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Page 1
Effect of Segment-Body Vibration on Strength Parameters.
Goebel RT, Kleinöder H, Yue Z, Gosh R, Mester J. Goebel RT, et al. Among authors: mester j. Sports Med Open. 2015;1(1):14. doi: 10.1186/s40798-015-0022-z. Epub 2015 Jul 3. Sports Med Open. 2015. PMID: 26258006 Free PMC article.
Erratum to: Effect of Segment-Body Vibration on Strength Parameters.
Goebel RT, Kleinöder H, Yue Z, Ghosh R, Mester J. Goebel RT, et al. Among authors: mester j. Sports Med Open. 2015 Dec;1(1):28. doi: 10.1186/s40798-015-0028-6. Epub 2015 Sep 9. Sports Med Open. 2015. PMID: 27747848 Free PMC article. No abstract available.
Vibration training: benefits and risks.
Mester J, Kleinöder H, Yue Z. Mester J, et al. J Biomech. 2006;39(6):1056-65. doi: 10.1016/j.jbiomech.2005.02.015. J Biomech. 2006. PMID: 15869759
Lactate Kinetics during Multiple Set Resistance Exercise.
Wirtz N, Wahl P, Kleinöder H, Mester J. Wirtz N, et al. Among authors: mester j. J Sports Sci Med. 2014 Jan 20;13(1):73-7. eCollection 2014 Jan. J Sports Sci Med. 2014. PMID: 24570608 Free PMC article.
Aqua Cycling Does Not Affect Recovery of Performance, Damage Markers, and Sensation of Pain.
Wahl P, Sanno M, Ellenberg K, Frick H, Böhm E, Haiduck B, Goldmann JP, Achtzehn S, Brüggemann GP, Mester J, Bloch W. Wahl P, et al. Among authors: mester j. J Strength Cond Res. 2017 Jan;31(1):162-170. doi: 10.1519/JSC.0000000000001462. J Strength Cond Res. 2017. PMID: 27135478 Clinical Trial.
Wahl, P, Sanno, M, Ellenberg, K, Frick, H, Bohm, E, Haiduck, B, Goldmann, J-P, Achtzehn, S, Bruggemann, G-P, Mester, J, and Bloch, W. Aqua cycling does not affect recovery of performance, damage markers, and sensation of pain. J Strength Cond Res 31(1) …
Wahl, P, Sanno, M, Ellenberg, K, Frick, H, Bohm, E, Haiduck, B, Goldmann, J-P, Achtzehn, S, Bruggemann, G-P, Mester, J, …
Accuracy of a Modified Lactate Minimum Test and Reverse Lactate Threshold Test to Determine Maximal Lactate Steady State.
Wahl P, Manunzio C, Vogt F, Strütt S, Volmary P, Bloch W, Mester J. Wahl P, et al. Among authors: mester j. J Strength Cond Res. 2017 Dec;31(12):3489-3496. doi: 10.1519/JSC.0000000000001770. J Strength Cond Res. 2017. PMID: 28033123
Wahl, P, Manunzio, C, Vogt, F, Strutt, S, Volmary, P, Bloch, W, and Mester, J. Accuracy of a modified lactate minimum test and reverse lactate threshold test to determine maximal lactate steady state. J Strength Cond Res 31(12): 3489-3496, 2017-This study eva …
Wahl, P, Manunzio, C, Vogt, F, Strutt, S, Volmary, P, Bloch, W, and Mester, J. Accuracy of a modified lactate minimum test and …
Low-Intensity Sprint Training With Blood Flow Restriction Improves 100-m Dash.
Behringer M, Behlau D, Montag JCK, McCourt ML, Mester J. Behringer M, et al. Among authors: mester j. J Strength Cond Res. 2017 Sep;31(9):2462-2472. doi: 10.1519/JSC.0000000000001746. J Strength Cond Res. 2017. PMID: 27941491 Clinical Trial.
Behringer, M, Behlau, D, Montag, JCK, McCourt, ML, and Mester, J. Low-intensity sprint training with blood flow restriction improves 100-m dash. J Strength Cond Res 31(9): 2462-2472, 2017-We investigated the effects of practical blood flow restriction (pBFR) …
Behringer, M, Behlau, D, Montag, JCK, McCourt, ML, and Mester, J. Low-intensity sprint training with blood flow restriction im …
Changes in muscle cross-sectional area, muscle force, and jump performance during 6 weeks of progressive whole-body vibration combined with progressive, high intensity resistance training.
