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Items: 1 to 50 of 88

1.

Can GBA1-Associated Parkinson Disease Be Modeled in the Mouse?

Farfel-Becker T, Do J, Tayebi N, Sidransky E.

Trends Neurosci. 2019 Sep;42(9):631-643. doi: 10.1016/j.tins.2019.05.010. Epub 2019 Jul 6. Review.

PMID:
31288942
2.

C-terminal α-synuclein truncations are linked to cysteine cathepsin activity in Parkinson's disease.

McGlinchey RP, Lacy SM, Huffer KE, Tayebi N, Sidransky E, Lee JC.

J Biol Chem. 2019 Jun 21;294(25):9973-9984. doi: 10.1074/jbc.RA119.008930. Epub 2019 May 15.

3.

Targeted next generation sequencing reveals genetic defects underlying inherited retinal disease in Iranian families.

Tayebi N, Akinrinade O, Khan MI, Hejazifar A, Dehghani A, Cremers FPM, Akhlaghi M.

Mol Vis. 2019 Feb 8;25:106-117. eCollection 2019.

4.

Scalable Nanogap Sensors for Non-Redox Enzyme Assays.

Su X, Tayebi N, Credo GM, Wu K, Elibol OH, Liu DJ, Daniels JS, Li H, Hall DA, Varma M.

ACS Sens. 2018 Sep 28;3(9):1773-1781. doi: 10.1021/acssensors.8b00500. Epub 2018 Sep 11.

PMID:
30156096
5.

The Relationship Between Body Mass Index (BMI) and Menstrual Disorders at Different Ages of Menarche and Sex Hormones.

Tayebi N, Yazdanpanahi Z, Yektatalab S, Pourahmad S, Akbarzadeh M.

J Natl Med Assoc. 2018 Oct;110(5):440-447. doi: 10.1016/j.jnma.2017.10.007. Epub 2017 Nov 23.

PMID:
30129516
6.

Exploring genetic modifiers of Gaucher disease: The next horizon.

Davidson BA, Hassan S, Garcia EJ, Tayebi N, Sidransky E.

Hum Mutat. 2018 Dec;39(12):1739-1751. doi: 10.1002/humu.23611. Epub 2018 Sep 11. Review.

PMID:
30098107
7.

Alleles with more than one mutation can complicate genotype/phenotype studies in Mendelian disorders: Lessons from Gaucher disease.

Hassan S, Lopez G, Stubblefield BK, Tayebi N, Sidransky E.

Mol Genet Metab. 2018 Sep;125(1-2):1-3. doi: 10.1016/j.ymgme.2018.06.013. Epub 2018 Jun 28.

8.

Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis.

Shang H, Yan D, Tayebi N, Saeidi K, Sahebalzamani A, Feng Y, Blanton S, Liu X.

Biomed Res Int. 2018 Jan 15;2018:3103986. doi: 10.1155/2018/3103986. eCollection 2018.

9.

ACE phenotyping in Gaucher disease.

Danilov SM, Tikhomirova VE, Metzger R, Naperova IA, Bukina TM, Goker-Alpan O, Tayebi N, Gayfullin NM, Schwartz DE, Samokhodskaya LM, Kost OA, Sidransky E.

Mol Genet Metab. 2018 Apr;123(4):501-510. doi: 10.1016/j.ymgme.2018.02.007. Epub 2018 Feb 17.

10.

Glucocerebrosidase haploinsufficiency in A53T α-synuclein mice impacts disease onset and course.

Tayebi N, Parisiadou L, Berhe B, Gonzalez AN, Serra-Vinardell J, Tamargo RJ, Maniwang E, Sorrentino Z, Fujiwara H, Grey RJ, Hassan S, Blech-Hermoni YN, Chen C, McGlinchey R, Makariou-Pikis C, Brooks M, Ginns EI, Ory DS, Giasson BI, Sidransky E.

Mol Genet Metab. 2017 Dec;122(4):198-208. doi: 10.1016/j.ymgme.2017.11.001. Epub 2017 Nov 21.

11.

Type 2 Gaucher disease in an infant despite a normal maternal glucocerebrosidase gene.

Hagege E, Grey RJ, Lopez G, Roshan Lal T, Sidransky E, Tayebi N.

