LIP1, a cytoplasmic protein functionally linked to the Peutz-Jeghers syndrome kinase LKB1

By Smith D.P.  

Human Molecular Genetics, Vol. 10, Iss. 25, 2001-12 ,pp. : 2869-2877

Oxford University Press

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The mouse Peutz–Jeghers syndrome gene Lkb1 encodes a nuclear protein kinase

By Smith Darrin P.   Spicer James   Smith Amanda   Swift Sally   Ashworth Alan   Peutz J.L.   Jeghers H.   Boardman M.D.   Spigelman A.D.   Hemminki A.   Hemminki A.   Nezu J.   Su J.-Y.   Jeanne D.E.   Mehenni H.   Ylikorkala A.   Kozak M.   Hall S.L.   Nagy E.   Williams T.   Laudet V.   Ashworth A.   Amariglio F.   Gusse M.   Smith D.P.   Yoneda Y.   Shaw P.J.   Jiang R   Randez Gil F.   Vincent O.   Polakis P.   Howe J.R.   He T.C.   Lorenzo M.J.   Thompson J.D.  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1479-1485

Oxford University Press

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Functional analysis of Peutz–Jeghers mutations reveals that the LKB1 C-terminal region exerts a crucial role in regulating both the AMPK pathway and the cell polarity

By Forcet Christelle  

Human Molecular Genetics, Vol. 14, Iss. 10, 2005-05 ,pp. : 1283-1292

Oxford University Press

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KVLQT1 Mutations in Three Families with Familial or Sporadic Long QT Syndrome

By Russell Mark W.   Dick Macdonald   Collins Francis S.   Brody Lawrence C.  

Human Molecular Genetics, Vol. 5, Iss. 9, 1996-01 ,pp. : 1319-1324

Oxford University Press

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Understanding familial and non-familial renal cell cancer

By Bodmer D.  

Human Molecular Genetics, Vol. 11, Iss. 20, 2002-10 ,pp. : 2489-2498

Oxford University Press

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