| Year |
Citation |
Score |
| 2023 |
Bernheim S, Borgel A, Le Garrec JF, Perthame E, Desgrange A, Michel C, Guillemot L, Sart S, Baroud CN, Krezel W, Raimondi F, Bonnet D, Zaffran S, Houyel L, Meilhac SM. Identification of Greb1l as a genetic determinant of crisscross heart in mice showing torsion of the heart tube by shortage of progenitor cells. Developmental Cell. PMID 37852253 DOI: 10.1016/j.devcel.2023.09.006 |
0.797 |
|
| 2023 |
Odelin G, Faucherre A, Marchese D, Pinard A, Jaouadi H, Le Scouarnec S, Chiarelli R, Achouri Y, Faure E, Herbane M, Théron A, Avierinos JF, Jopling C, Collod-Béroud G, Rezsohazy R, ... Zaffran S, et al. Variations in the poly-histidine repeat motif of HOXA1 contribute to bicuspid aortic valve in mouse and zebrafish. Nature Communications. 14: 1543. PMID 36941270 DOI: 10.1038/s41467-023-37110-x |
0.816 |
|
| 2023 |
Petolat E, Theron A, Resseguier N, Fabre C, Norscini G, Badaoui R, Habib G, Collart F, Zaffran S, Porto A, Avierinos JF. Prognostic value of forward flow indices in primary mitral regurgitation due to mitral valve prolapse. Frontiers in Cardiovascular Medicine. 10: 1076708. PMID 36910534 DOI: 10.3389/fcvm.2023.1076708 |
0.686 |
|
| 2023 |
Jaouadi H, Jopling C, Bajolle F, Théron A, Faucherre A, Gerard H, Al Dybiat S, Ovaert C, Bonnet D, Avierinos JF, Zaffran S. Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD. Journal of Translational Medicine. 21: 160. PMID 36855159 DOI: 10.1186/s12967-023-03994-y |
0.825 |
|
| 2023 |
Zaffran S, Kraoua L, Jaouadi H. Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy. International Journal of Molecular Sciences. 24. PMID 36834774 DOI: 10.3390/ijms24043365 |
0.311 |
|
| 2023 |
Jaouadi H, Theron A, Norscini G, Avierinos JF, Zaffran S. Genetic and phenotypic continuum of HOXA genes: A case with double HOXA9/HOXA13 mutations. Molecular Medicine Reports. 27. PMID 36734258 DOI: 10.3892/mmr.2023.12946 |
0.685 |
|
| 2022 |
Jaouadi H, Théron A, Hourdain J, Martel H, Nguyen K, Habachi R, Deharo JC, Collart F, Avierinos JF, Zaffran S. Variants as Genetic Arrhythmias Triggers for Familial Bileaflet Mitral Valve Prolapse. International Journal of Molecular Sciences. 23. PMID 36430924 DOI: 10.3390/ijms232214447 |
0.699 |
|
| 2022 |
Lin X, Swedlund B, Ton MN, Ghazanfar S, Guibentif C, Paulissen C, Baudelet E, Plaindoux E, Achouri Y, Calonne E, Dubois C, Mansfield W, Zaffran S, Marioni JC, Fuks F, et al. Mesp1 controls the chromatin and enhancer landscapes essential for spatiotemporal patterning of early cardiovascular progenitors. Nature Cell Biology. 24: 1114-1128. PMID 35817961 DOI: 10.1038/s41556-022-00947-3 |
0.789 |
|
| 2022 |
Kraoua L, Jaouadi H, Allouche M, Achour A, Kaouther H, Ahmed HB, Chaker L, Maazoul F, Ouarda F, Zaffran S, M'rad R. Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndrome. Molecular Genetics & Genomic Medicine. 10: e1954. PMID 35656879 DOI: 10.1002/mgg3.1954 |
0.305 |
|
| 2022 |
Jaouadi H, Gérard H, Théron A, Collod-Béroud G, Collart F, Avierinos JF, Zaffran S. Identification of non-synonymous variations in ROBO1 and GATA5 genes in a family with bicuspid aortic valve disease. Journal of Human Genetics. PMID 35534675 DOI: 10.1038/s10038-022-01036-x |
0.681 |
|
| 2022 |
Lescroart F, Zaffran S. Single Cell Approaches to Understand the Earliest Steps in Heart Development. Current Cardiology Reports. PMID 35384547 DOI: 10.1007/s11886-022-01681-w |
0.808 |
|
| 2021 |
Khasawneh RR, Kist R, Queen R, Hussain R, Coxhead J, Schneider JE, Mohun TJ, Zaffran S, Peters H, Phillips HM, Bamforth SD. Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype. Bmc Developmental Biology. 21: 14. PMID 34615475 DOI: 10.1186/s12861-021-00245-5 |
