Amy Chen

发表

Cripto is required for correct orientation of the anterior–posterior axis in the mouse embryo

A. Wynshaw-Boris, M. Shen, Jixiang Ding, 1998, Nature.

Knockout of Slc25a19 causes mitochondrial thiamine pyrophosphate depletion, embryonic lethality, CNS malformations, and anemia

L. Biesecker, P. Schwartzberg, C. Mathews, 2006, Proceedings of the National Academy of Sciences.

Addendum: An expressed pseudogene regulates the messenger-RNA stability of its homologous coding gene

A. Yoshiki, A. Wynshaw-Boris, Satoru Takahashi, 2003, Nature.

Increased Activity of Hypoxia-Inducible Factor 1 Is Associated with Early Embryonic Lethality in Commd1 Null Mice

C. Wijmenga, P. Muller, B. van de Sluis, 2007, Molecular and Cellular Biology.

Altered lymphocyte responses and cytokine production in mice deficient in the X-linked lymphoproliferative disease gene SH2D1A/DSHP/SAP

A. Sher, R. Ahmed, C. Duckett, 2001, Proceedings of the National Academy of Sciences of the United States of America.

The Adaptor Protein CIKS/Act1 Is Essential for IL-25-Mediated Allergic Airway Inflammation1

A. Leonardi, T. Wynn, A. Chariot, 2009, The Journal of Immunology.

Role of Cbfb in hematopoiesis and perturbations resulting from expression of the leukemogenic fusion gene Cbfb-MYH11.

L. Castilla, D. Bodine, M. Kundu, 2002, Blood.

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality

D. Ledbetter, A. Wynshaw-Boris, C. McBain, 1998, Nature Genetics.

Parkinson Phenotype in Aged PINK1-Deficient Mice Is Accompanied by Progressive Mitochondrial Dysfunction in Absence of Neurodegeneration

R. Nussbaum, A. Reichert, A. Kurz, 2009, PloS one.

Melanoma mouse model implicates metabotropic glutamate signaling in melanocytic neoplasia

P. Meltzer, P. Pollock, J. Trent, 2003, Nature Genetics.

Biochemical and Phenotypic Abnormalities in Kynurenine Aminotransferase II-Deficient Mice

R. Schwarcz, D. Tagle, P. Yu, 2004, Molecular and Cellular Biology.

Ascorbic-acid transporter Slc23a1 is essential for vitamin C transport into the brain and for perinatal survival

R. Nussbaum, O. Kwon, S. Guttentag, 2002, Nature Medicine.

An expressed pseudogene regulates the messenger-RNA stability of its homologous coding gene

Atsushi Yoshiki, Lisa Garrett, Amy Chen, 2003, Nature.

Chapter 3.1.2 Generation of transgenic mice by pronuclear DNA injection

C. Barlow, A. Wynshaw-Boris, Amy Chen, 1999 .

Chapter 3.1.1 Embryonic stem cells and gene targeting

C. Barlow, A. Wynshaw-Boris, Amy Chen, 1999 .

Complementation of melanocyte development in SOX10 mutant neural crest using lineage‐directed gene transfer

W. Pavan, S. Loftus, L. Hou, 2004, Developmental dynamics : an official publication of the American Association of Anatomists.

Acinar Cell Apoptosis in Serpini2-Deficient Mice Models Pancreatic Insufficiency

W. Pavan, L. Biesecker, J. Cannons, 2005, PLoS genetics.

Transgenic mice expressing mutant A53T human alpha-synuclein show neuronal dysfunction in the absence of aggregate formation

Georg Auburger, Lisa Garrett, Amy Chen, 2003, Molecular and Cellular Neuroscience.

Complete Loss of Ndel1 Results in Neuronal Migration Defects and Early Embryonic Lethality

N. Hiraiwa, A. Yoshiki, A. Wynshaw-Boris, 2005, Molecular and Cellular Biology.

RIF‐1, a novel nuclear receptor corepressor that associates with the nuclear matrix

Z. Haque, M. Mendelsohn, Amy Chen, 2007, Journal of cellular biochemistry.

Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.

P. Scambler, R. Paylor, A. Wynshaw-Boris, 1999, Human molecular genetics.

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

E. Green, B. Kachar, R. Cantos, 2001, Human molecular genetics.