β(2) Integrin Induces TCR ζ–Syk–PLC-γ Phosphorylation and Paxillin-dependent Granule Polarization in Human NK cells()

Por March, Michael E., Long, Eric O.
Publicado em 2011

Recruitment of Activation Receptors at Inhibitory NK Cell Immune Synapses

Por Schleinitz, Nicolas, March, Michael E., Long, Eric O.
Publicado em 2008

Genetic polymorphisms and associated susceptibility to asthma

Por March, Michael E, Sleiman, Patrick MA, Hakonarson, Hakon
Publicado em 2013

Use of transfected Drosophila S2 cells to study NK cell activation

Por March, Michael E., Gross, Catharina C., Long, Eric O.
Publicado em 2010

A Signaling Network Induced by β(2) Integrin Controls the Polarization of Lytic Granulesin Cytotoxic Cells

Por Zhang, Minggang, March, Michael E., Lane, William S., Long, Eric O.
Publicado em 2014

Synergy among receptors on resting NK cells for the activation of natural cytotoxicity and cytokine secretion

Por Bryceson, Yenan T., March, Michael E., Ljunggren, Hans-Gustaf, Long, Eric O.
Publicado em 2006

Activation, co–activation, and co–stimulation of resting human NK cells

Por Bryceson, Yenan T., March, Michael E., Ljunggren, Hans-Gustaf, Long, Eric O.
Publicado em 2006

Cytolytic granule polarization and degranulation controlled by different receptors in resting NK cells

Por Bryceson, Yenan T., March, Michael E., Barber, Domingo F., Ljunggren, Hans-Gustaf, Long, Eric O.
Publicado em 2005

Essential Role for the C-Terminal Noncatalytic Region of SHIP in FcγRIIB1-Mediated Inhibitory Signaling

Por Aman, M. Javad, Walk, Scott F., March, Michael E., Su, Hua-Poo, Carver, D. Jeannean, Ravichandran, Kodimangalam S.
Publicado em 2000

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

Por Liu, Yichuan, Li, Yun, March, Michael E., Kenny, Nguyen, Xu, Kexiang, Wang, Fengxiang, Guo, Yiran, Keating, Brendan, Glessner, Joseph, Li, Jiankang, Ganley, Theodore J., Zhang, Jianguo, Deardorff, Matthew A., Xu, Xun, Hakonarson, Hakon
Publicado no Hum Genomics (2015)

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

Por Liu, Yichuan, Li, Yun, March, Michael E., Nguyen, Kenny, Xu, Kexiang, Wang, Fengxiang, Guo, Yiran, Keating, Brendan, Glessner, Joseph, Li, Jiankang, Ganley, Theodore J., Zhang, Jianguo, Deardorff, Matthew A., Xu, Xun, Hakonarson, Hakon
Publicado no Hum Genomics (2016)

Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study

Por Cardinale, Christopher J., Li, Dong, Tian, Lifeng, Connolly, John J., March, Michael E., Hou, Cuiping, Wang, Fengxiang, Snyder, James, Kim, Cecilia E., Chiavacci, Rosetta M., Sleiman, Patrick M., Burnham, Jon M., Hakonarson, Hakon
Publicado no BMC Musculoskelet Disord (2016)

Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene

Por van Ingen, Gijs, Li, Jin, Goedegebure, André, Pandey, Rahul, Li, Yun Rose, March, Michael E., Jaddoe, Vincent W. V., Bakay, Marina, Mentch, Frank D., Thomas, Kelly, Wei, Zhi, Chang, Xiao, Hain, Heather S., Uitterlinden, André G., Moll, Henriette A., van Duijn, Cornelia M., Rivadeneira, Fernando, Raat, Hein, Baatenburg de Jong, Robert J., Sleiman, Patrick M., van der Schroeff, Marc P., Hakonarson, Hakon
Publicado no Nat Commun (2016)