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Items: 1 to 50 of 153

1.

Cell-to-Cell Variation in Gene Expression for Cultured Human Cells is Controlled in Trans by Diverse Genes: Implications for the Pathobiology of Aging.

Zhang J, Burnaevskiy N, Annis J, Han W, Hou D, Ladd P, Lee L, Mendenhall AR, Oshima J, Martin GM.

J Gerontol A Biol Sci Med Sci. 2020 Jan 20. pii: glaa027. doi: 10.1093/gerona/glaa027. [Epub ahead of print]

PMID:
31957802
2.

Free-flap reconstruction for full-thickness oral defects involving the oral commissure combined with oral modiolus reconstruction using a fascial sling.

Sasaki K, Sasaki M, Oshima J, Aihara Y, Nishijima A, Sekido M.

Microsurgery. 2019 Dec 23. doi: 10.1002/micr.30546. [Epub ahead of print]

PMID:
31868243
3.

Kinetics of Excimer Electrogenerated Chemiluminescence of Pyrene and 1-Pyrenebutyricacid 2-Ethylhexylester in Acetonitrile and an Ionic Liquid, Triethylpentylphosphonium Bis(trifluoromethanesulfonyl)imide.

Ishimatsu R, Tashiro S, Kasahara T, Oshima J, Mizuno J, Nakano K, Adachi C, Imato T.

J Phys Chem B. 2019 Dec 19;123(50):10825-10836. doi: 10.1021/acs.jpcb.9b08813. Epub 2019 Dec 5.

PMID:
31804083
4.

Inactivating Mutations in Exonuclease and Polymerase Domains in DNA Polymerase Delta Alter Sensitivities to Inhibitors of dNTP Synthesis.

Zhang J, Hou D, Annis J, Sargolzaeiaval F, Appelbaum J, Takahashi E, Martin GM, Herr A, Oshima J.

DNA Cell Biol. 2020 Jan;39(1):50-56. doi: 10.1089/dna.2019.5125. Epub 2019 Nov 21.

PMID:
31750734
5.

Spatiotemporal Dynamics of Hantavirus Cardiopulmonary Syndrome Transmission Risk in Brazil.

Muylaert RL, Sabino-Santos G Jr, Prist PR, Oshima JEF, Niebuhr BB, Sobral-Souza T, Oliveira SV, Bovendorp RS, Marshall JC, Hayman DTS, Ribeiro MC.

Viruses. 2019 Oct 31;11(11). pii: E1008. doi: 10.3390/v11111008.

6.

An intrinsic algorithm for viewing angle tolerance of object discrimination in human subjects.

Okamura JY, Oshima J, Yamaguchi R, Yamashita W, Wang G.

Can J Exp Psychol. 2019 Sep 19. doi: 10.1037/cep0000188. [Epub ahead of print]

PMID:
31535884
7.

[Malignant Mesothelioma of the Tunica Vaginalis Testis : A Case Report].

Oshima J, Inoue H, Fukuda S, Nishimura K, Hara T.

Hinyokika Kiyo. 2019 Jun;65(6):215-218. doi: 10.14989/ActaUrolJap_65_6_215. Japanese.

PMID:
31501388
8.

Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes.

Maierhofer A, Flunkert J, Oshima J, Martin GM, Poot M, Nanda I, Dittrich M, Müller T, Haaf T.

Aging Cell. 2019 Oct;18(5):e12995. doi: 10.1111/acel.12995. Epub 2019 Jul 1.

9.

Right on track? Performance of satellite telemetry in terrestrial wildlife research.

