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XB-GENEPAGE-5796324
Papers associated with fancf
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TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B, Borday C, Erkilic N, Mamaeva D, Donval A, Masson C, Parain K, Kaminska K, Quinodoz M, Perea-Romero I, Garcia-Garcia G, Jimenez-Medina C, Boukhaddaoui H, Coget A, Leboucq N, Calzetti G, Gandolfi S, Percesepe A, Barili V, Uliana V, Delsante M, Bozzetti F, Scholl HP, Corton M, Ayuso C, Millan JM, Rivolta C, Meunier I, Perron M, Kalatzis V., JCI Insight. November 8, 2023; 8 (21):  |
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Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channel., Henrion U, Zumhagen S, Steinke K, Strutz-Seebohm N, Stallmeyer B, Lang F, Schulze-Bahr E, Seebohm G., Cell Physiol Biochem. January 1, 2012; 29 (5-6): 809-18. |
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Identification, developmental expression and regulation of the Xenopus ortholog of human FANCG/XRCC9., Stone S, Sobeck A, van Kogelenberg M, de Graaf B, Joenje H, Christian J, Hoatlin ME., Genes Cells. July 1, 2007; 12 (7): 841-51.  |
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The Fanconi anemia gene product FANCF is a flexible adaptor protein., Léveillé F, Blom E, Medhurst AL, Bier P, Laghmani el H, Johnson M, Rooimans MA, Sobeck A, Waisfisz Q, Arwert F, Patel KJ, Hoatlin ME, Joenje H, de Winter JP., J Biol Chem. September 17, 2004; 279 (38): 39421-30. |
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Synthesis of biologically active fibroblast-activating factor (FAF) by xenopus oocytes injected with T lymphocyte mRNA., Agelli M, Wahl SM., Cell Immunol. November 1, 1987; 110 (1): 183-90. |
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