Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tchourbanov, Alexander"'
Autor:
Biesecker, Leslie G., Harrison, Steven M., Tayoun, Ahmad A., Berg, Jonathan S., Brenner, Steven E., Cutting, Garry R., Ellard, Sian, Greenblatt, Marc S., Kang, Peter, Karbassi, Izabela, Karchin, Rachel, Mester, Jessica, O’Donnell-Luria, Anne, Pesaran, Tina, Plon, Sharon E., Rehm, Heidi L., Strande, Natasha T., Tavtigian, Sean V., Topper, Scott, Walker, Logan C., Hoya, Miguel de la, Wiggins, George A.R., Lindy, Amanda, Vincent, Lisa M., Parsons, Michael T., Canson, Daffodil M., Bis-Brewer, Dana, Cass, Ashley, Tchourbanov, Alexander, Zimmermann, Heather, Byrne, Alicia B., Karam, Rachid, Spurdle, Amanda B.
Publikováno v:
In The American Journal of Human Genetics 6 July 2023 110(7):1046-1067
Autor:
Rhodes, Christopher J, Batai, Ken, Bleda, Marta, Haimel, Matthias, Southgate, Laura, Germain, Marine, Pauciulo, Michael W, Hadinnapola, Charaka, Aman, Jurjan, Girerd, Barbara, Arora, Amit, Knight, Jo, Hanscombe, Ken B, Karnes, Jason H, Kaakinen, Marika, Gall, Henning, Ulrich, Anna, Harbaum, Lars, Cebola, Inês, Ferrer, Jorge, Lutz, Katie, Swietlik, Emilia M, Ahmad, Ferhaan, Amouyel, Philippe, Archer, Stephen L, Argula, Rahul, Austin, Eric D, Badesch, David, Bakshi, Sahil, Barnett, Christopher, Benza, Raymond, Bhatt, Nitin, Bogaard, Harm J, Burger, Charles D, Chakinala, Murali, Church, Colin, Coghlan, John G, Condliffe, Robin, Corris, Paul A, Danesino, Cesare, Debette, Stéphanie, Elliott, C Gregory, Elwing, Jean, Eyries, Melanie, Fortin, Terry, Franke, Andre, Frantz, Robert P, Frost, Adaani, Garcia, Joe G N, Ghio, Stefano, Ghofrani, Hossein-Ardeschir, Gibbs, J Simon R, Harley, John, He, Hua, Hill, Nicholas S, Hirsch, Russel, Houweling, Arjan C, Howard, Luke S, Ivy, Dunbar, Kiely, David G, Klinger, James, Kovacs, Gabor, Lahm, Tim, Laudes, Matthias, Machado, Rajiv D, MacKenzie Ross, Robert V, Marsolo, Keith, Martin, Lisa J, Moledina, Shahin, Montani, David, Nathan, Steven D, Newnham, Michael, Olschewski, Andrea, Olschewski, Horst, Oudiz, Ronald J, Ouwehand, Willem H, Peacock, Andrew J, Pepke-Zaba, Joanna, Rehman, Zia, Robbins, Ivan, Roden, Dan M, Rosenzweig, Erika B, Saydain, Ghulam, Scelsi, Laura, Schilz, Robert, Seeger, Werner, Shaffer, Christian M, Simms, Robert W, Simon, Marc, Sitbon, Olivier, Suntharalingam, Jay, Tang, Haiyang, Tchourbanov, Alexander Y, Thenappan, Thenappan, Torres, Fernando, Toshner, Mark R, Treacy, Carmen M, Vonk Noordegraaf, Anton, Waisfisz, Quinten, Walsworth, Anna K, Walter, Robert E, Wharton, John, White, R James, Wilt, Jeffrey, Wort, Stephen J, Yung, Delphine, Lawrie, Allan, Humbert, Marc, Soubrier, Florent, Trégouët, David-Alexandre, Prokopenko, Inga, Kittles, Richard, Gräf, Stefan, Nichols, William C, Trembath, Richard C, Desai, Ankit A, Morrell, Nicholas W, Wilkins, Martin R
Publikováno v:
In The Lancet Respiratory Medicine March 2019 7(3):227-238
Akademický článek
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Autor:
Hammer, Michael F., Ishii, Atsushi, Johnstone, Laurel, Tchourbanov, Alexander, Lau, Branden, Sprissler, Ryan, Hallmark, Brian, Zhang, Miao, Zhou, Jin, Watkins, Joseph, Hirose, Shinichi