Hofman MPG, Hayward MW, Heim M, Marchand P, Rolandsen CM, Mattisson J, Urbano F, Heurich M, Mysterud A, Melzheimer J, Morellet N, Voigt U, Allen BL, Gehr B, Rouco C, Ullmann W, Holand Ø, Jørgensen NH, Steinheim G, Cagnacci F, Kroeschel M, Kaczensky P, Buuveibaatar B, Payne JC, Palmegiani I, Jerina K, Kjellander P, Johansson Ö, LaPoint S, Bayrakcismith R, Linnell JDC, Zaccaroni M, Jorge MLS, Oshima JEF, Songhurst A, Fischer C, Mc Bride RT Jr, Thompson JJ, Streif S, Sandfort R, Bonenfant C, Drouilly M, Klapproth M, Zinner D, Yarnell R, Stronza A, Wilmott L, Meisingset E, Thaker M, Vanak AT, Nicoloso S, Graeber R, Said S, Boudreau MR, Devlin A, Hoogesteijn R, May-Junior JA, Nifong JC, Odden J, Quigley HB, Tortato F, Parker DM, Caso A, Perrine J, Tellaeche C, Zieba F, Zwijacz-Kozica T, Appel CL, Axsom I, Bean WT, Cristescu B, Périquet S, Teichman KJ, Karpanty S, Licoppe A, Menges V, Black K, Scheppers TL, Schai-Braun SC, Azevedo FC, Lemos FG, Payne A, Swanepoel LH, Weckworth BV, Berger A, Bertassoni A, McCulloch G, Šustr P, Athreya V, Bockmuhl D, Casaer J, Ekori A, Melovski D, Richard-Hansen C, van de Vyver D, Reyna-Hurtado R, Robardet E, Selva N, Sergiel A, Farhadinia MS, Sunde P, Portas R, Ambarli H, Berzins R, Kappeler PM, Mann GK, Pyritz L, Bissett C, Grant T, Steinmetz R, Swedell L, Welch RJ, Armenteras D, Bidder OR, González TM, Rosenblatt A, Kachel S, Balkenhol N.

PLoS One. 2019 May 9;14(5):e0216223. doi: 10.1371/journal.pone.0216223. eCollection 2019.

10.

Changes in oxidative stress levels during two weeks of smoking cessation treatment and their association with nutritional characteristics in Japanese smokers.

Oba S, Inaba Y, Shibuya T, Oshima J, Seyama K, Kobayashi T, Kunugita N, Ino T.

Exp Ther Med. 2019 Apr;17(4):2757-2764. doi: 10.3892/etm.2019.7252. Epub 2019 Feb 7.

11.

ATLANTIC BIRD TRAITS: a data set of bird morphological traits from the Atlantic forests of South America.

Rodrigues RC, Hasui É, Assis JC, Pena JCC, Muylaert RL, Tonetti VR, Martello F, Regolin AL, Costa TVVD, Pichorim M, Carrano E, Lopes LE, de Vasconcelos MF, Fontana CS, Roos AL, Gonçalves F, Banks-Leite C, Cavarzere V, Efe MA, Alves MAS, Uezu A, Metzger JP, de Tarso Zuquim de Antas P, de Barros Ferraz KMPM, Calsavara LC, Bispo AA, Araujo HFP, Duca C, Piratelli AJ, Naka LN, Dias RA, Gatto CAFR, Vallejos MAV, Menezes GDR, Bugoni L, Rajão H, Zocche JJ, Willrich G, Silva ESD, Manica LT, de Camargo Guaraldo A, Althmann G, Serafini PP, Francisco MR, Lugarini C, Machado CG, Marques-Santos F, Bobato R, de Souza EA, Donatelli RJ, Ferreira CD, Morante-Filho JC, Paes-Macarrão ND, Macarrão A, Lima MR, Jacoboski LI, Candia-Gallardo C, Alegre VB, Jahn AE, de Camargo Barbosa KV, Cestari C, Silva JND, Silveira NSD, Crestani ACV, Petronetto AP, Bovo AAA, Viana AD, Araujo AC, Santos AHD, Amaral ACAD, Ferreira A, Vieira-Filho AH, Ribeiro BC, Missagia CCC, Bosenbecker C, Medolago CAB, Espínola CRR, Faxina C, Nunes CEC, Prates C, Luz DTAD, Moreno DJ, Mariz D, Faria D, Meyer D, Doná EA, Alexandrino ER, Fischer E, Girardi F, Giese FB, Shibuya FLS, Faria FA, de Farias FB, de Lima Favaro F, Freitas FJF, Chaves FG, Las-Casas FMG, Rosa GLM, Torre GM, Bochio GM, Bonetti GE, Kohler G, Toledo-Lima GS, Plucenio GP, Menezes Í, Torres IMD, Provinciato ICC, Viana IR, Roper JJ, Persegona JE, Barcik JJ, Martins-Silva J, Just JPG, Tavares-Damasceno JP, de Almeida Ferreira JR, Rosoni JRR, Falcon JET, Schaedler LM, Mathias LB, Deconto LR, Rodrigues LDC, Meyer MAP, Repenning M, Melo MA, de Carvalho MAS, Rodrigues M, Nunes MFC, Ogrzewalska MH, Gonçalves ML, Vecchi MB, Bettio M, Baptista MNDM, Arantes MS, Ruiz NL, de Andrade PGB, Ribeiro PHL, Junior PMG, Macario P, de Oliveira Fratoni R, Meurer R, Saint-Clair RS, Romagna RS, Lacerda RCA, Cerboncini RAS, Lyra RB, Lau R, Rodrigues RC, Faria RR, Laps RR, Althoff SL, de Jesus S, Namba S, Braga TV, Molin T, Câmara TPF, Enedino TR, Wischhoff U, de Oliveira VC, Leandro-Silva V, Araújo-Lima V, de Oliveira Lunardi V, de Gusmão RF, de Souza Correia JM, Gaspar LP, Fonseca RCB, Neto PAFP, de Aquino ACMM, de Camargo BB, Cezila BA, Costa LM, Paolino RM, Kanda CZ, Monteiro ECS, Oshima JEF, Alves-Eigenheer M, Pizo MA, Silveira LF, Galetti M, Ribeiro MC.

