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Items: 35

1.

Defects in the Exocyst-Cilia Machinery Cause Bicuspid Aortic Valve Disease and Aortic Stenosis.

Fulmer D, Toomer K, Guo L, Moore K, Glover J, Moore R, Stairley R, Lobo G, Zuo X, Dang Y, Su Y, Fogelgren B, Gerard P, Chung D, Heydarpour M, Mukherjee R, Body SC, Norris RA, Lipschutz JH.

Circulation. 2019 Aug 7. doi: 10.1161/CIRCULATIONAHA.119.038376. [Epub ahead of print]

PMID:
31387361
2.

Disruption of the exocyst induces podocyte loss and dysfunction.

Nihalani D, Solanki AK, Arif E, Srivastava P, Rahman B, Zuo X, Dang Y, Fogelgren B, Fermin D, Gillies CE, Sampson MG, Lipschutz JH.

J Biol Chem. 2019 Jun 28;294(26):10104-10119. doi: 10.1074/jbc.RA119.008362. Epub 2019 May 9.

PMID:
31073028
3.

Correction to: Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of Hearing.

Lee B, Baek JI, Min H, Bae SH, Moon K, Kim MA, Kim YR, Fogelgren B, Lipschutz JH, Lee KY, Bok J, Kim UK.

Mol Neurobiol. 2019 Mar;56(3):2300. doi: 10.1007/s12035-019-1470-0.

PMID:
30637586
4.

Transcriptional regulatory control of mammalian nephron progenitors revealed by multi-factor cistromic analysis and genetic studies.

O'Brien LL, Guo Q, Bahrami-Samani E, Park JS, Hasso SM, Lee YJ, Fang A, Kim AD, Guo J, Hong TM, Peterson KA, Lozanoff S, Raviram R, Ren B, Fogelgren B, Smith AD, Valouev A, McMahon AP.

PLoS Genet. 2018 Jan 29;14(1):e1007181. doi: 10.1371/journal.pgen.1007181. eCollection 2018 Jan.

5.

Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of Hearing.

Lee B, Baek JI, Min H, Bae SH, Moon K, Kim MA, Kim YR, Fogelgren B, Lipschutz JH, Lee KY, Bok J, Kim UK.

Mol Neurobiol. 2018 Aug;55(8):6518-6532. doi: 10.1007/s12035-017-0857-z. Epub 2018 Jan 11. Erratum in: Mol Neurobiol. 2019 Jan 14;:.

PMID:
29327200
6.

The exocyst is required for photoreceptor ciliogenesis and retinal development.

Lobo GP, Fulmer D, Guo L, Zuo X, Dang Y, Kim SH, Su Y, George K, Obert E, Fogelgren B, Nihalani D, Norris RA, Rohrer B, Lipschutz JH.

J Biol Chem. 2017 Sep 8;292(36):14814-14826. doi: 10.1074/jbc.M117.795674. Epub 2017 Jul 20.

7.

Regulation of Cell Polarity by Exocyst-Mediated Trafficking.

Polgar N, Fogelgren B.

Cold Spring Harb Perspect Biol. 2018 Mar 1;10(3). pii: a031401. doi: 10.1101/cshperspect.a031401. Review.

8.

Fibroproliferative response to urothelial failure obliterates the ureter lumen in a mouse model of prenatal congenital obstructive nephropathy.

Lee AJ, Polgar N, Napoli JA, Lui VH, Tamashiro KK, Fujimoto BA, Thompson KS, Fogelgren B.

Sci Rep. 2016 Aug 11;6:31137. doi: 10.1038/srep31137.

9.

Pan-Cancer Analyses Reveal Long Intergenic Non-Coding RNAs Relevant to Tumor Diagnosis, Subtyping and Prognosis.

Ching T, Peplowska K, Huang S, Zhu X, Shen Y, Molnar J, Yu H, Tiirikainen M, Fogelgren B, Fan R, Garmire LX.

EBioMedicine. 2016 May;7:62-72. doi: 10.1016/j.ebiom.2016.03.023. Epub 2016 Mar 19.

10.

A mutation in the tuft mouse disrupts TET1 activity and alters the expression of genes that are crucial for neural tube closure.

Fong KS, Hufnagel RB, Khadka VS, Corley MJ, Maunakea AK, Fogelgren B, Ahmed ZM, Lozanoff S.

Dis Model Mech. 2016 May 1;9(5):585-96. doi: 10.1242/dmm.024109. Epub 2016 Mar 17.

11.

Arl13b and the exocyst interact synergistically in ciliogenesis.