Dravet syndrome (DS) is a rare, devastating form of childhood epilepsy that is often associated with mutations in the voltage-gated sodium channel gene, SCN1A. There is considerable variability in expressivity within families, as well as among indivi
Externí odkaz:
http://hdl.handle.net/10150/625359
http://arizona.openrepository.com/arizona/handle/10150/625359
http://arizona.openrepository.com/arizona/handle/10150/625359
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Rhodes, Christopher J., Batai, Ken, Bleda, Marta, Haimel, Matthias, Southgate, Laura, Germain, Marine, Pauciulo, Michael W., Hadinnapola, Charaka, Aman, Jurjan, Girerd, Barbara, Arora, Amit, Knight, Jo, Hanscombe, Ken B., Karnes, Jason H., Kaakinen, Marika, Gall, Henning, Ulrich, Anna, Harbaum, Lars, Cebola, Inês, Ferrer, Jorge, Ahmad, Ferhaan, Amouyel, Philippe, Stephen L., Archer, Argula, Rahul, Eric D., Austin, Badesch, David, Bakshi, Sahil, Barnett, Christopher F., Benza, Raymond, Bhatt, Nitin, Bogaard, Harm J., Burger, Charles D., Chakinala, Murali M., Church, Colin, Coghlan, John G., Condliffe, Robin, Corris, Paul A., Danesino, Cesare, Debette, Stéphanie, Elliott, C. Gregory, Elwing, Jean, Eyries, Melanie, Fortin, Terry, Franke, Andre, Frantz, Robert P., Frost, Adaani, Garcia, Joe G.N., Ghio, Stefano, Ghofrani, Hossein-Ardeschir, Simon, J., Gibbs, R., Harley, John B., He, Hua, Hill, Nicholas S., Hirsch, Russel, Houweling, Arjan C., Howard, Luke S., Ivy, Dunbar, Kiely, David G., Klinger, James, Kovacs, Gabor, Lahm, Tim, Laudes, Matthias, Lutz, Katie, Machado, Rajiv D., MacKenzie Ross, Robert V., Marsolo, Keith, Martin, Lisa J., Moledina, Shahin, Montani, David, Nathan, Steven D., Newnham, Michael, Olschewski, Andrea, Olschewski, Horst, Oudiz, Ronald J., Ouwehand, Willem H., Peacock, Andrew J., Pepke-Zaba, Joanna, Rehman, Zia, Robbins, Ivan M., Roden, Dan M., Rosenzweig, Erika B., Saydain, Ghulam, Scelsi, Laura, Schilz, Robert, Seeger, Werner, Shaffer, Christian M., Simms, Robert W., Simon, Marc, Sitbon, Olivier, Suntharalingam, Jay, Swietlik, Emilia, Tang, Haiyang, Tchourbanov, Alexander Y., Thenappan, Thenappan, Torres, Fernando, Toshner, Mark R., Treacy, Carmen M., Noordegraaf, Anton Vonk, Waisfisz, Quinten, Walsworth, Anna K., Walter, Robert E, Wharton, John, White, R. James, Wilt, Jeffrey, Wort, Stephen J., Yung, Delphine, Lawrie, Allan, Humbert, Marc, Soubrier, Florent, Trégouët, David-Alexandre, Prokopenko, Inga, Kittles, Richard, Gräf, Stefan, Nichols, William C., Trembath, Richard C., Desai, Ankit A., Morrell, Nicholas W., Wilkins, Martin R.
BackgroundPulmonary arterial hypertension (PAH) is a rare disorder leading to premature death. Rare genetic variants contribute to disease etiology but the contribution of common genetic variation to disease risk and outcome remains poorly characteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0be038ddf6e6919ff713dc9dc62f637a
https://doi.org/10.1101/317164
https://doi.org/10.1101/317164
Autor:
Tchourbanov, Alexander.
