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1دورية أكاديمية
المؤلفون: Gielen, Marc, Barilone, Nathalie, Corringer, Pierre-Jean
المساهمون: Récepteurs Canaux - Channel Receptors, Institut Pasteur Paris (IP)-Centre National de la Recherche Scientifique (CNRS), Sorbonne Université (SU), Financial support by the Fondation de la Recherche Médicale (grant “Équipe FRM” DEQ20140329497 to P.-J.C.) and the European Commission Research Executive Agency (Marie Sklodowska-Curie Action, Individual Fellowship 659371 to M.G., ERC Advanced Grant GA788974 Dynacotine to P.-J.C.). M.G. is grateful to the Fondation Bettencourt Schueller for their support., European Project: 659371,H2020,H2020-MSCA-IF-2014,nAChR PAM-to-gate(2015), European Project: 788974,H2020
المصدر: ISSN: 2041-1723.
مصطلحات موضوعية: MESH: Animals, MESH: Computer Simulation, MESH: Protein Conformation, MESH: Protein Subunits, MESH: Receptors, GABA-A, MESH: Synaptic Transmission, MESH: Xenopus laevis, MESH: Ion Channels, MESH: Ion Transport, MESH: Kinetics, MESH: Models, Molecular, MESH: Molecular Conformation, MESH: Mutation, MESH: Nervous System, MESH: Oocytes, [SDV]Life Sciences [q-bio]
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33097732; info:eu-repo/grantAgreement//659371/EU/Gating mechanism and pharmacological modulation of nicotinic acetylcholine receptors/nAChR PAM-to-gate; info:eu-repo/grantAgreement//788974/EU/Signal transduction and allosteric modulation of nicotinic acetylcholine receptors:from ion channel electrophysiology to atomic 3D structures/Dynacotine; pasteur-03088067; https://pasteur.hal.science/pasteur-03088067Test; https://pasteur.hal.science/pasteur-03088067/documentTest; https://pasteur.hal.science/pasteur-03088067/file/Gielen.%202020.pdfTest; PUBMED: 33097732; PUBMEDCENTRAL: PMC7585415
الإتاحة: https://doi.org/10.1038/s41467-020-19218-6Test
https://pasteur.hal.science/pasteur-03088067Test
https://pasteur.hal.science/pasteur-03088067/documentTest
https://pasteur.hal.science/pasteur-03088067/file/Gielen.%202020.pdfTest -
2دورية أكاديمية
المؤلفون: Gielen, Marc, Barilone, Nathalie, Corringer, Pierre-Jean
المساهمون: Récepteurs Canaux - Channel Receptors, Institut Pasteur Paris (IP)-Centre National de la Recherche Scientifique (CNRS), Sorbonne Université (SU), Financial support by the Fondation de la Recherche Médicale (grant “Équipe FRM” DEQ20140329497 to P.-J.C.) and the European Commission Research Executive Agency (Marie Sklodowska-Curie Action, Individual Fellowship 659371 to M.G., ERC Advanced Grant GA788974 Dynacotine to P.-J.C.). M.G. is grateful to the Fondation Bettencourt Schueller for their support., European Project: 659371,H2020,H2020-MSCA-IF-2014,nAChR PAM-to-gate(2015), European Project: 788974,H2020
المصدر: ISSN: 2041-1723.