0.329 |
|
| 2021 |
Théron A, Touil A, Résseguier N, Collod-Beroud G, Norscini G, Simoni AS, Odelin G, Habib G, Collart F, Zaffran S, Avierinos JF. Clinical insights into a tertiary care center cohort of patients with bicuspid aortic valve. The International Journal of Cardiovascular Imaging. PMID 34374902 DOI: 10.1007/s10554-021-02366-1 |
0.788 |
|
| 2021 |
Stefanovic S, Etchevers HC, Zaffran S. Outflow Tract Formation-Embryonic Origins of Conotruncal Congenital Heart Disease. Journal of Cardiovascular Development and Disease. 8. PMID 33918884 DOI: 10.3390/jcdd8040042 |
0.747 |
|
| 2020 |
MacGrogan D, Martínez-Poveda B, Desvignes JP, Fernandez-Friera L, Gomez MJ, Gil Vilariño E, Callejas Alejano S, García-Pavía P, Solis J, Lucena J, Salgado D, Collod-Béroud G, Faure E, Théron A, Torrents J, ... ... Zaffran S, et al. Identification of a peripheral blood gene signature predicting aortic valve calcification. Physiological Genomics. PMID 33044885 DOI: 10.1152/physiolgenomics.00034.2020 |
0.688 |
|
| 2020 |
Faure E, Bertrand E, Gasté A, Plaindoux E, Deplano V, Zaffran S. Side-dependent effect in the response of valve endothelial cells to bidirectional shear stress. International Journal of Cardiology. PMID 32858136 DOI: 10.1016/J.Ijcard.2020.08.074 |
0.427 |
|
| 2020 |
Stefanovic S, Laforest B, Desvignes JP, Lescroart F, Argiro L, Maurel-Zaffran C, Salgado D, Plaindoux E, De Bono C, Pazur K, Théveniau-Ruissy M, Béroud C, Puceat M, Gavalas A, Kelly RG, ... Zaffran S, et al. -dependent coordination of mouse cardiac progenitor cell patterning and differentiation. Elife. 9. PMID 32804075 DOI: 10.7554/Elife.55124 |
0.851 |
|
| 2020 |
Faucherre A, Maati HMO, Nasr N, Pinard A, Theron A, Odelin G, Desvignes JP, Salgado D, Collod-Béroud G, Avierinos JF, Lebon G, Zaffran S, Jopling C. Piezo1 and outflow tract and aortic valve development. Journal of Molecular and Cellular Cardiology. PMID 32251670 DOI: 10.1016/J.Yjmcc.2020.03.013 |
0.795 |
|
| 2020 |
Jaouadi H, Bouyacoub Y, Chabrak S, Kraoua L, Zaroui A, Elouej S, Nagara M, Dallali H, Delague V, Levy N, Benkhalifa R, Mechmeche R, Zaffran S, Abdelhak S. Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young. Herz. PMID 31970460 DOI: 10.1007/S00059-019-04883-1 |
0.59 |
|
| 2020 |
Stefanovic S, Laforest B, Desvignes J, Lescroart F, Argiro L, Maurel-Zaffran C, Salgado D, Plaindoux E, Bono CD, Pazur K, Théveniau-Ruissy M, Béroud C, Puceat M, Gavalas A, Kelly RG, ... Zaffran S, et al. Author response: Hox-dependent coordination of mouse cardiac progenitor cell patterning and differentiation Elife. DOI: 10.7554/Elife.55124.Sa2 |
0.434 |
|
| 2020 |
Simoni A, Theron A, Faure E, Touil A, Collart F, Zaffran S, Avierinos JF. Myxomatous degeneration of the bicuspid aortic-valve Archives of Cardiovascular Diseases Supplements. 12: 84. DOI: 10.1016/J.Acvdsp.2019.09.179 |
0.4 |
|
| 2019 |
Odelin G, Faure E, Maurel-Zaffran C, Zaffran S. Krox20 Regulates Endothelial Nitric Oxide Signaling in Aortic Valve Development and Disease. Journal of Cardiovascular Development and Disease. 6. PMID 31684048 DOI: 10.3390/Jcdd6040039 |
0.825 |
|
| 2019 |
Jaouadi H, Chehida AB, Kraoua L, Etchevers HC, Argiro L, Kasdallah N, Blibech S, Delague V, Lévy N, Tebib N, Mrad R, Abdelhak S, Benkhalifa R, Zaffran S. A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation. Genetics Research. 101: e6. PMID 31030682 DOI: 10.1017/S0016672319000041 |
0.696 |
|
| 2019 |
Neri T, Hiriart E, van Vliet PP, Faure E, Norris RA, Farhat B, Jagla B, Lefrancois J, Sugi Y, Moore-Morris T, Zaffran S, Faustino RS, Zambon AC, Desvignes JP, Salgado D, et al. Human pre-valvular endocardial cells derived from pluripotent stem cells recapitulate cardiac pathophysiological valvulogenesis. Nature Communications. 10: 1929. PMID 31028265 DOI: 10.1038/S41467-019-09459-5 |
