Rajagopalan KV - Search Results

1

Isolated sulfite oxidase deficiency: identification of 12 novel SUOX mutations in 10 patients.

Johnson JL, Coyne KE, Garrett RM, Zabot MT, Dorche C, Kisker C, Rajagopalan KV. Johnson JL, et al. Among authors: rajagopalan kv. Hum Mutat. 2002 Jul;20(1):74. doi: 10.1002/humu.9038. Hum Mutat. 2002. PMID: 12112661

2

Molecular cloning of human liver sulfite oxidase.

Garrett RM, Bellissimo DB, Rajagopalan KV. Garrett RM, et al. Among authors: rajagopalan kv. Biochim Biophys Acta. 1995 Jun 9;1262(2-3):147-9. doi: 10.1016/0167-4781(95)00068-r. Biochim Biophys Acta. 1995. PMID: 7599189

3

An HPLC assay for detection of elevated urinary S-sulphocysteine, a metabolic marker of sulphite oxidase deficiency.

Johnson JL, Rajagopalan KV. Johnson JL, et al. Among authors: rajagopalan kv. J Inherit Metab Dis. 1995;18(1):40-7. doi: 10.1007/BF00711371. J Inherit Metab Dis. 1995. PMID: 7623441

4

Molecular cloning of rat liver sulfite oxidase. Expression of a eukaryotic Mo-pterin-containing enzyme in Escherichia coli.

Garrett RM, Rajagopalan KV. Garrett RM, et al. Among authors: rajagopalan kv. J Biol Chem. 1994 Jan 7;269(1):272-6. J Biol Chem. 1994. PMID: 8276806 Free article.

5

Site-directed mutagenesis of recombinant sulfite oxidase: identification of cysteine 207 as a ligand of molybdenum.

Garrett RM, Rajagopalan KV. Garrett RM, et al. Among authors: rajagopalan kv. J Biol Chem. 1996 Mar 29;271(13):7387-91. J Biol Chem. 1996. PMID: 8631762 Free article.

6

Human sulfite oxidase R160Q: identification of the mutation in a sulfite oxidase-deficient patient and expression and characterization of the mutant enzyme.

Garrett RM, Johnson JL, Graf TN, Feigenbaum A, Rajagopalan KV. Garrett RM, et al. Among authors: rajagopalan kv. Proc Natl Acad Sci U S A. 1998 May 26;95(11):6394-8. doi: 10.1073/pnas.95.11.6394. Proc Natl Acad Sci U S A. 1998. PMID: 9600976 Free PMC article.

7

Molybdopterin synthase mutations in a mild case of molybdenum cofactor deficiency.

Johnson JL, Coyne KE, Rajagopalan KV, Van Hove JL, Mackay M, Pitt J, Boneh A. Johnson JL, et al. Among authors: rajagopalan kv. Am J Med Genet. 2001 Nov 22;104(2):169-73. doi: 10.1002/1096-8628(20011122)104:2<169::aid-ajmg1603>3.0.co;2-8. Am J Med Genet. 2001. PMID: 11746050

8

Isolated sulfite oxidase deficiency: mutation analysis and DNA-based prenatal diagnosis.

Johnson JL, Rajagopalan KV, Renier WO, Van der Burgt I, Ruitenbeek W. Johnson JL, et al. Among authors: rajagopalan kv. Prenat Diagn. 2002 May;22(5):433-6. doi: 10.1002/pd.335. Prenat Diagn. 2002. PMID: 12001203

9

Prenatal diagnosis of molybdenum cofactor deficiency by assay of sulphite oxidase activity in chorionic villus samples.

Johnson JL, Rajagopalan KV, Lanman JT, Schutgens RB, van Gennip AH, Sorensen P, Applegarth DA. Johnson JL, et al. Among authors: rajagopalan kv. J Inherit Metab Dis. 1991;14(6):932-7. doi: 10.1007/BF01800477. J Inherit Metab Dis. 1991. PMID: 1779653

10

The structure of the molybdenum cofactor. Characterization of di-(carboxamidomethyl)molybdopterin from sulfite oxidase and xanthine oxidase.

Kramer SP, Johnson JL, Ribeiro AA, Millington DS, Rajagopalan KV. Kramer SP, et al. Among authors: rajagopalan kv. J Biol Chem. 1987 Dec 5;262(34):16357-63. J Biol Chem. 1987. PMID: 3680253 Free article.

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