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Pediatric Research|November 29, 2007
Mouse model of heterotaxy with single ventricle spectrum of cardiac anomaliesChristine N Aune, Bishwanath Chatterjee, Xiao-Qing Zhao, et al.
Virchows Archiv : an International Journal of Pathology|July 5, 2014
Malignant round cell tumor of bone with EWSR1-NFATC2 gene fusionNavid Sadri, Julieta Barroeta, Svetlana D Pack, et al.
The Journal of Clinical Investigation|June 24, 2021
Serine hydroxymethyltransferase 2 expression promotes tumorigenesis in rhabdomyosarcoma with 12q13-q14 amplificationThanh H Nguyen, Prasantha L Vemu, Gregory E Hoy, et al.
Molecular Cancer Therapeutics|November 20, 2025
Involvement of the FGF8/FGF receptor signaling pathway in the maintenance and progression of fusion-positive rhabdomyosarcomaSalah Boudjadi, Hana Kim, Bishwanath Chatterjee, et al.
European Journal of Endocrinology|July 21, 2022
Novel GLCCI1-BRAF fusion drives kinase signaling in a case of pheochromocytomatosisBenjamin L Green, Robert R C Grant, Christopher T Richie, et al.
Disease Models & Mechanisms|November 4, 2010
Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndromeCheng Cui, Bishwanath Chatterjee, Deanne Francis, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|May 17, 2005
Developmental regulation and expression of the zebrafish connexin43 geneBishwanath Chatterjee, Alvin J Chin, Gunnar Valdimarsson, et al.
Development (Cambridge, England)|November 19, 2004
ENU induced mutations causing congenital cardiovascular anomaliesQing Yu, Yuan Shen, Bishwanath Chatterjee, et al.
The Journal of Clinical Investigation|November 27, 2007
Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesiaSerena Y Tan, Julie Rosenthal, Xiao-Qing Zhao, et al.
Biology Open|February 18, 2016
Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defectsBrian C Gibbs, Rama Rao Damerla, Eszter K Vladar, et al.
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