1 - 10 toradh á dtaispeáint as 10 toradh san iomlán ar an gcuardach 'Javad NADAF', am iarratais: 0.04s Beachtaigh na torthaí
  1. 1
    Double Heterozygosity of BRCA2 and STK11 in Familial Breast Cancer Detected by Exome Sequencing

    Double Heterozygosity of BRCA2 and STK11 in Familial Breast Cancer Detected by Exome Sequencing de réir Mojgan ATAEI-KACHOUEI, Javad NADAF, Mohammad Taghi AKBARI, Morteza ATRI, Jacek MAJEWSKI, Yasser RIAZALHOSSEINI, Masoud GARSHASBI

    Foilsithe / Cruthaithe 2015-10-01
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  2. 2
    PRAME protein expression in DICER1‐related tumours

    PRAME protein expression in DICER1‐related tumours de réir Paul S Thorner, Anne‐Sophie Chong, Javad Nadaf, Naciba Benlimame, Paula Marrano, Rose Chami, Lili Fu, William D Foulkes

    Foilsithe / Cruthaithe 2022-05-01
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  3. 3
    PRAME protein expression in DICER1‐related tumours

    PRAME protein expression in DICER1‐related tumours de réir Paul S Thorner, Anne‐Sophie Chong, Javad Nadaf, Naciba Benlimame, Paula Marrano, Rose Chami, Lili Fu, William D Foulkes

    Foilsithe / Cruthaithe 2022-11-01
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  4. 4
    Exome sequencing study of partial agenesis of the corpus callosum in men with developmental delay, epilepsy, and microcephaly

    Exome sequencing study of partial agenesis of the corpus callosum in men with developmental delay, epilepsy, and microcephaly de réir Jolyane Meloche, Vanessa Brunet, Pierre‐Alexandre Gagnon, Marie‐Ève Lavoie, Jean‐Benoît Bouchard, Javad Nadaf, Jacek Majewski, Charles Morin, Catherine Laprise

    Foilsithe / Cruthaithe 2020-01-01
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  5. 5
    Identity and nature of neural stem cells in the adult human subventricular zone

    Identity and nature of neural stem cells in the adult human subventricular zone de réir Salma Baig, Javad Nadaf, Redouane Allache, Phuong U. Le, Michael Luo, Annisa Djedid, Andriniaina Nkili-Meyong, Maryam Safisamghabadi, Alex Prat, Jack Antel, Marie-Christine Guiot, Kevin Petrecca

    Foilsithe / Cruthaithe 2024-04-01
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  6. 6
    Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features

    Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features de réir Mariam Almuriekhi, Takafumi Shintani, Somayyeh Fahiminiya, Akihiro Fujikawa, Kazuya Kuboyama, Yasushi Takeuchi, Zafar Nawaz, Javad Nadaf, Hussein Kamel, Abu Khadija Kitam, Zaineddin Samiha, Laila Mahmoud, Tawfeg Ben-Omran, Jacek Majewski, Masaharu Noda

    Foilsithe / Cruthaithe 2015-03-01
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  7. 7
    Correction: Detection of a Cis eQTL Controlling Gene Expression Leads to the Identification of a QTG for Chicken Breast Meat Color.

    Correction: Detection of a Cis eQTL Controlling Gene Expression Leads to the Identification of a QTG for Chicken Breast Meat Color. de réir Elisabeth Le Bihan-Duval, Javad Nadaf, Cécile Berri, Frédérique Pitel, Benoît Graulet, Estelle Godet, Sophie Y. Leroux, Olivier Demeure, Sandrine Lagarrigue, Cécile Duby, Larry A. Cogburn, Catherine M. Beaumont, Michel J. Duclos

    Foilsithe / Cruthaithe 2011-01-01
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  8. 8
    Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy

    Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy de réir Charles P. Couturier, Shamini Ayyadhury, Phuong U. Le, Javad Nadaf, Jean Monlong, Gabriele Riva, Redouane Allache, Salma Baig, Xiaohua Yan, Mathieu Bourgey, Changseok Lee, Yu Chang David Wang, V. Wee Yong, Marie-Christine Guiot, Hamed Najafabadi, Bratislav Misic, Jack Antel, Guillaume Bourque, Jiannis Ragoussis, Kevin Petrecca

    Foilsithe / Cruthaithe 2020-07-01
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  9. 9
    Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients

    Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients de réir Jean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurélie Robert, Isabelle Koscinski, Isabelle Gastin, Pierre Filhine-Tresarrieu, Mihaela Pupavac, Alison Brebner, David Watkins, Tomi Pastinen, Alexandre Montpetit, Fadi Hariri, David Tregouët, Benjamin A Raby, Wendy K. Chung, Pierre-Emmanuel Morange, D. Sean Froese, Matthias R. Baumgartner, Jean-François Benoist, Can Ficicioglu, Virginie Marchand, Yuri Motorin, Chrystèle Bonnemains, François Feillet, Jacek Majewski, David S. Rosenblatt

    Foilsithe / Cruthaithe 2018-02-01
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  10. 10
    A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients

    A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients de réir Jean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurélie Robert, Isabelle Koscinski, Isabelle Gastin, Pierre Filhine-Tresarrieu, Mihaela Pupavac, Alison Brebner, David Watkins, Tomi Pastinen, Alexandre Montpetit, Fadi Hariri, David Tregouët, Benjamin A Raby, Wendy K. Chung, Pierre-Emmanuel Morange, D. Sean Froese, Matthias R. Baumgartner, Jean-François Benoist, Can Ficicioglu, Virginie Marchand, Yuri Motorin, Chrystèle Bonnemains, François Feillet, Jacek Majewski, David S. Rosenblatt

    Foilsithe / Cruthaithe 2018-01-01
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