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Nguyen HL, Chari S, Gruber D, Lue CM, Chapin SJ, Bulinski JC. Overexpression of full- or partial-length MAP4 stabilizes microtubules and alters cell growth. J Cell Sci. 1997 Jan;110 ( Pt 2):281-94. doi: 10.1242/jcs.110.2.281. PubMed PMID: 9044058.
Bulinski JC, McGraw TE, Gruber D, Nguyen HL, Sheetz MP. Overexpression of MAP4 inhibits organelle motility and trafficking in vivo. J Cell Sci. 1997 Dec;110 ( Pt 24):3055-64. doi: 10.1242/jcs.110.24.3055. PubMed PMID: 9365275.
Nguyen HL, Gruber D, McGraw T, Sheetz MP, Bulinski JC. Stabilization and functional modulation of microtubules by microtubule-associated protein 4. Biol Bull. 1998 Jun;194(3):354-7. doi: 10.2307/1543111. PubMed PMID: 9664661.
Faire K, Gruber D, Bulinski JC. Identification of kinesin-like molecules in myogenic cells. Eur J Cell Biol. 1998 Sep;77(1):27-34. doi: 10.1016/s0171-9335(98)80099-x. PubMed PMID: 9808286.
Nguyen HL, Gruber D, Bulinski JC. Microtubule-associated protein 4 (MAP4) regulates assembly, protomer-polymer partitioning and synthesis of tubulin in cultured cells. J Cell Sci. 1999 Jun;112 ( Pt 12):1813-24. doi: 10.1242/jcs.112.12.1813. PubMed PMID: 10341201.
Bulinski JC, Gruber D, Faire K, Prasad P, Chang W. GFP chimeras of E-MAP-115 (ensconsin) domains mimic behavior of the endogenous protein in vitro and in vivo. Cell Struct Funct. 1999 Oct;24(5):313-20. doi: 10.1247/csf.24.313. PubMed PMID: 15216888.
Faire K, Waterman-Storer CM, Gruber D, Masson D, Salmon ED, Bulinski JC. E-MAP-115 (ensconsin) associates dynamically with microtubules in vivo and is not a physiological modulator of microtubule dynamics. J Cell Sci. 1999 Dec;112 ( Pt 23):4243-55. doi: 10.1242/jcs.112.23.4243. PubMed PMID: 10564643.
Gruber D, Faire K, Bulinski JC. Abundant expression of the microtubule-associated protein, ensconsin (E-MAP-115), alters the cellular response to Taxol. Cell Motil Cytoskeleton. 2001 Jul;49(3):115-29. doi: 10.1002/cm.1026. PubMed PMID: 11668581.
Chang W, Gruber D, Chari S, Kitazawa H, Hamazumi Y, Hisanaga S, Bulinski JC. Phosphorylation of MAP4 affects microtubule properties and cell cycle progression. J Cell Sci. 2001 Aug;114(Pt 15):2879-87. doi: 10.1242/jcs.114.15.2879. PubMed PMID: 11683421.
Chang W, Webster DR, Salam AA, Gruber D, Prasad A, Eiserich JP, Bulinski JC. Alteration of the C-terminal amino acid of tubulin specifically inhibits myogenic differentiation. J Biol Chem. 2002 Aug 23;277(34):30690-8. doi: 10.1074/jbc.M204930200. Epub 2002 Jun 17. PubMed PMID: 12070174.
Finkelstein E, Chang W, Chao PH, Gruber D, Minden A, Hung CT, Bulinski JC. Roles of microtubules, cell polarity and adhesion in electric-field-mediated motility of 3T3 fibroblasts. J Cell Sci. 2004 Mar 15;117(Pt 8):1533-45. doi: 10.1242/jcs.00986. PubMed PMID: 15020680.
Gonzalez AM, Osorio JC, Manlhiot C, Gruber D, Homma S, Mital S. Hypertrophy signaling during peripartum cardiac remodeling. Am J Physiol Heart Circ Physiol. 2007 Nov;293(5):H3008-13. doi: 10.1152/ajpheart.00401.2007. Epub 2007 Aug 31. PubMed PMID: 17766481.
Kaufman BD, Auerbach S, Reddy S, Manlhiot C, Deng L, Prakash A, Printz BF, Gruber D, Papavassiliou DP, Hsu DT, Sehnert AJ, Chung WK, Mital S. RAAS gene polymorphisms influence progression of pediatric hypertrophic cardiomyopathy. Hum Genet. 2007 Dec;122(5):515-23. doi: 10.1007/s00439-007-0429-9. Epub 2007 Sep 13. PubMed PMID: 17851694.