مصطلحات موضوعية: MESH: Animals, MESH: Computer Simulation, MESH: Protein Conformation, MESH: Protein Subunits, MESH: Receptors, GABA-A, MESH: Synaptic Transmission, MESH: Xenopus laevis, MESH: Ion Channels, MESH: Ion Transport, MESH: Kinetics, MESH: Models, Molecular, MESH: Molecular Conformation, MESH: Mutation, MESH: Nervous System, MESH: Oocytes, [SDV]Life Sciences [q-bio]
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33097732; info:eu-repo/grantAgreement//659371/EU/Gating mechanism and pharmacological modulation of nicotinic acetylcholine receptors/nAChR PAM-to-gate; info:eu-repo/grantAgreement//788974/EU/Signal transduction and allosteric modulation of nicotinic acetylcholine receptors:from ion channel electrophysiology to atomic 3D structures/Dynacotine; pasteur-03088067; https://pasteur.hal.science/pasteur-03088067Test; https://pasteur.hal.science/pasteur-03088067/documentTest; https://pasteur.hal.science/pasteur-03088067/file/Gielen.%202020.pdfTest; PUBMED: 33097732; PUBMEDCENTRAL: PMC7585415
الإتاحة: https://doi.org/10.1038/s41467-020-19218-6Test
https://pasteur.hal.science/pasteur-03088067Test
https://pasteur.hal.science/pasteur-03088067/documentTest
https://pasteur.hal.science/pasteur-03088067/file/Gielen.%202020.pdfTest -
3دورية أكاديمية
المؤلفون: Gielen, Marc, Barilone, Nathalie, Corringer, Pierre-Jean
المساهمون: Récepteurs Canaux - Channel Receptors, Centre National de la Recherche Scientifique (CNRS)-Institut Pasteur Paris, Sorbonne Université (SU), Financial support by the Fondation de la Recherche Médicale (grant “Équipe FRM” DEQ20140329497 to P.-J.C.) and the European Commission Research Executive Agency (Marie Sklodowska-Curie Action, Individual Fellowship 659371 to M.G., ERC Advanced Grant GA788974 Dynacotine to P.-J.C.). M.G. is grateful to the Fondation Bettencourt Schueller for their support., European Project: 659371,H2020,H2020-MSCA-IF-2014,nAChR PAM-to-gate(2015), European Project: 788974,H2020
المصدر: ISSN: 2041-1723.
مصطلحات موضوعية: MESH: Animals, MESH: Computer Simulation, MESH: Protein Conformation, MESH: Protein Subunits, MESH: Receptors, GABA-A, MESH: Synaptic Transmission, MESH: Xenopus laevis, MESH: Ion Channels, MESH: Ion Transport, MESH: Kinetics, MESH: Models, Molecular, MESH: Molecular Conformation, MESH: Mutation, MESH: Nervous System, MESH: Oocytes, [SDV]Life Sciences [q-bio]
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33097732; info:eu-repo/grantAgreement//659371/EU/Gating mechanism and pharmacological modulation of nicotinic acetylcholine receptors/nAChR PAM-to-gate; info:eu-repo/grantAgreement//788974/EU/Signal transduction and allosteric modulation of nicotinic acetylcholine receptors:from ion channel electrophysiology to atomic 3D structures/Dynacotine; pasteur-03088067; https://hal-pasteur.archives-ouvertes.fr/pasteur-03088067Test; https://hal-pasteur.archives-ouvertes.fr/pasteur-03088067/documentTest; https://hal-pasteur.archives-ouvertes.fr/pasteur-03088067/file/Gielen.%202020.pdfTest; PUBMED: 33097732; PUBMEDCENTRAL: PMC7585415
الإتاحة: https://doi.org/10.1038/s41467-020-19218-6Test
https://hal-pasteur.archives-ouvertes.fr/pasteur-03088067Test
https://hal-pasteur.archives-ouvertes.fr/pasteur-03088067/documentTest
https://hal-pasteur.archives-ouvertes.fr/pasteur-03088067/file/Gielen.%202020.pdfTest -
4دورية أكاديمية
المؤلفون: Haccard, Olivier, Ciardo, Diletta, Narrissamprakash, Hemalatha, Bronchain, Odile, Kumagai, Akiko, Dunphy, William, Goldar, Arach, Marheineke, Kathrin
المساهمون: Institut de Biologie Intégrative de la Cellule (I2BC), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Institut de biologie de l'ENS Paris (IBENS), Département de Biologie - ENS Paris, École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Institut des Neurosciences Paris-Saclay (NeuroPSI), Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, 91125
المصدر: ISSN: 2399-3642 ; Communications Biology ; https://hal.science/hal-04223559Test ; Communications Biology, 2023, 6 (1), pp.788. ⟨10.1038/s42003-023-05172-8⟩.
