Search Page
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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2005 | 1 |
2006 | 1 |
2007 | 1 |
2009 | 2 |
2011 | 2 |
2012 | 1 |
2024 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Succinate links TCA cycle dysfunction to oncogenesis by inhibiting HIF-alpha prolyl hydroxylase.
Cancer Cell. 2005 Jan;7(1):77-85. doi: 10.1016/j.ccr.2004.11.022.
Cancer Cell. 2005.
PMID: 15652751
Free article.
Metabolic transformation in cancer.
Tennant DA, Durán RV, Boulahbel H, Gottlieb E.
Tennant DA, et al. Among authors: boulahbel h.
Carcinogenesis. 2009 Aug;30(8):1269-80. doi: 10.1093/carcin/bgp070. Epub 2009 Mar 25.
Carcinogenesis. 2009.
PMID: 19321800
Review.
Item in Clipboard
Prolyl hydroxylases as regulators of cell metabolism.
Boulahbel H, Durán RV, Gottlieb E.
Boulahbel H, et al.
Biochem Soc Trans. 2009 Feb;37(Pt 1):291-4. doi: 10.1042/BST0370291.
Biochem Soc Trans. 2009.
PMID: 19143649
Review.
Item in Clipboard
Mdm2 targets the p53 transcription cofactor JMY for degradation.
Coutts AS, Boulahbel H, Graham A, La Thangue NB.
Coutts AS, et al. Among authors: boulahbel h.
EMBO Rep. 2007 Jan;8(1):84-90. doi: 10.1038/sj.embor.7400855. Epub 2006 Dec 15.
EMBO Rep. 2007.
PMID: 17170761
Free PMC article.
Item in Clipboard
Rapidly progressive renal disease as part of Wolfram syndrome in a large inbred Turkish family due to a novel WFS1 mutation (p.Leu511Pro).
Yuca SA, Rendtorff ND, Boulahbel H, Lodahl M, Tranebjærg L, Cesur Y, Dogan M, Yilmaz C, Akgun C, Acikgoz M.
Yuca SA, et al. Among authors: boulahbel h.
Eur J Med Genet. 2012 Jan;55(1):37-42. doi: 10.1016/j.ejmg.2011.08.005. Epub 2011 Sep 23.
Eur J Med Genet. 2012.
PMID: 21968327
Item in Clipboard
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment.
Rendtorff ND, Lodahl M, Boulahbel H, Johansen IR, Pandya A, Welch KO, Norris VW, Arnos KS, Bitner-Glindzicz M, Emery SB, Mets MB, Fagerheim T, Eriksson K, Hansen L, Bruhn H, Möller C, Lindholm S, Ensgaard S, Lesperance MM, Tranebjaerg L.
Rendtorff ND, et al. Among authors: boulahbel h.
Am J Med Genet A. 2011 Jun;155A(6):1298-313. doi: 10.1002/ajmg.a.33970. Epub 2011 Apr 28.
Am J Med Genet A. 2011.
PMID: 21538838
Free PMC article.
Item in Clipboard
Cite
Cite