Rosenberger A, Beijer Å, Johannes B, Schoenau E, Mester J, Rittweger J, Zange J. Rosenberger A, et al. Among authors: mester j. J Musculoskelet Neuronal Interact. 2017 Jun 1;17(2):38-49. J Musculoskelet Neuronal Interact. 2017. PMID: 28574410 Free PMC article. Clinical Trial.
Dietary supplement use among elite young German athletes.
Braun H, Koehler K, Geyer H, Kleiner J, Mester J, Schanzer W. Braun H, et al. Among authors: mester j. Int J Sport Nutr Exerc Metab. 2009 Feb;19(1):97-109. doi: 10.1123/ijsnem.19.1.97. Int J Sport Nutr Exerc Metab. 2009. PMID: 19403956
Motor point map of upper body muscles.
Behringer M, Franz A, McCourt M, Mester J. Behringer M, et al. Among authors: mester j. Eur J Appl Physiol. 2014 Aug;114(8):1605-17. doi: 10.1007/s00421-014-2892-z. Epub 2014 Apr 29. Eur J Appl Physiol. 2014. PMID: 24777738
A mathematical model for lactate transport to red blood cells.
Wahl P, Yue Z, Zinner C, Bloch W, Mester J. Wahl P, et al. Among authors: mester j. J Physiol Sci. 2011 Mar;61(2):93-102. doi: 10.1007/s12576-010-0125-8. Epub 2010 Dec 22. J Physiol Sci. 2011. PMID: 21181323 Free PMC article.
Physical exercise modulates the homeostasis of human regulatory T cells.
Weinhold M, Shimabukuro-Vornhagen A, Franke A, Theurich S, Wahl P, Hallek M, Schmidt A, Schinköthe T, Mester J, von Bergwelt-Baildon M, Bloch W. Weinhold M, et al. Among authors: mester j. J Allergy Clin Immunol. 2016 May;137(5):1607-1610.e8. doi: 10.1016/j.jaci.2015.10.035. Epub 2016 Jan 7. J Allergy Clin Immunol. 2016. PMID: 26774657 No abstract available.
Physiological demands of hiking the Grand Canyon.
Sperlich B, Haegele M, de Marées M, Mester J, Linville J. Sperlich B, et al. Among authors: mester j. Wilderness Environ Med. 2010 Sep;21(3):276-8. doi: 10.1016/j.wem.2010.04.002. Epub 2010 Apr 9. Wilderness Environ Med. 2010. PMID: 20832712 No abstract available.
Vibration training intervention to maintain cartilage thickness and serum concentrations of cartilage oligometric matrix protein (COMP) during immobilization.
Liphardt AM, Mündermann A, Koo S, Bäcker N, Andriacchi TP, Zange J, Mester J, Heer M. Liphardt AM, et al. Among authors: mester j. Osteoarthritis Cartilage. 2009 Dec;17(12):1598-603. doi: 10.1016/j.joca.2009.07.007. Epub 2009 Sep 1. Osteoarthritis Cartilage. 2009. PMID: 19747585 Free article. Clinical Trial.
Urinary excretion of exogenous glycerol administration at rest.
Koehler K, Braun H, de Marees M, Geyer H, Thevis M, Mester J, Schaenzer W. Koehler K, et al. Among authors: mester j. Drug Test Anal. 2011 Nov-Dec;3(11-12):877-82. doi: 10.1002/dta.355. Epub 2011 Oct 19. Drug Test Anal. 2011. PMID: 22012747
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Paul MS, Michener SL, Pan H, Chan H, Pfliger JM, Rosenfeld JA, Lerma VC, Tran A, Longley MA, Lewis RA, Weisz-Hubshman M, Bekheirnia MR, Bekheirnia N, Massingham L, Zech M, Wagner M, Engels H, Cremer K, Mangold E, Peters S, Trautmann J, Perne C, Mester JL, Guillen Sacoto MJ, Person R, McDonnell PP, Cohen SR, Lusk L, Cohen ASA, Le Pichon JB, Pastinen T, Zhou D, Engleman K, Racine C, Faivre L, Moutton S, Denommé-Pichon AS, Koh HY, Poduri A, Bolton J, Knopp C, Julia Suh DS, Maier A, Toosi MB, Karimiani EG, Maroofian R, Schaefer GB, Ramakumaran V, Vasudevan P, Banos-Pinero B, Pagnamenta AT, Prasad C, Osmond M, Schuhmann S, Vasileiou G, Russ-Hall S, Scheffer IE, Carvill GL, Mefford H; Undiagnosed Diseases Network; Bacino CA, Lee BH, Chao HT. Paul MS, et al. Among authors: mester jl. Am J Hum Genet. 2024 Apr 4;111(4):805. doi: 10.1016/j.ajhg.2024.03.009. Epub 2024 Mar 20. Am J Hum Genet. 2024. PMID: 38508193 Free article. No abstract available.