0.486 |
|
| 2019 |
van Eif VWW, Stefanovic S, van Duijvenboden K, Bakker M, Wakker V, de Gier-de Vries C, Zaffran S, Verkerk AO, Boukens BJ, Christoffels VM. Transcriptome analysis of mouse and human sinoatrial node cells reveals a conserved genetic program. Development (Cambridge, England). 146. PMID 30936179 DOI: 10.1242/Dev.173161 |
0.405 |
|
| 2018 |
Lescroart F, Zaffran S. Hox and Tale transcription factors in heart development and disease. The International Journal of Developmental Biology. 62: 837-846. PMID 30604853 DOI: 10.1387/Ijdb.180192Sz |
0.824 |
|
| 2018 |
Zaffran S, Odelin G, Stefanovic S, Lescroart F, Etchevers HC. Ectopic expression of Hoxb1 induces cardiac and craniofacial malformations. Genesis (New York, N.Y. : 2000). 56: e23221. PMID 30134070 DOI: 10.1002/Dvg.23221 |
0.815 |
|
| 2018 |
Jaouadi H, Kraoua L, Chaker L, Atkinson A, Delague V, Levy N, Benkhalifa R, Mrad R, Abdelhak S, Zaffran S. Novel ALPK3 mutation in a Tunisian patient with pediatric cardiomyopathy and facio-thoraco-skeletal features. Journal of Human Genetics. PMID 30046096 DOI: 10.1038/S10038-018-0492-1 |
0.53 |
|
| 2018 |
De Bono C, Thellier C, Bertrand N, Sturny R, Jullian E, Cortes C, Stefanovic S, Zaffran S, Théveniau-Ruissy M, Kelly RG. T-box genes and retinoic acid signaling regulate the segregation of arterial and venous pole progenitor cells in the murine second heart field. Human Molecular Genetics. PMID 30016433 DOI: 10.1093/Hmg/Ddy266 |
0.861 |
|
| 2018 |
Pinard A, Eudes N, Mitchell J, Bajolle F, Grelet M, Okoronkwo J, Bonnet D, Collod-Béroud G, Zaffran S. Analysis of HOXB1 gene in a cohort of patients with sporadic ventricular septal defect. Molecular Biology Reports. PMID 29923154 DOI: 10.1007/S11033-018-4212-X |
0.804 |
|
| 2018 |
Papoutsi T, Luna-Zurita L, Prados B, Zaffran S, de la Pompa JL. Bmp2 and Notch cooperate to pattern the embryonic endocardium. Development (Cambridge, England). 145. PMID 29853617 DOI: 10.1242/Dev.163378 |
0.539 |
|
| 2018 |
Prados B, Gómez-Apiñániz P, Papoutsi T, Luxán G, Zaffran S, Pérez-Pomares JM, de la Pompa JL. Myocardial Bmp2 gain causes ectopic EMT and promotes cardiomyocyte proliferation and immaturity. Cell Death & Disease. 9: 399. PMID 29540665 DOI: 10.1038/S41419-018-0442-Z |
0.553 |
|
| 2018 |
Métais A, Lamsoul I, Melet A, Uttenweiler-Joseph S, Poincloux R, Stefanovic S, Valière A, Gonzalez de Peredo A, Stella A, Burlet-Schiltz O, Zaffran S, Lutz PG, Moog-Lutz C. Asb2α-Filamin A Axis Is Essential for Actin Cytoskeleton Remodeling During Heart Development. Circulation Research. 122: e34-e48. PMID 29374072 DOI: 10.1161/Circresaha.117.312015 |
0.524 |
|
| 2018 |
Etchevers HC, Rose C, Kahle B, Vorbringer H, Fina F, Heux P, Berger I, Schwarz B, Zaffran S, Macagno N, Krengel S. Giant congenital melanocytic nevus with vascular malformation and epidermal cysts associated with a somatic activating mutation in BRAF. Pigment Cell & Melanoma Research. PMID 29316280 DOI: 10.1111/Pcmr.12685 |
0.644 |
|
| 2018 |
Thellier C, Bono CD, Zaffran S, Theveniau-Ruissy M, Kelly R. Investigation of T-box gene function in patterning second heart field progenitor cells Archives of Cardiovascular Diseases Supplements. 10: 257. DOI: 10.1016/J.Acvdsp.2018.02.177 |
0.571 |
|
| 2018 |
Theron A, Touil A, Resseguier N, Faure E, Sumian M, Simoni AS, Habib G, Collart F, Zaffran S, Avierinos JF. Predictors of valve degeneration in 223 consecutive patients with bicuspid aortic valve: A single-center prospective study Archives of Cardiovascular Diseases Supplements. 10: 72-73. DOI: 10.1016/J.Acvdsp.2017.11.282 |
