Wang Y - Search Results

1

A missense mutation in the OCTN2 gene associated with residual carnitine transport activity.

Wang Y, Kelly MA, Cowan TM, Longo N. Wang Y, et al. Hum Mutat. 2000;15(3):238-45. doi: 10.1002/(SICI)1098-1004(200003)15:3<238::AID-HUMU4>3.0.CO;2-3. Hum Mutat. 2000. PMID: 10679939

2

Functional domains in the carnitine transporter OCTN2, defective in primary carnitine deficiency.

Amat di San Filippo C, Wang Y, Longo N. Amat di San Filippo C, et al. Among authors: wang y. J Biol Chem. 2003 Nov 28;278(48):47776-84. doi: 10.1074/jbc.M307911200. Epub 2003 Sep 23. J Biol Chem. 2003. PMID: 14506273 Free article.

3

Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency.

Wang Y, Ye J, Ganapathy V, Longo N. Wang Y, et al. Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2356-60. doi: 10.1073/pnas.96.5.2356. Proc Natl Acad Sci U S A. 1999. PMID: 10051646 Free PMC article.

4

Functional characterization of the carnitine transporter defective in primary carnitine deficiency.

Scaglia F, Wang Y, Longo N. Scaglia F, et al. Among authors: wang y. Arch Biochem Biophys. 1999 Apr 1;364(1):99-106. doi: 10.1006/abbi.1999.1118. Arch Biochem Biophys. 1999. PMID: 10087170

5

Abnormal sodium stimulation of carnitine transport in primary carnitine deficiency.

Wang Y, Meadows TA, Longo N. Wang Y, et al. J Biol Chem. 2000 Jul 7;275(27):20782-6. doi: 10.1074/jbc.M000194200. J Biol Chem. 2000. PMID: 10783384 Free article.

6

Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: lack of genotype-phenotype correlation.

Wang Y, Taroni F, Garavaglia B, Longo N. Wang Y, et al. Hum Mutat. 2000 Nov;16(5):401-7. doi: 10.1002/1098-1004(200011)16:5<401::AID-HUMU4>3.0.CO;2-J. Hum Mutat. 2000. PMID: 11058897

7

Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency.

Scaglia F, Wang Y, Singh RH, Dembure PP, Pasquali M, Fernhoff PM, Longo N. Scaglia F, et al. Among authors: wang y. Genet Med. 1998 Nov-Dec;1(1):34-9. doi: 10.1097/00125817-199811000-00008. Genet Med. 1998. PMID: 11261427 Free article.

8

Phenotype and genotype variation in primary carnitine deficiency.

Wang Y, Korman SH, Ye J, Gargus JJ, Gutman A, Taroni F, Garavaglia B, Longo N. Wang Y, et al. Genet Med. 2001 Nov-Dec;3(6):387-92. doi: 10.1097/00125817-200111000-00002. Genet Med. 2001. PMID: 11715001 Free article.

9

Genotype-phenotype correlation in inherited severe insulin resistance.

Longo N, Wang Y, Smith SA, Langley SD, DiMeglio LA, Giannella-Neto D. Longo N, et al. Among authors: wang y. Hum Mol Genet. 2002 Jun 1;11(12):1465-75. doi: 10.1093/hmg/11.12.1465. Hum Mol Genet. 2002. PMID: 12023989

10

Progressive decline in insulin levels in Rabson-Mendenhall syndrome.

Longo N, Wang Y, Pasquali M. Longo N, et al. Among authors: wang y. J Clin Endocrinol Metab. 1999 Aug;84(8):2623-9. doi: 10.1210/jcem.84.8.5902. J Clin Endocrinol Metab. 1999. PMID: 10443650

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

293,271 results

Search Page

Filters