Výsledky vyhledávání - Abdelkader Heddar
- Zobrazuji výsledky 1 - 4 z 4
-
1
Homozygous hypomorphic <i>BRCA2</i> variant in primary ovarian insufficiency without cancer or Fanconi anaemia trait Autor Sandrine Caburet, Abdelkader Heddar, Elodie Dardillac, H. Creux, Marie Lambert, Sébastien Messiaen, Sophie Tourpin, Gabriel Livera, Bernard S. López, Micheline Misrahi
Vydáno 2020Artigo -
2
Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency Autor Ilpo Huhtaniemi, Outi Hovatta, Antonio La Marca, Gabriel Livera, Danielle Monniaux, Luca Persani, Abdelkader Heddar, Katarzyna Jarząbek, Triin Laisk-Podar, Andres Salumets, Juha S. Tapanainen, Reiner A. Veitia, Jenny A. Visser, Peter Wieacker, Sławomir Wołczyński, Micheline Misrahi
Vydáno 2018Revisão -
3
Genetic Landscape of a Large Cohort of Primary Ovarian Insufficiency: New Genes and Pathways and Implications for Personalized Medicine Autor Abdelkader Heddar, Çağrı Oğur, Sabrina Corrêa da Costa, Inès Braham, Line Billaud-Rist, Necati Findlinki, Claire Bénéteau, Rachel Reynaud, Khaled Mahmoud, Stéphanie Legrand, Maud Marchand, Isabelle Cedrin Durnerin, Adèle Cantaloube, Maëliss Peigné, Marion Bretault, Bénédicte Dagher Hayeck, Sandrine Pérol, Céline Droumaguet, Sabri Cavkaytar, Carole Nicolas Bonne, Hanen Elloumi, Mohamed Khrouf, Charlotte Rougier Le Masle, Mélanie Fradin, Elsa Le Boette, Perrine Luigi, Anne‐Marie Guerrot, Emmanuelle Ginglinger, Amandine Zampa, Anaïs Fauconnier, Nathalie Auger, Françoise Paris, Elise Boucher, Christelle Cabrol, A. Brun, Laura Guyon, Melanie Berard, Axelle Rivière, Marion Gérard, Sylvie Odent, Brigitte Gilbert‐Dussardier, Bertrand Isidor, Juliette Piard, Laëtitia Lambert, S. Hamamah, Anne Marie Guedj, Aude Brac de la Perrière, Bertrand Godeau, H. Fernandez, Marie-Laure Raffin Sanson, Michel Polak, H. Letur, Sylvie Epelboin, Geneviève Plu‐Bureau, Sławomir Wołczyński, S. Hiéronimus, Kristiina Aittomäki, Sophie Catteau-Jonard, Micheline Misrahi
Vydáno 2022Artigo -
4
Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine Autor Abdelkader Heddar, Çağrı Oğur, Sabrina Corrêa da Costa, Inès Braham, Line Billaud-Rist, Necati Fındıklı, Claire Bénéteau, Rachel Reynaud, Khaled Mahmoud, Stéphanie Legrand, Maud Marchand, Isabelle Cédrin‐Durnerin, Adèle Cantalloube, Maëliss Peigné, Marion Bretault, Benedicte Dagher-Hayeck, Sandrine Pérol, Céline Droumaguet, Sabri Cavkaytar, Carole Nicolas-Bonne, Hanen Elloumi, Mohamed Khrouf, Charlotte Rougier-LeMasle, Mélanie Fradin, Elsa Le Boette, Perrine Luigi, Anne‐Marie Guerrot, Emmanuelle Ginglinger, Amandine Zampa, Anaïs Fauconnier, Nathalie Auger, Françoise Paris, Elise Brischoux‐Boucher, Christelle Cabrol, A. Brun, Laura Guyon, Melanie Berard, Axelle Rivière, Nicolas Gruchy, Sylvie Odent, Brigitte Gilbert‐Dussardier, Bertrand Isidor, Juliette Piard, Laëtitia Lambert, S. Hamamah, Anne Marie Guedj, Aude Brac de la Perrière, H. Fernandez, Marie‐Laure Raffin‐Sanson, Michel Polak, H. Letur, Sylvie Epelboin, Geneviève Plu‐Bureau, Sławomir Wołczyński, S. Hiéronimus, Kristiina Aittomäki, Sophie Catteau-Jonard, Micheline Misrahi
Vydáno 2022Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Bioinformatics
Internal medicine
Medicine
Phenotype
Genetic heterogeneity
Mutation
Premature ovarian insufficiency
BRCA2 Protein
Cancer
Cancer research
Cohort
Computational biology
DNA
DNA damage
DNA repair
Exome sequencing
Fanconi anemia
Genome instability
Germline mutation
Homologous recombination
Infertility
Missense mutation
Molecular genetics
Ovarian cancer
Ovarian reserve
PALB2
Personalized medicine