Schmidt B - Search Results

1

Guanidinoacetate methyltransferase deficiency: the first inborn error of creatine metabolism in man.

Stöckler S, Isbrandt D, Hanefeld F, Schmidt B, von Figura K. Stöckler S, et al. Among authors: schmidt b. Am J Hum Genet. 1996 May;58(5):914-22. Am J Hum Genet. 1996. PMID: 8651275 Free PMC article.

2

A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency.

Schmidt B, Selmer T, Ingendoh A, von Figura K. Schmidt B, et al. Cell. 1995 Jul 28;82(2):271-8. doi: 10.1016/0092-8674(95)90314-3. Cell. 1995. PMID: 7628016 Free article.

3

A novel protein modification generating an aldehyde group in sulfatases: its role in catalysis and disease.

von Figura K, Schmidt B, Selmer T, Dierks T. von Figura K, et al. Among authors: schmidt b. Bioessays. 1998 Jun;20(6):505-10. doi: 10.1002/(SICI)1521-1878(199806)20:6<505::AID-BIES9>3.0.CO;2-K. Bioessays. 1998. PMID: 9699462 Review.

4

Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme.

Dierks T, Schmidt B, Borissenko LV, Peng J, Preusser A, Mariappan M, von Figura K. Dierks T, et al. Among authors: schmidt b. Cell. 2003 May 16;113(4):435-44. doi: 10.1016/s0092-8674(03)00347-7. Cell. 2003. PMID: 12757705 Free article.

5

In vitro mutagenesis of potential N-glycosylation sites of arylsulfatase A. Effects on glycosylation, phosphorylation, and intracellular sorting.

Gieselmann V, Schmidt B, von Figura K. Gieselmann V, et al. Among authors: schmidt b. J Biol Chem. 1992 Jul 5;267(19):13262-6. J Biol Chem. 1992. PMID: 1352293 Free article.

6

The evolutionary conservation of a novel protein modification, the conversion of cysteine to serinesemialdehyde in arylsulfatase from Volvox carteri.

Selmer T, Hallmann A, Schmidt B, Sumper M, von Figura K. Selmer T, et al. Among authors: schmidt b. Eur J Biochem. 1996 Jun 1;238(2):341-5. doi: 10.1111/j.1432-1033.1996.0341z.x. Eur J Biochem. 1996. PMID: 8681943 Free article.

A novel post-translational protein modification has recently been described in two human sulfatases, by which a cysteine is replaced by a serinesemialdehyde (2-amino-3-oxopropionic acid) residue [Schmidt, B., Selmer, T., Ingendoh, A. & von Figura, K. (1995) Cell …

A novel post-translational protein modification has recently been described in two human sulfatases, by which a cysteine is replaced by a se …

7

The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes.

Landgrebe J, Dierks T, Schmidt B, von Figura K. Landgrebe J, et al. Among authors: schmidt b. Gene. 2003 Oct 16;316:47-56. doi: 10.1016/s0378-1119(03)00746-7. Gene. 2003. PMID: 14563551

8

The internalization signal in the cytoplasmic tail of lysosomal acid phosphatase consists of the hexapeptide PGYRHV.

Lehmann LE, Eberle W, Krull S, Prill V, Schmidt B, Sander C, von Figura K, Peters C. Lehmann LE, et al. Among authors: schmidt b. EMBO J. 1992 Dec;11(12):4391-9. doi: 10.1002/j.1460-2075.1992.tb05539.x. EMBO J. 1992. PMID: 1425575 Free PMC article.

9

Glycosylation of the Mr 46,000 mannose 6-phosphate receptor. Effect on ligand binding, stability, and conformation.

Wendland M, Waheed A, Schmidt B, Hille A, Nagel G, von Figura K, Pohlmann R. Wendland M, et al. Among authors: schmidt b. J Biol Chem. 1991 Mar 5;266(7):4598-604. J Biol Chem. 1991. PMID: 1847926 Free article.

10

Antibodies against the cytoplasmic tail can differentiate between the quaternary forms of the Mr 46,000 mannose 6-phosphate receptor.

Nadimpalli SK, Schmidt B, von Figura K, Hille A. Nadimpalli SK, et al. Among authors: schmidt b. FEBS Lett. 1991 Mar 11;280(1):61-4. doi: 10.1016/0014-5793(91)80204-g. FEBS Lett. 1991. PMID: 1849096 Free article.

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