Seixas C, Choi SY, Polgar N, Umberger NL, East MP, Zuo X, Moreiras H, Ghossoub R, Benmerah A, Kahn RA, Fogelgren B, Caspary T, Lipschutz JH, Barral DC.

Mol Biol Cell. 2016 Jan 15;27(2):308-20. doi: 10.1091/mbc.E15-02-0061. Epub 2015 Nov 18.

12.

Urothelial Defects from Targeted Inactivation of Exocyst Sec10 in Mice Cause Ureteropelvic Junction Obstructions.

Fogelgren B, Polgar N, Lui VH, Lee AJ, Tamashiro KK, Napoli JA, Walton CB, Zuo X, Lipschutz JH.

PLoS One. 2015 Jun 5;10(6):e0129346. doi: 10.1371/journal.pone.0129346. eCollection 2015.

13.

The exocyst gene Sec10 regulates renal epithelial monolayer homeostasis and apoptotic sensitivity.

Polgar N, Lee AJ, Lui VH, Napoli JA, Fogelgren B.

Am J Physiol Cell Physiol. 2015 Aug 1;309(3):C190-201. doi: 10.1152/ajpcell.00011.2015. Epub 2015 Jun 3.

14.

Exocyst Sec10 protects renal tubule cells from injury by EGFR/MAPK activation and effects on endocytosis.

Fogelgren B, Zuo X, Buonato JM, Vasilyev A, Baek JI, Choi SY, Chacon-Heszele MF, Palmyre A, Polgar N, Drummond I, Park KM, Lazzara MJ, Lipschutz JH.

Am J Physiol Renal Physiol. 2014 Dec 15;307(12):F1334-41. doi: 10.1152/ajprenal.00032.2014. Epub 2014 Oct 8.

15.

Exocyst Sec10 is involved in basolateral protein translation and translocation in the endoplasmic reticulum.

Choi SY, Fogelgren B, Zuo X, Huang L, McKenna S, Lingappa VR, Lipschutz JH.

Nephron Exp Nephrol. 2012;120(4):e134-40. doi: 10.1159/000342366. Epub 2012 Oct 4.

16.

Osmoregulatory defect in adult mice associated with deficient prenatal expression of six2.

Somponpun SJ, Wong B, Hynd TE, Fogelgren B, Lozanoff S.

Am J Physiol Regul Integr Comp Physiol. 2011 Sep;301(3):R682-9. doi: 10.1152/ajpregu.00187.2011. Epub 2011 Jun 8.

17.

The small GTPase Cdc42 is necessary for primary ciliogenesis in renal tubular epithelial cells.

Zuo X, Fogelgren B, Lipschutz JH.

J Biol Chem. 2011 Jun 24;286(25):22469-77. doi: 10.1074/jbc.M111.238469. Epub 2011 May 4.

18.

The exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypes.

Fogelgren B, Lin SY, Zuo X, Jaffe KM, Park KM, Reichert RJ, Bell PD, Burdine RD, Lipschutz JH.

PLoS Genet. 2011 Apr;7(4):e1001361. doi: 10.1371/journal.pgen.1001361. Epub 2011 Apr 7.

19.

Adeno-Associated Virus-Mediated Gene Transfer to Renal Tubule Cells via a Retrograde Ureteral Approach.

Chung DC, Fogelgren B, Park KM, Heidenberg J, Zuo X, Huang L, Bennett J, Lipschutz JH.

Nephron Extra. 2011 Jan;1(1):217-23. doi: 10.1159/000333071. Epub 2011 Nov 23.

20.

Exocyst Sec10 protects epithelial barrier integrity and enhances recovery following oxidative stress, by activation of the MAPK pathway.

Park KM, Fogelgren B, Zuo X, Kim J, Chung DC, Lipschutz JH.

Am J Physiol Renal Physiol. 2010 Mar;298(3):F818-26. doi: 10.1152/ajprenal.00596.2009. Epub 2010 Jan 6.

21.

Deficiency in Six2 during prenatal development is associated with reduced nephron number, chronic renal failure, and hypertension in Br/+ adult mice.

Fogelgren B, Yang S, Sharp IC, Huckstep OJ, Ma W, Somponpun SJ, Carlson EC, Uyehara CF, Lozanoff S.

Am J Physiol Renal Physiol. 2009 May;296(5):F1166-78. doi: 10.1152/ajprenal.90550.2008. Epub 2009 Feb 4.

22.

Misexpression of Six2 is associated with heritable frontonasal dysplasia and renal hypoplasia in 3H1 Br mice.

