Distinct expression profile in fumarate-hydratase-deficient uterine fibroids

Author： Vanharanta Sakari   Pollard Patrick J.   Lehtonen Heli J.   Laiho Päivi   Sjöberg Jari   Leminen Arto   Aittomäki Kristiina   Arola Johanna   Kruhoffer Mogens   Ørntoft Torben F.   Tomlinson Ian P.   Kiuru Maija   Arango Diego   Aaltonen Lauri A.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.15, Iss.1, 2006-01, pp. : 97-103

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency

By Alam N.A.  

Human Molecular Genetics, Vol. 12, Iss. 11, 2003-06 ,pp. : 1241-1252

Oxford University Press

Access to resources Recommend Favorite

Dysregulation of hypoxia pathways in fumarate hydratase-deficient cells is independent of defective mitochondrial metabolism

By O'Flaherty Linda   Adam Julie   Heather Lisa C.   Zhdanov Alexander V.   Chung Yuen-Li   Miranda Melroy X.   Croft Joanne   Olpin Simon   Clarke Kieran   Pugh Christopher W.   Griffiths John   Papkovsky Dmitri   Ashrafian Houman   Ratcliffe Peter J.   Pollard Patrick J.  

Human Molecular Genetics, Vol. 19, Iss. 19, 2010-10 ,pp. : 3844-3851

Oxford University Press

Access to resources Recommend Favorite

Expression profiling of uterine leiomyomata cytogenetic subgroups reveals distinct signatures in matched myometrium: transcriptional profiling of the t(12;14) and evidence in support of predisposing genetic heterogeneity

By Hodge Jennelle C.   Kim Tae-Min   Dreyfuss Jonathan M.   Somasundaram Priya   Christacos Nicole C.   Rousselle Marissa   Quade Bradley J.   Park Peter J.   Stewart Elizabeth A.   Morton Cynthia C.  

Human Molecular Genetics, Vol. 21, Iss. 10, 2012-05 ,pp. : 2312-2329

Oxford University Press

Access to resources Recommend Favorite

Neurofibroma-associated growth factors activate a distinct signaling network to alter the function of neurofibromin-deficient endothelial cells

By Munchhof Amy M.   Li Fang   Mead Laura E.   Krier Theresa R.   Fenoglio Amy   Li Xiaohong   Yuan Jin   Yang Feng-Chun   Ingram David A.  

Human Molecular Genetics, Vol. 15, Iss. 11, 2006-06 ,pp. : 1858-1869

Oxford University Press

Access to resources Recommend Favorite

Muscle-specific BCL2 expression ameliorates muscle disease in laminin α2-deficient, but not in dystrophin-deficient, mice

By Dominov Janice A.   Kravetz Amanda J.   Ardelt Magdalena   Kostek Christine A.   Beermann Mary Lou   Miller Jeffrey B.  

Human Molecular Genetics, Vol. 14, Iss. 8, 2005-04 ,pp. : 1029-1040

Oxford University Press

Access to resources Recommend Favorite