Ecology. 2019 Jun;100(6):e02647. doi: 10.1002/ecy.2647. Epub 2019 Apr 12.

12.

Characteristic Clinical Features of Werner Syndrome with a Novel Compound Heterozygous WRN Mutation c.1720+1G>A Plus c.3139-1G>C.

Matsumoto N, Ohta Y, Deguchi K, Kishida M, Sato K, Shang J, Takemoto M, Hishikawa N, Yamashita T, Watanabe A, Yokote K, Takemoto M, Oshima J, Abe K.

Intern Med. 2019 Apr 1;58(7):1033-1036. doi: 10.2169/internalmedicine.1816-18. Epub 2018 Dec 18.

13.

CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures.

Sargolzaeiaval F, Zhang J, Schleit J, Lessel D, Kubisch C, Precioso DR, Sillence D, Hisama FM, Dorschner M, Martin GM, Oshima J.

Mol Genet Genomic Med. 2018 Nov;6(6):1148-1156. doi: 10.1002/mgg3.495. Epub 2018 Nov 4.

14.

Biallelic WRN Mutations in Newly Identified Japanese Werner Syndrome Patients.

Maezawa Y, Kato H, Takemoto M, Watanabe A, Koshizaka M, Ishikawa T, Sargolzaeiaval F, Kuzuya M, Wakabayashi H, Kusaka T, Yokote K, Oshima J.

Mol Syndromol. 2018 Jul;9(4):214-218. doi: 10.1159/000489055. Epub 2018 May 15.

15.

Epigenetic clock for skin and blood cells applied to Hutchinson Gilford Progeria Syndrome and ex vivo studies.

Horvath S, Oshima J, Martin GM, Lu AT, Quach A, Cohen H, Felton S, Matsuyama M, Lowe D, Kabacik S, Wilson JG, Reiner AP, Maierhofer A, Flunkert J, Aviv A, Hou L, Baccarelli AA, Li Y, Stewart JD, Whitsel EA, Ferrucci L, Matsuyama S, Raj K.

Aging (Albany NY). 2018 Jul 26;10(7):1758-1775. doi: 10.18632/aging.101508.

16.

RECQ helicase disease and related progeroid syndromes: RECQ2018 meeting.

Oshima J, Kato H, Maezawa Y, Yokote K.

Mech Ageing Dev. 2018 Jul;173:80-83. doi: 10.1016/j.mad.2018.05.002. Epub 2018 May 9. Review.

