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Items: 1 to 20 of 30


The C-Terminal Extension Unique to the Long Isoform of the Shelterin Component TIN2 Enhances Its Interaction with TRF2 in a Phosphorylation- and Dyskeratosis Congenita Cluster-Dependent Fashion.

Nelson ND, Dodson LM, Escudero L, Sukumar AT, Williams CL, Mihalek I, Baldan A, Baird DM, Bertuch AA.

Mol Cell Biol. 2018 May 29;38(12). pii: e00025-18. doi: 10.1128/MCB.00025-18. Print 2018 Jun 15.


A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure.

Hung CY, Volkmar B, Baker JD, Bauer JW, Gussoni E, Hainzl S, Klausegger A, Lorenzo J, Mihalek I, Rittinger O, Tekin M, Dallman JE, Bodamer OA.

PLoS One. 2017 Dec 11;12(12):e0189324. doi: 10.1371/journal.pone.0189324. eCollection 2017.


Utility of rapid whole-exome sequencing in the diagnosis of Niemann-Pick disease type C presenting with fetal hydrops and acute liver failure.

Rohanizadegan M, Abdo SM, O'Donnell-Luria A, Mihalek I, Chen P, Sanders M, Leeman K, Cho M, Hung C, Bodamer O.

Cold Spring Harb Mol Case Stud. 2017 Nov 21;3(6). pii: a002147. doi: 10.1101/mcs.a002147. Print 2017 Nov.


Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype.

Koenighofer M, Hung CY, McCauley JL, Dallman J, Back EJ, Mihalek I, Gripp KW, Sol-Church K, Rusconi P, Zhang Z, Shi GX, Andres DA, Bodamer OA.

Clin Genet. 2016 Mar;89(3):359-66. doi: 10.1111/cge.12608. Epub 2015 Jun 4.


Active site coupling in PDE:PKA complexes promotes resetting of mammalian cAMP signaling.

Krishnamurthy S, Moorthy BS, Xin Xiang L, Xin Shan L, Bharatham K, Tulsian NK, Mihalek I, Anand GS.

Biophys J. 2014 Sep 16;107(6):1426-40. doi: 10.1016/j.bpj.2014.07.050.


Cube - an online tool for comparison and contrasting of protein sequences.

Zhang ZH, Khoo AA, Mihalek I.

PLoS One. 2013 Nov 20;8(11):e79480. doi: 10.1371/journal.pone.0079480. eCollection 2013.


ExoLocator--an online view into genetic makeup of vertebrate proteins.

Khoo AA, Ogrizek-Tomas M, Bulovic A, Korpar M, Gürler E, Slijepcevic I, Šikic M, Mihalek I.

Nucleic Acids Res. 2014 Jan;42(Database issue):D879-81. doi: 10.1093/nar/gkt1164. Epub 2013 Nov 23.


TRF2 interaction with Ku heterotetramerization interface gives insight into c-NHEJ prevention at human telomeres.

Ribes-Zamora A, Indiviglio SM, Mihalek I, Williams CL, Bertuch AA.

Cell Rep. 2013 Oct 17;5(1):194-206. doi: 10.1016/j.celrep.2013.08.040. Epub 2013 Oct 3.


Defining the phenotype in congenital disorder of glycosylation due to ALG1 mutations.

Morava E, Vodopiutz J, Lefeber DJ, Janecke AR, Schmidt WM, Lechner S, Item CB, Sykut-Cegielska J, Adamowicz M, Wierzba J, Zhang ZH, Mihalek I, Stockler S, Bodamer OA, Lehle L, Wevers RA.

Pediatrics. 2012 Oct;130(4):e1034-9. doi: 10.1542/peds.2011-2711. Epub 2012 Sep 10.


Cube-DB: detection of functional divergence in human protein families.

Zhang ZH, Bharatham K, Chee SM, Mihalek I.

Nucleic Acids Res. 2012 Jan;40(Database issue):D490-4. doi: 10.1093/nar/gkr1129. Epub 2011 Dec 1.


Determinants, discriminants, conserved residues--a heuristic approach to detection of functional divergence in protein families.

Bharatham K, Zhang ZH, Mihalek I.

PLoS One. 2011;6(9):e24382. doi: 10.1371/journal.pone.0024382. Epub 2011 Sep 12.


WLS-dependent secretion of WNT3A requires Ser209 acylation and vacuolar acidification.

Coombs GS, Yu J, Canning CA, Veltri CA, Covey TM, Cheong JK, Utomo V, Banerjee N, Zhang ZH, Jadulco RC, Concepcion GP, Bugni TS, Harper MK, Mihalek I, Jones CM, Ireland CM, Virshup DM.

J Cell Sci. 2010 Oct 1;123(Pt 19):3357-67. doi: 10.1242/jcs.072132. Epub 2010 Sep 7.


deconSTRUCT: general purpose protein database search on the substructure level.

Zhang ZH, Bharatham K, Sherman WA, Mihalek I.

Nucleic Acids Res. 2010 Jul;38(Web Server issue):W590-4. doi: 10.1093/nar/gkq489. Epub 2010 Jun 3.


Reduced representation of protein structure: implications on efficiency and scope of detection of structural similarity.

Zhang ZH, Lee HK, Mihalek I.

BMC Bioinformatics. 2010 Mar 26;11:155. doi: 10.1186/1471-2105-11-155.


Helix straightening as an activation mechanism in the gelsolin superfamily of actin regulatory proteins.

Wang H, Chumnarnsilpa S, Loonchanta A, Li Q, Kuan YM, Robine S, Larsson M, Mihalek I, Burtnick LD, Robinson RC.

J Biol Chem. 2009 Aug 7;284(32):21265-9. doi: 10.1074/jbc.M109.019760. Epub 2009 Jun 1.


pFlexAna: detecting conformational changes in remotely related proteins.

Nigham A, Tucker-Kellogg L, Mihalek I, Verma C, Hsu D.

Nucleic Acids Res. 2008 Jul 1;36(Web Server issue):W246-51. doi: 10.1093/nar/gkn259. Epub 2008 May 13.


Background frequencies for residue variability estimates: BLOSUM revisited.

Mihalek I, Res I, Lichtarge O.

BMC Bioinformatics. 2007 Dec 27;8:488.


Manifestation of hawkinsinuria in a patient compound heterozygous for hawkinsinuria and tyrosinemia III.

Item CB, Mihalek I, Lichtarge O, Jalan A, Vodopiutz J, Muhl A, Bodamer OA.

Mol Genet Metab. 2007 Aug;91(4):379-83. Epub 2007 Jun 7.


On itinerant water molecules and detectability of protein-protein interfaces through comparative analysis of homologues.

Mihalek I, Res I, Lichtarge O.

J Mol Biol. 2007 Jun 1;369(2):584-95. Epub 2007 Mar 24.


Distinct faces of the Ku heterodimer mediate DNA repair and telomeric functions.

Ribes-Zamora A, Mihalek I, Lichtarge O, Bertuch AA.

Nat Struct Mol Biol. 2007 Apr;14(4):301-7. Epub 2007 Mar 11.


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