検索結果 - Koscinski, Isabelle
- 検索結果 1 - 12 結果 / 12
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Minimal residual disease detection by multicolor flow cytometry in cryopreserved ovarian tissue from leukemia patients 著者: Zver, Tristan, Frontczak, Sophie, Poirot, Catherine, Rives-Feraille, Aurélie, Leroy-Martin, Brigitte, Koscinski, Isabelle, Arbez-Gindre, Francine, Garnache-Ottou, Francine, Roux, Christophe, Amiot, Clotilde
出版事項 2022テキスト -
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Multiorgan and Vascular Tropism of SARS-CoV-2 著者: Hartard, Cédric, Chaqroun, Ahlam, Settembre, Nicla, Gauchotte, Guillaume, Lefevre, Benjamin, Marchand, Elodie, Mazeaud, Charles, Nguyen, Duc Trung, Martrille, Laurent, Koscinski, Isabelle, Malikov, Sergueï, Schvoerer, Evelyne
出版事項 2022テキスト -
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Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia 著者: Dam, Anika H. D. M. , Koscinski, Isabelle , Kremer, Jan A. M. , Moutou, Céline , Jaeger, Anne-Sophie , Oudakker, Astrid R. , Tournaye, Herman , Charlet, Nicolas , Lagier-Tourenne, Clotilde , van Bokhoven, Hans , Viville, Stéphane
出版事項 2007テキスト -
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DPY19L2 Deletion as a Major Cause of Globozoospermia 著者: Koscinski, Isabelle, ElInati, Elias, Fossard, Camille, Redin, Claire, Muller, Jean, Velez de la Calle, Juan, Schmitt, Françoise, Ben Khelifa, Mariem, Ray, Pierre, Kilani, Zaid, Barratt, Christopher L.R., Viville, Stéphane
出版事項 2011テキスト -
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DPY19L2 Deletion as a Major Cause of Globozoospermia 著者: Koscinski, Isabelle, ElInati, Elias, Fossard, Camille, Redin, Claire, Muller, Jean, Velez de la Calle, Juan, Schmitt, Françoise, Ben Khelifa, Mariem, Ray, Pierre F., Kilani, Zaid, Barratt, Christopher L.R., Viville, Stéphane
出版事項 2011テキスト -
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A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation 著者: Harbuz, Radu, Zouari, Raoudha, Pierre, Virginie, Ben Khelifa, Mariem, Kharouf, Mahmoud, Coutton, Charles, Merdassi, Ghaya, Abada, Farid, Escoffier, Jessica, Nikas, Yorgos, Vialard, François, Koscinski, Isabelle, Triki, Chema, Sermondade, Nathalie, Schweitzer, Thérèse, Zhioua, Amel, Zhioua, Fethi, Latrous, Habib, Halouani, Lazhar, Ouafi, Marrakchi, Makni, Mounir, Jouk, Pierre-Simon, Sèle, Bernard, Hennebicq, Sylviane, Satre, Véronique, Viville, Stéphane, Arnoult, Christophe, Lunardi, Joël, Ray, Pierre F.
出版事項 2011テキスト -
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A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients 著者: Guéant, Jean-Louis, Chéry, Céline, Oussalah, Abderrahim, Nadaf, Javad, Coelho, David, Josse, Thomas, Flayac, Justine, Robert, Aurélie, Koscinski, Isabelle, Gastin, Isabelle, Filhine-Tresarrieu, Pierre, Pupavac, Mihaela, Brebner, Alison, Watkins, David, Pastinen, Tomi, Montpetit, Alexandre, Hariri, Fadi, Tregouët, David, Raby, Benjamin A, Chung, Wendy K., Morange, Pierre-Emmanuel, Froese, D. Sean, Baumgartner, Matthias R., Benoist, Jean-François, Ficicioglu, Can, Marchand, Virginie, Motorin, Yuri, Bonnemains, Chrystèle, Feillet, François, Majewski, Jacek, Rosenblatt, David S.
出版事項 2018テキスト -
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Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients 著者: Guéant, Jean-Louis, Chéry, Céline, Oussalah, Abderrahim, Nadaf, Javad, Coelho, David, Josse, Thomas, Flayac, Justine, Robert, Aurélie, Koscinski, Isabelle, Gastin, Isabelle, Filhine-Tresarrieu, Pierre, Pupavac, Mihaela, Brebner, Alison, Watkins, David, Pastinen, Tomi, Montpetit, Alexandre, Hariri, Fadi, Tregouët, David, Raby, Benjamin A, Chung, Wendy K., Morange, Pierre-Emmanuel, Froese, D. Sean, Baumgartner, Matthias R., Benoist, Jean-François, Ficicioglu, Can, Marchand, Virginie, Motorin, Yuri, Bonnemains, Chrystèle, Feillet, François, Majewski, Jacek, Rosenblatt, David S.
出版事項 2018テキスト