Fogelgren B, Kuroyama MC, McBratney-Owen B, Spence AA, Malahn LE, Anawati MK, Cabatbat C, Alarcon VB, Marikawa Y, Lozanoff S.

Dev Dyn. 2008 Jul;237(7):1767-79. doi: 10.1002/dvdy.21587.

23.

Mutation in Mpzl3, a novel [corrected] gene encoding a predicted [corrected] adhesion protein, in the rough coat (rc) mice with severe skin and hair abnormalities.

Cao T, Racz P, Szauter KM, Groma G, Nakamatsu GY, Fogelgren B, Pankotai E, He QP, Csiszar K.

J Invest Dermatol. 2007 Jun;127(6):1375-86. Epub 2007 Feb 1. Erratum in: J Invest Dermatol. 2007 Nov;127(11):2678.

24.

Lysyl oxidase interacts with hormone placental lactogen and synergistically promotes breast epithelial cell proliferation and migration.

Polgar N, Fogelgren B, Shipley JM, Csiszar K.

J Biol Chem. 2007 Feb 2;282(5):3262-72. Epub 2006 Nov 27.

25.

Lysyl oxidase regulates breast cancer cell migration and adhesion through a hydrogen peroxide-mediated mechanism.

Payne SL, Fogelgren B, Hess AR, Seftor EA, Wiley EL, Fong SF, Csiszar K, Hendrix MJ, Kirschmann DA.

Cancer Res. 2005 Dec 15;65(24):11429-36.

26.

Cellular fibronectin binds to lysyl oxidase with high affinity and is critical for its proteolytic activation.

Fogelgren B, Polgár N, Szauter KM, Ujfaludi Z, Laczkó R, Fong KS, Csiszar K.

J Biol Chem. 2005 Jul 1;280(26):24690-7. Epub 2005 Apr 19.

27.

Drosophila lysyl oxidases Dmloxl-1 and Dmloxl-2 are differentially expressed and the active DmLOXL-1 influences gene expression and development.

Molnar J, Ujfaludi Z, Fong SF, Bollinger JA, Waro G, Fogelgren B, Dooley DM, Mink M, Csiszar K.

J Biol Chem. 2005 Jun 17;280(24):22977-85. Epub 2005 Apr 4.

28.

Progressive hair loss and myocardial degeneration in rough coat mice: reduced lysyl oxidase-like (LOXL) in the skin and heart.

Hayashi K, Cao T, Passmore H, Jourdan-Le Saux C, Fogelgren B, Khan S, Hornstra I, Kim Y, Hayashi M, Csiszar K.

J Invest Dermatol. 2004 Nov;123(5):864-71.

29.

Structural and functional diversity of lysyl oxidase and the LOX-like proteins.

Molnar J, Fong KS, He QP, Hayashi K, Kim Y, Fong SF, Fogelgren B, Szauter KM, Mink M, Csiszar K.

Biochim Biophys Acta. 2003 Apr 11;1647(1-2):220-4. Review.

PMID:
12686136
30.

A novel human lysyl oxidase-like gene (LOXL4) on chromosome 10q24 has an altered scavenger receptor cysteine rich domain.

Asuncion L, Fogelgren B, Fong KS, Fong SF, Kim Y, Csiszar K.

Matrix Biol. 2001 Nov;20(7):487-91.

PMID:
11691588
32.

Mutations of the INI1 rhabdoid tumor suppressor gene in medulloblastomas and primitive neuroectodermal tumors of the central nervous system.

Biegel JA, Fogelgren B, Zhou JY, James CD, Janss AJ, Allen JC, Zagzag D, Raffel C, Rorke LB.

Clin Cancer Res. 2000 Jul;6(7):2759-63.

33.

Germline INI1 mutation in a patient with a central nervous system atypical teratoid tumor and renal rhabdoid tumor.

Biegel JA, Fogelgren B, Wainwright LM, Zhou JY, Bevan H, Rorke LB.

Genes Chromosomes Cancer. 2000 May;28(1):31-7.

PMID:
10738300
34.

Isolation of genes from the rhabdoid tumor deletion region in chromosome band 22q11.2.

Zhou J, Fogelgren B, Wang Z, Roe BA, Biegel JA.

Gene. 2000 Jan 4;241(1):133-41.

PMID:
10607907
35.

Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors.

Biegel JA, Zhou JY, Rorke LB, Stenstrom C, Wainwright LM, Fogelgren B.

Cancer Res. 1999 Jan 1;59(1):74-9.

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