Papers associated with apob

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	A secretory cell type develops alongside multiciliated cells, ionocytes and goblet cells, and provides a protective, anti-infective function in the frog embryonic mucociliary epidermis., Dubaissi E, Rousseau K, Lea R, Soto X, Nardeosingh S, Schweickert A, Amaya E, Thornton DJ, Papalopulu N., Development. April 1, 2014; 141 (7): 1514-25.
	Conservation of a vitellogenin gene cluster in oviparous vertebrates and identification of its traces in the platypus genome., Babin PJ., Gene. April 30, 2008; 413 (1-2): 76-82.
	A non-canonical Grb2-PLC-gamma1-Sos cascade triggered by lipovitellin 1, an apolipoprotein B homologue., Browaeys-Poly E, Broutin I, Antoine AF, Marin M, Lescuyer A, Vilain JP, Ducruix A, Cailliau K., Cell Signal. December 1, 2007; 19 (12): 2540-8.
	Microsomal triglyceride transfer protein promotes the secretion of Xenopus laevis vitellogenin A1., Sellers JA, Hou L, Schoenberg DR, Batistuzzo de Medeiros SR, Wahli W, Shelness GS., J Biol Chem. April 8, 2005; 280 (14): 13902-5.
	An atlas of differential gene expression during early Xenopus embryogenesis., Pollet N, Muncke N, Verbeek B, Li Y, Fenger U, Delius H, Niehrs C., Mech Dev. March 1, 2005; 122 (3): 365-439.
	A common binding site on the microsomal triglyceride transfer protein for apolipoprotein B and protein disulfide isomerase., Bradbury P, Mann CJ, Köchl S, Anderson TA, Chester SA, Hancock JM, Ritchie PJ, Amey J, Harrison GB, Levitt DG, Banaszak LJ, Scott J, Shoulders CC., J Biol Chem. January 29, 1999; 274 (5): 3159-64.
	Evaluation of a clinically applicable mutation screening technique for genetic diagnosis of familial hypercholesterolemia and familial defective apolipoprotein B., Nissen H, Hansen AB, Guldberg P, Hansen TS, Petersen NE, Hørder M., Clin Genet. June 1, 1998; 53 (6): 433-9.
	Characterization of the platelet-activating factor acetylhydrolase from human plasma by heterologous expression in Xenopus laevis oocytes., Yamada Y, Stafforini DM, Imaizumi T, Zimmerman GA, McIntyre TM, Prescott SM., Proc Natl Acad Sci U S A. October 25, 1994; 91 (22): 10320-4.
	Expression and characterization of p27, the catalytic subunit of the apolipoprotein B mRNA editing enzyme., Driscoll DM, Zhang Q., J Biol Chem. August 5, 1994; 269 (31): 19843-7.
	Complementation of apolipoprotein B mRNA editing by human liver accompanied by secretion of apolipoprotein B48., Giannoni F, Bonen DK, Funahashi T, Hadjiagapiou C, Burant CF, Davidson NO., J Biol Chem. February 25, 1994; 269 (8): 5932-6.
	Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein., Shoulders CC, Brett DJ, Bayliss JD, Narcisi TM, Jarmuz A, Grantham TT, Leoni PR, Bhattacharya S, Pease RJ, Cullen PM., Hum Mol Genet. December 1, 1993; 2 (12): 2109-16.
	Analysis of a pause transfer sequence from apolipoprotein B., Chuck SL, Lingappa VR., J Biol Chem. October 25, 1993; 268 (30): 22794-801.
	The p27 catalytic subunit of the apolipoprotein B mRNA editing enzyme is a cytidine deaminase., Navaratnam N, Morrison JR, Bhattacharya S, Patel D, Funahashi T, Giannoni F, Teng BB, Davidson NO, Scott J., J Biol Chem. October 5, 1993; 268 (28): 20709-12.
	The low density lipoprotein receptor in Xenopus laevis. II. Feedback repression mediated by conserved sterol regulatory element., Mehta KD, Brown MS, Bilheimer DW, Goldstein JL., J Biol Chem. June 5, 1991; 266 (16): 10415-9.
	Vitellogenin--homologs of mammalian apolipoproteins?, Perez LE, Fenton MJ, Callard IP., Comp Biochem Physiol B. January 1, 1991; 100 (4): 821-6.
	Is vitellogenin an ancestor of apolipoprotein B-100 of human low-density lipoprotein and human lipoprotein lipase?, Baker ME., Biochem J. November 1, 1988; 255 (3): 1057-60.

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