0.349 |
|
| 2017 |
Odelin G, Faure E, Coulpier F, Di Bonito M, Bajolle F, Studer M, Avierinos JF, Charnay P, Topilko P, Zaffran S. Krox20 defines a subpopulation of cardiac neural crest cells contributing to arterial valves and bicuspid aortic valve. Development (Cambridge, England). PMID 29158447 DOI: 10.1242/Dev.151944 |
0.829 |
|
| 2017 |
Rambeau P, Faure E, Théron A, Avierinos JF, Jopling C, Zaffran S, Faucherre A. Reduced aggrecan expression affects cardiac outflow tract development in zebrafish and is associated with bicuspid aortic valve disease in humans. International Journal of Cardiology. PMID 28986054 DOI: 10.1016/J.Ijcard.2017.09.174 |
0.758 |
|
| 2017 |
Ovaert C, Busa T, Faure E, Missirian C, Philip N, Paoli F, Milh M, Macé L, Zaffran S. FOXC1 haploinsufficiency due to 6p25 deletion in a patient with rapidly progressing aortic valve disease. American Journal of Medical Genetics. Part A. PMID 28657660 DOI: 10.1002/Ajmg.A.38331 |
0.445 |
|
| 2017 |
Labbé P, Faure E, Lecointe S, Le Scouarnec S, Kyndt F, Marrec M, Le Tourneau T, Offmann B, Duplaà C, Zaffran S, Schott JJ, Merot J. The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/β-catenin transcription pathway. Biochimica Et Biophysica Acta. PMID 28322931 DOI: 10.1016/J.Bbamcr.2017.03.008 |
0.354 |
|
| 2017 |
Stefanovic S, Zaffran S. Mechanisms of retinoic acid signaling during cardiogenesis. Mechanisms of Development. 143: 9-19. PMID 28007475 DOI: 10.1016/J.Mod.2016.12.002 |
0.48 |
|
| 2017 |
Bono CD, Théveniau-Ruissy M, Bertrand N, Sturny R, Stefanovic S, Zaffran S, Kelly RG. Tbx1 and Retinoic acid-dependent Tbx5 expression coordinate second heart field progenitor cell addition to alternate cardiac poles Archives of Cardiovascular Diseases Supplements. 9: 212. DOI: 10.1016/S1878-6480(17)30525-6 |
0.519 |
|
| 2017 |
Theron A, Faure E, Pistol A, Desvignes JP, Collod-Beroud G, Avierinos JF, Collart F, Zaffran S. Aortic valve disease acquired after left ventricular assist device implantation: an outstanding in vivo model of valvular heart disease pathophysiology and remodeling Archives of Cardiovascular Diseases Supplements. 9: 98. DOI: 10.1016/S1878-6480(17)30294-X |
0.429 |
|
| 2016 |
Roux M, Zaffran S. Hox Genes in Cardiovascular Development and Diseases. Journal of Developmental Biology. 4. PMID 29615581 DOI: 10.3390/jdb4020014 |
0.804 |
|
| 2016 |
Roux M, Laforest B, Eudes N, Bertrand N, Stefanovic S, Zaffran S. Hoxa1 and Hoxb1 are required for pharyngeal arch artery development. Mechanisms of Development. PMID 27956219 DOI: 10.1016/J.Mod.2016.11.006 |
0.839 |
|
| 2016 |
Pinard A, Salgado D, Desvignes JP, Rai G, Hanna N, Arnaud P, Guien C, Martinez M, Faivre L, Jondeau G, Boileau C, Zaffran S, Béroud C, Collod-Béroud G. WES/WGS Reporting of Mutations from Cardiovascular "Actionable" Genes in Clinical Practice: A Key Role for UMD Knowledgebases in the era of Big Databases. Human Mutation. PMID 27647783 DOI: 10.1002/Humu.23119 |
0.735 |
|
| 2016 |
Pinard A, Miltgen M, Blanchard A, Mathieu H, Desvignes JP, Fabre A, Arnaud P, Barré L, Krahn M, Grandval P, Olschwang S, Zaffran S, Boileau C, Béroud C, Collod-Béroud G. Actionable Genes, Core Databases and LOCUS Specific Databases (LSDBs). Human Mutation. PMID 27600092 DOI: 10.1002/Humu.23112 |
0.735 |
|
| 2016 |
Escot S, Blavet C, Faure E, Zaffran S, Duband JL, Fournier-Thibault C. Disruption of CXCR4 signaling in pharyngeal neural crest cells causes DiGeorge syndrome-like malformations. Development (Cambridge, England). 143: 582-8. PMID 26755698 DOI: 10.1242/Dev.126573 |
0.461 |
|
| 2016 |
