Prolyl hydroxylases as regulators of cell metabolism
Boulahbel, Houda, Durán, Raúl V, Gottlieb, Eyal
Published in Biochemical Society transactions (01.02.2009)
Published in Biochemical Society transactions (01.02.2009)
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Journal Article
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment
Rendtorff, Nanna D., Lodahl, Marianne, Boulahbel, Houda, Johansen, Ida R., Pandya, Arti, Welch, Katherine O., Norris, Virginia W., Arnos, Kathleen S., Bitner-Glindzicz, Maria, Emery, Sarah B., Mets, Marilyn B., Fagerheim, Toril, Eriksson, Kristina, Hansen, Lars, Bruhn, Helene, Möller, Claes, Lindholm, Sture, Ensgaard, Stefan, Lesperance, Marci M., Tranebjaerg, Lisbeth
Published in American journal of medical genetics. Part A (01.06.2011)
Published in American journal of medical genetics. Part A (01.06.2011)
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Journal Article
Mdm2 targets the p53 transcription cofactor JMY for degradation
Coutts, Amanda S, Boulahbel, Houda, Graham, Anne, La Thangue, Nicholas B
Published in EMBO reports (01.01.2007)
Published in EMBO reports (01.01.2007)
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Journal Article
Metabolic transformation in cancer
Tennant, Daniel A., Durán, Raúl V., Boulahbel, Houda, Gottlieb, Eyal
Published in Carcinogenesis (New York) (01.08.2009)
Published in Carcinogenesis (New York) (01.08.2009)
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Journal Article
Succinate links TCA cycle dysfunction to oncogenesis by inhibiting HIF-α prolyl hydroxylase
Selak, Mary A., Armour, Sean M., MacKenzie, Elaine D., Boulahbel, Houda, Watson, David G., Mansfield, Kyle D., Pan, Yi, Simon, M.Celeste, Thompson, Craig B., Gottlieb, Eyal
Published in Cancer cell (2005)
Published in Cancer cell (2005)
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Journal Article
Rapidly progressive renal disease as part of Wolfram syndrome in a large inbred Turkish family due to a novel WFS1 mutation (p.Leu511Pro)
Yuca, Sevil Ari, Rendtorff, Nanna Dahl, Boulahbel, Houda, Lodahl, Marianne, Tranebjærg, Lisbeth, Cesur, Yasar, Dogan, Murat, Yilmaz, Cahide, Akgun, Cihangir, Acikgoz, Mehmet
Published in European journal of medical genetics (01.01.2012)
Published in European journal of medical genetics (01.01.2012)
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Journal Article