مصطلحات موضوعية: MESH: Animals, MESH: Cell Cycle, MESH: Cell Cycle Proteins, MESH: Chromatin, MESH: Replication Origin, MESH: Xenopus laevis, [SDV]Life Sciences [q-bio]
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37516798; hal-04223559; https://hal.science/hal-04223559Test; PUBMED: 37516798; PUBMEDCENTRAL: PMC10387115
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5دورية أكاديمية
المؤلفون: Gordon, Christopher, Xue, Shifeng, Yigit, Gökhan, Filali, Hicham, Chen, Kelan, Rosin, Nadine, Yoshiura, Koh-Ichiro, Oufadem, Myriam, Beck, Tamara J, Mcgowan, Ruth, Magee, Alex C, Altmüller, Janine, Dion, Camille, Thiele, Holger, Gurzau, Alexandra D, Nurnberg, Peter, Meschede, Dieter, Mühlbauer, Wolfgang, Okamoto, Nobuhiko, Varghese, Vinod, Irving, Rachel, Sigaudy, Sabine, Williams, Denise, Ahmed, S Faisal, Bonnard, Carine, Kong, Mung Kei, Ratbi, Ilham, Fejjal, Nawfal, Fikri, Meriem, Elalaoui, Siham Chafai, Reigstad, Hallvard, Bole-Feysot, Christine, Nitschke, Patrick, Ragge, Nicola, Lévy, Nicolas, Tunçbilek, Gökhan, Teo, Audrey S M, Cunningham, Michael L, Sefiani, Abdelaziz, Kayserili, Hulya, Murphy, James M, Chatdokmaiprai, Chalermpong, Hillmer, Axel M, Wattanasirichaigoon, Duangrurdee, Lyonnet, Stanislas, Magdinier, Frédérique, Javed, Asif, Blewitt, Marnie E, Amiel, Jeanne, Wollnik, Bernd, Reversade, Bruno
المساهمون: Imagine - Institut des maladies génétiques (IMAGINE - U1163), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Human Genetics, Nagasaki University, Department of Clinical Genetics, Leicester Royal Infirmary, University Hospitals Leicester-University Hospitals Leicester, Universität zu Köln = University of Cologne, Génétique Médicale et Génomique Fonctionnelle (GMGF), Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Département de génétique médicale Hôpital de la Timone - APHM, Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Plate Forme Paris Descartes de Bioinformatique (BIP-D), Université Paris Descartes - Paris 5 (UPD5), Department of Medical Genetics, Istanbul University, Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement (Inserm U781), ANR-10-IAHU-0001,Imagine,Institut Hospitalo-Universitaire Imagine(2010)
المصدر: ISSN: 1061-4036.
