Kelly Lammerts Van Bueren - Cardiovascular Research Institute, University of California

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论文共 26 篇作者统计合作学者相似作者

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Corrigendum to "HIC2 regulates isoform switching during maturation of the cardiovascular system" [Journal of Molecular and Cellular Cardiology volume 114 (2018) P29-37/ https://doi.org/10.1016/j.yjmcc.2017.10.007]

Iain M Dykes,Kelly Lammerts van Bueren,Peter J Scambler

Journal of molecular and cellular cardiology (2023): 102-102

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HIC2 regulates isoform switching during maturation of the cardiovascular system (vol 114,, P29-37, 2018 )

Iain M. Dykes,Kelly Lammerts van Bueren,Peter J. Scambler

JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2023): 102-102

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Differential Etv2 Threshold Requirement for Endothelial and Erythropoietic Development

Tanvi Sinha,Kelly Lammerts van Bueren,Diane E. Dickel,Ivana Zlatanova,Reuben Thomas,Carlos O. Lizama,Shan-Mei Xu,Ann C. Zovein,Kohta Ikegami,Ivan P. Moskowitz,Katherine S. Pollard,Len A. Pennacchio,Brian L. Black

Cell Reports（2022）

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Cardiovascular Development and Survival Require Mef2c Function in the Myocardial but Not the Endothelial Lineage

Stefan C. Materna,Tanvi Sinha,Ralston M. Barnes,Kelly Lammerts van Bueren,Brian L. Black

Developmental Biology（2019）

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HIC2 Regulates Isoform Switching During Maturation of the Cardiovascular System

Lain M. Dykes,Kelly Lammerts van Bueren,Peter J. Scambler

Journal of Molecular and Cellular Cardiology (2018): 29-37

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HIC2 is a Novel Dosage-Dependent Regulator of Cardiac Development Located Within the Distal 22q11 Deletion Syndrome Region

Iain M. Dykes,Kelly Lammerts van Bueren, Rebekah J. Ashmore,Thomas Floss,Wolfgang Wurst,Dorota Szumska,Shoumo Bhattacharya,Peter J. Scambler

CIRCULATION RESEARCHno. 1 (2014): 23-31

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Chromatin Stretch Enhancer States Drive Cell-Specific Gene Regulation And Harbor Human Disease Risk Variants

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA（2013）

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692

Transcriptional regulation of Etv2 during vascular development

Lammerts Kelly van Bueren,Xu Shan-Mei,Brian L. Black

ANGIOGENESIS（2013）

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Cyp26b1 null embryos display a 22q11 deletion syndrome-like cardiovascular phenotype which is modified by the presence of an additional Tbx1(+/-) allele

Catherine Roberts,Sarah Ivins,Kelly Lammerts Van Bueren,Bertrand Vernay,Kenta Yashiro,Peter J. Scambler

GENETICS RESEARCH（2013）

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