Lars Schlotawa und Thomas Dierks - Info zur Person

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Der Schlüssel zur TherapieDetmolder Zeitung

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— Lars Schlotawa, Michaela Wachs, Olaf Bernhard, Franz J. Mayer, Thomas Dierks, Bernhard Schmidt, Karthikeyan Radhakrishnan: Recognition and — Lars Schlotawa, Michaela Wachs, Olaf Bernhard, Franz J. Mayer, Thomas Dierks, Bernhard Schmidt, Karthikeyan Radhakrishnan: Recognition and ...

uni.aktuell-Archiv: Der Schlüssel zur Therapie

blogs.uni-bielefeld.de

Nettet20. mai · Lars Schlotawa, Michaela Wachs, Olaf Bernhard, Franz J. Mayer, Thomas Dierks, Bernhard Schmidt, Karthikeyan Radhakrishnan: Recognition and ER quality …

Pressemitteilungen: Der Schlüssel zur Therapie (Nr )

blogs.uni-bielefeld.de

Lars Schlotawa, Michaela Wachs, Olaf Bernhard, Franz J. Mayer, Thomas Dierks, Bernhard Schmidt, Karthikeyan Radhakrishnan: Recognition and ER quality control of ...

Recognition and ER Quality Control of Misfolded Formylglycine ...www.cell.com › cell-reports › pdfExtended

www.cell.com

· Lars Schlotawa,1,5 Michaela Wachs,2 Olaf Bernhard,3 Franz J. Mayer,4 Thomas Dierks,2,6,* Bernhard Schmidt,3,* and Karthikeyan Radhakrishnan2 ...

Complex care of individuals with multiple sulfatase deficiencyjournals.scholarsportal.info › details

journals.scholarsportal.info

Lars Schlotawa · ORCID ID · Andrea Ballabio · ORCID ID · Nicola Brunetti-Pierri · ORCID ID · Mauricio De Castro · ORCID ID · Thomas Dierks · Florian Eichler ...

Thomas Dierks | Scinapsewww.scinapse.io › authors

www.scinapse.io

Lars Schlotawa. h-index: 13. University of Göttingen · Torben Lübke. h-index: 20. Bielefeld University · Ina Kalus. h-index: 9. Bielefeld University · Norbert ...

SUMF1 mutations affecting stability and activity of ...Archive ouverte HAL

hal.science

von T Dierks · · Zitiert von: 70 — Thomas Dierks, Lars Schlotawa, Eva Charlotte Ennemann, Karthikeyan Radhakrishnan, Bernhard. Schmidt, et al.. SUMF1 mutations affecting ... von T Dierks · · Zitiert von: 70 — Thomas Dierks, Lars Schlotawa, Eva Charlotte Ennemann, Karthikeyan Radhakrishnan, Bernhard. Schmidt, et al.. SUMF1 mutations affecting ...

A homozygous missense variant of SUMF1 in the Bedouin ...

europepmc.org

von O Staretz-Chacham · · Zitiert von: 3 — 1 , 2 , 3 Lars Schlotawa, 4 Ohad Wormser, 5 , 6 Inbal Golan‐Tripto, 3 Ohad S. Birk, 5 , 6 , 7 Carlos R. Ferreira, 8 Thomas Dierks, 9 and Karthikeyan ... › articles › bin

method for the treatment of diseases associated with sulfatase ...patents.justia.com › patent

patents.justia.com

— Inventors: Lars SCHLOTAWA (Gottingen), Matthias KETTWIG (Gottingen), Karthikeyan RADHAKRISHNAN (Bielefeld), Thomas DIERKS (Bielefeld), ...

Biochimica et Biophysica Acta (BBA) - Molecular Cell Research |...

www.sciencedirect.com

Open archive - Review article: Pages Thomas Dierks, Lars Schlotawa, Marc-André Frese, Karthikeyan Radhakrishnan, ... Bernhard Schmidt. Download ...

application/xml - PUBpub.uni-bielefeld.de › record

pub.uni-bielefeld.de

... Lars Schlotawa Lars Dierks, Thomas Dierks Thomas Ohlenbusch, Andreas Ohlenbusch Andreas Koppenhoefer, Dominique Koppenhoefer Dominique Babicz, Mariusz ...

Molecular Genetics and Metabolism | Vol 121, Issue 3, Pages www.sciencedirect.com › journal › vol › issue

www.sciencedirect.com

Ilona Jaszczuk, Lars Schlotawa, Thomas Dierks, Andreas Ohlenbusch, ... Agnieszka Ługowska. Pages : Download PDF. Article preview.

A novel SUMF1 variant in a patient displaying a severe late ...Uniwersytet Medyczny w Lublinie

ppm.umlub.pl

Lars Schlotawa,; Thomas Dierks,; Andreas Ohlenbusch,; Dominique Koppenhöfer,; Mariusz Babicz,; Monika Lejman,; Karthikeyan Radhakrishnan,; Agnieszka Ługowska ... Lars Schlotawa,; Thomas Dierks,; Andreas Ohlenbusch,; Dominique Koppenhöfer,; Mariusz Babicz,; Monika Lejman,; Karthikeyan Radhakrishnan,; Agnieszka Ługowska ...