مصطلحات موضوعية: Bosma arhinia microphthalmia syndrome, SMCHD1, nasal development, FSHD, Epigenetics, Medical genetics, Genetic linkage study, Embryology, MESH: Animals, MESH: Cell Line, MESH: Female, MESH: Genetic Predisposition to Disease, MESH: Humans, MESH: Male, MESH: Mice, Inbred C57BL, MESH: Microphthalmos, MESH: Muscular Dystrophy, Facioscapulohumeral, MESH: Mutation, Missense, MESH: Nose, MESH: Xenopus laevis, MESH: Child, Preschool, MESH: Choanal Atresia, MESH: Chromosomal Proteins, Non-Histone, MESH: Epigenesis, Genetic
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28067911; hal-01617529; https://hal.science/hal-01617529Test; https://hal.science/hal-01617529/documentTest; https://hal.science/hal-01617529/file/ng.3765.pdfTest; PUBMED: 28067911
الإتاحة: https://doi.org/10.1038/ng.3765Test
https://hal.science/hal-01617529Test
https://hal.science/hal-01617529/documentTest
https://hal.science/hal-01617529/file/ng.3765.pdfTest -
6دورية أكاديمية
المؤلفون: Gordon, Christopher, Xue, Shifeng, Yigit, Gökhan, Filali, Hicham, Chen, Kelan, Rosin, Nadine, Yoshiura, Koh-Ichiro, Oufadem, Myriam, Beck, Tamara J, Mcgowan, Ruth, Magee, Alex C, Altmüller, Janine, Dion, Camille, Thiele, Holger, Gurzau, Alexandra D, Nurnberg, Peter, Meschede, Dieter, Mühlbauer, Wolfgang, Okamoto, Nobuhiko, Varghese, Vinod, Irving, Rachel, Sigaudy, Sabine, Williams, Denise, Ahmed, S Faisal, Bonnard, Carine, Kong, Mung Kei, Ratbi, Ilham, Fejjal, Nawfal, Fikri, Meriem, Elalaoui, Siham Chafai, Reigstad, Hallvard, Bole-Feysot, Christine, Nitschke, Patrick, Ragge, Nicola, Lévy, Nicolas, Tunçbilek, Gökhan, Teo, Audrey S M, Cunningham, Michael L, Sefiani, Abdelaziz, Kayserili, Hulya, Murphy, James M, Chatdokmaiprai, Chalermpong, Hillmer, Axel M, Wattanasirichaigoon, Duangrurdee, Lyonnet, Stanislas, Magdinier, Frédérique, Javed, Asif, Blewitt, Marnie E, Amiel, Jeanne, Wollnik, Bernd, Reversade, Bruno
المساهمون: Imagine - Institut des maladies génétiques (IMAGINE - U1163), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Human Genetics, Nagasaki University, Department of Clinical Genetics, Leicester Royal Infirmary, University Hospitals Leicester-University Hospitals Leicester, Universität zu Köln = University of Cologne, Génétique Médicale et Génomique Fonctionnelle (GMGF), Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Département de génétique médicale Hôpital de la Timone - APHM, Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Plate Forme Paris Descartes de Bioinformatique (BIP-D), Université Paris Descartes - Paris 5 (UPD5), Department of Medical Genetics, Istanbul University, Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement (Inserm U781), ANR-10-IAHU-0001,Imagine,Institut Hospitalo-Universitaire Imagine(2010)
المصدر: ISSN: 1061-4036.
مصطلحات موضوعية: Bosma arhinia microphthalmia syndrome, SMCHD1, nasal development, FSHD, Epigenetics, Medical genetics, Genetic linkage study, Embryology, MESH: Animals, MESH: Cell Line, MESH: Female, MESH: Genetic Predisposition to Disease, MESH: Humans, MESH: Male, MESH: Mice, Inbred C57BL, MESH: Microphthalmos, MESH: Muscular Dystrophy, Facioscapulohumeral, MESH: Mutation, Missense, MESH: Nose, MESH: Xenopus laevis, MESH: Child, Preschool, MESH: Choanal Atresia, MESH: Chromosomal Proteins, Non-Histone, MESH: Epigenesis, Genetic
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28067911; hal-01617529; https://hal.science/hal-01617529Test; https://hal.science/hal-01617529/documentTest; https://hal.science/hal-01617529/file/ng.3765.pdfTest; PUBMED: 28067911
الإتاحة: https://doi.org/10.1038/ng.3765Test
https://hal.science/hal-01617529Test
https://hal.science/hal-01617529/documentTest