Am J Med Genet A. 2017 Dec;173(12):3211-3215. doi: 10.1002/ajmg.a.38487. Epub 2017 Nov 1.

12.

The role of epigenetics in lysosomal storage disorders: Uncharted territory.

Hassan S, Sidransky E, Tayebi N.

Mol Genet Metab. 2017 Nov;122(3):10-18. doi: 10.1016/j.ymgme.2017.07.012. Epub 2017 Aug 1. Review.

PMID:
28918065
13.

Pattern of menarche age (normal, early and late) and its relationship with some demographic characteristics in girls and their parents.

Tayebi N, Yazdznpanahi Z, Yektatalab S, Akbarzadeh M, Zare N.

Int J Adolesc Med Health. 2016 Aug 26;30(3). pii: /j/ijamh.2018.30.issue-3/ijamh-2016-0048/ijamh-2016-0048.xml. doi: 10.1515/ijamh-2016-0048.

PMID:
27564696
14.

A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease.

Westbroek W, Nguyen M, Siebert M, Lindstrom T, Burnett RA, Aflaki E, Jung O, Tamargo R, Rodriguez-Gil JL, Acosta W, Hendrix A, Behre B, Tayebi N, Fujiwara H, Sidhu R, Renvoise B, Ginns EI, Dutra A, Pak E, Cramer C, Ory DS, Pavan WJ, Sidransky E.

Dis Model Mech. 2016 Jul 1;9(7):769-78. doi: 10.1242/dmm.024588. Epub 2016 May 19.

15.

Clinical course and prognosis in patients with Gaucher disease and parkinsonism.

Lopez G, Kim J, Wiggs E, Cintron D, Groden C, Tayebi N, Mistry PK, Pastores GM, Zimran A, Goker-Alpan O, Sidransky E.

Neurol Genet. 2016 Mar 4;2(2):e57. doi: 10.1212/NXG.0000000000000057. eCollection 2016 Apr.

16.

Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice.

Spielmann M, Kakar N, Tayebi N, Leettola C, Nürnberg G, Sowada N, Lupiáñez DG, Harabula I, Flöttmann R, Horn D, Chan WL, Wittler L, Yilmaz R, Altmüller J, Thiele H, van Bokhoven H, Schwartz CE, Nürnberg P, Bowie JU, Ahmad J, Kubisch C, Mundlos S, Borck G.

Genome Res. 2016 Feb;26(2):183-91. doi: 10.1101/gr.199430.115. Epub 2016 Jan 11.

17.

A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation.

Ibrahim DM, Tayebi N, Knaus A, Stiege AC, Sahebzamani A, Hecht J, Mundlos S, Spielmann M.

Am J Med Genet A. 2016 Mar;170(3):615-21. doi: 10.1002/ajmg.a.37464. Epub 2015 Nov 18.

PMID:
26581570
18.

Deletions of exons with regulatory activity at the DYNC1I1 locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families.

Tayebi N, Jamsheer A, Flöttmann R, Sowinska-Seidler A, Doelken SC, Oehl-Jaschkowitz B, Hülsemann W, Habenicht R, Klopocki E, Mundlos S, Spielmann M.

Orphanet J Rare Dis. 2014 Jul 29;9:108. doi: 10.1186/s13023-014-0108-6.

19.

Macrophage models of Gaucher disease for evaluating disease pathogenesis and candidate drugs.

Aflaki E, Stubblefield BK, Maniwang E, Lopez G, Moaven N, Goldin E, Marugan J, Patnaik S, Dutra A, Southall N, Zheng W, Tayebi N, Sidransky E.

Sci Transl Med. 2014 Jun 11;6(240):240ra73. doi: 10.1126/scitranslmed.3008659.

20.

Reduced glucocerebrosidase is associated with increased α-synuclein in sporadic Parkinson's disease.

Murphy KE, Gysbers AM, Abbott SK, Tayebi N, Kim WS, Sidransky E, Cooper A, Garner B, Halliday GM.

Brain. 2014 Mar;137(Pt 3):834-48. doi: 10.1093/brain/awt367. Epub 2014 Jan 28.

21.

Lysosomal integral membrane protein-2: a new player in lysosome-related pathology.

