Transmission device and drive device for electrically driven vehicle von LUBKE ECKHARD, WEHLEN TIMO, SCHAER STEPHAN, TEER MARK

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Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases von Pierson, Tyler Mark, Adams, David, Bonn, Florian, Martinelli, Paola, Cherukuri, Praveen F, Teer, Jamie K, Hansen, Nancy F, Cruz, Pedro, Mullikin For The Nisc Comparative Sequencing Program, James C, Blakesley, Robert W, Golas, Gretchen, Kwan, Justin, Sandler, Anthony, Fuentes Fajardo, Karin, Markello, Thomas, Tifft, Cynthia, Blackstone, Craig, Rugarli, Elena I, Langer, Thomas, Gahl, William A, Toro, Camilo

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Modeling phenotypic heterogeneity towards evolutionarily inspired osteosarcoma therapy von Welch, Darcy L., Fridley, Brooke L., Cen, Ling, Teer, Jamie K., Yoder, Sean J., Pettersson, Fredrik, Xu, Liping, Cheng, Chia-Ho, Zhang, Yonghong, Alexandrow, Mark G., Xiang, Shengyan, Robertson-Tessi, Mark, Brown, Joel S., Metts, Jonathan, Brohl, Andrew S., Reed, Damon R.

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The Florida Pancreas Collaborative Next-Generation Biobank: Infrastructure to Reduce Disparities and Improve Survival for a Diverse Cohort of Patients with Pancreatic Cancer von Permuth, Jennifer B, Dezsi, Kaleena B, Vyas, Shraddha, Ali, Karla N, Basinski, Toni L, Utuama, Ovie A, Denbo, Jason W, Klapman, Jason, Dam, Aamir, Carballido, Estrella, Kim, Dae Won, Pimiento, Jose M, Powers, Benjamin D, Otto, Amy K, Choi, Jung W, Chen, Dung-Tsa, Teer, Jamie K, Beato, Francisca, Ward, Alina, Cortizas, Elena M, Whisner, Suzanne Y, Williams, Iverson E, Riner, Andrea N, Tardif, Kenneth, Velanovich, Vic, Karachristos, Andreas, Douglas, Wade G, Legaspi, Adrian, Allan, Bassan J, Meredith, Kenneth, Molina-Vega, Manual A, Bao, Philip, St Julien, Jamii, Huguet, Kevin L, Green, Lee, Odedina, Folakemi T, Kumar, Nagi B, Simmons, Vani N, George, Thomas J, Vadaparampil, Susan T, Hodul, Pamela J, Arnoletti, J Pablo, Awad, Ziad T, Bose, Debashish, Jiang, Kun, Centeno, Barbara A, Gwede, Clement K, Malafa, Mokenge, Judge, Sarah M, Judge, Andrew R, Jeong, Daniel, Bloomston, Mark, Merchant, Nipun B, Fleming, Jason B, Trevino, Jose G, On Behalf Of The Florida Pancreas Collaborative

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Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM1-gangliosidosis von MARK PIERSON, Tyler, ADAMS, David A, CRUZ, Pedro, TEER, Jamie K, MULLIKIN, James C, BOERKOEL, Cornelius F, GAHL, William A, TIFFT, Cynthia J, MARKELLO, Thomas, GOLAS, Gretchen, YANG, Sandra, SINCAN, Murat, SIMEONOV, Dimitre R, FUENTES FAJARDO, Karin, HANSEN, Nancy F, CHERUKURI, Praveen F

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Plasma cell dependence on histone/protein deacetylase 11 reveals a therapeutic target in multiple myeloma von Mostofa, Agm, Distler, Allison, Meads, Mark B, Sahakian, Eva, Powers, John J, Achille, Alexandra, Noyes, David, Wright, Gabriela, Fang, Bin, Izumi, Victoria, Koomen, John, Rampakrishnan, Rupal, Nguyen, Tuan P, De Avila, Gabriel, Silva, Ariosto S, Sudalagunta, Praneeth, Canevarolo, Rafael Renatino, Siqueira Silva, Maria D Coelho, Alugubelli, Raghunandan Reddy, Dai, Hongyue A, Kulkarni, Amit, Dalton, William S, Hampton, Oliver A, Welsh, Eric A, Teer, Jamie K, Tungesvik, Alexandre, Wright, Kenneth L, Pinilla-Ibarz, Javier, Sotomayor, Eduardo M, Shain, Kenneth H, Brayer, Jason

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A CK1δ/CK1ε Regulated Metabolic Circuit Is a Therapeutic Vulnerability for Multiple Myeloma von Burger, Karen L, Meads, Mark B., Berglund, Anders, Oliveira, Paula S., Distler, Allison, Sudalagunta, Praneeth Reddy, Jacobson, Timothy, Teer, Jamie, Welsh, Eric A., Dai, Hongyue, Koomen, John M., Raghunandan Reddy, Alugubelli, De Avila, Gabriel, Tungesvik, Alexandre, Roush, William, Siqueira Silva, Ariosto, Shain, Kenneth H., Cleveland, John

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Re-Constructing and Exploiting Transcriptional Regulatory Networks in Multiple Myeloma Drug Resistance von Renatino-Canevarolo, Rafael, Sudalagunta, Praneeth Reddy, Coelho Siqueira Silva, Maria D, Meads, Mark B., Tungesvik, Alexandre, De Avila, Gabriel, Raghunandan Reddy, Alugubelli, Nong, Minerva, Teer, Jamie, Welsh, Eric A., Lwin, Tint, Kulkarni, Amit, Dai, Hongyue, Dalton, William S., Shain, Kenneth H., Siqueira Silva, Ariosto

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A CK1δ/CK1ε-to-Wnt/β-Catenin Circuit Is a Therapeutic Vulnerability in Primary and Drug Resistant Multiple Myeloma von Burger, Karen L., Meads, Mark B, Silva, Ariosto, Distler, Allison, Silva, Maria Coelho Siqueira, Jacobson, Timothy, Teer, Jamie K, Roush, William R., Shain, Kenneth H., Cleveland, John L.