https://hal.science/hal-01617529/file/ng.3765.pdfTest -
7دورية أكاديمية
المؤلفون: Gordon, Christopher, Xue, Shifeng, Yigit, Gökhan, Filali, Hicham, Chen, Kelan, Rosin, Nadine, Yoshiura, Koh-Ichiro, Oufadem, Myriam, Beck, Tamara J, Mcgowan, Ruth, Magee, Alex C, Altmüller, Janine, Dion, Camille, Thiele, Holger, Gurzau, Alexandra D, Nurnberg, Peter, Meschede, Dieter, Mühlbauer, Wolfgang, Okamoto, Nobuhiko, Varghese, Vinod, Irving, Rachel, Sigaudy, Sabine, Williams, Denise, Ahmed, S Faisal, Bonnard, Carine, Kong, Mung Kei, Ratbi, Ilham, Fejjal, Nawfal, Fikri, Meriem, Elalaoui, Siham Chafai, Reigstad, Hallvard, Bole-Feysot, Christine, Nitschke, Patrick, Ragge, Nicola, Lévy, Nicolas, Tunçbilek, Gökhan, Teo, Audrey S M, Cunningham, Michael L, Sefiani, Abdelaziz, Kayserili, Hulya, Murphy, James M, Chatdokmaiprai, Chalermpong, Hillmer, Axel M, Wattanasirichaigoon, Duangrurdee, Lyonnet, Stanislas, Magdinier, Frédérique, Javed, Asif, Blewitt, Marnie E, Amiel, Jeanne, Wollnik, Bernd, Reversade, Bruno
المساهمون: Imagine - Institut des maladies génétiques (IMAGINE - U1163), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Human Genetics, Nagasaki University, Department of Clinical Genetics, Leicester Royal Infirmary, University Hospitals Leicester-University Hospitals Leicester, Universität zu Köln = University of Cologne, Génétique Médicale et Génomique Fonctionnelle (GMGF), Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Département de génétique médicale Hôpital de la Timone - APHM, Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Plate Forme Paris Descartes de Bioinformatique (BIP-D), Université Paris Descartes - Paris 5 (UPD5), Department of Medical Genetics, Istanbul University, Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement (Inserm U781), ANR-10-IAHU-0001,Imagine,Institut Hospitalo-Universitaire Imagine(2010)
المصدر: ISSN: 1061-4036.
مصطلحات موضوعية: Bosma arhinia microphthalmia syndrome, SMCHD1, nasal development, FSHD, Epigenetics, Medical genetics, Genetic linkage study, Embryology, MESH: Animals, MESH: Cell Line, MESH: Female, MESH: Genetic Predisposition to Disease, MESH: Humans, MESH: Male, MESH: Mice, Inbred C57BL, MESH: Microphthalmos, MESH: Muscular Dystrophy, Facioscapulohumeral, MESH: Mutation, Missense, MESH: Nose, MESH: Xenopus laevis, MESH: Child, Preschool, MESH: Choanal Atresia, MESH: Chromosomal Proteins, Non-Histone, MESH: Epigenesis, Genetic
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28067911; hal-01617529; https://hal.science/hal-01617529Test; https://hal.science/hal-01617529/documentTest; https://hal.science/hal-01617529/file/ng.3765.pdfTest; PUBMED: 28067911
الإتاحة: https://doi.org/10.1038/ng.3765Test
https://hal.science/hal-01617529Test
https://hal.science/hal-01617529/documentTest
https://hal.science/hal-01617529/file/ng.3765.pdfTest -
8دورية أكاديمية
المؤلفون: Gordon, Christopher, Xue, Shifeng, Yigit, Gökhan, Filali, Hicham, Chen, Kelan, Rosin, Nadine, Yoshiura, Koh-Ichiro, Oufadem, Myriam, Beck, Tamara J, McGowan, Ruth, Magee, Alex C, Altmüller, Janine, Dion, Camille, Thiele, Holger, Gurzau, Alexandra D, Nurnberg, Peter, Meschede, Dieter, Mühlbauer, Wolfgang, Okamoto, Nobuhiko, Varghese, Vinod, Irving, Rachel, Sigaudy, Sabine, Williams, Denise, Ahmed, S Faisal, Bonnard, Carine, Kong, Mung Kei, Ratbi, Ilham, Fejjal, Nawfal, Fikri, Meriem, Elalaoui, Siham Chafai, Reigstad, Hallvard, Bole-Feysot, Christine, Nitschke, Patrick, Ragge, Nicola, Lévy, Nicolas, Tunçbilek, Gökhan, Teo, Audrey S M, Cunningham, Michael L, Sefiani, Abdelaziz, Kayserili, Hulya, Murphy, James M, Chatdokmaiprai, Chalermpong, Hillmer, Axel M, Wattanasirichaigoon, Duangrurdee, Lyonnet, Stanislas, Magdinier, Frédérique, Javed, Asif, Blewitt, Marnie E, Amiel, Jeanne, Wollnik, Bernd, Reversade, Bruno
