J. Northrop

发表

Single cell assay of a transcription factor reveals a threshold in transcription activated by signals emanating from the T-cell antigen receptor.

G. Nolan, G. Crabtree, S. Fiering, 1990, Genes & development.

Lipofection: a highly efficient, lipid-mediated DNA-transfection procedure.

J. Northrop, P. Felgner, T. Gadek, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Rapid shuttling of NF-AT in discrimination of Ca2+ signals and immunosuppression

G. Crabtree, S. Ho, J. Northrop, 1996, Nature.

A chemical biology toolbox to study protein methyltransferases and epigenetic signaling

Jian Jin, Matthieu Schapira, Jennifer A. Ward, 2019, Nature Communications.

Jun family members are controlled by a calcium-regulated, cyclosporin A-sensitive signaling pathway in activated T lymphocytes.

G. Crabtree, A. Admon, J. Northrop, 1993, Genes & development.

Transmission of signals from the T lymphocyte antigen receptor to the genes responsible for cell proliferation and immune function: the missing link.

G. Crabtree, J. Northrop, C. Verweij, 1990, Annual review of immunology.

Drugs and probes: the symbiotic relationship between pharmaceutical discovery and imaging science.

J. Northrop, D. Maclean, J. Walsh, 2003, Molecular imaging and biology : MIB : the official publication of the Academy of Molecular Imaging.

Characterization of wild type and mutant glucocorticoid receptors from rat hepatoma and mouse lymphoma cells.

R. Harrison, J. Northrop, G. Ringold, 1985, The Journal of biological chemistry.

TNF alpha-mediated inhibition and reversal of adipocyte differentiation is accompanied by suppressed expression of PPARgamma without effects on Pref-1 expression.

J. Northrop, K. Kilpatrick, G. Ringold, 1997, Endocrinology.

Cell surface expression of single chain antibodies with applications to imaging of gene expression in vivo

J. Star-Lack, King Li, M. Bednarski, 2003, European Journal of Nuclear Medicine and Molecular Imaging.

Compositions et methodes de detection des interactions dependant de ligands entre un recepteur nucleaire et un co-activateur

J. Northrop, Charles P. Hart, P. Schatz, 1999 .

Characterization of the nuclear and cytoplasmic components of the lymphoid-specific nuclear factor of activated T cells (NF-AT) complex.

G. Crabtree, J. Northrop, K. Ullman, 1993, The Journal of biological chemistry.

Glucocorticoid Receptors and the Control of Gene Expression

J. Northrop, G. Ringold, M. Danielsen, 1987 .

Analysis of glucocorticoid unresponsive cell variants using a mouse glucocorticoid receptor complementary DNA clone.

J. Northrop, G. Ringold, M. Danielsen, 1986, The Journal of biological chemistry.

TNF (cid:97) -Mediated Inhibition and Reversal of Adipocyte Differentiation Is Accompanied by Suppressed Expression of PPAR (cid:103) without Effects on Pref-1 Expression*

J. Northrop, K. Kilpatrick, G. Ringold, 1997 .

The mouse glucocorticoid receptor: mapping of functional domains by cloning, sequencing and expression of wild‐type and mutant receptor proteins.

J. Northrop, G. Ringold, M. Danielsen, 1986, The EMBO journal.

The mechanism of action of cyclosporin A and FK506.

L Timmermann, I. Graef, G. Crabtree, 1996, Clinical immunology and immunopathology.

Cloning and characterization of NF-ATc and NF-ATp: the cytoplasmic components of NF-AT.

G. Crabtree, S. Ho, J. Northrop, 1994, Advances in experimental medicine and biology.

TNFα-Mediated Inhibition and Reversal of Adipocyte Differentiation Is Accompanied by Suppressed Expression of PPARγ without Effects on Pref-1 Expression.

J. Northrop, K. Kilpatrick, G. Ringold, 1997, Endocrinology.

Histone H3 Lysine 9 Methyltransferase G9a Is a Transcriptional Coactivator for Nuclear Receptors*

J. Northrop, M. Stallcup, M. Kuo, 2006, Journal of Biological Chemistry.

Activating and inhibitory functions for the histone lysine methyltransferase G9a in T helper cell differentiation and function

S. Mullaly, F. Rossi, J. Northrop, 2010, The Journal of experimental medicine.

Domains of the glucocorticoid receptor involved in specific and nonspecific deoxyribonucleic acid binding, hormone activation, and transcriptional enhancement.

J. Jonklaas, J. Northrop, G. Ringold, 1987, Molecular endocrinology.

Potent inhibitory ligands of the GRB2 SH2 domain from recombinant peptide libraries.

J. Northrop, D. Patel, C. Hart, 1999, Cellular signalling.

Characterization of the roles of SH2 domain-containing proteins in T-lymphocyte activation by using dominant negative SH2 domains

J. Northrop, A. T. Lu, J. Grove, 1996, Molecular and cellular biology.

Expression of cre recombinase as a reporter of signal transduction in mammalian cells.

J. Northrop, L. Mattheakis, S. E. Olivan, 1999, Chemistry & biology.

High level expression of wild type and variant mouse glucocorticoid receptors in Chinese hamster ovary cells.

J. Northrop, G. Ringold, M. Danielsen, 1990, Molecular endocrinology.

NF-AT components define a family of transcription factors targeted in T-cell activation

G. Nolan, Daryl J. Thomas, G. Crabtree, 1994, Nature.

The ankyrin repeats of G9a and GLP histone methyltransferases are mono- and dimethyllysine binding modules

Xing Zhang, Robert E Collins, Xiaodong Cheng, 2008, Nature Structural &Molecular Biology.

Negative regulation of interleukin 2 transcription by the glucocorticoid receptor

G. Crabtree, J. Northrop, P. Mattila, 1992, The Journal of experimental medicine.

Selection of Estrogen Receptor β- and Thyroid Hormone Receptor β-Specific Coactivator-Mimetic Peptides Using Recombinant Peptide Libraries

J. Northrop, P. Schatz, C. Hart, 2000 .

Control of the hippo pathway by Set7-dependent methylation of Yap.

Amber L. Couzens, A. Gingras, M. Gold, 2013, Developmental cell.

A chemical biology toolbox to study protein methyltransferases and epigenetic signaling

Jennifer A. Ward, P. Richardson, C. Arrowsmith, 2018, bioRxiv.

Activating and inhibitory functions for the histone lysine methyltransferase G9a in T helper cell differentiation and function

S. Mullaly, F. Rossi, J. Northrop, 2010, The Journal of experimental medicine.