Challenges and approaches to calibrating patient phenotype as evidence for cancer gene variant classification under ACMG/AMP guidelines.
Fortuno C, Michailidou K, Parsons M, Dolinsky JS, Pesaran T, Yussuf A, Mester JL, Hruska KS, Hiraki S, O'Connor R, Chan RC, Kim S, Tavtigian SV, Goldgar D, James PA, Spurdle AB. Fortuno C, et al. Among authors: mester jl. Hum Mol Genet. 2024 Apr 8;33(8):724-732. doi: 10.1093/hmg/ddae009. Hum Mol Genet. 2024. PMID: 38271184
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Paul MS, Michener SL, Pan H, Chan H, Pfliger JM, Rosenfeld JA, Lerma VC, Tran A, Longley MA, Lewis RA, Weisz-Hubshman M, Bekheirnia MR, Bekheirnia N, Massingham L, Zech M, Wagner M, Engels H, Cremer K, Mangold E, Peters S, Trautmann J, Mester JL, Guillen Sacoto MJ, Person R, McDonnell PP, Cohen SR, Lusk L, Cohen ASA, Le Pichon JB, Pastinen T, Zhou D, Engleman K, Racine C, Faivre L, Moutton S, Denommé-Pichon AS, Koh HY, Poduri A, Bolton J, Knopp C, Julia Suh DS, Maier A, Toosi MB, Karimiani EG, Maroofian R, Schaefer GB, Ramakumaran V, Vasudevan P, Prasad C, Osmond M, Schuhmann S, Vasileiou G, Russ-Hall S, Scheffer IE, Carvill GL, Mefford H; Undiagnosed Diseases Network; Bacino CA, Lee BH, Chao HT. Paul MS, et al. Among authors: mester jl. Am J Hum Genet. 2024 Jan 4;111(1):96-118. doi: 10.1016/j.ajhg.2023.12.004. Am J Hum Genet. 2024. PMID: 38181735
Specifications of the ACMG/AMP Variant Classification Guidelines for Germline DICER1 Variant Curation.
Hatton JN, Frone MN, Cox HC, Crowley SB, Hiraki S, Yokoyama NN, Abul-Husn NS, Amatruda JF, Anderson MJ, Bofill-De Ros X, Carr AG, Chao EC, Chen KS, Gu S, Higgs C, Machado J, Ritter D, Schultz KA, Soper ER, Wu MK, Mester JL, Kim J, Foulkes WD, Witkowski L, Stewart DR. Hatton JN, et al. Among authors: mester jl. Hum Mutat. 2023;2023:9537832. doi: 10.1155/2023/9537832. Epub 2023 Mar 29. Hum Mutat. 2023. PMID: 38084291 Free PMC article.
Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group.
Schmidt RJ, Steeves M, Bayrak-Toydemir P, Benson KA, Coe BP, Conlin LK, Ganapathi M, Garcia J, Gollob MH, Jobanputra V, Luo M, Ma D, Maston G, McGoldrick K, Palculict TB, Pesaran T, Pollin TI, Qian E, Rehm HL, Riggs ER, Schilit SLP, Sergouniotis PI, Tvrdik T, Watkins N, Zec L, Zhang W, Lebo MS; ClinGen Low Penetrance/Risk Allele Working Group. Schmidt RJ, et al. Genet Med. 2024 Mar;26(3):101036. doi: 10.1016/j.gim.2023.101036. Epub 2023 Dec 3. Genet Med. 2024. PMID: 38054408
Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup.
Walker LC, Hoya M, Wiggins GAR, Lindy A, Vincent LM, Parsons MT, Canson DM, Bis-Brewer D, Cass A, Tchourbanov A, Zimmermann H, Byrne AB, Pesaran T, Karam R, Harrison SM, Spurdle AB; ClinGen Sequence Variant Interpretation Working Group. Walker LC, et al. Am J Hum Genet. 2023 Jul 6;110(7):1046-1067. doi: 10.1016/j.ajhg.2023.06.002. Epub 2023 Jun 22. Am J Hum Genet. 2023. PMID: 37352859 Free PMC article.