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A CK1δ/CK1ε-to-β-Catenin Circuit Is a Therapeutic Vulnerability for Primary and Drug Resistant Multiple Myeloma von Burger, Karen L, Meads, Mark B., Siqueira Silva, Ariosto, Oliveira, Paula, Nguyen, Tuan, Distler, Allison, Siqueira Silva, Maria Coelho, Jacobson, Timothy, Teer, Jamie, Dai, Hongyue, Roush, William, Cleveland, John, Shain, Kenneth H

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A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk von Lu, Yingchang, Beeghly-Fadiel, Alicia, Wu, Lang, Guo, Xingyi, Li, Bingshan, Schildkraut, Joellen M, Im, Hae Kyung, Chen, Yian A, Permuth, Jennifer B, Reid, Brett M, Teer, Jamie K, Moysich, Kirsten B, Andrulis, Irene L, Anton-Culver, Hoda, Arun, Banu K, Bandera, Elisa V, Barkardottir, Rosa B, Barnes, Daniel R, Benitez, Javier, Bjorge, Line, Brenton, James, Butzow, Ralf, Caldes, Trinidad, Caligo, Maria A, Campbell, Ian, Chang-Claude, Jenny, Claes, Kathleen B.M, Couch, Fergus J, Cramer, DanielW, Daly, Mary B, deFazio, Anna, Dennis, Joe, Diez, Orland, Domchek, Susan M, Doerk, Thilo, Easton, Douglas F, Eccles, Diana M, Fasching, Peter A, Fortner, Renee T, Fountzilas, George, Friedman, Eitan, Ganz, Patricia A, Garber, Judy, Giles, Graham G, Godwin, Andrew K, Goldgar, David E, Goodman, Marc T, Greene, Mark H, Gronwald, Jacek, Hamann, Ute, Heitz, Florian, Hildebrandt, Michelle A.T, Hogdall, Claus K, Hollestelle, Antoinette, Hulick, Peter J, Huntsman, David G, Imyanitov, Evgeny N, Isaacs, Claudine, Jakubowska, Anna, James, Paul, Karlan, Beth Y, Kelemen, Linda E, Kiemeney, Lambertus A, Kjaer, Susanne K, Kwong, Ava, Le, Nhu D, Leslie, Goska, Lesueur, Fabienne, Levine, Douglas A, Mattiello, Amalia, May, Taymaa, McGuffog, Lesley, McNeish, Iain A, Merritt, Melissa A, Modugno, Francesmary, Montagna, Marco, Neuhausen, Susan L, Nevanlinna, Heli, Nielsen, Finn C, Nikitina-Zake, Liene, Nussbaum, Robert L, Offit, Kenneth, Olah, Edith, Olopade, Olufunmilayo I, Olson, Sara H, Olsson, Hakan, Osorio, Ana, Park, Sue K, Parsons, Michael T, Peeters, Petra H.M, Pejovic, Tanja, Peterlongo, Paolo, Phelan, Catherine M, Pujana, Miquel Angel, Ramus, Susan J, Rennert, Gad, Risch, Harvey, Rodriguez, Gustavo C, Rodriguez-Antona, Cristina, Romieu, Isabelle

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Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases von Pierson, Tyler Mark, Adams, David, Bonn, Florian, Martinelli, Paola, Cherukuri, Praveen F., Teer, Jamie K., Hansen, Nancy F., Cruz, Pedro, Mullikin, James C., Blakesley, Robert W., Golas, Gretchen, Kwan, Justin, Sandler, Anthony, Fuentes Fajardo, Karin, Markello, Thomas, Tifft, Cynthia, Blackstone, Craig, Rugarli, Elena I., Langer, Thomas, Gahl, William A., Toro, Camilo

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Correction: Whole-Exome Sequencing Identifies Homozygous Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial -AAA Proteases von Tyler Mark Pierson, David Adams, Florian Bonn, Paola Martinelli, Praveen F. Cherukuri, Jamie K. Teer, Nancy F. Hansen, Pedro Cruz, James C. Mullikin, Robert W. Blakesley, Gretchen Golas, Justin Kwan, Anthony Sandler, Karin Fuentes Fajardo, Thomas Markello, Cynthia Tifft, Craig Blackstone, Elena I. Rugarli, Thomas Langer, William A. Gahl, Camilo Toro

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Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM 1 -gangliosidosis von Pierson, Tyler Mark, Adams, David A., Markello, Thomas, Golas, Gretchen, Yang, Sandra, Sincan, Murat, Simeonov, Dimitre R., Fuentes Fajardo, Karin, Hansen, Nancy F., Cherukuri, Praveen F., Cruz, Pedro, Teer, Jamie K., Mullikin, James C., Boerkoel, Cornelius F., Gahl, William A., Tifft, Cynthia J.

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Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases: e1002325 von Pierson, Tyler Mark, Adams, David, Bonn, Florian, Martinelli, Paola, Cherukuri, Praveen F, Teer, Jamie K, Hansen, Nancy F, Cruz, Pedro, Program, NISC ComparativeSequencing, Blakesley, Robert W, Golas, Gretchen, Kwan, Justin, Sandler, Anthony, Fajardo, Karin Fuentes, Markello, Thomas, Tifft, Cynthia, Blackstone, Craig, Rugarli, Elena I, Langer, Thomas, Gahl, William A, Toro, Camilo

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Adwatch von Tomblin, Mark

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