المساهمون: Imagine - Institut des maladies génétiques (IMAGINE - U1163), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Human Genetics, Nagasaki University, Department of Clinical Genetics, Leicester Royal Infirmary, University Hospitals Leicester-University Hospitals Leicester, Universität zu Köln, Génétique Médicale et Génomique Fonctionnelle (GMGF), Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Département de génétique médicale Hôpital de la Timone - APHM, Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Plate Forme Paris Descartes de Bioinformatique (BIP-D), Université Paris Descartes - Paris 5 (UPD5), Department of Medical Genetics, Istanbul University, Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement (Inserm U781)
المصدر: ISSN: 1061-4036.
مصطلحات موضوعية: Medical genetics, Genetic linkage study, Embryology, Epigenetics, FSHD, nasal development, SMCHD1, Bosma arhinia microphthalmia syndrome, MESH: Animals, MESH: Cell Line, MESH: Female, MESH: Genetic Predisposition to Disease, MESH: Humans, MESH: Male, MESH: Mice, Inbred C57BL, MESH: Microphthalmos, MESH: Muscular Dystrophy, Facioscapulohumeral, MESH: Mutation, Missense, MESH: Nose, MESH: Xenopus laevis, MESH: Child, Preschool, MESH: Choanal Atresia, MESH: Chromosomal Proteins, Non-Histone, MESH: Epigenesis, Genetic
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28067911; hal-01617529; https://hal.archives-ouvertes.fr/hal-01617529Test; https://hal.archives-ouvertes.fr/hal-01617529/documentTest; https://hal.archives-ouvertes.fr/hal-01617529/file/ng.3765.pdfTest; PUBMED: 28067911
الإتاحة: https://doi.org/10.1038/ng.3765Test
https://hal.archives-ouvertes.fr/hal-01617529Test
https://hal.archives-ouvertes.fr/hal-01617529/documentTest
https://hal.archives-ouvertes.fr/hal-01617529/file/ng.3765.pdfTest -
9دورية أكاديمية
المؤلفون: Gordon, Christopher, Xue, Shifeng, Yigit, Gökhan, Filali, Hicham, Chen, Kelan, Rosin, Nadine, Yoshiura, Koh-Ichiro, Oufadem, Myriam, Beck, Tamara J, Mcgowan, Ruth, Magee, Alex C, Altmüller, Janine, Dion, Camille, Thiele, Holger, Gurzau, Alexandra D, Nurnberg, Peter, Meschede, Dieter, Mühlbauer, Wolfgang, Okamoto, Nobuhiko, Varghese, Vinod, Irving, Rachel, Sigaudy, Sabine, Williams, Denise, Ahmed, S Faisal, Bonnard, Carine, Kong, Mung Kei, Ratbi, Ilham, Fejjal, Nawfal, Fikri, Meriem, Elalaoui, Siham Chafai, Reigstad, Hallvard, Bole-Feysot, Christine, Nitschke, Patrick, Ragge, Nicola, Lévy, Nicolas, Tunçbilek, Gökhan, Teo, Audrey S M, Cunningham, Michael L, Sefiani, Abdelaziz, Kayserili, Hulya, Murphy, James M, Chatdokmaiprai, Chalermpong, Hillmer, Axel M, Wattanasirichaigoon, Duangrurdee, Lyonnet, Stanislas, Magdinier, Frédérique, Javed, Asif, Blewitt, Marnie E, Amiel, Jeanne, Wollnik, Bernd, Reversade, Bruno
المساهمون: Imagine - Institut des maladies génétiques (IMAGINE - U1163), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Human Genetics, Nagasaki University, Department of Clinical Genetics, Leicester Royal Infirmary, University Hospitals Leicester-University Hospitals Leicester, Universität zu Köln = University of Cologne, Génétique Médicale et Génomique Fonctionnelle (GMGF), Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Département de génétique médicale Hôpital de la Timone - APHM, Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Plate Forme Paris Descartes de Bioinformatique (BIP-D), Université Paris Descartes - Paris 5 (UPD5), Department of Medical Genetics, Istanbul University, Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement (Inserm U781), ANR-10-IAHU-0001,Imagine,Institut Hospitalo-Universitaire Imagine(2010)
المصدر: ISSN: 1061-4036.
