Ngā hua rapu kaituhi

1

Loss of Gata5 in mice leads to bicuspid aortic valve mā Brigitte Laforest, Grégor Andelfinger, Mona Nemer

I whakaputaina 2011

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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I tiakina i:
2

Genetic testing in congenital heart disease: A clinical approach mā Marie Chaix, Grégor Andelfinger, Paul Khairy

I whakaputaina 2016

Whiwhi kuputuhi katoa
Revisão

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I tiakina i:
3

The expanding phenotypes of cohesinopathies: one ring to rule them all! mā Jessica Piché, Patrick van Vliet, Michel Pucéat, Grégor Andelfinger

I whakaputaina 2019

Whiwhi kuputuhi katoa
Revisão

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4

Role of Epigenetics in Cardiac Development and Congenital Diseases mā Thomas Moore‐Morris, Patrick van Vliet, Grégor Andelfinger, Michel Pucéat

I whakaputaina 2018

Whiwhi kuputuhi katoa
Revisão

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5

New prospectives on treatment opportunities in <scp>RASopathies</scp> mā Bruce D. Gelb, Marielle E. Yohe, Cordula M. Wolf, Grégor Andelfinger

I whakaputaina 2022

Whiwhi kuputuhi katoa
Revisão

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6

Age-Dependent Recombination Rates in Human Pedigrees mā Julie Hussin, Marie‐Hélène Roy‐Gagnon, Roxanne Gendron, Grégor Andelfinger, Philip Awadalla

I whakaputaina 2011

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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7

Bicuspid aortic valve is heritable mā Linda Cripe, Grégor Andelfinger, Lisa J. Martin, Kerry A. Shooner, D. Woodrow Benson

I whakaputaina 2004

Whiwhi kuputuhi katoa
Artigo

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8

The Kruppel-like transcription factor KLF13 is a novel regulator of heart development mā Geneviève Lavallée, Gregor Andelfinger, Mathieu Nadeau, Chantal Lefèbvre, Georges Nemer, Marko E. Horb, Mona Nemer

I whakaputaina 2006

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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9

KCNJ2 Mutation Results in Andersen Syndrome with Sex-Specific Cardiac and Skeletal Muscle Phenotypes mā Grégor Andelfinger, Andrew R. Tapper, Richard C. Welch, Carlos G. Vanoye, Alfred L. George, D. Woodrow Benson

I whakaputaina 2002

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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10

Prenatal Head Growth and White Matter Injury in Hypoplastic Left Heart Syndrome mā Robert B. Hinton, Grégor Andelfinger, Priya Sekar, Andrea C. Hinton, Roxanne Gendron, Erik Michelfelder, Yves Robitaille, D. Woodrow Benson

I whakaputaina 2008

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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11

Genetic interaction between members of the Vangl family causes neural tube defects in mice mā Elena Torban, Anne‐Marie Patenaude, Séverine Leclerc, Staci M. Rakowiecki, Susan A. Gauthier, Grégor Andelfinger, Douglas J. Epstein, Philippe Gros

I whakaputaina 2008

Whiwhi kuputuhi katoa
Artigo

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12

An endocardial pathway involving Tbx5, Gata4, and Nos3 required for atrial septum formation mā Mathieu Nadeau, Romain O. Georges, Brigitte Laforest, Abir Yamak, Chantal Lefèbvre, Janie Beauregard, Pierre Paradis, Benoit G. Bruneau, Grégor Andelfinger, Mona Nemer

I whakaputaina 2010

Whiwhi kuputuhi katoa
Artigo

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13

Functional Zebrafish Studies Based on Human Genotyping Point to Netrin-1 as a Link Between Aberrant Cardiovascular Development and Thyroid Dysgenesis mā Robert Opitz, Marc‐Phillip Hitz, Isabelle Vandernoot, Achim Trubiroha, Rasha Abu‐Khudir, Mark E. Samuels, Valérie Désilets, Sabine Costagliola, Grégor Andelfinger, Johnny Deladoëy

I whakaputaina 2014

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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14

Hypertrophic Cardiomyopathy in Noonan Syndrome Treated by MEK-Inhibition mā Grégor Andelfinger, Christopher Marquis, Marie‐Josée Raboisson, Yves Théorêt, Stephan Waldmüller, G. Wiegand, Bruce D. Gelb, Martin Zenker, Marie‐Ange Delrue, Michael Hofbeck

I whakaputaina 2019

Whiwhi kuputuhi katoa
Carta

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15

Characterization of PGE<sub>2</sub>receptors in fetal and newborn lamb ductus arteriosus mā Asmàa Bouayad, Hiroki Kajino, Nahid Waleh, Jean‐Claude Fouron, Grégor Andelfinger, Daya R. Varma, Amanda Skoll, Alejandro Vázquez, Fernand Gobeil, Ronald I. Clyman, Sylvain Chemtob

I whakaputaina 2001

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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16

Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease mā Christoph Preuß, M. Capredon, Florian Wünnemann, Philippe Chétaille, Andrea Prince, Béatrice Godard, Séverine Leclerc, Nara Sobreira, Hua Ling, Philip Awadalla, Maryse Thibeault, Paul Khairy, Mark E. Samuels, Grégor Andelfinger

I whakaputaina 2016

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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17

