Yu P - Search Results

1

Praja1, a novel gene encoding a RING-H2 motif in mouse development.

Mishra L, Tully RE, Monga SP, Yu P, Cai T, Makalowski W, Mezey E, Pavan WJ, Mishra B. Mishra L, et al. Among authors: yu p. Oncogene. 1997 Nov 6;15(19):2361-8. doi: 10.1038/sj.onc.1201405. Oncogene. 1997. PMID: 9393880

2

Identification of mouse itih-4 encoding a glycoprotein with two EF-hand motifs from early embryonic liver.

Cai T, Yu P, Monga SP, Mishra B, Mishra L. Cai T, et al. Among authors: yu p. Biochim Biophys Acta. 1998 May 29;1398(1):32-7. doi: 10.1016/s0167-4781(98)00049-9. Biochim Biophys Acta. 1998. PMID: 9602042

3

Genomic structure, chromosomal mapping, and muscle-specific expression of a PH domain-associated intronless gene, cded/lior.

Mishra L, Yu P, Cai T, Monga SP, Mishra B. Mishra L, et al. Among authors: yu p. Mamm Genome. 1999 Jan;10(1):62-7. doi: 10.1007/s003359900944. Mamm Genome. 1999. PMID: 9892736

4

Elf3 encodes a novel 200-kD beta-spectrin: role in liver development.

Mishra L, Cai T, Yu P, Monga SP, Mishra B. Mishra L, et al. Among authors: yu p. Oncogene. 1999 Jan 14;18(2):353-64. doi: 10.1038/sj.onc.1202313. Oncogene. 1999. PMID: 9927192

5

A novel isoform of beta-spectrin II localizes to cerebellar Purkinje-cell bodies and interacts with neurofibromatosis type 2 gene product schwannomin.

Chen Y, Yu P, Lu D, Tagle DA, Cai T. Chen Y, et al. Among authors: yu p. J Mol Neurosci. 2001 Aug;17(1):59-70. doi: 10.1385/JMN:17:1:59. J Mol Neurosci. 2001. PMID: 11665863

6

Trinucleotide repeat expansion of spinocerebellar ataxia (SCA1) found in a Chinese family.

Cai T, Yu P, Chen X, Lopa M. Cai T, et al. Among authors: yu p. Chin Med J (Engl). 1998 Feb;111(2):160-2. Chin Med J (Engl). 1998. PMID: 10374379

7

Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.

Cai T, Yu P, Tagle DA, Xia J. Cai T, et al. Among authors: yu p. Am J Med Genet. 1999 Oct 8;86(4):305-11. Am J Med Genet. 1999. PMID: 10494083 Review.

8

A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility.

Cai T, Yu P, Tagle DA, Lu D, Chen Y, Xia J. Cai T, et al. Among authors: yu p. Hum Reprod. 2001 Jan;16(1):59-62. doi: 10.1093/humrep/16.1.59. Hum Reprod. 2001. PMID: 11139537

9

A novel case of unilateral blepharophimosis syndrome and mental retardation associated with de novo trisomy for chromosome 3q.

Cai T, Tagle DA, Xia X, Yu P, He XX, Li LY, Xia JH. Cai T, et al. Among authors: yu p. J Med Genet. 1997 Sep;34(9):772-6. doi: 10.1136/jmg.34.9.772. J Med Genet. 1997. PMID: 9321768 Free PMC article. Review.

10

Genomic organization and expression analysis of mouse kynurenine aminotransferase II, a possible factor in the pathophysiology of Huntington's disease.

Yu P, Mosbrook DM, Tagle DA. Yu P, et al. Mamm Genome. 1999 Sep;10(9):845-52. doi: 10.1007/s003359901102. Mamm Genome. 1999. PMID: 10441733

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