Zhang V - Search Results

1

Human surfactant protein D: SP-D contains a C-type lectin carbohydrate recognition domain.

Rust K, Grosso L, Zhang V, Chang D, Persson A, Longmore W, Cai GZ, Crouch E. Rust K, et al. Among authors: zhang v. Arch Biochem Biophys. 1991 Oct;290(1):116-26. doi: 10.1016/0003-9861(91)90597-c. Arch Biochem Biophys. 1991. PMID: 1898081

2

Molecular cloning, functional expression, and selective regulation of ovine prostaglandin H synthase-2.

Zhang V, O'Sullivan M, Hussain H, Roswit WT, Holtzman MJ. Zhang V, et al. Biochem Biophys Res Commun. 1996 Oct 14;227(2):499-506. doi: 10.1006/bbrc.1996.1536. Biochem Biophys Res Commun. 1996. PMID: 8878543

3

Prostaglandin H synthase and lipoxygenase gene families in the epithelial cell barrier.

Holtzman MJ, Zhang V, Hussain H, Roswit WT, Wilson JD. Holtzman MJ, et al. Among authors: zhang v. Ann N Y Acad Sci. 1994 Nov 15;744:58-77. doi: 10.1111/j.1749-6632.1994.tb52724.x. Ann N Y Acad Sci. 1994. PMID: 7825863 Review.

4

FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome.

Dai H, Zhang VW, El-Hattab AW, Ficicioglu C, Shinawi M, Lines M, Schulze A, McNutt M, Gotway G, Tian X, Chen S, Wang J, Craigen WJ, Wong LJ. Dai H, et al. Among authors: zhang vw. Clin Genet. 2017 Apr;91(4):634-639. doi: 10.1111/cge.12894. Epub 2017 Jan 5. Clin Genet. 2017. PMID: 27743463

5

An integrated approach for classifying mitochondrial DNA variants: one clinical diagnostic laboratory's experience.

Wang J, Schmitt ES, Landsverk ML, Zhang VW, Li FY, Graham BH, Craigen WJ, Wong LJ. Wang J, et al. Genet Med. 2012 Jun;14(6):620-6. doi: 10.1038/gim.2012.4. Epub 2012 Mar 8. Genet Med. 2012. PMID: 22402757 Free article.

6

Clinical application of massively parallel sequencing in the molecular diagnosis of glycogen storage diseases of genetically heterogeneous origin.

Wang J, Cui H, Lee NC, Hwu WL, Chien YH, Craigen WJ, Wong LJ, Zhang VW. Wang J, et al. Genet Med. 2013 Feb;15(2):106-14. doi: 10.1038/gim.2012.104. Epub 2012 Aug 16. Genet Med. 2013. PMID: 22899091 Free article.

7

Biochemical, molecular, and clinical diagnoses of patients with cerebral creatine deficiency syndromes.

Comeaux MS, Wang J, Wang G, Kleppe S, Zhang VW, Schmitt ES, Craigen WJ, Renaud D, Sun Q, Wong LJ. Comeaux MS, et al. Mol Genet Metab. 2013 Jul;109(3):260-8. doi: 10.1016/j.ymgme.2013.04.006. Epub 2013 Apr 17. Mol Genet Metab. 2013. PMID: 23660394

8

Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene.

Chanprasert S, Wang J, Weng SW, Enns GM, Boué DR, Wong BL, Mendell JR, Perry DA, Sahenk Z, Craigen WJ, Alcala FJ, Pascual JM, Melancon S, Zhang VW, Scaglia F, Wong LJ. Chanprasert S, et al. Mol Genet Metab. 2013 Sep-Oct;110(1-2):153-61. doi: 10.1016/j.ymgme.2013.07.009. Epub 2013 Jul 17. Mol Genet Metab. 2013. PMID: 23932787

9

Interpretation of mitochondrial tRNA variants.

Wong LC, Chen T, Wang J, Tang S, Schmitt ES, Landsverk M, Li F, Wang Y, Zhang S, Zhang VW, Craigen WJ. Wong LC, et al. Genet Med. 2020 May;22(5):917-926. doi: 10.1038/s41436-019-0746-0. Epub 2020 Jan 22. Genet Med. 2020. PMID: 31965079 Free article.

10

Added value of next generation gene panel analysis for patients with elevated methylmalonic acid and no clinical diagnosis following functional studies of vitamin B12 metabolism.

Pupavac M, Tian X, Chu J, Wang G, Feng Y, Chen S, Fenter R, Zhang VW, Wang J, Watkins D, Wong LJ, Rosenblatt DS. Pupavac M, et al. Mol Genet Metab. 2016 Mar;117(3):363-8. doi: 10.1016/j.ymgme.2016.01.008. Epub 2016 Jan 23. Mol Genet Metab. 2016. PMID: 26827111

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