17.

Precision Medicine and Progress in the Treatment of Hutchinson-Gilford Progeria Syndrome.

Hisama FM, Oshima J.

JAMA. 2018 Apr 24;319(16):1663-1664. doi: 10.1001/jama.2018.2199. No abstract available.

18.

[A Case of Retroperitoneal Cavernous Hemangioma Difficult to Differentiate from Retroperitoneal Liposarcoma].

Fujimoto K, Oshima J, Katayma K, Tei N, Harada Y, Nishimura K, Kiyokawa H, Kodama Y, Mano M.

Hinyokika Kiyo. 2017 Dec;63(12):521-524. doi: 10.14989/ActaUrolJap_63_12_521. Japanese.

19.
20.

ERCC4 variants identified in a cohort of patients with segmental progeroid syndromes.

Mori T, Yousefzadeh MJ, Faridounnia M, Chong JX, Hisama FM, Hudgins L, Mercado G, Wade EA, Barghouthy AS, Lee L, Martin GM, Nickerson DA, Bamshad MJ; University of Washington Center for Mendelian Genomics, Niedernhofer LJ, Oshima J.

Hum Mutat. 2018 Feb;39(2):255-265. doi: 10.1002/humu.23367. Epub 2017 Nov 17.

21.

[Inflammatory Pseudotumor of the Ureter : A Case Report and a Review].

Oshima J, Kinoshita T, Tei N, Harada Y, Oka S, Nishimura K, Mori K.

Hinyokika Kiyo. 2017 Oct;63(10):403-406. doi: 10.14989/ActaUrolJap_63_10_403. Review. Japanese.

22.

Dysfunction of the MDM2/p53 axis is linked to premature aging.

Lessel D, Wu D, Trujillo C, Ramezani T, Lessel I, Alwasiyah MK, Saha B, Hisama FM, Rading K, Goebel I, Schütz P, Speit G, Högel J, Thiele H, Nürnberg G, Nürnberg P, Hammerschmidt M, Zhu Y, Tong DR, Katz C, Martin GM, Oshima J, Prives C, Kubisch C.

J Clin Invest. 2017 Oct 2;127(10):3598-3608. doi: 10.1172/JCI92171. Epub 2017 Aug 28.

23.

Uncommon cause of cirrhosis-A case of Werner syndrome with a novel WRN mutation.

Amalnath SD, Sargolzaeiaval F, Oshima J, Baskar D.

Indian J Gastroenterol. 2017 Jul;36(4):323-325. doi: 10.1007/s12664-017-0781-1. Epub 2017 Aug 9.

24.

Accelerated epigenetic aging in Werner syndrome.

Maierhofer A, Flunkert J, Oshima J, Martin GM, Haaf T, Horvath S.

Aging (Albany NY). 2017 Apr;9(4):1143-1152. doi: 10.18632/aging.101217.

25.

[Nonischemic Priapism Following Brachytherapy : A Case Report and a Review].

Oshima J, Fujita K, Kishimoto K, Osuga K, Suzuki O, Soda T, Nakai Y, Kiuchi H, Takao T, Miyagawa Y, Tsujimura A, Nonomura N.

Hinyokika Kiyo. 2016 Nov;62(11):605-607. doi: 10.14989/ActaUrolJap_62_11_605. Japanese.

26.

High incidence of BSCL2 intragenic recombinational mutation in Peruvian type 2 Berardinelli-Seip syndrome.

Purizaca-Rosillo N, Mori T, Benites-Cóndor Y, Hisama FM, Martin GM, Oshima J.

Am J Med Genet A. 2017 Feb;173(2):471-478. doi: 10.1002/ajmg.a.38053. Epub 2016 Nov 21.

27.

Werner Syndrome.

Oshima J, Martin GM, Hisama FM.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020.
2002 Dec 2 [updated 2016 Sep 29].

28.

WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.