Rare variants in PPFIA3 cause delayed development, intellectual disability, autism, and epilepsy.
Paul MS, Michener SL, Pan H, Pfliger JM, Rosenfeld JA, Lerma VC, Tran A, Longley MA, Lewis RA, Weisz-Hubshman M, Bekheirnia MR, Bekheirnia N, Massingham L, Zech M, Wagner M, Engels H, Cremer K, Mangold E, Peters S, Trautmann J, Mester JL, Guillen Sacoto MJ, Person R, McDonnell PP, Cohen SR, Lusk L, Cohen ASA, Pichon JL, Pastinen T, Zhou D, Engleman K, Racine C, Faivre L, Moutton S, Pichon AD, Schuhmann S, Vasileiou G, Russ-Hall S, Scheffer IE, Carvill GL, Mefford H, Network UD, Bacino CA, Lee BH, Chao HT. Paul MS, et al. Among authors: mester jl. medRxiv [Preprint]. 2023 Mar 29:2023.03.27.23287689. doi: 10.1101/2023.03.27.23287689. medRxiv. 2023. PMID: 37034625 Free PMC article. Preprint.
Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria.
Pejaver V, Byrne AB, Feng BJ, Pagel KA, Mooney SD, Karchin R, O'Donnell-Luria A, Harrison SM, Tavtigian SV, Greenblatt MS, Biesecker LG, Radivojac P, Brenner SE; ClinGen Sequence Variant Interpretation Working Group. Pejaver V, et al. Am J Hum Genet. 2022 Dec 1;109(12):2163-2177. doi: 10.1016/j.ajhg.2022.10.013. Epub 2022 Nov 21. Am J Hum Genet. 2022. PMID: 36413997 Free PMC article.
Ascl1 phospho-site mutations enhance neuronal conversion of adult cortical astrocytes in vivo.
Ghazale H, Park E, Vasan L, Mester J, Saleh F, Trevisiol A, Zinyk D, Chinchalongporn V, Liu M, Fleming T, Prokopchuk O, Klenin N, Kurrasch D, Faiz M, Stefanovic B, McLaurin J, Schuurmans C. Ghazale H, et al. Among authors: mester j. Front Neurosci. 2022 Aug 18;16:917071. doi: 10.3389/fnins.2022.917071. eCollection 2022. Front Neurosci. 2022. PMID: 36061596 Free PMC article.
ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines.
Preston CG, Wright MW, Madhavrao R, Harrison SM, Goldstein JL, Luo X, Wand H, Wulf B, Cheung G, Mandell ME, Tong H, Cheng S, Iacocca MA, Pineda AL, Popejoy AB, Dalton K, Zhen J, Dwight SS, Babb L, DiStefano M, O'Daniel JM, Lee K, Riggs ER, Zastrow DB, Mester JL, Ritter DI, Patel RY, Subramanian SL, Milosavljevic A, Berg JS, Rehm HL, Plon SE, Cherry JM, Bustamante CD, Costa HA; Clinical Genome Resource (ClinGen). Preston CG, et al. Among authors: mester jl. Genome Med. 2022 Jan 18;14(1):6. doi: 10.1186/s13073-021-01004-8. Genome Med. 2022. PMID: 35039090 Free PMC article.
Effects of Acquisition Matrix Size on the Accuracy and Repeatability of Parameters of Left Ventricular Function: A Phantom Study for ECG-gated Myocardial SPECT.
Gersdorf D, Rambow F, Weise R, Apostolova I, Kobayashi Y, Yamamura J, Tecklenburg K, Zsebe Z, Klutmann S, Nakajima K, Mester J. Gersdorf D, et al. Among authors: mester j. Ann Nucl Cardiol. 2021;7(1):43-48. doi: 10.17996/anc.21-00140. Epub 2021 Aug 31. Ann Nucl Cardiol. 2021. PMID: 36994135 Free PMC article.
Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants.
Fortuno C, Lee K, Olivier M, Pesaran T, Mai PL, de Andrade KC, Attardi LD, Crowley S, Evans DG, Feng BJ, Foreman AKM, Frone MN, Huether R, James PA, McGoldrick K, Mester J, Seifert BA, Slavin TP, Witkowski L, Zhang L, Plon SE, Spurdle AB, Savage SA; ClinGen TP53 Variant Curation Expert Panel. Fortuno C, et al. Among authors: mester j. Hum Mutat. 2021 Mar;42(3):223-236. doi: 10.1002/humu.24152. Epub 2020 Dec 25. Hum Mutat. 2021. PMID: 33300245 Free PMC article.
