Bartsch I - Search Results

1

Characterization of human septin interactions.

Sandrock K, Bartsch I, Bläser S, Busse A, Busse E, Zieger B. Sandrock K, et al. Among authors: bartsch i. Biol Chem. 2011 Aug;392(8-9):751-61. doi: 10.1515/BC.2011.081. Epub 2011 Jul 19. Biol Chem. 2011. PMID: 21767235

2

Human endothelial cell septins: SEPT11 is an interaction partner of SEPT5.

Bläser S, Röseler S, Rempp H, Bartsch I, Bauer H, Lieber M, Lessmann E, Weingarten L, Busse A, Huber M, Zieger B. Bläser S, et al. Among authors: bartsch i. J Pathol. 2006 Sep;210(1):103-10. doi: 10.1002/path.2013. J Pathol. 2006. PMID: 16767699

3

Septin expression in proliferative retinal membranes.

Xin X, Pache M, Zieger B, Bartsch I, Prünte C, Flammer J, Meyer P. Xin X, et al. Among authors: bartsch i. J Histochem Cytochem. 2007 Nov;55(11):1089-94. doi: 10.1369/jhc.7A7188.2007. Epub 2007 Jul 11. J Histochem Cytochem. 2007. PMID: 17625225 Free PMC article.

4

A large Swiss family with Bernard-Soulier syndrome - Correlation phenotype and genotype.

Zieger B, Jenny A, Tsakiris DA, Bartsch I, Sandrock K, Schubart C, Schäfer S, Busse A, Wuillemin WA. Zieger B, et al. Among authors: bartsch i. Hamostaseologie. 2009 May;29(2):161-7. Hamostaseologie. 2009. PMID: 19404517

5

Septins, a novel group of GTP-binding proteins: relevance in hemostasis, neuropathology and oncogenesis.

Roeseler S, Sandrock K, Bartsch I, Zieger B. Roeseler S, et al. Among authors: bartsch i. Klin Padiatr. 2009 May-Jun;221(3):150-5. doi: 10.1055/s-0029-1220706. Epub 2009 May 12. Klin Padiatr. 2009. PMID: 19437362 Review.

6

Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type I.

Vannier C, Behnisch W, Bartsch I, Sandrock K, Ertle F, Schmidt K, Busse A, Superti-Furga A, Kulozik A, Santoso S, Zieger B. Vannier C, et al. Among authors: bartsch i. Klin Padiatr. 2010 May;222(3):150-3. doi: 10.1055/s-0030-1249064. Epub 2010 May 31. Klin Padiatr. 2010. PMID: 20514618

7

Compound heterozygous mutations in 2 siblings with Hermansky-Pudlak syndrome type 1 (HPS1).

Sandrock K, Bartsch I, Rombach N, Schmidt K, Nakamura L, Hainmann I, Busse A, Zieger B. Sandrock K, et al. Among authors: bartsch i. Klin Padiatr. 2010 May;222(3):168-74. doi: 10.1055/s-0030-1249628. Epub 2010 May 31. Klin Padiatr. 2010. PMID: 20514622

8

Human endothelial and platelet septin SEPT11: cloning of novel variants and characterisation of interaction partners.

Bartsch I, Bläser S, Röseler S, Sandrock K, Busse A, Huber M, Rempp H, Lieber M, Horn J, Brendle C, Zieger B. Bartsch I, et al. Thromb Haemost. 2010 Dec;104(6):1201-10. doi: 10.1160/TH10-07-0472. Epub 2010 Oct 26. Thromb Haemost. 2010. PMID: 20978712

9

Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay.

Bartsch I, Sandrock K, Lanza F, Nurden P, Hainmann I, Pavlova A, Greinacher A, Tacke U, Barth M, Busse A, Oldenburg J, Bommer M, Strahm B, Superti-Furga A, Zieger B. Bartsch I, et al. Thromb Haemost. 2011 Sep;106(3):475-83. doi: 10.1160/TH11-05-0305. Epub 2011 Jul 28. Thromb Haemost. 2011. PMID: 21800012

10

Lethal phenotype of mice carrying a Sept11 null mutation.

Röseler S, Sandrock K, Bartsch I, Busse A, Omran H, Loges NT, Zieger B. Röseler S, et al. Among authors: bartsch i. Biol Chem. 2011 Aug;392(8-9):779-81. doi: 10.1515/BC.2011.093. Biol Chem. 2011. PMID: 21824005

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