Théron A, Odelin G, Faure E, Avierinos JF, Zaffran S. Krox20 heterozygous mice: A model of aortic regurgitation associated with decreased expression of fibrillar collagen genes. Archives of Cardiovascular Diseases. 109: 188-98. PMID 26711547 DOI: 10.1016/J.Acvd.2015.10.002 |
0.804 |
|
| 2016 |
Theron A, Pinard A, Riberi A, Zaffran S. An uncommon cause of tricuspid regurgitation: three-dimensional echocardiographic incremental value, surgical and genetic insights. European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association For Cardio-Thoracic Surgery. 50: 180-2. PMID 26670804 DOI: 10.1093/Ejcts/Ezv423 |
0.823 |
|
| 2016 |
Theron A, Odelin G, Faure E, Avierinos J, Zaffran S. 0352: Decrease of Krox20 expression leads to aortic valve dysfunction and thickening of the valve leaflets Archives of Cardiovascular Diseases Supplements. 8: 55. DOI: 10.1016/S1878-6480(16)30166-5 |
0.422 |
|
| 2015 |
El Robrini N, Etchevers HC, Ryckebüsch L, Faure E, Eudes N, Niederreither K, Zaffran S, Bertrand N. Cardiac outflow morphogenesis depends on effects of retinoic acid signaling on multiple cell lineages. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 26442704 DOI: 10.1002/Dvdy.24357 |
0.791 |
|
| 2015 |
Roux M, Laforest B, Capecchi M, Bertrand N, Zaffran S. Hoxb1 regulates proliferation and differentiation of second heart field progenitors in pharyngeal mesoderm and genetically interacts with Hoxa1 during cardiac outflow tract development. Developmental Biology. 406: 247-58. PMID 26284287 DOI: 10.1016/J.Ydbio.2015.08.015 |
0.859 |
|
| 2015 |
Papoutsi T, Odelin G, Moore-Morris T, Pucéat M, de la Pompa JL, Robert B, Zaffran S. Msx1CreERT2 knock-In allele: A useful tool to target embryonic and adult cardiac valves. Genesis (New York, N.Y. : 2000). 53: 337-45. PMID 25950518 DOI: 10.1002/Dvg.22856 |
0.853 |
|
| 2015 |
Labbé P, Faure E, Lecointe S, Kyndt F, Tourneau TL, Pompa JLDL, Duplaà C, Zaffran S, Schott J, Merot J. 0268 : Involvement of LRRFip1 gene and canonical Wnt pathway in Mitral Valve Prolapse (MVP) Archives of Cardiovascular Diseases Supplements. 7: 204. DOI: 10.1016/S1878-6480(15)30200-7 |
0.461 |
|
| 2014 |
Odelin G, Faure E, Kober F, Maurel-Zaffran C, Théron A, Coulpier F, Guillet B, Bernard M, Avierinos JF, Charnay P, Topilko P, Zaffran S. Loss of Krox20 results in aortic valve regurgitation and impaired transcriptional activation of fibrillar collagen genes. Cardiovascular Research. 104: 443-55. PMID 25344368 DOI: 10.1093/Cvr/Cvu233 |
0.826 |
|
| 2014 |
Rana MS, Théveniau-Ruissy M, De Bono C, Mesbah K, Francou A, Rammah M, Domínguez JN, Roux M, Laforest B, Anderson RH, Mohun T, Zaffran S, Christoffels VM, Kelly RG. Tbx1 coordinates addition of posterior second heart field progenitor cells to the arterial and venous poles of the heart. Circulation Research. 115: 790-9. PMID 25190705 DOI: 10.1161/Circresaha.115.305020 |
0.857 |
|
| 2014 |
Laforest B, Bertrand N, Zaffran S. Genetic lineage tracing analysis of anterior Hox expressing cells. Methods in Molecular Biology (Clifton, N.J.). 1196: 37-48. PMID 25151156 DOI: 10.1007/978-1-4939-1242-1_3 |
0.7 |
|
| 2014 |
Zaffran S, Robrini N, Bertrand N. Retinoids and Cardiac Development Journal of Developmental Biology. 2: 50-71. DOI: 10.3390/JDB2010050 |
0.341 |
|
| 2014 |
Laforest B, Bertrand N, Zaffran S. Anterior Hox Genes in Cardiac Development and Great Artery Patterning Journal of Cardiovascular Development and Disease. 1: 3-13. DOI: 10.3390/Jcdd1010003 |
0.589 |
|
| 2014 |
Labbé P, Kyndt F, Tourneau TL, Zaffran S, Duplaà C, Schott J, Merot J. 0174: LRRFip1 and Wnt pathway involvement in mitral valve prolapse Archives of Cardiovascular Diseases Supplements. 6: 72. DOI: 10.1016/S1878-6480(14)71460-0 |