Suggested application of HER2+ breast tumor phenotype for germline TP53 variant classification within ACMG/AMP guidelines.
Fortuno C, Mester J, Pesaran T, Weitzel JN, Dolinsky J, Yussuf A, McGoldrick K, Garber JE, Savage SA, Khincha PP, Gareth Evans D, Achatz MI, Nichols KE, Maxwell KN, Schiffman JD, Sandoval R; Li-Fraumeni Exploration (LIFE) Consortium; James PA, Spurdle AB. Fortuno C, et al. Among authors: mester j. Hum Mutat. 2020 Sep;41(9):1555-1562. doi: 10.1002/humu.24060. Epub 2020 Jun 12. Hum Mutat. 2020. PMID: 32485079 Free PMC article.
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework.
Brnich SE, Abou Tayoun AN, Couch FJ, Cutting GR, Greenblatt MS, Heinen CD, Kanavy DM, Luo X, McNulty SM, Starita LM, Tavtigian SV, Wright MW, Harrison SM, Biesecker LG, Berg JS; Clinical Genome Resource Sequence Variant Interpretation Working Group. Brnich SE, et al. Genome Med. 2019 Dec 31;12(1):3. doi: 10.1186/s13073-019-0690-2. Genome Med. 2019. PMID: 31892348 Free PMC article.
Rural nurse recruitment.
Mester JS. Mester JS. Nurs Manage. 2018 Dec;49(12):51-53. doi: 10.1097/01.NUMA.0000544468.98484.b7. Nurs Manage. 2018. PMID: 30499859 No abstract available.
ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretation.
Rivera-Muñoz EA, Milko LV, Harrison SM, Azzariti DR, Kurtz CL, Lee K, Mester JL, Weaver MA, Currey E, Craigen W, Eng C, Funke B, Hegde M, Hershberger RE, Mao R, Steiner RD, Vincent LM, Martin CL, Plon SE, Ramos E, Rehm HL, Watson M, Berg JS. Rivera-Muñoz EA, et al. Hum Mutat. 2018 Nov;39(11):1614-1622. doi: 10.1002/humu.23645. Hum Mutat. 2018. PMID: 30311389 Free PMC article.
Neurogliovascular dysfunction in a model of repeated traumatic brain injury.
Adams C, Bazzigaluppi P, Beckett TL, Bishay J, Weisspapir I, Dorr A, Mester JR, Steinman J, Hirschler L, Warnking JM, Barbier EL, McLaurin J, Sled JG, Stefanovic B. Adams C, et al. Among authors: mester jr. Theranostics. 2018 Sep 9;8(17):4824-4836. doi: 10.7150/thno.24747. eCollection 2018. Theranostics. 2018. PMID: 30279740 Free PMC article.
Disruption of cardiac cholinergic neurons enhances susceptibility to ventricular arrhythmias.
Jungen C, Scherschel K, Eickholt C, Kuklik P, Klatt N, Bork N, Salzbrunn T, Alken F, Angendohr S, Klene C, Mester J, Klöcker N, Veldkamp MW, Schumacher U, Willems S, Nikolaev VO, Meyer C. Jungen C, et al. Among authors: mester j. Nat Commun. 2017 Jan 27;8:14155. doi: 10.1038/ncomms14155. Nat Commun. 2017. PMID: 28128201 Free PMC article.
Detection rate of PET/CT in patients with biochemical relapse of prostate cancer using [68Ga]PSMA I&T and comparison with published data of [68Ga]PSMA HBED-CC.
Berliner C, Tienken M, Frenzel T, Kobayashi Y, Helberg A, Kirchner U, Klutmann S, Beyersdorff D, Budäus L, Wester HJ, Mester J, Bannas P. Berliner C, et al. Among authors: mester j. Eur J Nucl Med Mol Imaging. 2017 Apr;44(4):670-677. doi: 10.1007/s00259-016-3572-5. Epub 2016 Nov 28. Eur J Nucl Med Mol Imaging. 2017. PMID: 27896369
Your views on leader visibility.
Lomack K, Dickens D, Mester J, Covert K. Lomack K, et al. Among authors: mester j. Nurs Manage. 2016 Oct;47(10):8-9. doi: 10.1097/01.NUMA.0000499566.57021.22. Nurs Manage. 2016. PMID: 27683161 No abstract available.