Gonzalez A, Valeiras M, Sidransky E, Tayebi N.

Mol Genet Metab. 2014 Feb;111(2):84-91. doi: 10.1016/j.ymgme.2013.12.005. Epub 2013 Dec 11. Review.

22.

Mechanical model of vertical nanowire cell penetration.

Xie X, Xu AM, Angle MR, Tayebi N, Verma P, Melosh NA.

Nano Lett. 2013;13(12):6002-8. doi: 10.1021/nl403201a. Epub 2013 Nov 20.

PMID:
24237230
23.

Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.

Yang SK, Hong M, Zhao W, Jung Y, Baek J, Tayebi N, Kim KM, Ye BD, Kim KJ, Park SH, Lee I, Lee EJ, Kim WH, Cheon JH, Kim YH, Jang BI, Kim HS, Choi JH, Koo JS, Lee JH, Jung SA, Lee YJ, Jang JY, Shin HD, Kang D, Youn HS, Liu J, Song K.

Gut. 2014 Jan;63(1):80-7. doi: 10.1136/gutjnl-2013-305193. Epub 2013 Jul 14.

PMID:
23850713
24.

Association of CETP Taq1B and -629C > A polymorphisms with coronary artery disease and lipid levels in the multi-ethnic Singaporean population.

Lu Y, Tayebi N, Li H, Saha N, Yang H, Heng CK.

Lipids Health Dis. 2013 Jun 8;12:85. doi: 10.1186/1476-511X-12-85.

25.

A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies.

Nalls MA, Duran R, Lopez G, Kurzawa-Akanbi M, McKeith IG, Chinnery PF, Morris CM, Theuns J, Crosiers D, Cras P, Engelborghs S, De Deyn PP, Van Broeckhoven C, Mann DM, Snowden J, Pickering-Brown S, Halliwell N, Davidson Y, Gibbons L, Harris J, Sheerin UM, Bras J, Hardy J, Clark L, Marder K, Honig LS, Berg D, Maetzler W, Brockmann K, Gasser T, Novellino F, Quattrone A, Annesi G, De Marco EV, Rogaeva E, Masellis M, Black SE, Bilbao JM, Foroud T, Ghetti B, Nichols WC, Pankratz N, Halliday G, Lesage S, Klebe S, Durr A, Duyckaerts C, Brice A, Giasson BI, Trojanowski JQ, Hurtig HI, Tayebi N, Landazabal C, Knight MA, Keller M, Singleton AB, Wolfsberg TG, Sidransky E.

JAMA Neurol. 2013 Jun;70(6):727-35. doi: 10.1001/jamaneurol.2013.1925.

26.

Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians.

Yang SK, Hong M, Zhao W, Jung Y, Tayebi N, Ye BD, Kim KJ, Park SH, Lee I, Shin HD, Cheong HS, Kim LH, Kim HJ, Jung SA, Kang D, Youn HS, Liu J, Song K.

Inflamm Bowel Dis. 2013 Apr;19(5):954-66. doi: 10.1097/MIB.0b013e3182802ab6.

PMID:
23511034
27.

Is Parkinson disease associated with lysosomal integral membrane protein type-2?: challenges in interpreting association data.

Maniwang E, Tayebi N, Sidransky E.

Mol Genet Metab. 2013 Apr;108(4):269-71. doi: 10.1016/j.ymgme.2013.01.012. Epub 2013 Jan 29.

28.

Association of single nucleotide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean population.

Tayebi N, Ke T, Foo JN, Friedlander Y, Liu J, Heng CK.

Clin Biochem. 2013 Jun;46(9):755-9. doi: 10.1016/j.clinbiochem.2013.01.004. Epub 2013 Jan 18.

PMID:
23337689
29.

A case of primary systemic amyloidosis.

Mirfeizi Z, Hatef MR, Hashemzadeh K, Hashemzadeh S, Tayebi N.

Int J Rheum Dis. 2012 Oct;15(5):e134-5. doi: 10.1111/j.1756-185X.2011.01605.x. Epub 2011 Mar 14. No abstract available.

PMID:
23083051
30.

Induced pluripotent stem cell model recapitulates pathologic hallmarks of Gaucher disease.

