa, Rajala, Michael, Lidov, Hart G.W., McNally, Elizabeth M., Watkins, Simon, Kunkel, Louis M.
Pubblicazione 2000

AIFM1 mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant

di Morton, Sarah U., Prabhu, Sanjay P., Lidov, Hart G.W., Shi, Jiahai, Anselm, Irina, Brownstein, Catherine A., Bainbridge, Matthew N., Beggs, Alan H., Vargas, Sara O., Agrawal, Pankaj B.
Pubblicato in Cold Spring Harb Mol Case Stud (2017)

Inefficient dystrophin expression after cord blood transplantation in DMD

di Kang, Peter B., Lidov, Hart G.W., White, Alexander J., Mitchell, Matthew, Balasubramanian, Anuradha, Estrella, Elicia, Bennett, Richard R., Darras, Basil T., Shapiro, Frederic D., Bambach, Barbara J., Kurtzberg, Joanne, Gussoni, Emanuela, Kunkel, Louis M.
Pubblicazione 2010

The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States

di Reddy, Hemakumar M., Cho, Kyung-Ah, Lek, Monkol, Estrella, Elicia, Valkanas, Elise, Jones, Michael D., Mitsuhashi, Satomi, Darras, Basil T., Amato, Anthony A., Lidov, Hart G.W., Brownstein, Catherine A., Margulies, David M., Yu, Timothy W., Salih, Mustafa A., Kunkel, Louis M., MacArthur, Daniel G., Kang, Peter B.
Pubblicato in J Hum Genet (2016)

Spatially Heterogeneous Choroid Plexus Transcriptomes Encode Positional Identity and Contribute to Regional CSF Production

di Lun, Melody P., Johnson, Matthew B., Broadbelt, Kevin G., Watanabe, Momoko, Kang, Young-jin, Chau, Kevin F., Springel, Mark W., Malesz, Alexandra, Sousa, André M.M., Pletikos, Mihovil, Adelita, Tai, Calicchio, Monica L., Zhang, Yong, Holtzman, Michael J., Lidov, Hart G.W., Sestan, Nenad, Steen, Hanno, Monuki, Edwin S., Lehtinen, Maria K.
Pubblicato in J Neurosci (2015)

Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia

di Boisson, Bertrand, Laplantine, Emmanuel, Dobbs, Kerry, Cobat, Aurélie, Tarantino, Nadine, Hazen, Melissa, Lidov, Hart G.W., Hopkins, Gregory, Du, Likun, Belkadi, Aziz, Chrabieh, Maya, Itan, Yuval, Picard, Capucine, Fournet, Jean-Christophe, Eibel, Hermann, Tsitsikov, Erdyni, Pai, Sung-Yun, Abel, Laurent, Al-Herz, Waleed, Casanova, Jean-Laurent, Israel, Alain, Notarangelo, Luigi D.
Pubblicato in J Exp Med (2015)

Perioperatively Inhaled Hydrogen Gas Diminishes Neurologic Injury Following Experimental Circulatory Arrest in Swine

di Cole, Alexis R., Perry, Dorothy A., Raza, Ali, Nedder, Arthur P., Pollack, Elizabeth, Regan, William L., van den Bosch, Sarah J., Polizzotti, Brian D., Yang, Edward, Davila, Daniel, Afacan, Onur, Warfield, Simon K., Ou, Yangming, Sefton, Brenda, Everett, Allen D., Neil, Jeffrey J., Lidov, Hart G.W., Mayer, John E., Kheir, John N.
Pubblicato in JACC Basic Transl Sci (2019)

The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles

di Coulter, Michael E., Dorobantu, Cristina M., Lodewijk, Gerrald A., Delalande, François, Cianferani, Sarah, Ganesh, Vijay S., Smith, Richard S., Lim, Elaine T., Xu, C. Shan, Pang, Song, Wong, Eric T., Lidov, Hart G.W., Calicchio, Monica L., Yang, Edward, Gonzalez, Dilenny M., Schlaeger, Thorsten M., Mochida, Ganeshwaran H., Hess, Harald, Allen Lee, Wei-Chung, Lehtinen, Maria K., Kirchhausen, Tomas, Haussler, David, Jacobs, Frank M.J., Gaudin, Raphael, Walsh, Christopher A.
Pubblicato in Cell Rep (2018)

Exome sequencing identifies BRAF mutations in papillary craniopharyngiomas

di Brastianos, Priscilla K., Taylor-Weiner, Amaro, Manley, Peter E., Jones, Robert T., Dias-Santagata, Dora, Thorner, Aaron R., Rodriguez, Fausto J., Bernardo, Lindsay A., Schubert, Laura, Sunkavalli, Ashwini, Shillingford, Nick, Calicchio, Monica L., Lidov, Hart G.W., Taha, Hala, Martinez-Lage, Maria, Santi, Mariarita, Storm, Phillip B., Lee, John Y. K., Palmer, James N., Adappa, Nithin D., Scott, R. Michael, Dunn, Ian F., Laws, Edward R., Stewart, Chip, Ligon, Keith L., Hoang, Mai P., Van Hummelen, Paul, Hahn, William C., Louis, David N., Resnick, Adam C., Kieran, Mark W., Getz, Gad, Santagata, Sandro
Pubblicazione 2014

Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy

di Winawer, Melodie R., Griffin, Nicole G., Samanamud, Jorge, Baugh, Evan H., Rathakrishnan, Dinesh, Ramalingam, Senthilmurugan, Zagzag, David, Schevon, Catherine A., Dugan, Patricia, Hegde, Manu, Sheth, Sameer A., McKhann, Guy M., Doyle, Werner K., Grant, Gerald A., Porter, Brenda E., Mikati, Mohamad A., Muh, Carrie R., Malone, Colin D., Bergin, Ann Marie R., Peters, Jurriaan M., McBrian, Danielle K., Pack, Alison M., Akman, Cigdem I., LaCoursiere, Christopher M., Keever, Katherine M., Madsen, Joseph R., Yang, Edward, Lidov, Hart G.W., Shain, Catherine, Allen, Andrew S., Canoll, Peter, Crino, Peter B., Poduri, Annapurna H., Heinzen, Erin L.
Pubblicato in Ann Neurol (2018)