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5 results for author:"Bechtel S."Drop in Literature Citations

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The full-ORF clone resource of the German cDNA consortium.

Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U., Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H. et al.

BMC Genomics 8:399-399(2007) · UniProtKB (2,241)

An anthropoid-specific segmental duplication on human chromosome 1q22.

Kuryshev V.Y., Vorobyov E., Zink D., Schmitz J., Rozhdestvensky T.S., Muenstermann E., Ernst U., Wellenreuther R., Moosmayer P., Bechtel S. et al.

Genomics 88:143-151(2006) · UniProtKB (1) · Mapped (1)

The systematic functional characterisation of Xq28 genes prioritises candidate disease genes.

Kolb-Kokocinski A., Mehrle A., Bechtel S., Simpson J.C., Kioschis P., Wiemann S., Wellenreuther R., Poustka A.

BMC Genomics 7:29-29(2006) · UniProtKB (2)

The effect of amino-acid substitutions I112P, D147E and K152N in CYP11B2 on the catalytic activities of the enzyme.

Bechtel S., Belkina N., Bernhardt R.

Eur. J. Biochem. 269:1118-1127(2002) · Mapped (5)

Mutations in aldosterone synthase gene of Milan hypertensive rats: phenotypic consequences.

Lloyd-MacGilp S.A., Torielli L., Bechtel S., Tripodi G., Gomez-Sanchez C.E., Zagato L., Bernhardt R., Kenyon C.J.

Am. J. Physiol. Endocrinol. Metab. 282:E608-17(2002) · Mapped (1)

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