Panicker LM, Miller D, Park TS, Patel B, Azevedo JL, Awad O, Masood MA, Veenstra TD, Goldin E, Stubblefield BK, Tayebi N, Polumuri SK, Vogel SN, Sidransky E, Zambidis ET, Feldman RA.

Proc Natl Acad Sci U S A. 2012 Oct 30;109(44):18054-9. doi: 10.1073/pnas.1207889109. Epub 2012 Oct 15.

31.

Tuning the built-in electric field in ferroelectric Pb(Zr(0.2)Ti(0.8))O3 films for long-term stability of single-digit nanometer inverted domains.

Tayebi N, Kim S, Chen RJ, Tran Q, Franklin N, Nishi Y, Ma Q, Rao V.

Nano Lett. 2012 Nov 14;12(11):5455-63. doi: 10.1021/nl302911k. Epub 2012 Oct 12.

PMID:
23043427
32.

A germline or de novo mutation in two families with Gaucher disease: implications for recessive disorders.

Saranjam H, Chopra SS, Levy H, Stubblefield BK, Maniwang E, Cohen IJ, Baris H, Sidransky E, Tayebi N.

Eur J Hum Genet. 2013 Jan;21(1):115-7. doi: 10.1038/ejhg.2012.105. Epub 2012 Jun 20.

33.

A Rare Case of Pericentric Inversion, Inv (21) (p12;q22) in Repeated Pregnancy Loss: A Case Report.

Tayebi N, Khodaei H.

Oman Med J. 2011 Nov;26(6):441-3. doi: 10.5001/omj.2011.112.

34.

Skin ultrastructural findings in type 2 Gaucher disease: diagnostic implications.

Chan A, Holleran WM, Ferguson T, Crumrine D, Goker-Alpan O, Schiffmann R, Tayebi N, Ginns EI, Elias PM, Sidransky E.

Mol Genet Metab. 2011 Dec;104(4):631-6. doi: 10.1016/j.ymgme.2011.09.008. Epub 2011 Sep 16.

35.

Gaucher disease type 2: homozygosity for the mutation F331S in two unrelated consanguineous Muslim Arab patients with Gaucher disease from the Gaza and Jenin regions.

Baris HN, Raas-Rothschild A, Garty BZ, Tor R, Klontz S, Tayebi N, Sidransky E, Cohen IJ.

Blood Cells Mol Dis. 2011 Dec 15;47(4):262-3. doi: 10.1016/j.bcmd.2011.08.002. Epub 2011 Sep 1. No abstract available.

36.

A mutation in SCARB2 is a modifier in Gaucher disease.

Velayati A, DePaolo J, Gupta N, Choi JH, Moaven N, Westbroek W, Goker-Alpan O, Goldin E, Stubblefield BK, Kolodny E, Tayebi N, Sidransky E.

Hum Mutat. 2011 Nov;32(11):1232-8. doi: 10.1002/humu.21566. Epub 2011 Sep 15.

37.

Secondary amenorrhea associated with 46,X,der(X)t(X;X)(p22;p22).

Tayebi N, Khodaei H.

Taiwan J Obstet Gynecol. 2011 Jun;50(2):223-4. doi: 10.1016/j.tjog.2010.12.001. No abstract available.

38.

Aggregation of α-synuclein in brain samples from subjects with glucocerebrosidase mutations.

Choi JH, Stubblefield B, Cookson MR, Goldin E, Velayati A, Tayebi N, Sidransky E.

Mol Genet Metab. 2011 Sep-Oct;104(1-2):185-8. doi: 10.1016/j.ymgme.2011.06.008. Epub 2011 Jun 17.

39.

Identification of recombinant alleles using quantitative real-time PCR implications for Gaucher disease.

Velayati A, Knight MA, Stubblefield BK, Sidransky E, Tayebi N.

J Mol Diagn. 2011 Jul;13(4):401-5. doi: 10.1016/j.jmoldx.2011.02.005.

40.

The association between second-trimester maternal serum alpha-fetoprotein in 14-22 weeks and adverse pregnancy outcome.

Dehghani-Firouzabadi R, Tayebi N, Ghasemi N, Tahmasbi Z.

Acta Med Iran. 2010 Jul-Aug;48(4):234-8.

41.

