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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Endothelial function evaluation in patients with anorexia nervosa.
Journal of integrative cardiology. 2016 May; 2(3):287. doi: 10.15761/JIC.1000161.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Implementing a specialized cardiogenomics team for lipid disorders: Insights from a single large health system.
Journal of Preventive Cardiology. 2025 September; 23.
What would you like to do?