Yokote K, Chanprasert S, Lee L, Eirich K, Takemoto M, Watanabe A, Koizumi N, Lessel D, Mori T, Hisama FM, Ladd PD, Angle B, Baris H, Cefle K, Palanduz S, Ozturk S, Chateau A, Deguchi K, Easwar TK, Federico A, Fox A, Grebe TA, Hay B, Nampoothiri S, Seiter K, Streeten E, Piña-Aguilar RE, Poke G, Poot M, Posmyk R, Martin GM, Kubisch C, Schindler D, Oshima J.

Hum Mutat. 2017 Jan;38(1):7-15. doi: 10.1002/humu.23128. Epub 2016 Oct 7. Review.

29.

Werner syndrome through the lens of tissue and tumour genomics.

Tokita M, Kennedy SR, Risques RA, Chun SG, Pritchard C, Oshima J, Liu Y, Bryant-Greenwood PK, Welcsh P, Monnat RJ.

Sci Rep. 2016 Aug 25;6:32038. doi: 10.1038/srep32038.

30.

Ageing: Dietary protection for genes.

Oshima J, Martin GM.

Nature. 2016 Sep 15;537(7620):316-317. doi: 10.1038/nature19427. Epub 2016 Aug 24. No abstract available.

31.

Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions.

Oshima J, Sidorova JM, Monnat RJ Jr.

Ageing Res Rev. 2017 Jan;33:105-114. doi: 10.1016/j.arr.2016.03.002. Epub 2016 Mar 15. Review.

32.

The Werner syndrome RECQ helicase targets G4 DNA in human cells to modulate transcription.

Tang W, Robles AI, Beyer RP, Gray LT, Nguyen GH, Oshima J, Maizels N, Harris CC, Monnat RJ Jr.

Hum Mol Genet. 2016 May 15;25(10):2060-2069. Epub 2016 Mar 16.

33.

How Research on Human Progeroid and Antigeroid Syndromes Can Contribute to the Longevity Dividend Initiative.

Hisama FM, Oshima J, Martin GM.

Cold Spring Harb Perspect Med. 2016 Apr 1;6(4):a025882. doi: 10.1101/cshperspect.a025882. Review.

34.

Serum Albumin Concentrations Predict hypovolaemia Caused by Polyethylene Glycol Plus Ascorbic Acid Prior to Colonoscopy in Elderly Patients.

Ogino N, Aridome G, Oshima J, Shibata M, Watanabe T, Kume K, Yoshikawa I, Harada M.

Drugs Aging. 2016 May;33(5):355-63. doi: 10.1007/s40266-016-0355-4.

PMID:
26895453
35.

Aβ 1-40 enhances the proliferation of human diploid fibroblasts.

Theda L, Drews MK, Zitnik G, Oshima J, Martin GM.

Neurobiol Aging. 2016 Feb;38:11-13. doi: 10.1016/j.neurobiolaging.2015.10.027. Epub 2015 Nov 2.

36.

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).