A monozygotic twin pair with highly discordant Gaucher phenotypes.

Biegstraaten M, van Schaik IN, Aerts JM, Langeveld M, Mannens MM, Bour LJ, Sidransky E, Tayebi N, Fitzgibbon E, Hollak CE.

Blood Cells Mol Dis. 2011 Jan 15;46(1):39-41. doi: 10.1016/j.bcmd.2010.10.007. Epub 2010 Nov 5.

42.

An ultraclean tip-wear reduction scheme for ultrahigh density scanning probe-based data storage.

Tayebi N, Zhang Y, Chen RJ, Tran Q, Chen R, Nishi Y, Ma Q, Rao V.

ACS Nano. 2010 Oct 26;4(10):5713-20. doi: 10.1021/nn1013512.

PMID:
20929239
43.

Type 2 Gaucher disease: phenotypic variation and genotypic heterogeneity.

Gupta N, Oppenheim IM, Kauvar EF, Tayebi N, Sidransky E.

Blood Cells Mol Dis. 2011 Jan 15;46(1):75-84. doi: 10.1016/j.bcmd.2010.08.012. Epub 2010 Sep 28. Review.

44.

Coinheritance of Gaucher disease and α-thalassemia resulting in confusion between two inherited hematologic diseases.

Miri-Moghaddam E, Velayati A, Naderi M, Tayebi N, Sidransky E.

Blood Cells Mol Dis. 2011 Jan 15;46(1):88-91. doi: 10.1016/j.bcmd.2010.08.007. Epub 2010 Sep 16.

45.

False-positive results using a Gaucher diagnostic kit--RecTL and N370S.

Choi JH, Velayati A, Stubblefield BK, Orr-Urtreger A, Gan-Or Z, Tayebi N, Sidransky E.

Mol Genet Metab. 2010 May;100(1):100-2. doi: 10.1016/j.ymgme.2009.12.017. Epub 2010 Jan 4.

46.

The prevalence of congenital malformations and its correlation with consanguineous marriages.

Tayebi N, Yazdani K, Naghshin N.

Oman Med J. 2010 Jan;25(1):37-40. doi: 10.5001/omj.2010.9.

47.

Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset.

Sidransky E, Samaddar T, Tayebi N.

Neurology. 2009 Oct 27;73(17):1424-5, author reply 1425-6. doi: 10.1212/WNL.0b013e3181b28601. No abstract available.

PMID:
19858467
48.

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

Sidransky E, Nalls MA, Aasly JO, Aharon-Peretz J, Annesi G, Barbosa ER, Bar-Shira A, Berg D, Bras J, Brice A, Chen CM, Clark LN, Condroyer C, De Marco EV, Dürr A, Eblan MJ, Fahn S, Farrer MJ, Fung HC, Gan-Or Z, Gasser T, Gershoni-Baruch R, Giladi N, Griffith A, Gurevich T, Januario C, Kropp P, Lang AE, Lee-Chen GJ, Lesage S, Marder K, Mata IF, Mirelman A, Mitsui J, Mizuta I, Nicoletti G, Oliveira C, Ottman R, Orr-Urtreger A, Pereira LV, Quattrone A, Rogaeva E, Rolfs A, Rosenbaum H, Rozenberg R, Samii A, Samaddar T, Schulte C, Sharma M, Singleton A, Spitz M, Tan EK, Tayebi N, Toda T, Troiano AR, Tsuji S, Wittstock M, Wolfsberg TG, Wu YR, Zabetian CP, Zhao Y, Ziegler SG.

N Engl J Med. 2009 Oct 22;361(17):1651-61. doi: 10.1056/NEJMoa0901281.

49.

Glucocerebrosidase mutation H255Q appears to be exclusively in cis with D409H: structural implications.

Vithayathil J, Gibney G, Baxevanis AD, Stubblefield BK, Sidransky E, Tayebi N.

Clin Genet. 2009 May;75(5):503-4. doi: 10.1111/j.1399-0004.2009.01163.x. No abstract available.

50.

Bloom's syndrome in a 12-year-old Iranian girl.

Tayebi N, Khodaei H.

Indian J Hum Genet. 2008 Sep;14(3):103-5. doi: 10.4103/0971-6866.45003.

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