Results
|
|
41.
|
|
|
|
42.
|
|
|
|
43.
|
|
|
|
44.
|
|
|
|
45.
|
|
|
|
46.
|
|
|
|
47.
|
Novel ALPK3 mutation in a Tunisian patient with pediatric cardiomyopathy and facio-thoraco-skeletal features. [electronic resource] by
- Jaouadi, Hager
- Kraoua, Lilia
- Chaker, Lilia
- Atkinson, Alexandre
- Delague, Valérie
- Levy, Nicolas
- Benkhalifa, Rym
- Mrad, Ridha
- Abdelhak, Sonia
- Zaffran, Stéphane
Producer: 20181211
In:
Journal of human genetics vol. 63
Availability: No items available.
|
|
|
48.
|
|
|
|
49.
|
ISL1 directly regulates FGF10 transcription during human cardiac outflow formation. [electronic resource] by
- Golzio, Christelle
- Havis, Emmanuelle
- Daubas, Philippe
- Nuel, Gregory
- Babarit, Candice
- Munnich, Arnold
- Vekemans, Michel
- Zaffran, Stéphane
- Lyonnet, Stanislas
- Etchevers, Heather C
Producer: 20120611
In:
PloS one vol. 7
Availability: No items available.
|
|
|
50.
|
Krox20 defines a subpopulation of cardiac neural crest cells contributing to arterial valves and bicuspid aortic valve. [electronic resource] by
- Odelin, Gaëlle
- Faure, Emilie
- Coulpier, Fanny
- Di Bonito, Maria
- Bajolle, Fanny
- Studer, Michèle
- Avierinos, Jean-François
- Charnay, Patrick
- Topilko, Piotr
- Zaffran, Stéphane
Producer: 20180329
In:
Development (Cambridge, England) vol. 145
Availability: No items available.
|
|
|
51.
|
T-box genes and retinoic acid signaling regulate the segregation of arterial and venous pole progenitor cells in the murine second heart field. [electronic resource] by
- De Bono, Christopher
- Thellier, Charlotte
- Bertrand, Nicolas
- Sturny, Rachel
- Jullian, Estelle
- Cortes, Claudio
- Stefanovic, Sonia
- Zaffran, Stéphane
- Théveniau-Ruissy, Magali
- Kelly, Robert G
Producer: 20190422
In:
Human molecular genetics vol. 27
Availability: No items available.
|
|
|
52.
|
Giant congenital melanocytic nevus with vascular malformation and epidermal cysts associated with a somatic activating mutation in BRAF. [electronic resource] by
- Etchevers, Heather C
- Rose, Christian
- Kahle, Birgit
- Vorbringer, Helmuth
- Fina, Frédéric
- Heux, Pauline
- Berger, Irina
- Schwarz, Benjamin
- Zaffran, Stéphane
- Macagno, Nicolas
- Krengel, Sven
Producer: 20190130
In:
Pigment cell & melanoma research vol. 31
Availability: No items available.
|
|
|
53.
|
Expression of Slit and Robo genes in the developing mouse heart. [electronic resource] by
- Medioni, Caroline
- Bertrand, Nicolas
- Mesbah, Karim
- Hudry, Bruno
- Dupays, Laurent
- Wolstein, Orit
- Washkowitz, Andrew J
- Papaioannou, Virginia E
- Mohun, Timothy J
- Harvey, Richard P
- Zaffran, Stéphane
Producer: 20110315
In:
Developmental dynamics : an official publication of the American Association of Anatomists vol. 239
Availability: No items available.
|
|
|
54.
|
Loss of Krox20 results in aortic valve regurgitation and impaired transcriptional activation of fibrillar collagen genes. [electronic resource] by
- Odelin, Gaëlle
- Faure, Emilie
- Kober, Frank
- Maurel-Zaffran, Corinne
- Théron, Alexis
- Coulpier, Fanny
- Guillet, Benjamin
- Bernard, Monique
- Avierinos, Jean-François
- Charnay, Patrick
- Topilko, Piotr
- Zaffran, Stéphane
Producer: 20151026
In:
Cardiovascular research vol. 104
Availability: No items available.
|
|
|
55.
|
The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/β-catenin transcription pathway. [electronic resource] by
- Labbé, Pauline
- Faure, Emilie
- Lecointe, Simon
- Le Scouarnec, Solena
- Kyndt, Florence
- Marrec, Marie
- Le Tourneau, Thierry
- Offmann, Bernard
- Duplaà, Cécile
- Zaffran, Stéphane
- Schott, Jean Jacques
- Merot, Jean
Producer: 20171024
In:
Biochimica et biophysica acta. Molecular cell research vol. 1864
Availability: No items available.
|
|
|
56.
|
Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young. [electronic resource] by
- Jaouadi, Hager
- Bouyacoub, Yosra
- Chabrak, Sonia
- Kraoua, Lilia
- Zaroui, Amira
- Elouej, Sahar
- Nagara, Majdi
- Dallali, Hamza
- Delague, Valérie
- Levy, Nicolas
- Benkhalifa, Rym
- Mechmeche, Rachid
- Zaffran, Stéphane
- Abdelhak, Sonia
Producer: 20210415
In:
Herz vol. 46
Availability: No items available.
|
|
|
57.
|
Value of in vivo T2 measurement for myocardial fibrosis assessment in diabetic mice at 11.75 T. [electronic resource] by
- Bun, Sok-Sithikun
- Kober, Frank
- Jacquier, Alexis
- Espinosa, Leon
- Kalifa, Jérôme
- Bonzi, Marie-France
- Kopp, Francis
- Lalevee, Nathalie
- Zaffran, Stephane
- Deharo, Jean-Claude
- Cozzone, Patrick J
- Bernard, Monique
Producer: 20120820
In:
Investigative radiology vol. 47
Availability: No items available.
|
|
|
58.
|
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation. [electronic resource] by
- Jaouadi, Hager
- Chehida, Amel Ben
- Kraoua, Lilia
- Etchevers, Heather C
- Argiro, Laurent
- Kasdallah, Nadia
- Blibech, Sonia
- Delague, Valérie
- Lévy, Nicolas
- Tebib, Néji
- Mrad, Ridha
- Abdelhak, Sonia
- Benkhalifa, Rym
- Zaffran, Stéphane
Producer: 20200511
In:
Genetics research vol. 101
Availability: No items available.
|
|
|
59.
|
Transcriptome analysis of mouse and human sinoatrial node cells reveals a conserved genetic program. [electronic resource] by
- van Eif, Vincent W W
- Stefanovic, Sonia
- van Duijvenboden, Karel
- Bakker, Martijn
- Wakker, Vincent
- de Gier-de Vries, Corrie
- Zaffran, Stéphane
- Verkerk, Arie O
- Boukens, Bas J
- Christoffels, Vincent M
Producer: 20200309
In:
Development (Cambridge, England) vol. 146
Availability: No items available.
|
|
|
60.
|
WES/WGS Reporting of Mutations from Cardiovascular "Actionable" Genes in Clinical Practice: A Key Role for UMD Knowledgebases in the Era of Big Databases. [electronic resource] by
- Pinard, Amélie
- Salgado, David
- Desvignes, Jean-Pierre
- Rai, Ghadi
- Hanna, Nadine
- Arnaud, Pauline
- Guien, Céline
- Martinez, Maria
- Faivre, Laurence
- Jondeau, Guillaume
- Boileau, Catherine
- Zaffran, Stéphane
- Béroud, Christophe
- Collod-Béroud, Gwenaëlle
Producer: 20171107
In:
Human mutation vol. 37
Availability: No items available.
|