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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 1
2004 1
2005 3
2006 1
2007 2
2008 1
2011 1
2012 2
2013 2
2016 3
2018 2
2020 2
2021 6
2022 3
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28 results
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Page 1
Wolfram syndrome: MAMs' connection?
Delprat B, Maurice T, Delettre C. Delprat B, et al. Cell Death Dis. 2018 Mar 6;9(3):364. doi: 10.1038/s41419-018-0406-3. Cell Death Dis. 2018. PMID: 29511163 Free PMC article. Review.
Editorial: Organelles Relationships and Interactions: A Cancer Perspective.
Patergnani S, Marchi S, Delprat B, Wieckowski MR. Patergnani S, et al. Among authors: delprat b. Front Cell Dev Biol. 2021 Apr 8;9:678307. doi: 10.3389/fcell.2021.678307. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33898471 Free PMC article. No abstract available.
Use of Zebrafish Models to Boost Research in Rare Genetic Diseases.
Crouzier L, Richard EM, Sourbron J, Lagae L, Maurice T, Delprat B. Crouzier L, et al. Among authors: delprat b. Int J Mol Sci. 2021 Dec 12;22(24):13356. doi: 10.3390/ijms222413356. Int J Mol Sci. 2021. PMID: 34948153 Free PMC article. Review.
[FXYD proteins: novel regulators of Na,K-ATPase].
Delprat B, Bibert S, Geering K. Delprat B, et al. Med Sci (Paris). 2006 Jun-Jul;22(6-7):633-8. doi: 10.1051/medsci/20062267633. Med Sci (Paris). 2006. PMID: 16828040 Free article. Review. French.
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss.
Bassani S, van Beelen E, Rossel M, Voisin N, Morgan A, Arribat Y, Chatron N, Chrast J, Cocca M, Delprat B, Faletra F, Giannuzzi G, Guex N, Machavoine R, Pradervand S, Smits JJ, van de Kamp JM, Ziegler A, Amati F, Marlin S, Kremer H, Locher H, Maurice T, Gasparini P, Girotto G, Reymond A. Bassani S, et al. Among authors: delprat b. Hum Mol Genet. 2021 Sep 15;30(19):1785-1796. doi: 10.1093/hmg/ddab145. Hum Mol Genet. 2021. PMID: 34059922
28 results