Arama Sonuçları - Koscinski, Isabelle
- Gösterilen 1 - 12 sonuçlar arası kayıtlar. 12
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1
Hypogonadotropic hypogonadism in men with hereditary hemochromatosis Yazar: El Osta, Rabih, Grandpre, Nicolas, Monnin, Nicolas, Hubert, Jacques, Koscinski, Isabelle
Baskı/Yayın Bilgisi 2017Metin -
2
Ovarian Telomerase and Female Fertility Yazar: Toupance, Simon, Fattet, Anne-Julie, Thornton, Simon N., Benetos, Athanase, Guéant, Jean-Louis, Koscinski, Isabelle
Baskı/Yayın Bilgisi 2021Metin -
3
Telomere length in granulosa cells and leukocytes: a potential marker of female fertility? A systematic review of the literature Yazar: Fattet, Anne-Julie, Toupance, Simon, Thornton, Simon N., Monnin, Nicolas, Guéant, Jean-Louis, Benetos, Athanase, Koscinski, Isabelle
Baskı/Yayın Bilgisi 2020Metin -
4
Reproduction Function in Male Patients With Bardet Biedl Syndrome Yazar: Koscinski, Isabelle, Mark, Manuel, Messaddeq, Nadia, Braun, Jean Jacques, Celebi, Catherine, Muller, Jean, Zinetti-Bertschy, Anna, Goetz, Nathalie, Dollfus, Hélène, Rossignol, Sylvie
Baskı/Yayın Bilgisi 2020Metin -
5
Minimal residual disease detection by multicolor flow cytometry in cryopreserved ovarian tissue from leukemia patients Yazar: Zver, Tristan, Frontczak, Sophie, Poirot, Catherine, Rives-Feraille, Aurélie, Leroy-Martin, Brigitte, Koscinski, Isabelle, Arbez-Gindre, Francine, Garnache-Ottou, Francine, Roux, Christophe, Amiot, Clotilde
Baskı/Yayın Bilgisi 2022Metin -
6
Multiorgan and Vascular Tropism of SARS-CoV-2 Yazar: 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
Baskı/Yayın Bilgisi 2022Metin -
7
Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia Yazar: 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
Baskı/Yayın Bilgisi 2007Metin -
8
DPY19L2 Deletion as a Major Cause of Globozoospermia Yazar: 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
Baskı/Yayın Bilgisi 2011Metin -
9
DPY19L2 Deletion as a Major Cause of Globozoospermia Yazar: 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
Baskı/Yayın Bilgisi 2011Metin -
10
A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation Yazar: 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.
Baskı/Yayın Bilgisi 2011Metin -
11
A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients Yazar: 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.
Baskı/Yayın Bilgisi 2018Metin -
12
Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients Yazar: 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.
Baskı/Yayın Bilgisi 2018Metin