0.476 |
|
| 2012 |
Watanabe Y, Zaffran S, Kuroiwa A, Higuchi H, Ogura T, Harvey RP, Kelly RG, Buckingham M. Fibroblast growth factor 10 gene regulation in the second heart field by Tbx1, Nkx2-5, and Islet1 reveals a genetic switch for down-regulation in the myocardium. Proceedings of the National Academy of Sciences of the United States of America. 109: 18273-80. PMID 23093675 DOI: 10.1073/Pnas.1215360109 |
0.857 |
|
| 2012 |
Van Vliet P, Wu SM, Zaffran S, Pucéat M. Early cardiac development: a view from stem cells to embryos. Cardiovascular Research. 96: 352-62. PMID 22893679 DOI: 10.1093/Cvr/Cvs270 |
0.44 |
|
| 2012 |
Zaffran S, Kelly RG. New developments in the second heart field. Differentiation; Research in Biological Diversity. 84: 17-24. PMID 22521611 DOI: 10.1016/J.Diff.2012.03.003 |
0.798 |
|
| 2012 |
Golzio C, Havis E, Daubas P, Nuel G, Babarit C, Munnich A, Vekemans M, Zaffran S, Lyonnet S, Etchevers HC. ISL1 directly regulates FGF10 transcription during human cardiac outflow formation. Plos One. 7: e30677. PMID 22303449 DOI: 10.1371/Journal.Pone.0030677 |
0.725 |
|
| 2012 |
Odelin G, Kober F, Avierinos JF, Arab S, Topilko P, Charnay P, Cozzone P, Bernard M, Zaffran S. 289 Role of Krox20 during cardiac valve development, remodeling and maturation Archives of Cardiovascular Diseases Supplements. 4: 92. DOI: 10.1016/S1878-6480(12)70685-7 |
0.497 |
|
| 2011 |
Diman NY, Remacle S, Bertrand N, Picard JJ, Zaffran S, Rezsohazy R. A retinoic acid responsive Hoxa3 transgene expressed in embryonic pharyngeal endoderm, cardiac neural crest and a subdomain of the second heart field. Plos One. 6: e27624. PMID 22110697 DOI: 10.1371/Journal.Pone.0027624 |
0.75 |
|
| 2011 |
Bertrand N, Roux M, Ryckebüsch L, Niederreither K, Dollé P, Moon A, Capecchi M, Zaffran S. Hox genes define distinct progenitor sub-domains within the second heart field. Developmental Biology. 353: 266-74. PMID 21385575 DOI: 10.1016/J.Ydbio.2011.02.029 |
0.832 |
|
| 2010 |
Medioni C, Bertrand N, Mesbah K, Hudry B, Dupays L, Wolstein O, Washkowitz AJ, Papaioannou VE, Mohun TJ, Harvey RP, Zaffran S. Expression of Slit and Robo genes in the developing mouse heart. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 239: 3303-11. PMID 20941780 DOI: 10.1002/Dvdy.22449 |
0.77 |
|
| 2010 |
Lin SC, Dollé P, Ryckebüsch L, Noseda M, Zaffran S, Schneider MD, Niederreither K. Endogenous retinoic acid regulates cardiac progenitor differentiation. Proceedings of the National Academy of Sciences of the United States of America. 107: 9234-9. PMID 20439714 DOI: 10.1073/Pnas.0910430107 |
0.844 |
|
| 2010 |
Ryckebüsch L, Bertrand N, Mesbah K, Bajolle F, Niederreither K, Kelly RG, Zaffran S. Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome. Circulation Research. 106: 686-94. PMID 20110535 DOI: 10.1161/Circresaha.109.205732 |
0.804 |
|
| 2009 |
Bonnet D, Zaffran S, Kelly R, Bajolle F. [Embryological and genetic mechanisms of cardiac great arteries malformations]. Journal De La Societe De Biologie. 203: 161-5. PMID 19527629 DOI: 10.1051/Jbio/2009019 |
0.851 |
|
| 2009 |
Bajolle F, Zaffran S, Losay J, Ou P, Buckingham M, Bonnet D. Conotruncal defects associated with anomalous pulmonary venous connections. Archives of Cardiovascular Diseases. 102: 105-10. PMID 19303577 DOI: 10.1016/J.Acvd.2008.04.010 |
0.815 |
|
| 2009 |
Bajolle F, Zaffran S, Bonnet D. Genetics and embryological mechanisms of congenital heart diseases. Archives of Cardiovascular Diseases. 102: 59-63. PMID 19233110 DOI: 10.1016/J.Acvd.2008.06.020 |
0.742 |
|
| 2008 |
Bajolle F, Zaffran S. [Haemodynamic induces aortic arch asymmetry]. Medecine Sciences : M/S. 24: 354-6. PMID 18405626 DOI: 10.1051/Medsci/2008244354 |
