M. Puri

发表

Proteome adaptation in cell reprogramming proceeds via distinct transcriptional networks

David L. A. Wood, S. Grimmond, A. Heck, 2014, Nature Communications.

Requisite Role for Nck Adaptors in Cardiovascular Development, Endothelial-to-Mesenchymal Transition, and Directed Cell Migration

Derek L. Clouthier, N. Jones, M. Puri, 2015, Molecular and Cellular Biology.

VEGFR2-targeted molecular imaging in the mouse embryo: an alternative to the tumor model.

F. Foster, J. Hudson, M. Puri, 2014, Ultrasound in medicine & biology.

Identification of Sokotrasterol Sulfate As a Novel Proangiogenic Steroid

T. Veenstra, A. Karsan, David E. Williams, 2006, Circulation research.

Contrast-enhanced molecular ultrasound differentiates endoglin genotypes in mouse embryos

J. J. Lee, F. Foster, F. S. Foster, 2014, Angiogenesis.

Cell autonomous functions of the receptor tyrosine kinase TIE in a late phase of angiogenic capillary growth and endothelial cell survival during murine development.

J. Rossant, J. Partanen, A. Bernstein, 1996, Development.

Abnormal embryonic lymphatic vessel development in Tie1 hypomorphic mice

H. Baldwin, Lorene E Batts, Xianghu Qu, 2014, Development.

Abnormal embryonic lymphatic vessel development in Tie1 hypomorphic mice

H. Baldwin, Lorene E Batts, Xianghu Qu, 2010, Development.

A UNIQUE PATTERN OF Tie1 EXPRESSION IN THE DEVELOPING MURINE LUNG

D. Taichman, A. Bernstein, Yixun Li, 2003, Experimental lung research.

Divergent reprogramming routes lead to alternative stem-cell states

David L. A. Wood, S. Grimmond, T. Preiss, 2014, Nature.

Vascularization of the mouse embryo: A study of flk‐1, tek, tie, and vascular endothelial growth factor expression during development

K. Alitalo, D. Dumont, G. Fong, 1995, Developmental dynamics : an official publication of the American Association of Anatomists.

The receptor tyrosine kinase TIE is required for integrity and survival of vascular endothelial cells.

J. Rossant, J. Partanen, K. Alitalo, 1995, The EMBO journal.

Corrigendum: Genome-wide characterization of the routes to pluripotency

David L. A. Wood, W. Ritchie, J. Rasko, 2015, Nature.

Genome-wide characterization of the routes to pluripotency

William Ritchie, Jeong-Sun Seo, Rowland Mosbergen, 2014, Nature.

Vascular system defects and neuronal apoptosis in mice lacking Ras GTPase-activating protein

T. Pawson, T. Jacks, Derrick J. Rossi, 1995, Nature.

Fluctuations in histone H4 isoforms during cellular reprogramming monitored by middle‐down proteomics

A. Heck, A. Nagy, J. Muñoz, 2015, Proteomics.

Corrigendum: Divergent reprogramming routes lead to alternative stem-cell states

David L. A. Wood, S. Grimmond, T. Preiss, 2015, Nature.

CD24 tracks divergent pluripotent states in mouse and human cells

Yonatan Y Lipsitz, J. Hanna, A. Heck, 2015, Nature Communications.

Small RNA changes en route to distinct cellular states of induced pluripotency

David L. A. Wood, J. Rasko, S. Grimmond, 2014, Nature Communications.

An epigenomic roadmap to induced pluripotency reveals DNA methylation as a reprogramming modulator

David L. A. Wood, S. Grimmond, T. Preiss, 2014, Nature Communications.

Cell competition during reprogramming gives rise to dominant clones

D. van der Kooy, J. Wrana, P. Zandstra, 2019, Science.

EMBRYONIC STEM CELLS / INDUCED PLURIPOTENT STEM CELLS Concise Review : Embryonic Stem Cells Versus Induced Pluripotent Stem Cells : The Game Is On

A. Nagy, M. Puri, Mira C. Puri, 2011 .

Requirement for the TIE family of receptor tyrosine kinases in adult but not fetal hematopoiesis

A. Bernstein, M. Puri, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Interaction of the TEK and TIE receptor tyrosine kinases during cardiovascular development.

J. Rossant, J. Partanen, A. Bernstein, 1999, Development.

Dominant-negative and targeted null mutations in the endothelial receptor tyrosine kinase, tek, reveal a critical role in vasculogenesis of the embryo.

M. Gertsenstein, D. Dumont, A. Auerbach, 1994, Genes & development.

Contrast imaging in mouse embryos using high-frequency ultrasound.

F. Foster, M. Puri, J. Denbeigh, 2015, Journal of Visualized Experiments.

Selective Role of a Distinct Tyrosine Residue on Tie2 in Heart Development and Early Hematopoiesis

A. Bernstein, D. Dumont, N. Jones, 2005, Molecular and Cellular Biology.

The role of TEK and TIE receptor tyrosine kinases in murine cardiovascular development

M. Puri, 1999 .

Novel zinc finger proteins that interact with the mouse gamma F-crystallin promoter and are expressed in the sclerotome during early somitogenesis.

F. Shalaby, Q R Liu, S. Tang, 1994, Developmental biology.

Endoglin is dispensable for angiogenesis, but required for endocardial cushion formation in the midgestation mouse embryo.

M. Letarte, A. Nomura-Kitabayashi, M. Puri, 2009, Developmental biology.

Differentiation of vascular smooth muscle cells from local precursors during embryonic and adult arteriogenesis requires Notch signaling

A. Karsan, M. Noseda, D. Dumont, 2012, Proceedings of the National Academy of Sciences.

Contrast-enhanced molecular ultrasound differentiates endoglin genotypes in mouse embryos

F. Foster, P. Marsden, M. Letarte, 2014, Angiogenesis.

Highly efficient reprogrammable mouse lines with integrated reporters to track the route to pluripotency

P. Zandstra, Leann Nguyen, M. Faiz, 2022, Proceedings of the National Academy of Sciences of the United States of America.

Differentiation of vascular smooth muscle cells from local precursors during embryonic and adult arteriogenesis requires Notch signaling

A. Karsan, M. Noseda, D. Dumont, 2012, Proceedings of the National Academy of Sciences.

Proteome adaptation in cell reprogramming proceeds via distinct transcriptional networks

David L. A. Wood, S. Grimmond, A. Heck, 2014, Nature Communications.