Neurovascular unit remodelling in the subacute stage of stroke recovery.
Lake EMR, Bazzigaluppi P, Mester J, Thomason LAM, Janik R, Brown M, McLaurin J, Carlen PL, Corbett D, Stanisz GJ, Stefanovic B. Lake EMR, et al. Among authors: mester j. Neuroimage. 2017 Feb 1;146:869-882. doi: 10.1016/j.neuroimage.2016.09.016. Epub 2016 Sep 21. Neuroimage. 2017. PMID: 27664828
Assessment of clinical workload for general and specialty genetic counsellors at an academic medical center: a tool for evaluating genetic counselling practices.
Heald B, Rybicki L, Clements D, Marquard J, Mester J, Noss R, Nardini M, Polk J, Psensky B, Rigelsky C, Schreiber A, Shealy A, Smith M, Eng C. Heald B, et al. Among authors: mester j. NPJ Genom Med. 2016 May 11;1:16010. doi: 10.1038/npjgenmed.2016.10. eCollection 2016. NPJ Genom Med. 2016. PMID: 29263811 Free PMC article.
PTEN hamartoma tumor syndrome.
Mester J, Charis E. Mester J, et al. Handb Clin Neurol. 2015;132:129-37. doi: 10.1016/B978-0-444-62702-5.00009-3. Handb Clin Neurol. 2015. PMID: 26564076 Review.
KLLN epigenotype-phenotype associations in Cowden syndrome.
Nizialek EA, Mester JL, Dhiman VK, Smiraglia DJ, Eng C. Nizialek EA, et al. Among authors: mester jl. Eur J Hum Genet. 2015 Nov;23(11):1538-43. doi: 10.1038/ejhg.2015.8. Epub 2015 Feb 11. Eur J Hum Genet. 2015. PMID: 25669429 Free PMC article.
A novel germline mutation in BAP1 predisposes to familial clear-cell renal cell carcinoma.
Farley MN, Schmidt LS, Mester JL, Pena-Llopis S, Pavia-Jimenez A, Christie A, Vocke CD, Ricketts CJ, Peterson J, Middelton L, Kinch L, Grishin N, Merino MJ, Metwalli AR, Xing C, Xie XJ, Dahia PLM, Eng C, Linehan WM, Brugarolas J. Farley MN, et al. Among authors: mester jl. Mol Cancer Res. 2013 Sep;11(9):1061-1071. doi: 10.1158/1541-7786.MCR-13-0111. Epub 2013 May 24. Mol Cancer Res. 2013. PMID: 23709298 Free PMC article.
When overgrowth bumps into cancer: the PTEN-opathies.
Mester J, Eng C. Mester J, et al. Am J Med Genet C Semin Med Genet. 2013 May;163C(2):114-21. doi: 10.1002/ajmg.c.31364. Am J Med Genet C Semin Med Genet. 2013. PMID: 23613428 Review.
Cognitive characteristics of PTEN hamartoma tumor syndromes.
Busch RM, Chapin JS, Mester J, Ferguson L, Haut JS, Frazier TW, Eng C. Busch RM, et al. Among authors: mester j. Genet Med. 2013 Jul;15(7):548-53. doi: 10.1038/gim.2013.1. Epub 2013 Mar 7. Genet Med. 2013. PMID: 23470840 Free PMC article.
Prevalence of germline PTEN, BMPR1A, SMAD4, STK11, and ENG mutations in patients with moderate-load colorectal polyps.
Ngeow J, Heald B, Rybicki LA, Orloff MS, Chen JL, Liu X, Yerian L, Willis J, Lehtonen HJ, Lehtonen R, Mester JL, Moline J, Burke CA, Church J, Aaltonen LA, Eng C. Ngeow J, et al. Among authors: mester jl. Gastroenterology. 2013 Jun;144(7):1402-9, 1409.e1-5. doi: 10.1053/j.gastro.2013.02.001. Epub 2013 Feb 8. Gastroenterology. 2013. PMID: 23399955 Free PMC article.
Lifetime cancer risks in individuals with germline PTEN mutations.
Tan MH, Mester JL, Ngeow J, Rybicki LA, Orloff MS, Eng C. Tan MH, et al. Among authors: mester jl. Clin Cancer Res. 2012 Jan 15;18(2):400-7. doi: 10.1158/1078-0432.CCR-11-2283. Clin Cancer Res. 2012. PMID: 22252256 Free PMC article.
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