Vreugde S - Search Results

1

Colloidal silver against macrophage infections and biofilms of atypical mycobacteria.

Feizi S, Cooksley CM, Ramezanpour M, Nepal R, Psaltis AJ, Wormald PJ, Vreugde S. Feizi S, et al. Among authors: vreugde s. Biometals. 2023 Aug;36(4):913-925. doi: 10.1007/s10534-023-00494-w. Epub 2023 Feb 2. Biometals. 2023. PMID: 36729280 Free PMC article.

2

SPPL2a and SPPL2b promote intramembrane proteolysis of TNFalpha in activated dendritic cells to trigger IL-12 production.

Friedmann E, Hauben E, Maylandt K, Schleeger S, Vreugde S, Lichtenthaler SF, Kuhn PH, Stauffer D, Rovelli G, Martoglio B. Friedmann E, et al. Among authors: vreugde s. Nat Cell Biol. 2006 Aug;8(8):843-8. doi: 10.1038/ncb1440. Epub 2006 Jul 9. Nat Cell Biol. 2006. PMID: 16829952

3

Metastasis of a renal cell carcinoma to the nose and paranasal sinuses.

Vreugde S, Duttmann R, Halama A, Deron P. Vreugde S, et al. Acta Otorhinolaryngol Belg. 1999;53(2):129-31. Acta Otorhinolaryngol Belg. 1999. PMID: 10427366

4

USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses.

Adato A, Vreugde S, Joensuu T, Avidan N, Hamalainen R, Belenkiy O, Olender T, Bonne-Tamir B, Ben-Asher E, Espinos C, Millán JM, Lehesjoki AE, Flannery JG, Avraham KB, Pietrokovski S, Sankila EM, Beckmann JS, Lancet D. Adato A, et al. Among authors: vreugde s. Eur J Hum Genet. 2002 Jun;10(6):339-50. doi: 10.1038/sj.ejhg.5200831. Eur J Hum Genet. 2002. PMID: 12080385

5

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

Vreugde S, Erven A, Kros CJ, Marcotti W, Fuchs H, Kurima K, Wilcox ER, Friedman TB, Griffith AJ, Balling R, Hrabé De Angelis M, Avraham KB, Steel KP. Vreugde S, et al. Nat Genet. 2002 Mar;30(3):257-8. doi: 10.1038/ng848. Epub 2002 Feb 19. Nat Genet. 2002. PMID: 11850623

6

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population.

Sobe T, Vreugde S, Shahin H, Berlin M, Davis N, Kanaan M, Yaron Y, Orr-Urtreger A, Frydman M, Shohat M, Avraham KB. Sobe T, et al. Among authors: vreugde s. Hum Genet. 2000 Jan;106(1):50-7. doi: 10.1007/s004390051009. Hum Genet. 2000. PMID: 10982182

7

Nuclear myosin VI enhances RNA polymerase II-dependent transcription.

Vreugde S, Ferrai C, Miluzio A, Hauben E, Marchisio PC, Crippa MP, Bussi M, Biffo S. Vreugde S, et al. Mol Cell. 2006 Sep 1;23(5):749-55. doi: 10.1016/j.molcel.2006.07.005. Mol Cell. 2006. PMID: 16949370 Free article.

8

Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor.

Frydman M, Vreugde S, Nageris BI, Weiss S, Vahava O, Avraham KB. Frydman M, et al. Among authors: vreugde s. Arch Otolaryngol Head Neck Surg. 2000 May;126(5):633-7. doi: 10.1001/archotol.126.5.633. Arch Otolaryngol Head Neck Surg. 2000. PMID: 10807331

9

Calcific tendinitis of the longus colli muscle.

De Maeseneer M, Vreugde S, Laureys S, Sartoris DJ, De Ridder F, Osteaux M. De Maeseneer M, et al. Among authors: vreugde s. Head Neck. 1997 Sep;19(6):545-8. doi: 10.1002/(sici)1097-0347(199709)19:6<545::aid-hed13>3.0.co;2-4. Head Neck. 1997. PMID: 9278764

10

High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim.

Sobe T, Erlich P, Berry A, Korostichevsky M, Vreugde S, Avraham KB, Bonné-Tamir B, Shohat M. Sobe T, et al. Among authors: vreugde s. Am J Med Genet. 1999 Oct 29;86(5):499-500. Am J Med Genet. 1999. PMID: 10508996 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

179 results

Search Page