0.652 |
|
| 2008 |
Ryckebusch L, Wang Z, Bertrand N, Lin SC, Chi X, Schwartz R, Zaffran S, Niederreither K. Retinoic acid deficiency alters second heart field formation. Proceedings of the National Academy of Sciences of the United States of America. 105: 2913-8. PMID 18287057 DOI: 10.1073/Pnas.0712344105 |
0.825 |
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| 2008 |
Galli D, Domínguez JN, Zaffran S, Munk A, Brown NA, Buckingham ME. Atrial myocardium derives from the posterior region of the second heart field, which acquires left-right identity as Pitx2c is expressed. Development (Cambridge, England). 135: 1157-67. PMID 18272591 DOI: 10.1242/Dev.014563 |
0.712 |
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| 2008 |
Bajolle F, Zaffran S, Meilhac SM, Dandonneau M, Chang T, Kelly RG, Buckingham ME. Myocardium at the base of the aorta and pulmonary trunk is prefigured in the outflow tract of the heart and in subdomains of the second heart field. Developmental Biology. 313: 25-34. PMID 18005956 DOI: 10.1016/J.Ydbio.2007.09.023 |
0.831 |
|
| 2007 |
Lo PC, Zaffran S, Sénatore S, Frasch M. The Drosophila Hand gene is required for remodeling of the developing adult heart and midgut during metamorphosis. Developmental Biology. 311: 287-96. PMID 17904115 DOI: 10.1016/J.Ydbio.2007.08.024 |
0.685 |
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| 2007 |
Prall OW, Menon MK, Solloway MJ, Watanabe Y, Zaffran S, Bajolle F, Biben C, McBride JJ, Robertson BR, Chaulet H, Stennard FA, Wise N, Schaft D, Wolstein O, Furtado MB, et al. An Nkx2-5/Bmp2/Smad1 negative feedback loop controls heart progenitor specification and proliferation. Cell. 128: 947-59. PMID 17350578 DOI: 10.1016/J.Cell.2007.01.042 |
0.832 |
|
| 2006 |
Zaffran S, Reim I, Qian L, Lo PC, Bodmer R, Frasch M. Cardioblast-intrinsic Tinman activity controls proper diversification and differentiation of myocardial cells in Drosophila. Development (Cambridge, England). 133: 4073-83. PMID 16987868 DOI: 10.1242/Dev.02586 |
0.708 |
|
| 2006 |
Marguerie A, Bajolle F, Zaffran S, Brown NA, Dickson C, Buckingham ME, Kelly RG. Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice. Cardiovascular Research. 71: 50-60. PMID 16687131 DOI: 10.1016/J.Cardiores.2006.03.021 |
0.843 |
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| 2006 |
Bajolle F, Zaffran S, Kelly RG, Hadchouel J, Bonnet D, Brown NA, Buckingham ME. Rotation of the myocardial wall of the outflow tract is implicated in the normal positioning of the great arteries. Circulation Research. 98: 421-8. PMID 16397144 DOI: 10.1161/01.Res.0000202800.85341.6E |
0.831 |
|
| 2006 |
Relaix F, Montarras D, Zaffran S, Gayraud-Morel B, Rocancourt D, Tajbakhsh S, Mansouri A, Cumano A, Buckingham M. Pax3 and Pax7 have distinct and overlapping functions in adult muscle progenitor cells. The Journal of Cell Biology. 172: 91-102. PMID 16380438 DOI: 10.1083/Jcb.200508044 |
0.792 |
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| 2006 |
Buckingham M, Bajolle F, Bonnet D, Brown N, Meilhac S, Kelly R, Zaffran S. Myocardial cell lineages in the mammalian embryo: The second heart field Journal of Molecular and Cellular Cardiology. 40: 992. DOI: 10.1016/J.Yjmcc.2006.03.213 |
0.481 |
|
| 2005 |
Buckingham M, Meilhac S, Zaffran S. Building the mammalian heart from two sources of myocardial cells. Nature Reviews. Genetics. 6: 826-35. PMID 16304598 DOI: 10.1038/Nrg1710 |
0.838 |
|
| 2005 |
Montarras D, Morgan J, Colins C, Relaix F, Zaffran S, Cumano A, Partridge T, Buckingham M. Developmental biology: Direct isolation of satellite cells for skeletal muscle regeneration Science. 309: 2064-2067. PMID 16141372 DOI: 10.1126/Science.1114758 |