مصطلحات موضوعية: Bosma arhinia microphthalmia syndrome, SMCHD1, nasal development, FSHD, Epigenetics, Medical genetics, Genetic linkage study, Embryology, MESH: Animals, MESH: Cell Line, MESH: Female, MESH: Genetic Predisposition to Disease, MESH: Humans, MESH: Male, MESH: Mice, Inbred C57BL, MESH: Microphthalmos, MESH: Muscular Dystrophy, Facioscapulohumeral, MESH: Mutation, Missense, MESH: Nose, MESH: Xenopus laevis, MESH: Child, Preschool, MESH: Choanal Atresia, MESH: Chromosomal Proteins, Non-Histone, MESH: Epigenesis, Genetic
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28067911; hal-01617529; https://hal.science/hal-01617529Test; https://hal.science/hal-01617529/documentTest; https://hal.science/hal-01617529/file/ng.3765.pdfTest; PUBMED: 28067911
الإتاحة: https://doi.org/10.1038/ng.3765Test
https://hal.science/hal-01617529Test
https://hal.science/hal-01617529/documentTest
https://hal.science/hal-01617529/file/ng.3765.pdfTest -
10دورية أكاديمية
المؤلفون: Hoffmann, Céline, Mazari, Elsa, Lallet, Sylvie, Le Borgne, Roland, Marchi, Valérie, Gosse, Charlie, Gueroui, Zoher
المساهمون: Processus d'Activation Sélective par Transfert d'Energie Uni-électronique ou Radiatif (UMR 8640) (PASTEUR), Université Pierre et Marie Curie - Paris 6 (UPMC)-Département de Chimie - ENS Paris, École normale supérieure - Paris (ENS-PSL), Université Paris Sciences et Lettres (PSL)-Université Paris Sciences et Lettres (PSL)-École normale supérieure - Paris (ENS-PSL), Université Paris Sciences et Lettres (PSL)-Université Paris Sciences et Lettres (PSL)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de photonique et de nanostructures (LPN), Centre National de la Recherche Scientifique (CNRS), Institut de Génétique et Développement de Rennes (IGDR), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Institut des Sciences Chimiques de Rennes (ISCR), Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)
المصدر: ISSN: 1748-3387.
مصطلحات موضوعية: MESH: Animals, MESH: Cell Cycle Proteins, MESH: ran GTP-Binding Protein, MESH: Cell Differentiation, MESH: Cell Nucleus, MESH: Cytoskeleton, MESH: Guanine Nucleotide Exchange Factors, MESH: Magnetite Nanoparticles, MESH: Nuclear Proteins, MESH: Signal Transduction, MESH: Xenopus laevis, [SDV.GEN]Life Sciences [q-bio]/Genetics
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23334169; inserm-00869559; https://inserm.hal.science/inserm-00869559Test; PUBMED: 23334169
