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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.
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.
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HIF-independent role of prolyl hydroxylases in the cellular response to amino acids.
Durán RV, MacKenzie ED, Boulahbel H, Frezza C, Heiserich L, Tardito S, Bussolati O, Rocha S, Hall MN, Gottlieb E.
Durán RV, et al. Among authors: boulahbel h.
Oncogene. 2013 Sep 19;32(38):4549-56. doi: 10.1038/onc.2012.465. Epub 2012 Oct 22.
Oncogene. 2013.
PMID: 23085753
Free PMC article.
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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.
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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.
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Solar photodegradation of Rhodamine B dye by Cu2O/TiO2 heterostructure: experimental and computational studies of degradation and toxicity.
Messaadia L, Kiamouche S, Lahmar H, Masmoudi R, Boulahbel H, Trari M, Benamira M.
Messaadia L, et al. Among authors: boulahbel h.
J Mol Model. 2023 Jan 14;29(2):38. doi: 10.1007/s00894-023-05449-z.
J Mol Model. 2023.
PMID: 36639544
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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
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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.
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