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Enhancement of IRES-mediated translation of the c-myc and BiP mRNAs by the poly(A) tail is independent of intact eIF4G and PABP.
Thoma C, Bergamini G, Galy B, Hundsdoerfer P, Hentze MW. Thoma C, et al. Among authors: hundsdoerfer p. Mol Cell. 2004 Sep 24;15(6):925-35. doi: 10.1016/j.molcel.2004.08.021. Mol Cell. 2004. PMID: 15383282
Eukaryotic translation initiation factor 4GI and p97 promote cellular internal ribosome entry sequence-driven translation.
Hundsdoerfer P, Thoma C, Hentze MW. Hundsdoerfer P, et al. Proc Natl Acad Sci U S A. 2005 Sep 20;102(38):13421-6. doi: 10.1073/pnas.0506536102. Epub 2005 Sep 7. Proc Natl Acad Sci U S A. 2005. PMID: 16174738 Free PMC article.
The prothrombin 3'end formation signal reveals a unique architecture that is sensitive to thrombophilic gain-of-function mutations.
Danckwardt S, Gehring NH, Neu-Yilik G, Hundsdoerfer P, Pforsich M, Frede U, Hentze MW, Kulozik AE. Danckwardt S, et al. Among authors: hundsdoerfer p. Blood. 2004 Jul 15;104(2):428-35. doi: 10.1182/blood-2003-08-2894. Epub 2004 Apr 1. Blood. 2004. PMID: 15059842
Increased efficiency of mRNA 3' end formation: a new genetic mechanism contributing to hereditary thrombophilia.
Gehring NH, Frede U, Neu-Yilik G, Hundsdoerfer P, Vetter B, Hentze MW, Kulozik AE. Gehring NH, et al. Among authors: hundsdoerfer p. Nat Genet. 2001 Aug;28(4):389-92. doi: 10.1038/ng578. Nat Genet. 2001. PMID: 11443298
Chronic haemolytic anaemia and glucose-6 phosphate dehydrogenase deficiency. Case report and review of the literature.
Hundsdoerfer P, Vetter B, Kulozik AE. Hundsdoerfer P, et al. Acta Haematol. 2002;108(2):102-5. doi: 10.1159/000064749. Acta Haematol. 2002. PMID: 12187030 Review.
Design of a prospective neonatal cohort study of homozygous and double heterozygous factor V Leiden and factor II G20210A.
Hundsdoerfer P, Vetter B, Stöver B, Bassir C, Mönch E, Ziemer S, Kulozik AE. Hundsdoerfer P, et al. Klin Padiatr. 2000 Jul-Aug;212(4):159-62. doi: 10.1055/s-2000-9670. Klin Padiatr. 2000. PMID: 10994543
Proximal and distal 15q25.2 microdeletions-genotype-phenotype delineation of two neurodevelopmental susceptibility loci.
Doelken SC, Seeger K, Hundsdoerfer P, Weber-Ferro W, Klopocki E, Graul-Neumann L. Doelken SC, et al. Among authors: hundsdoerfer p. Am J Med Genet A. 2013 Jan;161A(1):218-24. doi: 10.1002/ajmg.a.35695. Epub 2012 Dec 14. Am J Med Genet A. 2013. PMID: 23239641
FDG-PET in 10 children with non-Hodgkin's lymphoma: initial experience in staging and follow-up.
Amthauer H, Furth C, Denecke T, Hundsdoerfer P, Voelker T, Seeger K, Stöver B, Henze G. Amthauer H, et al. Among authors: hundsdoerfer p. Klin Padiatr. 2005 Nov-Dec;217(6):327-33. doi: 10.1055/s-2005-872517. Klin Padiatr. 2005. PMID: 16307418
Homozygous and double heterozygous Factor V Leiden and Factor II G20210A genotypes predispose infants to thromboembolism but are not associated with an increase of foetal loss.
Hundsdoerfer P, Vetter B, Stöver B, Bassir C, Scholz T, Grimmer I, Mönch E, Ziemer S, Rossi R, Kulozik AE. Hundsdoerfer P, et al. Thromb Haemost. 2003 Oct;90(4):628-35. doi: 10.1160/TH03-02-0096. Thromb Haemost. 2003. PMID: 14515183
2017 GPOH Guidelines for Diagnosis and Treatment of Patients with Neuroblastic Tumors.
Simon T, Hero B, Schulte JH, Deubzer H, Hundsdoerfer P, von Schweinitz D, Fuchs J, Schmidt M, Prasad V, Krug B, Timmermann B, Leuschner I, Fischer M, Langer T, Astrahantseff K, Berthold F, Lode H, Eggert A. Simon T, et al. Among authors: hundsdoerfer p. Klin Padiatr. 2017 May;229(3):147-167. doi: 10.1055/s-0043-103086. Epub 2017 May 30. Klin Padiatr. 2017. PMID: 28561228 English.
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