S. Huang

发表

Targeted point mutagenesis of mouse Kcnq1: phenotypic analysis of mice with point mutations that cause Romano-Ward syndrome in humans.

M. Casimiro, A. Grinberg, K. Pfeifer, 2004, Genomics.

Vasopressin receptor 1a-mediated negative regulation of B cell receptor signaling

H. Westphal, A. Grinberg, P. Gold, 2003, Journal of Neuroimmunology.

Defects in enteric innervation and kidney development in mice lacking GDNF

Mart Saarma, Hannu Sariola, Barry J. Hoffer, 1996, Nature.

The H19 Differentially Methylated Region Marks the Parental Origin of a Heterologous Locus without Gametic DNA Methylation

A. Grinberg, K. Pfeifer, Kye-yoon Park, 2004, Molecular and Cellular Biology.

Specification of Pituitary Cell Lineages by the LIM Homeobox Gene Lhx3

B. Mosinger, H. Westphal, A. Grinberg, 1996, Science.

The LIM homeobox gene Lhx9 is essential for mouse gonad formation

O. Birk, Liping Zhao, J. Kreidberg, 2000, Nature.

Functional ablation of the mouse Ldb1 gene results in severe patterning defects during gastrulation

A. Teufel, H. Westphal, D. Dorward, 2003, Development.

H 19 and Igf 2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H 19

M. Srivastava, S. Hsieh, A. Grinberg, 2022 .

Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange– Nielsen Syndrome

M. Franz, B. Knollmann, M. Casimiro, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development.

F. Alt, D. Bodine, J. Drago, 1997, Development.

Dickkopf1 is required for embryonic head induction and limb morphogenesis in the mouse.

J. I. Izpisúa Belmonte, C. Niehrs, Concepción Rodríguez-Esteban, 2001, Developmental cell.

Isolated cleft palate in mice with a targeted mutation of the LIM homeobox gene lhx8.

H. Westphal, A. Grinberg, S. Huang, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Altered striatal function in a mutant mouse lacking D1A dopamine receptors.

C. Gerfen, H. Steiner, J. Lachowicz, 1994, Proceedings of the National Academy of Sciences of the United States of America.

T cell development in mice that lack the zeta chain of the T cell antigen receptor complex.

A. Singer, M. Tremblay, H. Westphal, 1993, Science.

Glial cell line-derived neurotrophic factor receptor α1 availability regulates glial cell line-derived neurotrophic factor signaling: evidence from mice carrying one or two mutated alleles

B. Hoffer, H. Westphal, A. Grinberg, 1999, Neuroscience.

Control of hippocampal morphogenesis and neuronal differentiation by the LIM homeobox gene Lhx5.

H. Westphal, A. Grinberg, S. Huang, 1999, Science.

H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19.

M. Srivastava, S. Hsieh, A. Grinberg, 2000, Genes & development.