Malhiot C, Auerbach SR, McCrindle BW, Dipchand AI, Kinnear C, Chan JM, Gruber D, Addonizio L, Chun WK, Mital S. Renin Angiotensin Aldosterone (RAAS) Gene Polymorphisms Mediate Cardiac Allograft Dysfunction through Cytokine Upregulation in Pediatric Patients. International Society for Heart and Lung Transplantation -Annual Meeting and Scientific Session. International Society for Heart and Lung Transplantation Twenty-Ninth Annual Meeting and Scientific Sessions, Palais des Congres, Paris, France; 2009 January; Paris, France. DOI:10.1016/j.healun.2008.11.173: The Journal of Heart and Lung Transplantation; c2009.
Auerbach SR, Manlhiot C, Reddy S, Kinnear C, Richmond ME, Gruber D, McCrindle BW, Deng L, Chen JM, Addonizio LJ, Chung WK, Mital S. Recipient genotype is a predictor of allograft cytokine expression and outcomes after pediatric cardiac transplantation. J Am Coll Cardiol. 2009 May 19;53(20):1909-17. doi: 10.1016/j.jacc.2009.02.027. PubMed PMID: 19442892.
Cadeiras M, Shahzad K, John MM, Gruber D, Bayern Mv, Auerbach S, Sinha A, Latif F, Unniachan S, Memon S, Mital S, Restaino S, Marboe CC, Addonizio LJ, Deng MC. Relationship between a validated molecular cardiac transplant rejection classifier and routine organ function parameters. Clin Transplant. 2010 May-Jun;24(3):321-7. doi: 10.1111/j.1399-0012.2009.01063.x. Epub 2009 Aug 27. PubMed PMID: 19712087.
Gupta-Malhotra M, Gruber D, Abraham SS, Roman MJ, Zabriskie JB, Hudgins LC, Flynn PA, Levine DM, Okorie U, Baday A, Schiller MS, Maturi J, Meehan D, Dyme J, Parker TS, Wittkowski KM, Gersony WM, Cooper RS. Atherosclerosis in survivors of Kawasaki disease. J Pediatr. 2009 Oct;155(4):572-7. doi: 10.1016/j.jpeds.2009.04.054. PubMed PMID: 19595365.
Pediatric Cardiac Genomics Consortium, Gelb B, Brueckner M, Chung W, Goldmuntz E, Kaltman J, Kaski JP, Kim R, Kline J, Mercer-Rosa L, Porter G, Roberts A, Rosenberg E, Seiden H, Seidman C, Sleeper L, Tennstedt S, Kaltman J, Schramm C, Burns K, Pearson G, Rosenberg E. The Congenital Heart Disease Genetic Network Study: rationale, design, and early results. Circ Res. 2013 Feb 15;112(4):698-706. doi: 10.1161/CIRCRESAHA.111.300297. PubMed PMID: 23410879; PubMed Central PMCID: PMC3679175.
Patel M, Blaufox A, Gruber D, Akerman M, Meyer D, Parnell V, Bakar A. Predictors of the utilization of temporary pacing wires in pediatric patients after cardiac surgery. Critical Care Congress- Cardiovascular 6. Critical Care Medicine; 2014 December; Phoenix, AZ, USA. doi: 10.1097/01.ccm.0000457695.87657.f9: Critical Care Medicine; c2014.
Suntharos P, Aleida Jones ME, Seiden HS, Fisher M, Gruber D, Rosen LM, Blaufox AD, Cooper RS. Endothelial function evaluation in patients with anorexia nervosa. Journal of integrative cardiology. 2016 May; 2(3):287. doi: 10.15761/JIC.1000161.
Richardson C, Amirtharaj C, Gruber D, Hayes DA. Assessing Myocardial Function in Infants with Pulmonary Hypertension: The Role of Tissue Doppler Imaging and Tricuspid Annular Plane Systolic Excursion. Pediatr Cardiol. 2017 Mar;38(3):558-565. doi: 10.1007/s00246-016-1548-7. Epub 2016 Dec 19. PubMed PMID: 27995291.
Zablah JE, Gruber D, Stoffels G, Cabezas EG, Hayes DA. Subclinical Decrease in Myocardial Function in Asymptomatic Infants of Diabetic Mothers: A Tissue Doppler Study. Pediatr Cardiol. 2017 Apr;38(4):801-806. doi: 10.1007/s00246-017-1584-y. Epub 2017 Feb 14. PubMed PMID: 28197645.
Zablah JE, Misra N, Gruber D, Kholwadwala D, Epstein S. Comparison of Patients Undergoing Surgical Versus Transcatheter Pulmonary Valve Replacement: Criteria for Referral and Mid-Term Outcome. Pediatr Cardiol. 2017 Mar;38(3):603-607. doi: 10.1007/s00246-016-1554-9. Epub 2017 Feb 25. PubMed PMID: 28236163.
