2001 - Albert Lasker Award for Basic Medical Research, Lasker Foundation
1993 - Fellow of the Royal Society, United Kingdom
Martin J. Evans mainly focuses on Cell biology, Genetics, Cancer research, Cystic fibrosis and Mutation. His research in Cell biology intersects with topics in Cell culture, Endoderm, Induced pluripotent stem cell and Eomesodermin. The various areas that Martin J. Evans examines in his Cell culture study include Cellular differentiation, Chimera, Blastocyst, Embryo and Embryoid body.
His Induced pluripotent stem cell study often links to related topics such as Tissue culture. His study on Stem cell, Germ layer, Mesoderm and Epiblast is often connected to Trophoblast as part of broader study in Genetics. His biological study spans a wide range of topics, including BRCA2 Protein and DNA repair.
Cell biology, Molecular biology, Genetics, Gene and Embryonic stem cell are his primary areas of study. His work deals with themes such as Cell, Germ layer and Embryoid body, which intersect with Cell biology. Martin J. Evans combines subjects such as Embryonal carcinoma, KOSR and Teratocarcinoma with his study of Embryoid body.
His Molecular biology study incorporates themes from Endoderm, Cystic fibrosis, Cystic fibrosis transmembrane conductance regulator and Mutant, Null allele. His Embryonic stem cell research focuses on Stem cell and how it connects with Adult stem cell. The Embryo study combines topics in areas such as Ploidy, Induced pluripotent stem cell and Tissue culture.
His primary scientific interests are in Internal medicine, Cell biology, Embryonic stem cell, Molecular biology and Cardiology. Martin J. Evans works in the field of Cell biology, focusing on Progenitor in particular. His work on Endoderm as part of general Embryonic stem cell research is frequently linked to Media optimization, bridging the gap between disciplines.
Martin J. Evans has researched Molecular biology in several fields, including Complementary DNA, Gene expression, Gene and Embryoid body. The concepts of his Embryoid body study are interwoven with issues in Hemoglobin, Cell aggregation, Developmental biology and KOSR. Martin J. Evans has included themes like Cell culture, Regenerative medicine, Adult stem cell, Gene targeting and Tissue culture in his Mammalian Genetics study.
Martin J. Evans mostly deals with Molecular biology, Internal medicine, Endocrinology, Stem cell and Embryonic stem cell. His Molecular biology research integrates issues from Microarray, Regulation of gene expression, Gene expression and Gene. His work on Knockout mouse, Metabolism and Bone remodeling as part of general Internal medicine study is frequently linked to Osteonectin, bridging the gap between disciplines.
His Endocrinology research is multidisciplinary, incorporating elements of Wild type, Biochemistry, Calcium and Tartrate-resistant acid phosphatase. His Stem cell research includes elements of Cellular differentiation, KOSR, Developmental biology, Cell aggregation and Embryoid body. His research integrates issues of Embryo, Cell biology, Mammalian Genetics and Tissue culture in his study of Embryonic stem cell.
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Establishment in culture of pluripotential cells from mouse embryos
M. J. Evans;M. H. Kaufman.
Nature (1981)
Formation of germ-line chimaeras from embryo-derived teratocarcinoma cell lines
Allan Bradley;Martin Evans;Matthew H. Kaufman;Elizabeth Robertson.
Nature (1984)
Germ-line transmission of genes introduced into cultured pluripotential cells by retroviral vector
Elizabeth Robertson;Allan Bradley;Michael Kuehn;Martin Evans.
Nature (1986)
Involvement of Brca2 in DNA repair.
Ketan J Patel;Veronica P.C.C Yu;Hyunsook Lee;Anne Corcoran.
Molecular Cell (1998)
THE ONCOGENIC CYSTEINE-RICH LIM DOMAIN PROTEIN RBTN2 IS ESSENTIAL FOR ERYTHROID DEVELOPMENT
Alan J. Warren;William H. Colledge;Mark B.L. Carlton;Martin J. Evans.
Cell (1994)
A potential animal model for Lesch–Nyhan syndrome through introduction of HPRT mutations into mice
Michael R. Kuehn;Allan Bradley;Elizabeth J. Robertson;Martin J. Evans.
Nature (1987)
Eomesodermin is required for mouse trophoblast development and mesoderm formation
Andreas P. Russ;Andreas P. Russ;Sigrid Wattler;William H. Colledge;Samuel A. J. R. Aparicio;Samuel A. J. R. Aparicio.
Nature (2000)
Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy
Stephen C. Hyde;Deborah R. Gill;Christopher F. Higgins;Ann E. O. Trezise.
Nature (1993)
Salmonella typhi uses CFTR to enter intestinal epithelial cells.
Gerald B. Pier;Martha Grout;Tanweer Zaidi;Gloria Meluleni.
Nature (1998)
Mice lacking tartrate-resistant acid phosphatase (Acp 5) have disrupted endochondral ossification and mild osteopetrosis
Alison R. Hayman;Sheila J. Jones;Alan Boyde;Diane Foster.
Development (1996)
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