Klionsky DJ, Abdelmohsen K, Abe A, Abedin MJ, Abeliovich H, Acevedo Arozena A, Adachi H, Adams CM, Adams PD, Adeli K, Adhihetty PJ, Adler SG, Agam G, Agarwal R, Aghi MK, Agnello M, Agostinis P, Aguilar PV, Aguirre-Ghiso J, Airoldi EM, Ait-Si-Ali S, Akematsu T, Akporiaye ET, Al-Rubeai M, Albaiceta GM, Albanese C, Albani D, Albert ML, Aldudo J, Algül H, Alirezaei M, Alloza I, Almasan A, Almonte-Beceril M, Alnemri ES, Alonso C, Altan-Bonnet N, Altieri DC, Alvarez S, Alvarez-Erviti L, Alves S, Amadoro G, Amano A, Amantini C, Ambrosio S, Amelio I, Amer AO, Amessou M, Amon A, An Z, Anania FA, Andersen SU, Andley UP, Andreadi CK, Andrieu-Abadie N, Anel A, Ann DK, Anoopkumar-Dukie S, Antonioli M, Aoki H, Apostolova N, Aquila S, Aquilano K, Araki K, Arama E, Aranda A, Araya J, Arcaro A, Arias E, Arimoto H, Ariosa AR, Armstrong JL, Arnould T, Arsov I, Asanuma K, Askanas V, Asselin E, Atarashi R, Atherton SS, Atkin JD, Attardi LD, Auberger P, Auburger G, Aurelian L, Autelli R, Avagliano L, Avantaggiati ML, Avrahami L, Awale S, Azad N, Bachetti T, Backer JM, Bae DH, Bae JS, Bae ON, Bae SH, Baehrecke EH, Baek SH, Baghdiguian S, Bagniewska-Zadworna A, Bai H, Bai J, Bai XY, Bailly Y, Balaji KN, Balduini W, Ballabio A, Balzan R, Banerjee R, Bánhegyi G, Bao H, Barbeau B, Barrachina MD, Barreiro E, Bartel B, Bartolomé A, Bassham DC, Bassi MT, Bast RC Jr, Basu A, Batista MT, Batoko H, Battino M, Bauckman K, Baumgarner BL, Bayer KU, Beale R, Beaulieu JF, Beck GR Jr, Becker C, Beckham JD, Bédard PA, Bednarski PJ, Begley TJ, Behl C, Behrends C, Behrens GM, Behrns KE, Bejarano E, Belaid A, Belleudi F, Bénard G, Berchem G, Bergamaschi D, Bergami M, Berkhout B, Berliocchi L, Bernard A, Bernard M, Bernassola F, Bertolotti A, Bess AS, Besteiro S, Bettuzzi S, Bhalla S, Bhattacharyya S, Bhutia SK, Biagosch C, Bianchi MW, Biard-Piechaczyk M, Billes V, Bincoletto C, Bingol B, Bird SW, Bitoun M, Bjedov I, Blackstone C, Blanc L, Blanco GA, Blomhoff HK, Boada-Romero E, Böckler S, Boes M, Boesze-Battaglia K, Boise LH, Bolino A, Boman A, Bonaldo P, Bordi M, Bosch J, Botana LM, Botti J, Bou G, Bouché M, Bouchecareilh M, Boucher MJ, Boulton ME, Bouret SG, Boya P, Boyer-Guittaut M, Bozhkov PV, Brady N, Braga VM, Brancolini C, Braus GH, Bravo-San Pedro JM, Brennan LA, Bresnick EH, Brest P, Bridges D, Bringer MA, Brini M, Brito GC, Brodin B, Brookes PS, Brown EJ, Brown K, Broxmeyer HE, Bruhat A, Brum PC, Brumell JH, Brunetti-Pierri N, Bryson-Richardson RJ, Buch S, Buchan AM, Budak H, Bulavin DV, Bultman SJ, Bultynck G, Bumbasirevic V, Burelle Y, Burke RE, Burmeister M, Bütikofer P, Caberlotto L, Cadwell K, Cahova M, Cai D, Cai J, Cai Q, Calatayud S, Camougrand N, Campanella M, Campbell GR, Campbell M, Campello S, Candau R, Caniggia I, Cantoni L, Cao L, Caplan AB, Caraglia M, Cardinali C, Cardoso SM, Carew JS, Carleton LA, Carlin CR, Carloni S, Carlsson SR, Carmona-Gutierrez D, Carneiro LA, Carnevali O, Carra S, Carrier A, Carroll B, Casas C, Casas J, Cassinelli G, Castets P, Castro-Obregon S, Cavallini G, Ceccherini I, Cecconi F, Cederbaum AI, Ceña V, Cenci S, Cerella C, Cervia D, Cetrullo S, Chaachouay H, Chae HJ, Chagin AS, Chai CY, Chakrabarti G, Chamilos G, Chan EY, Chan MT, Chandra D, Chandra P, Chang CP, Chang RC, Chang TY, Chatham JC, Chatterjee S, Chauhan S, Che Y, Cheetham ME, Cheluvappa R, Chen CJ, Chen G, Chen GC, Chen G, Chen H, Chen JW, Chen JK, Chen M, Chen M, Chen P, Chen Q, Chen Q, Chen SD, Chen S, Chen SS, Chen W, