Hasil Pencarian - Alex V. Postma

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  1. 1
    Genetics of sinoatrial node function and heart rate disorders

    Genetics of sinoatrial node function and heart rate disorders oleh Lieve E. van der Maarel, Alex V. Postma, Vincent M. Christoffels

    Diterbitkan 2023-05-01
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  2. 2
    <em>GMDS</em> Intragenic Deletions Associate with Congenital Heart Disease including Ebstein Anomaly

    <em>GMDS</em> Intragenic Deletions Associate with Congenital Heart Disease including Ebstein Anomaly oleh Shirley M. Lo-A-Njoe, Eline A. Verberne, Lars T. van der Veken, Eric Arends, J. Peter van Tintelen, Alex V. Postma, Mieke M. van Haelst

    Diterbitkan 2023-07-01
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  3. 3
    Identifying the evolutionary building blocks of the cardiac conduction system.

    Identifying the evolutionary building blocks of the cardiac conduction system. oleh Bjarke Jensen, Bastiaan J D Boukens, Alex V Postma, Quinn D Gunst, Maurice J B van den Hoff, Antoon F M Moorman, Tobias Wang, Vincent M Christoffels

    Diterbitkan 2012-01-01
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  4. 4
    The ambiguous role of NKX2-5 mutations in thyroid dysgenesis.

    The ambiguous role of NKX2-5 mutations in thyroid dysgenesis. oleh Klaartje van Engelen, Mathilda T M Mommersteeg, Marieke J H Baars, Jan Lam, Aho Ilgun, A S Paul van Trotsenburg, Anne M J B Smets, Vincent M Christoffels, Barbara J M Mulder, Alex V Postma

    Diterbitkan 2012-01-01
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  5. 5
    Specialized impulse conduction pathway in the alligator heart

    Specialized impulse conduction pathway in the alligator heart oleh Bjarke Jensen, Bastiaan J Boukens, Dane A Crossley II, Justin Conner, Rajiv A Mohan, Karel van Duijvenboden, Alex V Postma, Christopher R Gloschat, Ruth M Elsey, David Sedmera, Igor R Efimov, Vincent M Christoffels

    Diterbitkan 2018-03-01
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  6. 6
    <i>TGFBR1</i> Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy

    <i>TGFBR1</i> Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy oleh Manal Alaamery, Nour Albesher, Fahad Alhabshan, Phil Barnett, Mohamed Salim Kabbani, Farah Chaikhouni, Aho Ilgun, Olaf R. F. Mook, Hessa Alsaif, Vincent M. Christoffels, Peter van Tintelen, Arthur A. M. Wilde, Arjan C. Houweling, Salam Massadeh, Alex V. Postma

    Diterbitkan 2023-11-01
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  7. 7
    No prominent role for complement C1-esterase inhibitor in Marfan syndrome mice

    No prominent role for complement C1-esterase inhibitor in Marfan syndrome mice oleh Stijntje Hibender, Siyu Li, Alex V Postma, Myrthe E Hoogeland, Denise Klaver, Richard B Pouw, Hans W Niessen, Antoine HG Driessen, David R Koolbergen, Carlie JM de Vries, Marieke JH Baars, Arjan C Houweling, Paul A Krijnen, Vivian de Waard

    Diterbitkan 2022-11-01
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  8. 8
    A validated heart-specific model for splice-disrupting variants in childhood heart disease

    A validated heart-specific model for splice-disrupting variants in childhood heart disease oleh Robert Lesurf, Jeroen Breckpot, Jade Bouwmeester, Nour Hanafi, Anjali Jain, Yijing Liang, Tanya Papaz, Jane Lougheed, Tapas Mondal, Mahmoud Alsalehi, Luis Altamirano-Diaz, Erwin Oechslin, Enrique Audain, Gregor Dombrowsky, Alex V. Postma, Odilia I. Woudstra, Berto J. Bouma, Marc-Phillip Hitz, Connie R. Bezzina, Gillian M. Blue, David S. Winlaw, Seema Mital

    Diterbitkan 2024-10-01
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  9. 9
    Biallelic variants in the calpain regulatory subunit CAPNS1 cause pulmonary arterial hypertension

    Biallelic variants in the calpain regulatory subunit CAPNS1 cause pulmonary arterial hypertension oleh Alex V. Postma, Christina K. Rapp, Katrin Knoflach, Alexander E. Volk, Johannes R. Lemke, Maximilian Ackermann, Nicolas Regamey, Philipp Latzin, Lucas Celant, Samara M.A. Jansen, Harm J. Bogaard, Aho Ilgun, Mariëlle Alders, Karin Y. van Spaendonck-Zwarts, Danny Jonigk, Christoph Klein, Stefan Gräf, Christian Kubisch, Arjan C. Houweling, Matthias Griese

