Mutations and impaired function of LKB1 in familial and non-familial Peutz–Jeghers syndrome and a sporadic testicular cancer

By Markie D.  

Human Molecular Genetics, Vol. 8, Iss. 1, 1999-01 ,pp. : 45-51

Oxford University Press

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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 BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families

By Olsson H.  

Human Molecular Genetics, Vol. 10, Iss. 4, 2001-02 ,pp. : 353-360

Oxford University Press

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Altered LKB1/AMPK/TSC1/TSC2/mTOR signaling causes disruption of Sertoli cell polarity and spermatogenesis

By Tanwar Pradeep S.   Kaneko-Tarui Tomoko   Zhang LiHua   Teixeira Jose M.  

Human Molecular Genetics, Vol. 21, Iss. 20, 2012-10 ,pp. : 4394-4405

Oxford University Press

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