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Dielectrophoretic studies of the activation of human T lymphocytes using a newly developed cell profiling system. [electronic resource] by
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- Chen, Yan
- Foster-Haje, Linda
- García-Ojeda, Marcos E
- Lee, Richard S
- Lock, Gary M
- Talary, Mark S
- Tate, Keri M
Producer: 20030212
In:
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A Pilot Study of Inspiratory Muscle Training to Improve Exercise Capacity in Patients with Fontan Physiology. [electronic resource] by
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- Shafer, Keri M
- Valente, Anne Marie
- Uluer, Ahmet Z
- Rhodes, Jonathan
Producer: 20190114
In:
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Zika Inquiries Made to the CDC-INFO System, December 2015-September 2017. [electronic resource] by
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- Watson, Crystal
- Meyer, Diane
- Snyder, Michael R
- Ravi, Sanjana J
- McGinty, Emma E
- Pechta, Laura E
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- Podgornik, Michelle N
- Lubell, Keri M
Producer: 20210618
In:
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Characterization of X chromosome inactivation using integrated analysis of whole-exome and mRNA sequencing. [electronic resource] by
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- Kurdoglu, Ahmet A
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- Trent, Jeffrey M
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The Disaster Information Needs of Families of Children with Special Healthcare Needs: A Scoping Review. [electronic resource] by
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- Lubell, Keri M
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Producer: 20181015
In:
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Academic Advancement in the Current Era: Integrating and Empowering Clinician Educators. [electronic resource] by
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- Abudayyeh, Islam
- Feldman, Dmitriy N
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- Damp, Julie
- Gopinathannair, Rakesh
- Valente, Anne Marie
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Producer: 20200120
In:
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Escherichia coli O123 O antigen genes and polysaccharide structure are conserved in some Salmonella enterica serogroups. [electronic resource] by
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- Trout-Yakel, Keri M
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- Ng, Lai-King
- Paramonov, Nikolay A
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In:
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Reducing radiation dose from myocardial perfusion imaging in subjects with complex congenital heart disease. [electronic resource] by
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- Bruyere, John
- Rosica, Dillenia
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- Landzberg, Michael J
- Taqueti, Viviany R
- Blankstein, Ron
- Skali, Hicham
- Kwatra, Neha
- DiCarli, Marcelo F
- Grant, Frederick D
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Producer: 20220216
In:
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How did Ebola information spread on twitter: broadcasting or viral spreading? [electronic resource] by
- Liang, Hai
- Fung, Isaac Chun-Hai
- Tse, Zion Tsz Ho
- Yin, Jingjing
- Chan, Chung-Hong
- Pechta, Laura E
- Smith, Belinda J
- Marquez-Lameda, Rossmary D
- Meltzer, Martin I
- Lubell, Keri M
- Fu, King-Wa
Producer: 20190625
In:
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Relationship of non-invasive quantification of myocardial blood flow to arrhythmic events in patients with implantable cardiac defibrillators. [electronic resource] by
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- Yun, Hong Jun
- Lazarus, John J
- Konerman, Matthew
- Saleh, Ashraf
- Weinberg, Richard L
- Cunnane, Ryan
- Shah, Ravi V
- Hiller, Keri M
- Ficaro, Edward P
- Corbett, James R
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Producer: 20200819
In:
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Effects of age and aerobic fitness on myocardial lipid content. [electronic resource] by
- Sarma, Satyam
- Carrick-Ranson, Graeme
- Fujimoto, Naoki
- Adams-Huet, Beverley
- Bhella, Paul S
- Hastings, Jeffrey L
- Shafer, Keri M
- Shibata, Shigeki
- Boyd, Kara
- Palmer, Dean
- Szczepaniak, Edward W
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Producer: 20140122
In:
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Cardiovascular effects of 1 year of alagebrium and endurance exercise training in healthy older individuals. [electronic resource] by
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- Hastings, Jeffrey L
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- Shafer, Keri M
- Shibata, Shigeki
- Bhella, Paul S
- Abdullah, Shuaib M
- Barkley, Kyler W
- Adams-Huet, Beverley
- Boyd, Kara N
- Livingston, Sheryl A
- Palmer, Dean
- Levine, Benjamin D
Producer: 20140122
In:
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Lessons of Risk Communication and Health Promotion - West Africa and United States. [electronic resource] by
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- Young, Cathy E
- Smith, Laura A
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- Manning, Craig
- Pechta, Laura
- Telfer, Jana L
- Gaines-McCollom, Molly
- Harben, Kathy
- Holmes, Wendy
- Lubell, Keri M
- McQuiston, Jennifer H
- Nordlund, Kristen
- O'Connor, John
- Reynolds, Barbara S
- Schindelar, Jessica A
- Shelley, Gene
- Daniel, Katherine Lyon
Producer: 20170123
In:
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Intra- and Inter-cellular Rewiring of the Human Colon during Ulcerative Colitis. [electronic resource] by
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- Biton, Moshe
- Ordovas-Montanes, Jose
- Sullivan, Keri M
- Burgin, Grace
- Graham, Daniel B
- Herbst, Rebecca H
- Rogel, Noga
- Slyper, Michal
- Waldman, Julia
- Sud, Malika
- Andrews, Elizabeth
- Velonias, Gabriella
- Haber, Adam L
- Jagadeesh, Karthik
- Vickovic, Sanja
- Yao, Junmei
- Stevens, Christine
- Dionne, Danielle
- Nguyen, Lan T
- Villani, Alexandra-Chloé
- Hofree, Matan
- Creasey, Elizabeth A
- Huang, Hailiang
- Rozenblatt-Rosen, Orit
- Garber, John J
- Khalili, Hamed
- Desch, A Nicole
- Daly, Mark J
- Ananthakrishnan, Ashwin N
- Shalek, Alex K
- Xavier, Ramnik J
- Regev, Aviv
Producer: 20200427
In:
Cell vol. 178
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Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease. [electronic resource] by
- Rice, Gillian I
- Kitabayashi, Naoki
- Barth, Magalie
- Briggs, Tracy A
- Burton, Annabel C E
- Carpanelli, Maria Luisa
- Cerisola, Alfredo M
- Colson, Cindy
- Dale, Russell C
- Danti, Federica Rachele
- Darin, Niklas
- De Azua, Begoña
- De Giorgis, Valentina
- De Goede, Christian G L
- Desguerre, Isabelle
- De Laet, Corinne
- Eslahi, Atieh
- Fahey, Michael C
- Fallon, Penny
- Fay, Alex
- Fazzi, Elisa
- Gorman, Mark P
- Gowrinathan, Nirmala Rani
- Hully, Marie
- Kurian, Manju A
- Leboucq, Nicolas
- Lin, Jean-Pierre S-M
- Lines, Matthew A
- Mar, Soe S
- Maroofian, Reza
- Martí-Sanchez, Laura
- McCullagh, Gary
- Mojarrad, Majid
- Narayanan, Vinodh
- Orcesi, Simona
- Ortigoza-Escobar, Juan Dario
- Pérez-Dueñas, Belén
- Petit, Florence
- Ramsey, Keri M
- Rasmussen, Magnhild
- Rivier, François
- Rodríguez-Pombo, Pilar
- Roubertie, Agathe
- Stödberg, Tommy I
- Toosi, Mehran Beiraghi
- Toutain, Annick
- Uettwiller, Florence
- Ulrick, Nicole
- Vanderver, Adeline
- Waldman, Amy
- Livingston, John H
- Crow, Yanick J
Producer: 20180312
In:
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A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis. [electronic resource] by
- Olson, Heather E
- Jean-Marçais, Nolwenn
- Yang, Edward
- Heron, Delphine
- Tatton-Brown, Katrina
- van der Zwaag, Paul A
- Bijlsma, Emilia K
- Krock, Bryan L
- Backer, E
- Kamsteeg, Erik-Jan
- Sinnema, Margje
- Reijnders, Margot R F
- Bearden, David
- Begtrup, Amber
- Telegrafi, Aida
- Lunsing, Roelineke J
- Burglen, Lydie
- Lesca, Gaetan
- Cho, Megan T
- Smith, Lacey A
- Sheidley, Beth R
- El Achkar, Christelle Moufawad
- Pearl, Phillip L
- Poduri, Annapurna
- Skraban, Cara M
- Tarpinian, Jennifer
- Nesbitt, Addie I
- Fransen van de Putte, Dietje E
- Ruivenkamp, Claudia A L
- Rump, Patrick
- Chatron, Nicolas
- Sabatier, Isabelle
- De Bellescize, Julitta
- Guibaud, Laurent
- Sweetser, David A
- Waxler, Jessica L
- Wierenga, Klaas J
- Donadieu, Jean
- Narayanan, Vinodh
- Ramsey, Keri M
- Nava, Caroline
- Rivière, Jean-Baptiste
- Vitobello, Antonio
- Mau-Them, Frédéric Tran
- Philippe, Christophe
- Bruel, Ange-Line
- Duffourd, Yannis
- Thomas, Laurel
- Lelieveld, Stefan H
- Schuurs-Hoeijmakers, Janneke
- Brunner, Han G
- Keren, Boris
- Thevenon, Julien
- Faivre, Laurence
- Thomas, Gary
- Thauvin-Robinet, Christel
Publication details: American journal of human genetics 10 2018
In:
American journal of human genetics vol. 103
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58.