Molecular analysis of SUMF1 mutationsRead by QxMD

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Lars Schlotawa, Robert Steinfeld, Kurt von Figura, Thomas Dierks, Jutta Gärtner. Human Mutation January. Multiple Sulfatase Deficiency (MSD) is a rare ... Lars Schlotawa, Robert Steinfeld, Kurt von Figura, Thomas Dierks, Jutta Gärtner. Human Mutation January. Multiple Sulfatase Deficiency (MSD) is a rare ...

Molecular basis of multiple sulfatase deficiency ...Read by QxMD

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Thomas Dierks, Lars Schlotawa, Marc-André Frese, Karthikeyan Radhakrishnan, Kurt von Figura, Bernhard Schmidt. Biochimica et Biophysica Acta April. Thomas Dierks, Lars Schlotawa, Marc-André Frese, Karthikeyan Radhakrishnan, Kurt von Figura, Bernhard Schmidt. Biochimica et Biophysica Acta April.

Rapid degradation of an active formylglycine generating ...Europe PMC

europepmc.org

von L Schlotawa · · Zitiert von: 24 — ... Lars Schlotawa,1,6 Karthikeyan Radhakrishnan,2,3,6 Matthias Baumgartner,4 Regula Schmid,5 Bernhard Schmidt,3 Thomas Dierks,2,* and Jutta Gärtner1. Lars ... von L Schlotawa · · Zitiert von: 24 — ... Lars Schlotawa,1,6 Karthikeyan Radhakrishnan,2,3,6 Matthias Baumgartner,4 Regula Schmid,5 Bernhard Schmidt,3 Thomas Dierks,2,* and Jutta Gärtner1. Lars ...

Severe neonatal multiple sulfatase deficiency presenting ...Akademie věd

katalog.lib.cas.cz

Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient. Autor: Lars Schlotawa, Thomas Dierks, Sophie ... Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient. Autor: Lars Schlotawa, Thomas Dierks, Sophie ...

Der Schlüssel zur TherapieMedWiss.Online

www.medwiss.de

— Originalveröffentlichung: Lars Schlotawa, Michaela Wachs, Olaf Bernhard, Franz J. Mayer, Thomas Dierks, Bernhard Schmidt, Karthikeyan — Originalveröffentlichung: Lars Schlotawa, Michaela Wachs, Olaf Bernhard, Franz J. Mayer, Thomas Dierks, Bernhard Schmidt, Karthikeyan ...

Jutta Gärtner
Alrun Hotz
Thomas Dierks

Hans-Jürgen Christen
Andreas Ohlenbusch
Christiane Kehrer

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Vorname "Lars" (24476)
Name "Schlotawa" (8)

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Lars Schlotawa und Thomas Dierks Person-Info

Der Schlüssel zur TherapieDetmolder Zeitung

uni.aktuell-Archiv: Der Schlüssel zur Therapie

Pressemitteilungen: Der Schlüssel zur Therapie (Nr )

Recognition and ER Quality Control of Misfolded Formylglycine ...www.cell.com › cell-reports › pdfExtended

Complex care of individuals with multiple sulfatase deficiencyjournals.scholarsportal.info › details

Thomas Dierks | Scinapsewww.scinapse.io › authors

SUMF1 mutations affecting stability and activity of ...Archive ouverte HAL

A homozygous missense variant of SUMF1 in the Bedouin ...

method for the treatment of diseases associated with sulfatase ...patents.justia.com › patent

Biochimica et Biophysica Acta (BBA) - Molecular Cell Research |...

application/xml - PUBpub.uni-bielefeld.de › record

Molecular Genetics and Metabolism | Vol 121, Issue 3, Pages www.sciencedirect.com › journal › vol › issue

A novel SUMF1 variant in a patient displaying a severe late ...Uniwersytet Medyczny w Lublinie

Molecular analysis of SUMF1 mutationsRead by QxMD

Molecular basis of multiple sulfatase deficiency ...Read by QxMD

Rapid degradation of an active formylglycine generating ...Europe PMC

Severe neonatal multiple sulfatase deficiency presenting ...Akademie věd

Der Schlüssel zur TherapieMedWiss.Online

Der Schlüssel zur Therapie • DGP

Proteine: Fehlfaltung mit Folgen - Vogel

A homozygous missense variant of SUMF1 in the Bedouin ...cris.bgu.ac.il › publications › a-homozygous-missen...

Ohad Birk - Publications List

Kurt von Figura: د Z-Library مفت الکترونیکی کتابتون

Molecular basis of multiple sulfatase deficiency, mucolipidosis...

Molecular analysis of SUMF1 mutations: stability and residual ...read.qxmd.com › read › molecular-analysis-of-sumf...

SUMF1 mutations affecting stability and activity of formylglycine ...hal.archives-ouvertes.fr › hal

Science Bulletin. der Fakultät VI Medizin und DocPlayer.org

Severe neonatal multiple sulfatase deficiency Cureuswww.cureus.com › pmc_articles

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