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Works by Pan, Yanzhen

Results: 4

1

Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3.

Published in:

Human Molecular Genetics, 2011, v. 20, n. 15, p. 3093, doi. 10.1093/hmg/ddr212

By:

Wang, Xiaoming;
McCoy, Portia A.;
Rodriguiz, Ramona M.;
Pan, Yanzhen;
Je, H. Shawn;
Roberts, Adam C.;
Kim, Caroline J.;
Berrios, Janet;
Colvin, Jennifer S.;
Bousquet-Moore, Danielle;
Lorenzo, Isabel;
Wu, Gangyi;
Weinberg, Richard J.;
Ehlers, Michael D.;
Philpot, Benjamin D.;
Beaudet, Arthur L.;
Wetsel, William C.;
Jiang, Yong-hui

Publication type:

Article

2

Altered Ultrasonic Vocalization and Impaired Learning and Memory in Angelman Syndrome Mouse Model with a Large Maternal Deletion from Ube3a to Gabrb3.

Published in:

PLoS ONE, 2010, v. 5, n. 8, p. 1, doi. 10.1371/journal.pone.0012278

By:

Yong-hui Jiang;
Yanzhen Pan;
Li Zhu;
Landa, Luis;
Jong Yoo;
Spencer, Corinne;
Lorenzo, Isabel;
Brilliant, Murray;
Noebels, Jeffrey;
Beaudet, Arthur L.

Publication type:

Article

3

Identification of Two Mutations in a Compound Heterozygous Child with Dihydrolipoamide Dehydrogenase Deficiency.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 12, p. 1925, doi. 10.1093/hmg/5.12.1925

By:

Hong, Young Soo;
Kerr, Douglas S.;
Craigen, William J.;
Tan, Jie;
Pan, Yanzhen;
Lusk, Marilyn;
Patel, Mulchand S.

Publication type:

Article

4

Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region.

Published in:

BMC Genomics, 2008, v. 9, p. 1, doi. 10.1186/1471-2164-9-50

By:

Yong-hui Jiang;
Wauki, Kekio;
Qian Liu;
Bressler, Jan;
Yanzhen Pan;
Kashork, Catherine D.;
Shaffer, Lisa G.;
Beaudet, Arthur L.

Publication type:

Article