Intramembrane-cleaving aspartic proteases and disease: presenilins, signal peptide peptidase and their homologs

By Martoglio Bruno  

Human Molecular Genetics, Vol. 12, Iss. 2, 2003-10 ,pp. : 201-206

Oxford University Press

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Disruption of the WFS1 gene in mice causes progressive -cell loss and impaired stimulus–secretion coupling in insulin secretion

By Ishihara Hisamitsu   Takeda Satoshi   Tamura Akira   Takahashi Rui   Yamaguchi Suguru   Takei Daisuke   Yamada Takahiro   Inoue Hiroshi   Soga Hiroyuki   Katagiri Hideki   Tanizawa Yukio   Oka Yoshitomo  

Human Molecular Genetics, Vol. 13, Iss. 11, 2004-06 ,pp. : 1159-1170

Oxford University Press

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Loss of Cited2 causes congenital heart disease by perturbing left–right patterning of the body axis

By Lopes Floro Kylie   Artap Stanley T.   Preis Jost I.   Fatkin Diane   Chapman Gavin   Furtado Milena B.   Harvey Richard P.   Hamada Hiroshi   Sparrow Duncan B.   Dunwoodie Sally L.  

Human Molecular Genetics, Vol. 20, Iss. 6, 2011-03 ,pp. : 1097-1110

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Loss of Tsc1 , but not Pten , in renal tubular cells causes polycystic kidney disease by activating mTORC1

By Zhou Jing   Brugarolas James   Parada Luis F.  

Human Molecular Genetics, Vol. 18, Iss. 22, 2009-11 ,pp. : 4428-4441

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A retroviral gene trap insertion into the histone 3.3A gene causes partial neonatal lethality, stunted growth, neuromuscular deficits and male sub-fertility in transgenic mice

By Couldrey Christine   Carlton Mark B.L.  

Human Molecular Genetics, Vol. 8, Iss. 13, 1999-12 ,pp. : 2489-2495

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