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Items: 14

1.

Flagellin-induced NADPH oxidase 4 activation is involved in atherosclerosis.

Kim J, Seo M, Kim SK, Bae YS.

Sci Rep. 2016 May 5;6:25437. doi: 10.1038/srep25437.

2.

Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta.

Garbes L, Kim K, Rieß A, Hoyer-Kuhn H, Beleggia F, Bevot A, Kim MJ, Huh YH, Kweon HS, Savarirayan R, Amor D, Kakadia PM, Lindig T, Kagan KO, Becker J, Boyadjiev SA, Wollnik B, Semler O, Bohlander SK, Kim J, Netzer C.

Am J Hum Genet. 2015 Mar 5;96(3):432-9. doi: 10.1016/j.ajhg.2015.01.002.

3.

Overexpression of TLR7 promotes cell-intrinsic expansion and autoantibody production by transitional T1 B cells.

Giltiay NV, Chappell CP, Sun X, Kolhatkar N, Teal TH, Wiedeman AE, Kim J, Tanaka L, Buechler MB, Hamerman JA, Imanishi-Kari T, Clark EA, Elkon KB.

J Exp Med. 2013 Nov 18;210(12):2773-89. doi: 10.1084/jem.20122798.

4.

MAPK/ERK Signaling Pathway Analysis in Primary Osteoblasts From Patients With Nonsyndromic Sagittal Craniosynostosis.

Kim SD, Yagnik G, Cunningham ML, Kim J, Boyadjiev SA.

Cleft Palate Craniofac J. 2014 Jan;51(1):115-9. doi: 10.1597/12-136.

5.

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.

Justice CM, Yagnik G, Kim Y, Peter I, Jabs EW, Erazo M, Ye X, Ainehsazan E, Shi L, Cunningham ML, Kimonis V, Roscioli T, Wall SA, Wilkie AO, Stoler J, Richtsmeier JT, Heuzé Y, Sanchez-Lara PA, Buckley MF, Druschel CM, Mills JL, Caggana M, Romitti PA, Kay DM, Senders C, Taub PJ, Klein OD, Boggan J, Zwienenberg-Lee M, Naydenov C, Kim J, Wilson AF, Boyadjiev SA.

Nat Genet. 2012 Dec;44(12):1360-4. doi: 10.1038/ng.2463.

6.

ALX4 gain-of-function mutations in nonsyndromic craniosynostosis.

Yagnik G, Ghuman A, Kim S, Stevens CG, Kimonis V, Stoler J, Sanchez-Lara PA, Bernstein JA, Naydenov C, Drissi H, Cunningham ML, Kim J, Boyadjiev SA.

Hum Mutat. 2012 Dec;33(12):1626-9. doi: 10.1002/humu.22166.

7.

Leucine-rich repeat, immunoglobulin-like and transmembrane domain 3 (LRIT3) is a modulator of FGFR1.

Kim SD, Liu JL, Roscioli T, Buckley MF, Yagnik G, Boyadjiev SA, Kim J.

FEBS Lett. 2012 May 21;586(10):1516-21. doi: 10.1016/j.febslet.2012.04.010.

8.

The [corrected] SEC23-SEC31 [corrected] interface plays critical role for export of procollagen from the endoplasmic reticulum.

Kim SD, Pahuja KB, Ravazzola M, Yoon J, Boyadjiev SA, Hammamoto S, Schekman R, Orci L, Kim J.

J Biol Chem. 2012 Mar 23;287(13):10134-44. doi: 10.1074/jbc.M111.283382. Erratum in: J Biol Chem. 2012 Sep 21;287(39):32860.

9.

Mice deficient in LMAN1 exhibit FV and FVIII deficiencies and liver accumulation of α1-antitrypsin.

Zhang B, Zheng C, Zhu M, Tao J, Vasievich MP, Baines A, Kim J, Schekman R, Kaufman RJ, Ginsburg D.

Blood. 2011 Sep 22;118(12):3384-91. doi: 10.1182/blood-2011-05-352815.

10.

Cranio-lenticulo-sutural dysplasia associated with defects in collagen secretion.

Boyadjiev SA, Kim SD, Hata A, Haldeman-Englert C, Zackai EH, Naydenov C, Hamamoto S, Schekman RW, Kim J.

Clin Genet. 2011 Aug;80(2):169-76. doi: 10.1111/j.1399-0004.2010.01550.x.

11.

Sequence analyses of presenilin mutations linked to familial Alzheimer's disease.

Kim SD, Kim J.

Cell Stress Chaperones. 2008 Dec;13(4):401-12. doi: 10.1007/s12192-008-0046-0. Review.

12.

Biogenesis of gamma-secretase early in the secretory pathway.

Kim J, Kleizen B, Choy R, Thinakaran G, Sisodia SS, Schekman RW.

J Cell Biol. 2007 Dec 3;179(5):951-63.

13.

Chloroplast SecA and Escherichia coli SecA have distinct lipid and signal peptide preferences.

Sun C, Rusch SL, Kim J, Kendall DA.

J Bacteriol. 2007 Feb;189(3):1171-5.

14.

The ins and outs of presenilin 1 membrane topology.

Kim J, Schekman R.

Proc Natl Acad Sci U S A. 2004 Jan 27;101(4):905-6. No abstract available.

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