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4161.
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Absence of cardiovascular manifestations in a haploinsufficient Tgfbr1 mouse model. [electronic resource] by
- Renard, Marjolijn
- Trachet, Bram
- Casteleyn, Christophe
- Campens, Laurence
- Cornillie, Pieter
- Callewaert, Bert
- Deleye, Steven
- Vandeghinste, Bert
- van Heijningen, Paula M
- Dietz, Harry
- De Vos, Filip
- Essers, Jeroen
- Staelens, Steven
- Segers, Patrick
- Loeys, Bart
- Coucke, Paul
- De Paepe, Anne
- De Backer, Julie
Producer: 20150122
In:
PloS one vol. 9
Availability: No items available.
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4162.
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4163.
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4164.
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4165.
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4166.
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4167.
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4168.
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4169.
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4170.
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4171.
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4172.
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4173.
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4174.
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Molecular analysis of PRKAG2, LAMP2, and NKX2-5 genes in a cohort of 125 patients with accessory atrioventricular connection. [electronic resource] by
- Esposito, Giorgia
- Grutter, Giorgia
- Drago, Fabrizio
- Costa, Mauro W
- De Santis, Antonella
- Bosco, Giovanna
- Marino, Bruno
- Bellacchio, Emanuele
- Lepri, Francesca
- Harvey, Richard P
- Sarkozy, Anna
- Dallapiccola, Bruno
Producer: 20090923
In:
American journal of medical genetics. Part A vol. 149A
Availability: No items available.
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4175.
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GLUT10 is required for the development of the cardiovascular system and the notochord and connects mitochondrial function to TGFβ signaling. [electronic resource] by
- Willaert, Andy
- Khatri, Sandeep
- Callewaert, Bert L
- Coucke, Paul J
- Crosby, Seth D
- Lee, Joseph G H
- Davis, Elaine C
- Shiva, Sruti
- Tsang, Michael
- De Paepe, Anne
- Urban, Zsolt
Producer: 20120807
In:
Human molecular genetics vol. 21
Availability: No items available.
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4176.
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Atypical aortic arch branching variants: A novel marker for thoracic aortic disease. [electronic resource] by
- Dumfarth, Julia
- Chou, Alan S
- Ziganshin, Bulat A
- Bhandari, Rohan
- Peterss, Sven
- Tranquilli, Maryann
- Mojibian, Hamid
- Fang, Hai
- Rizzo, John A
- Elefteriades, John A
Producer: 20150817
In:
The Journal of thoracic and cardiovascular surgery vol. 149
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4177.
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4178.
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Constitutive activation of the PI3K-AKT pathway and cardiovascular abnormalities in an individual with Kosaki overgrowth syndrome. [electronic resource] by
- Zarate, Yuri A
- Boccuto, Luigi
- Srikanth, Sujata
- Pauly, Rini
- Ocal, Eylem
- Balmakund, Tonya
- Hinkle, Kevin
- Stefans, Vikki
- Schaefer, Gerald B
- Collins, Ronnie Thomas
Producer: 20200610
In:
American journal of medical genetics. Part A vol. 179
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4179.
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Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. [electronic resource] by
- Liu, Ning
- Schoch, Kelly
- Luo, Xi
- Pena, Loren D M
- Bhavana, Venkata Hemanjani
- Kukolich, Mary K
- Stringer, Sarah
- Powis, Zöe
- Radtke, Kelly
- Mroske, Cameron
- Deak, Kristen L
- McDonald, Marie T
- McConkie-Rosell, Allyn
- Markert, M Louise
- Kranz, Peter G
- Stong, Nicholas
- Need, Anna C
- Bick, David
- Amaral, Michelle D
- Worthey, Elizabeth A
- Levy, Shawn
- Wangler, Michael F
- Bellen, Hugo J
- Shashi, Vandana
- Yamamoto, Shinya
Producer: 20190312
In:
Human molecular genetics vol. 27
Availability: No items available.
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4180.
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