Thesis (Ph.D.)--University of Nebraska-Lincoln, 2006.
Title from title screen (site viewed on September 12, 2006). PDF text of dissertation: 172 p. : ill. (some col.) ; 2.15Mb. UMI publication number: AAT 3209964. Includes bibliographical refere
Title from title screen (site viewed on September 12, 2006). PDF text of dissertation: 172 p. : ill. (some col.) ; 2.15Mb. UMI publication number: AAT 3209964. Includes bibliographical refere
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Rhodes, Christopher J, Batai, Ken, Bleda, Marta, Haimel, Matthias, Southgate, Laura, Germain, Marine, Pauciulo, Michael W, Hadinnapola, Charaka, Aman, Jurjan, Girerd, Barbara, Arora, Amit, Knight, Jo, Hanscombe, Ken B, Karnes, Jason H, Kaakinen, Marika, Gall, Henning, Ulrich, Anna, Harbaum, Lars, Cebola, Inês, Ferrer, Jorge, Lutz, Katie, Swietlik, Emilia M, Ahmad, Ferhaan, Amouyel, Philippe, Archer, Stephen L, Argula, Rahul, Austin, Eric D, Badesch, David, Bakshi, Sahil, Barnett, Christopher, Benza, Raymond, Bhatt, Nitin, Bogaard, Harm J, Burger, Charles D, Chakinala, Murali, Church, Colin, Coghlan, John G, Condliffe, Robin, Corris, Paul A, Danesino, Cesare, Debette, Stéphanie, Elliott, C Gregory, Elwing, Jean, Eyries, Melanie, Fortin, Terry, Franke, Andre, Frantz, Robert P, Frost, Adaani, Garcia, Joe GN, Ghio, Stefano, Ghofrani, Hossein-Ardeschir, Gibbs, J Simon R, Harley, John, He, Hua, Hill, Nicholas S, Hirsch, Russel, Houweling, Arjan C, Howard, Luke S, Ivy, Dunbar, Kiely, David G, Klinger, James, Kovacs, Gabor, Lahm, Tim, Laudes, Matthias, Machado, Rajiv D, MacKenzie Ross, Robert V, Marsolo, Keith, Martin, Lisa J, Moledina, Shahin, Montani, David, Nathan, Steven D, Newnham, Michael, Olschewski, Andrea, Olschewski, Horst, Oudiz, Ronald J, Ouwehand, Willem H, Peacock, Andrew J, Pepke-Zaba, Joanna, Rehman, Zia, Robbins, Ivan, Roden, Dan M, Rosenzweig, Erika B, Saydain, Ghulam, Scelsi, Laura, Schilz, Robert, Seeger, Werner, Shaffer, Christian M, Simms, Robert W, Simon, Marc, Sitbon, Olivier, Suntharalingam, Jay, Tang, Haiyang, Tchourbanov, Alexander Y, Thenappan, Thenappan, Torres, Fernando, Toshner, Mark R, Treacy, Carmen M, Vonk Noordegraaf, Anton, Waisfisz, Quinten, Walsworth, Anna K, Walter, Robert E, Wharton, John, White, R James, Wilt, Jeffrey, Wort, Stephen J, Yung, Delphine, Lawrie, Allan, Humbert, Marc, Soubrier, Florent, Trégouët, David-Alexandre, Prokopenko, Inga, Kittles, Richard, Gräf, Stefan, Nichols, William C, Trembath, Richard C, Desai, Ankit A, Morrell, Nicholas W, Wilkins, Martin R, UK NIHR BioResource Rare Diseases Consortium, UK PAH Cohort Study Consortium, US PAH Biobank Consortium
BACKGROUND: Rare genetic variants cause pulmonary arterial hypertension, but the contribution of common genetic variation to disease risk and natural history is poorly characterised. We tested for genome-wide association for pulmonary arterial hypert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c3aad566d9f4bd78b66b888f4bc3cae
Akademický článek
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