Pironkova RP, Giamelli J, Seiden H, Parnell VA, Gruber D, Sison CP, Kowal C, Ojamaa K. Brain injury with systemic inflammation in newborns with congenital heart disease undergoing heart surgery. Exp Ther Med. 2017 Jul;14(1):228-238. doi: 10.3892/etm.2017.4493. Epub 2017 May 22. PubMed PMID: 28672919; PubMed Central PMCID: PMC5488503.
Yaari J, Gruber D, Blaufox AD. Usefulness of Routine Transtelephonic Monitoring for Supraventricular Tachycardia in Infants. J Pediatr. 2018 Feb;193:109-113. doi: 10.1016/j.jpeds.2017.10.014. Epub 2017 Dec 1. PubMed PMID: 29198533.
Vlachos A, Osorio DS, Atsidaftos E, Kang J, Lababidi ML, Seiden HS, Gruber D, Glader BE, Onel K, Farrar JE, Bodine DM, Aspesi A, Dianzani I, Ramenghi U, Ellis SR, Lipton JM. Increased Prevalence of Congenital Heart Disease in Children With Diamond Blackfan Anemia Suggests Unrecognized Diamond Blackfan Anemia as a Cause of Congenital Heart Disease in the General Population: A Report of the Diamond Blackfan Anemia Registry. Circ Genom Precis Med. 2018 May;11(5):e002044. doi: 10.1161/CIRCGENETICS.117.002044. PubMed PMID: 29748317; PubMed Central PMCID: PMC5951415.
Amirtharaj CR, Palmeri LC, Gradwohl G, Adar Y, Nitzan M, Gruber D, Blaufox A, Meyer DB, Kwon EN, Koppel R. Photoplethysmographic assessment of pulse transit time correlates with echocardiographic measurement of stroke volume in preterm infants with patent ductus arteriosus. J Perinatol. 2018 Sep;38(9):1220-1226. doi: 10.1038/s41372-018-0165-0. Epub 2018 Jul 2. PubMed PMID: 29961764.
McPhillips L, Kholwadwala D, Sison CP, Gruber D, Ojamaa K. A Novel Brain Injury Biomarker Correlates with Cyanosis in Infants with Congenital Heart Disease. Pediatr Cardiol. 2019 Mar;40(3):546-553. doi: 10.1007/s00246-018-2023-4. Epub 2018 Nov 14. PubMed PMID: 30430186.
Pashun RA, Azari BM, Achar A, Gruber D, Epstein LM, Geraci AP, Saba SG. Intramyocardial Fat in Family With Limb-Girdle Muscular Dystrophy Type 2E Cardiomyopathy and Sudden Cardiac Death. Circ Cardiovasc Imaging. 2020 Jul;13(7):e010104. doi: 10.1161/CIRCIMAGING.119.010104. Epub 2020 Jul 8. PubMed PMID: 32635746.
Martin-Trujillo A, Patel N, Richter F, Jadhav B, Garg P, Morton SU, McKean DM, DePalma SR, Goldmuntz E, Gruber D, Kim R, Newburger JW, Porter GA Jr, Giardini A, Bernstein D, Tristani-Firouzi M, Seidman JG, Seidman CE, Chung WK, Gelb BD, Sharp AJ. Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles. PLoS Genet. 2020 Nov;16(11):e1009189. doi: 10.1371/journal.pgen.1009189. eCollection 2020 Nov. PubMed PMID: 33216750; PubMed Central PMCID: PMC7679001.
Dhar A, Leung TM, Appiah-Kubi A, Gruber D, Aygun B, Serigano O, Mitchell E. Longitudinal analysis of cardiac abnormalities in pediatric patients with sickle cell anemia and effect of hydroxyurea therapy. Blood Adv. 2021 Nov 9;5(21):4406-4412. doi: 10.1182/bloodadvances.2021005076. PubMed PMID: 34529023; PubMed Central PMCID: PMC8579269.
Loke J, Alim I, Yam S, Klugman S, Xia LC, Gruber D, Tegay D, LaBella A, Onel K, Ostrer H. Prediction of breast cancer risk based on flow variant analysis of circulating peripheral blood mononuclear cells. HGG Adv. 2022 Apr 14;3(2):100085. doi: 10.1016/j.xhgg.2022.100085. eCollection 2022 Apr 14. PubMed PMID: 35146455; PubMed Central PMCID: PMC8801379.
Simon D, Broadbridge E, Baker M, Gaviglio A, Gruber D, Piper KN, Tavakoli NP, Sullivan J, Kennedy A. Common Challenges and Identified Solutions for State Newborn Screening Programs during COVID-19 Pandemic. Int J Neonatal Screen. 2022 Jan 18;8(1). doi: 10.3390/ijns8010007. PubMed PMID: 35225930; PubMed Central PMCID: PMC8883950.
