Cellular differentiation, Genetics, Embryonic stem cell, Cell biology and Stem cell are his primary areas of study. As a part of the same scientific study, William L. Stanford usually deals with the Cellular differentiation, concentrating on Stem cell marker and frequently concerns with Reverse genetics, Somatic cell, Ploidy and Genetic screen. In general Genetics study, his work on Genome, Mutagenesis, Induced pluripotent stem cell and Epigenetics often relates to the realm of Histone methylation, thereby connecting several areas of interest.
His Embryonic stem cell research integrates issues from Myogenesis, Function and Gene regulatory network. His work on Stem cell factor and Receptor tyrosine kinase as part of general Cell biology study is frequently linked to AXL receptor tyrosine kinase and C-Mer Tyrosine Kinase, bridging the gap between disciplines. He combines subjects such as Endothelial stem cell and Mesenchymal stem cell with his study of Stem cell.
Cell biology, Stem cell, Embryonic stem cell, Cancer research and Induced pluripotent stem cell are his primary areas of study. His Cell biology research incorporates elements of Endothelial stem cell, Cell, Cell culture, Cellular differentiation and Cell fate determination. His work carried out in the field of Stem cell brings together such families of science as Molecular biology and Mesenchymal stem cell.
His study on Embryonic stem cell is covered under Genetics. His study explores the link between Cancer research and topics such as Immunology that cross with problems in Progenitor and Phenotype. His research on Induced pluripotent stem cell also deals with topics like
His scientific interests lie mostly in Cell biology, Induced pluripotent stem cell, Lymphangioleiomyomatosis, Cancer research and Stem cell. His study in Cell biology is interdisciplinary in nature, drawing from both Mesoderm, Genetically modified organism and Smooth muscle. His Induced pluripotent stem cell study contributes to a more complete understanding of Embryonic stem cell.
His studies in Cancer research integrate themes in fields like Cell, Haematopoiesis, Mdm2, Lung cancer and Self-healing hydrogels. He studies Stem cell, focusing on Progenitor cell in particular. His research in Somatic cell intersects with topics in Germline mutation and Immunology.
His primary scientific interests are in Cell biology, Induced pluripotent stem cell, Cancer research, Mesenchymal stem cell and Stem cell. His biological study spans a wide range of topics, including Epigenetics and Locus. His Induced pluripotent stem cell research is multidisciplinary, incorporating elements of Reprogramming, Lamin and Cellular differentiation.
His Mesenchymal stem cell study incorporates themes from Cell therapy, Bioinformatics and Bone marrow. His Cell therapy study integrates concerns from other disciplines, such as Embryonic stem cell, Progenitor cell, Pathology and Lung injury, Lung. His studies deal with areas such as Phenotype, Virus, Genetic enhancement and Transgene as well as Stem cell.
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Essential role of the mitochondrial apoptosis-inducing factor in programmed cell death
Nicholas Joza;Nicholas Joza;Santos A. Susin;Eric Daugas;William L. Stanford.
Function of PI3Kγ in Thymocyte Development, T Cell Activation, and Neutrophil Migration
Takehiko Sasaki;Junko Irie-Sasaki;Russell G. Jones;Antonio J. Oliveira-dos-Santos.
A requirement for Flk1 in primitive and definitive hematopoiesis and vasculogenesis.
Fouad Shalaby;Jacqueline Ho;William L Stanford;Klaus-Dieter Fischer.
Prevention Conference V Beyond Secondary Prevention : Identifying the High-Risk Patient for Primary Prevention : Noninvasive Tests of Atherosclerotic Burden : Writing Group III
Philip Greenland;Jonathan Abrams;Gerard P. Aurigemma;M. Gene Bond.
Gene-trap mutagenesis: past, present and beyond.
William L. Stanford;Jason B. Cohn;Jason B. Cohn;Sabine P. Cordes;Sabine P. Cordes.
Nature Reviews Genetics (2001)
Concise review: stem cell antigen-1: expression, function, and enigma.
Christina Holmes;William L. Stanford.
Stem Cells (2007)
Combinatorial effects of Flk1 and Tal1 on vascular and hematopoietic development in the mouse.
Masatsugu Ema;Patrick Faloon;Wen Jie Zhang;Masanori Hirashima.
Genes & Development (2003)
Human Mesenchymal Stem Cells Self-Renew and Differentiate According to a Deterministic Hierarchy
Rahul Sarugaser;Lorraine Hanoun;Armand Keating;William L. Stanford.
PLOS ONE (2009)
Mesenchymal progenitor self-renewal deficiency leads to age-dependent osteoporosis in Sca-1/Ly-6A null mice
Mortaza Bonyadi;Stephen D. Waldman;Danmei Liu;Jane E. Aubin.
Proceedings of the National Academy of Sciences of the United States of America (2003)
The mammalian gene function resource: the international knockout mouse consortium
Allan Bradley;Konstantinos Anastassiadis;Abdelkader Ayadi;James F. Battey.
Mammalian Genome (2012)
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