    Diterbitkan 2023-01-01
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  10. 10
    Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly

    Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly oleh Najim Lahrouchi, Aman George, Ilham Ratbi, Ronen Schneider, Siham C. Elalaoui, Shahida Moosa, Sanita Bharti, Ruchi Sharma, Mones Abu-Asab, Felix Onojafe, Najlae Adadi, Elisabeth M. Lodder, Fatima-Zahra Laarabi, Yassine Lamsyah, Hamza Elorch, Imane Chebbar, Alex V. Postma, Vassilios Lougaris, Alessandro Plebani, Janine Altmueller, Henriette Kyrieleis, Vardiella Meiner, Helen McNeill, Kapil Bharti, Stanislas Lyonnet, Bernd Wollnik, Alexandra Henrion-Caude, Amina Berraho, Friedhelm Hildebrandt, Connie R. Bezzina, Brian P. Brooks, Abdelaziz Sefiani

    Diterbitkan 2019-03-01
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  11. 11
    Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human

    Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human oleh Julia E. Niskanen, Åsa Ohlsson, Ingrid Ljungvall, Michaela Drögemüller, Robert F. Ernst, Dennis Dooijes, Hanneke W. M. van Deutekom, J. Peter van Tintelen, Christian J. B. Snijders Blok, Marion van Vugt, Jessica van Setten, Folkert W. Asselbergs, Aleksandra Domanjko Petrič, Milla Salonen, Sruthi Hundi, Matthias Hörtenhuber, DoGA consortium, Juha Kere, W. Glen Pyle, Jonas Donner, Alex V. Postma, Tosso Leeb, Göran Andersson, Marjo K. Hytönen, Jens Häggström, Maria Wiberg, Jana Friederich, Jenny Eberhard, Magdalena Harakalova, Frank G. van Steenbeek, Gerhard Wess, Hannes Lohi

    Diterbitkan 2023-09-01
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  12. 12
    Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.

    Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. oleh Enrique Audain, Anna Wilsdon, Jeroen Breckpot, Jose M G Izarzugaza, Tomas W Fitzgerald, Anne-Karin Kahlert, Alejandro Sifrim, Florian Wünnemann, Yasset Perez-Riverol, Hashim Abdul-Khaliq, Mads Bak, Anne S Bassett, D Woodrow Benson, Felix Berger, Ingo Daehnert, Koenraad Devriendt, Sven Dittrich, Piers Ef Daubeney, Vidu Garg, Karl Hackmann, Kirstin Hoff, Philipp Hofmann, Gregor Dombrowsky, Thomas Pickardt, Ulrike Bauer, Bernard D Keavney, Sabine Klaassen, Hans-Heiner Kramer, Christian R Marshall, Dianna M Milewicz, Scott Lemaire, Joseph S Coselli, Michael E Mitchell, Aoy Tomita-Mitchell, Siddharth K Prakash, Karl Stamm, Alexandre F R Stewart, Candice K Silversides, Reiner Siebert, Brigitte Stiller, Jill A Rosenfeld, Inga Vater, Alex V Postma, Almuth Caliebe, J David Brook, Gregor Andelfinger, Matthew E Hurles, Bernard Thienpont, Lars Allan Larsen, Marc-Phillip Hitz

    Diterbitkan 2021-07-01
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  13. 13
    Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.

    Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. oleh Enrique Audain, Anna Wilsdon, Jeroen Breckpot, Jose M G Izarzugaza, Tomas W Fitzgerald, Anne-Karin Kahlert, Alejandro Sifrim, Florian Wünnemann, Yasset Perez-Riverol, Hashim Abdul-Khaliq, Mads Bak, Anne S Bassett, D Woodrow Benson, Felix Berger, Ingo Daehnert, Koenraad Devriendt, Sven Dittrich, Piers Ef Daubeney, Vidu Garg, Karl Hackmann, Kirstin Hoff, Philipp Hofmann, Gregor Dombrowsky, Thomas Pickardt, Ulrike Bauer, Bernard D Keavney, Sabine Klaassen, Hans-Heiner Kramer, Christian R Marshall, Dianna M Milewicz, Scott Lemaire, Joseph S Coselli, Michael E Mitchell, Aoy Tomita-Mitchell, Siddharth K Prakash, Karl Stamm, Alexandre F R Stewart, Candice K Silversides, Reiner Siebert, Brigitte Stiller, Jill A Rosenfeld, Inga Vater, Alex V Postma, Almuth Caliebe, J David Brook, Gregor Andelfinger, Matthew E Hurles, Bernard Thienpont, Lars Allan Larsen, Marc-Phillip Hitz

    Diterbitkan 2021-09-01
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