Specialized endothelial tip cells guide neuroretina vascularization and blood-retina-barrier formation mā Georgia Zarkada, Joel P. Howard, Xue Xiao, Hyojin Park, Mathilde Bizou, Séverine Leclerc, Steffen E. Künzel, Blanche Boisseau, Jinyu Li, Gaël Cagnone, Jean Sébastien Joyal, Grégor Andelfinger, Anne Eichmann, Alexandre Dubrac

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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18

eNOS controls angiogenic sprouting and retinal neovascularization through the regulation of endothelial cell polarity mā Tracy L. Smith, Malika Oubaha, Gaël Cagnone, Cécile Boscher, Jin Sung Kim, Yassine El Bakkouri, Ying Zhang, Rony Chidiac, Jeanne Corriveau, Chantal Delisle, Grégor Andelfinger, Przemysław Sapieha, Jean‐Sébastien Joyal, Jean‐Philippe Gratton

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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19

Acan downregulation in parvalbumin GABAergic cells reduces spontaneous recovery of fear memories mā Marisol Lavertu-Jolin, Bidisha Chattopadhyaya, Pegah Chehrazi, Denise Carrier, Florian Wünnemann, Séverine Leclerc, Félix Dumouchel, Derek N. Robertson, Hicham Affia, Kamal Saba, Vijaya Gopal, Anant B. Patel, Grégor Andelfinger, Graciela Piñeyro, Graziella Di Cristo

I whakaputaina 2023

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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20

Electrocardiographic Features in Andersen-Tawil Syndrome Patients With <i>KCNJ2</i> Mutations mā Li Zhang, D. Woodrow Benson, Martin Tristani‐Firouzi, Louis J. Ptáček, Rabi Tawil, Peter J. Schwartz, Alfred L. George, Minoru Horie, Grégor Andelfinger, Gregory L. Snow, Ying‐Hui Fu, Michael J. Ackerman, G. Michael Vincent

I whakaputaina 2005

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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Ngā hua rapu - Grégor Andelfinger

Loss of Gata5 in mice leads to bicuspid aortic valve mā Brigitte Laforest, Grégor Andelfinger, Mona Nemer

Genetic testing in congenital heart disease: A clinical approach mā Marie Chaix, Grégor Andelfinger, Paul Khairy

The expanding phenotypes of cohesinopathies: one ring to rule them all! mā Jessica Piché, Patrick van Vliet, Michel Pucéat, Grégor Andelfinger

Role of Epigenetics in Cardiac Development and Congenital Diseases mā Thomas Moore‐Morris, Patrick van Vliet, Grégor Andelfinger, Michel Pucéat

New prospectives on treatment opportunities in <scp>RASopathies</scp> mā Bruce D. Gelb, Marielle E. Yohe, Cordula M. Wolf, Grégor Andelfinger

Age-Dependent Recombination Rates in Human Pedigrees mā Julie Hussin, Marie‐Hélène Roy‐Gagnon, Roxanne Gendron, Grégor Andelfinger, Philip Awadalla

Bicuspid aortic valve is heritable mā Linda Cripe, Grégor Andelfinger, Lisa J. Martin, Kerry A. Shooner, D. Woodrow Benson

The Kruppel-like transcription factor KLF13 is a novel regulator of heart development mā Geneviève Lavallée, Gregor Andelfinger, Mathieu Nadeau, Chantal Lefèbvre, Georges Nemer, Marko E. Horb, Mona Nemer

KCNJ2 Mutation Results in Andersen Syndrome with Sex-Specific Cardiac and Skeletal Muscle Phenotypes mā Grégor Andelfinger, Andrew R. Tapper, Richard C. Welch, Carlos G. Vanoye, Alfred L. George, D. Woodrow Benson

Prenatal Head Growth and White Matter Injury in Hypoplastic Left Heart Syndrome mā Robert B. Hinton, Grégor Andelfinger, Priya Sekar, Andrea C. Hinton, Roxanne Gendron, Erik Michelfelder, Yves Robitaille, D. Woodrow Benson

Genetic interaction between members of the Vangl family causes neural tube defects in mice mā Elena Torban, Anne‐Marie Patenaude, Séverine Leclerc, Staci M. Rakowiecki, Susan A. Gauthier, Grégor Andelfinger, Douglas J. Epstein, Philippe Gros

An endocardial pathway involving Tbx5, Gata4, and Nos3 required for atrial septum formation mā Mathieu Nadeau, Romain O. Georges, Brigitte Laforest, Abir Yamak, Chantal Lefèbvre, Janie Beauregard, Pierre Paradis, Benoit G. Bruneau, Grégor Andelfinger, Mona Nemer

Hypertrophic Cardiomyopathy in Noonan Syndrome Treated by MEK-Inhibition mā Grégor Andelfinger, Christopher Marquis, Marie‐Josée Raboisson, Yves Théorêt, Stephan Waldmüller, G. Wiegand, Bruce D. Gelb, Martin Zenker, Marie‐Ange Delrue, Michael Hofbeck

Characterization of PGE<sub>2</sub>receptors in fetal and newborn lamb ductus arteriosus mā Asmàa Bouayad, Hiroki Kajino, Nahid Waleh, Jean‐Claude Fouron, Grégor Andelfinger, Daya R. Varma, Amanda Skoll, Alejandro Vázquez, Fernand Gobeil, Ronald I. Clyman, Sylvain Chemtob

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