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Bruce D Gelb

Showing results (21-30 of 284) with videos related to

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Stem Cells Translational Medicine|February 5, 2014
Concise review: drug discovery in the age of the induced pluripotent stem cellHuaising C Ko, Bruce D Gelb
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 17, 2022
The molecular genetics of RASopathies: An update on novel disease genes and new disordersMarco Tartaglia, Yoko Aoki, Bruce D Gelb
Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
Noonan syndrome and clinically related disordersMarco Tartaglia, Bruce D Gelb, Martin Zenker
Gene Expression Patterns : GEP|April 25, 2003
Expression of Tfap2d, the gene encoding the transcription factor Ap-2 delta, during mouse embryogenesisFeng Zhao, Thomas Lufkin, Bruce D Gelb
Progress in Pediatric Cardiology|September 19, 2015
Cardiomyopathies in Noonan syndrome and the other RASopathiesBruce D Gelb, Amy E Roberts, Marco Tartaglia
Human Mutation|February 20, 2004
Noonan syndrome-associated SHP2/PTPN11 mutants cause EGF-dependent prolonged GAB1 binding and sustained ERK2/MAPK1 activationAlessandra Fragale, Marco Tartaglia, Jie Wu, et al.
Plos One|January 5, 2010
Fgfr3 is a transcriptional target of Ap2delta and Ash2l-containing histone methyltransferase complexesCheryl C Tan, Martin J Walsh, Bruce D Gelb
Pediatrics|March 21, 2012
Role of copy number variants in structural birth defectsAbigail E Southard, Lisa J Edelmann, Bruce D Gelb
Anadolu Kardiyoloji Dergisi : AKD = the Anatolian Journal of Cardiology|June 26, 2012
Char syndrome, a familial form of patent ductus arteriosus, with a new finding: hypoplasia [corrected] of the 3rd fingerKadir Babaoğlu, Meral Oruç, Ayla Günlemez, et al.
Congenital Heart Disease|April 2, 2008
Evaluation of pulmonary artery banding in the setting of ventricular septal defects and severely elevated pulmonary vascular resistanceSadaf A Khan, Bruce D Gelb, Khanh H Nguyen
Pageof 29

Showing results (21-30 of 284) with videos related to

Sort By:
Pageof 29
Stem Cells Translational Medicine|February 5, 2014
Concise review: drug discovery in the age of the induced pluripotent stem cellHuaising C Ko, Bruce D Gelb
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 17, 2022
The molecular genetics of RASopathies: An update on novel disease genes and new disordersMarco Tartaglia, Yoko Aoki, Bruce D Gelb
Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
Noonan syndrome and clinically related disordersMarco Tartaglia, Bruce D Gelb, Martin Zenker
Gene Expression Patterns : GEP|April 25, 2003
Expression of Tfap2d, the gene encoding the transcription factor Ap-2 delta, during mouse embryogenesisFeng Zhao, Thomas Lufkin, Bruce D Gelb
Progress in Pediatric Cardiology|September 19, 2015
Cardiomyopathies in Noonan syndrome and the other RASopathiesBruce D Gelb, Amy E Roberts, Marco Tartaglia
Human Mutation|February 20, 2004
Noonan syndrome-associated SHP2/PTPN11 mutants cause EGF-dependent prolonged GAB1 binding and sustained ERK2/MAPK1 activationAlessandra Fragale, Marco Tartaglia, Jie Wu, et al.
Plos One|January 5, 2010
Fgfr3 is a transcriptional target of Ap2delta and Ash2l-containing histone methyltransferase complexesCheryl C Tan, Martin J Walsh, Bruce D Gelb
Pediatrics|March 21, 2012
Role of copy number variants in structural birth defectsAbigail E Southard, Lisa J Edelmann, Bruce D Gelb
Anadolu Kardiyoloji Dergisi : AKD = the Anatolian Journal of Cardiology|June 26, 2012
Char syndrome, a familial form of patent ductus arteriosus, with a new finding: hypoplasia [corrected] of the 3rd fingerKadir Babaoğlu, Meral Oruç, Ayla Günlemez, et al.
Congenital Heart Disease|April 2, 2008
Evaluation of pulmonary artery banding in the setting of ventricular septal defects and severely elevated pulmonary vascular resistanceSadaf A Khan, Bruce D Gelb, Khanh H Nguyen
Pageof 29