Wynn J, Tavakoli NP, Armstrong N, Gomez J, Koval C, Lai C, Tang S, Quevedo Prince A, Quevedo Y, Rufino K, Palacio Morales L, Pena A, Grossman S, Monfiletto M, Ruda E, Jimenez V, Verdade L, Jones A, Barriga MG, Karan N, Puma A, Sarker S, Chin S, Duarte K, Tegay DH, Bacchus I, Julooru R, Maloney B, Park S, Saami AM, Cohen L, Shapiro N, Caggana M, Chung WK, Gruber D. Improving Recruitment for a Newborn Screening Pilot Study with Adaptations in Response to the COVID-19 Pandemic. Int J Neonatal Screen. 2022 Mar 22;8(2). doi: 10.3390/ijns8020023. PubMed PMID: 35466194; PubMed Central PMCID: PMC9036248.
Gruber D, Lloyd-Puryear M, Armstrong N, Scavina M, Tavakoli NP, Brower AM, Caggana M, Chung WK. Newborn screening for Duchenne muscular dystrophy-early detection and diagnostic algorithm for female carriers of Duchenne muscular dystrophy. Am J Med Genet C Semin Med Genet. 2022 Jun;190(2):197-205. doi: 10.1002/ajmg.c.32000. Epub 2022 Sep 24. Review. PubMed PMID: 36152336; PubMed Central PMCID: PMC9826042.
Hartnett MJ, Lloyd-Puryear MA, Tavakoli NP, Wynn J, Koval-Burt CL, Gruber D, Trotter T, Caggana M, Chung WK, Armstrong N, Brower AM. Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot. Int J Neonatal Screen. 2022 Sep 22;8(4). doi: 10.3390/ijns8040050. PubMed PMID: 36278620; PubMed Central PMCID: PMC9589949.
Tavakoli NP, Gruber D, Armstrong N, Chung WK, Maloney B, Park S, Wynn J, Koval-Burt C, Verdade L, Tegay DH, Cohen LL, Shapiro N, Kennedy A, Noritz G, Ciafaloni E, Weinberger B, Ellington M Jr, Schleien C, Spinazzola R, Sood S, Brower A, Lloyd-Puryear M, Caggana M, Duchenne Muscular Dystrophy Pilot Study Group. Newborn screening for Duchenne muscular dystrophy: A two-year pilot study. Ann Clin Transl Neurol. 2023 Aug;10(8):1383-1396. doi: 10.1002/acn3.51829. Epub 2023 Jun 23. PubMed PMID: 37350320; PubMed Central PMCID: PMC10424650.
Maloney B, Park S, Sowizral M, Brackett I, Moslehi R, Chung WK, Gruber D, Brower A, Lloyd-Puryear M, Caggana M, Tavakoli NP. Factors influencing creatine kinase-MM concentrations in newborns and implications for newborn screening for Duchenne muscular dystrophy. Clin Biochem. 2023 Aug;118:110614. doi: 10.1016/j.clinbiochem.2023.110614. Epub 2023 Jul 19. PubMed PMID: 37479106.
Guntaka S, Alston MR, Gruber D, Azari BM. Isolated ventricular noncompaction in a patient with a sarcomeric gene mutation: A case report. HeartRhythm Case Rep. 2024 Jul;10(7):456-459. doi: 10.1016/j.hrcr.2024.03.017. eCollection 2024 Jul. PubMed PMID: 39129736; PubMed Central PMCID: PMC11312041.
Jnani J, Gruber D, Mtisi T, Saleh M, Azari BM. Identification of a SCN5A Genetic Variant Associated With Type 1 Brugada Syndrome (BrS) in a Family. Cureus. 2024 Jul;16(7):e64883. doi: 10.7759/cureus.64883. eCollection 2024 Jul. PubMed PMID: 39156269; PubMed Central PMCID: PMC11330683.
Lozinsky SM, Iezzi CA, Gruber D, Onel K, Fein Levy C. The Diagnostic Yield of Panel Versus Exome Sequencing to Identify Hereditary Cancer Disorders in Pediatric Cancer. J Pediatr Hematol Oncol. 2025 Mar 1;47(2):74-79. doi: 10.1097/MPH.0000000000003000. Epub 2025 Jan 30. PubMed PMID: 39899692.
Vortak N, Gruber D, Azari B, Ahmad Z, Huang X, Fishbein J, Hirsh B, Frangeskos J, Gianos E. Implementing a specialized cardiogenomics team for lipid disorders: Insights from a single large health system. Journal of Preventive Cardiology. 2025 September; 23.
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