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A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis. [electronic resource] by
- Olson, Heather E
- Jean-Marçais, Nolwenn
- Yang, Edward
- Heron, Delphine
- Tatton-Brown, Katrina
- van der Zwaag, Paul A
- Bijlsma, Emilia K
- Krock, Bryan L
- Backer, E
- Kamsteeg, Erik-Jan
- Sinnema, Margje
- Reijnders, Margot R F
- Bearden, David
- Begtrup, Amber
- Telegrafi, Aida
- Lunsing, Roelineke J
- Burglen, Lydie
- Lesca, Gaetan
- Cho, Megan T
- Smith, Lacey A
- Sheidley, Beth R
- Moufawad El Achkar, Christelle
- Pearl, Phillip L
- Poduri, Annapurna
- Skraban, Cara M
- Tarpinian, Jennifer
- Nesbitt, Addie I
- Fransen van de Putte, Dietje E
- Ruivenkamp, Claudia A L
- Rump, Patrick
- Chatron, Nicolas
- Sabatier, Isabelle
- De Bellescize, Julitta
- Guibaud, Laurent
- Sweetser, David A
- Waxler, Jessica L
- Wierenga, Klaas J
- Donadieu, Jean
- Narayanan, Vinodh
- Ramsey, Keri M
- Nava, Caroline
- Rivière, Jean-Baptiste
- Vitobello, Antonio
- Tran Mau-Them, Frédéric
- Philippe, Christophe
- Bruel, Ange-Line
- Duffourd, Yannis
- Thomas, Laurel
- Lelieveld, Stefan H
- Schuurs-Hoeijmakers, Janneke
- Brunner, Han G
- Keren, Boris
- Thevenon, Julien
- Faivre, Laurence
- Thomas, Gary
- Thauvin-Robinet, Christel
Producer: 20181211
In:
American journal of human genetics vol. 102
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Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency. [electronic resource] by
- Zawerton, Ash
- Mignot, Cyril
- Sigafoos, Ashley
- Blackburn, Patrick R
- Haseeb, Abdul
- McWalter, Kirsty
- Ichikawa, Shoji
- Nava, Caroline
- Keren, Boris
- Charles, Perrine
- Marey, Isabelle
- Tabet, Anne-Claude
- Levy, Jonathan
- Perrin, Laurence
- Hartmann, Andreas
- Lesca, Gaetan
- Schluth-Bolard, Caroline
- Monin, Pauline
- Dupuis-Girod, Sophie
- Guillen Sacoto, Maria J
- Schnur, Rhonda E
- Zhu, Zehua
- Poisson, Alice
- El Chehadeh, Salima
- Alembik, Yves
- Bruel, Ange-Line
- Lehalle, Daphné
- Nambot, Sophie
- Moutton, Sébastien
- Odent, Sylvie
- Jaillard, Sylvie
- Dubourg, Christèle
- Hilhorst-Hofstee, Yvonne
- Barbaro-Dieber, Tina
- Ortega, Lucia
- Bhoj, Elizabeth J
- Masser-Frye, Diane
- Bird, Lynne M
- Lindstrom, Kristin
- Ramsey, Keri M
- Narayanan, Vinodh
- Fassi, Emily
- Willing, Marcia
- Cole, Trevor
- Salter, Claire G
- Akilapa, Rhoda
- Vandersteen, Anthony
- Canham, Natalie
- Rump, Patrick
- Gerkes, Erica H
- Klein Wassink-Ruiter, Jolien S
- Bijlsma, Emilia
- Hoffer, Mariëtte J V
- Vargas, Marcelo
- Wojcik, Antonina
- Cherik, Florian
- Francannet, Christine
- Rosenfeld, Jill A
- Machol, Keren
- Scott, Daryl A
- Bacino, Carlos A
- Wang, Xia
- Clark, Gary D
- Bertoli, Marta
- Zwolinski, Simon
- Thomas, Rhys H
- Akay, Ela
- Chang, Richard C
- Bressi, Rebekah
- Sanchez Russo, Rossana
- Srour, Myriam
- Russell, Laura
- Goyette, Anne-Marie E
- Dupuis, Lucie
- Mendoza-Londono, Roberto
- Karimov, Catherine
- Joseph, Maries
- Nizon, Mathilde
- Cogné, Benjamin
- Kuechler, Alma
- Piton, Amélie
- Klee, Eric W
- Lefebvre, Véronique
- Clark, Karl J
- Depienne, Christel
Producer: 20210203
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 22
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