0.707 |
|
| 2005 |
Zaffran S, Frasch M. The homeodomain of Tinman mediates homo- and heterodimerization of NK proteins. Biochemical and Biophysical Research Communications. 334: 361-9. PMID 16004970 DOI: 10.1016/J.Bbrc.2005.06.090 |
0.621 |
|
| 2005 |
Mailleux AA, Kelly R, Veltmaat JM, De Langhe SP, Zaffran S, Thiery JP, Bellusci S. Fgf10 expression identifies parabronchial smooth muscle cell progenitors and is required for their entry into the smooth muscle cell lineage. Development (Cambridge, England). 132: 2157-66. PMID 15800000 DOI: 10.1242/Dev.01795 |
0.716 |
|
| 2004 |
Zaffran S, Kelly RG, Meilhac SM, Buckingham ME, Brown NA. Right ventricular myocardium derives from the anterior heart field. Circulation Research. 95: 261-8. PMID 15217909 DOI: 10.1161/01.Res.0000136815.73623.Be |
0.845 |
|
| 2003 |
Kelly RG, Lemonnier M, Zaffran S, Munk A, Buckingham ME. Cell history determines the maintenance of transcriptional differences between left and right ventricular cardiomyocytes in the developing mouse heart. Journal of Cell Science. 116: 5005-13. PMID 14625394 DOI: 10.1242/Jcs.00824 |
0.825 |
|
| 2003 |
Zaffran S, Kelly R, Munk A, Brown N, Buckingham M. [The mouse as a model for heart morphogenesis in mammals: the origin of myocytes and studies with cardiac explants]. Journal De La SociéTé De Biologie. 197: 187-94. PMID 12910634 |
0.837 |
|
| 2002 |
Zaffran S, Xu X, Lo PC, Lee HH, Frasch M. Cardiogenesis in the Drosophila model: control mechanisms during early induction and diversification of cardiac progenitors. Cold Spring Harbor Symposia On Quantitative Biology. 67: 1-12. PMID 12858517 DOI: 10.1101/Sqb.2002.67.1 |
0.665 |
|
| 2002 |
Zaffran S, Frasch M. Early signals in cardiac development. Circulation Research. 91: 457-69. PMID 12242263 DOI: 10.1161/01.Res.0000034152.74523.A8 |
0.726 |
|
| 2002 |
Zaffran S, Frasch M. The beta 3 tubulin gene is a direct target of bagpipe and biniou in the visceral mesoderm of Drosophila. Mechanisms of Development. 114: 85-93. PMID 12175492 DOI: 10.1016/S0925-4773(02)00063-1 |
0.591 |
|
| 2002 |
Chartier A, Zaffran S, Astier M, Sémériva M, Gratecos D. Pericardin, a Drosophila type IV collagen-like protein is involved in the morphogenesis and maintenance of the heart epithelium during dorsal ectoderm closure. Development (Cambridge, England). 129: 3241-53. PMID 12070098 |
0.432 |
|
| 2001 |
Zaffran S, Küchler A, Lee HH, Frasch M. biniou (FoxF), a central component in a regulatory network controlling visceral mesoderm development and midgut morphogenesis in Drosophila. Genes & Development. 15: 2900-15. PMID 11691840 DOI: 10.1101/Gad.917101 |
0.636 |
|
| 2000 |
Zaffran S, Das G, Frasch M. The NK-2 homeobox gene scarecrow (scro) is expressed in pharynx, ventral nerve cord and brain of Drosophila embryos. Mechanisms of Development. 94: 237-41. PMID 10842079 DOI: 10.1016/S0925-4773(00)00298-7 |
0.587 |
|
| 2000 |
Zaffran S. Molecular cloning and embryonic expression of dFKBP59, a novel Drosophila FK506-binding protein. Gene. 246: 103-109. PMID 10767531 DOI: 10.1016/S0378-1119(00)00058-5 |
0.334 |
|
| 1999 |
Frémion F, Astier M, Zaffran S, Guillèn A, Homburger V, Sémériva M. The Heterotrimeric Protein Go Is Required for the Formation of Heart Epithelium in Drosophila Journal of Cell Biology. 145: 1063-1076. PMID 10352022 DOI: 10.1083/Jcb.145.5.1063 |
0.513 |
|
| 1995 |
Zaffran S, Astier M, Gratecos D, Guillen A, Sémériva M. Cellular interactions during heart morphogenesis in the Drosophila embryo Biology of the Cell. 84: 13-24. PMID 8574195 DOI: 10.1016/0248-4900(96)81314-1 |
0.511 |
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