Wang Y - Search Results

1

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.

2

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.

3

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

4

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

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

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.

8

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.

9

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

10

Insulin increases the turnover rate of Na+-K+-ATPase in human fibroblasts.

Longo N, Scaglia F, Wang Y. Longo N, et al. Among authors: wang y. Am J Physiol Cell Physiol. 2001 Apr;280(4):C912-9. doi: 10.1152/ajpcell.2001.280.4.C912. Am J Physiol Cell Physiol. 2001. PMID: 11245608 Free article.

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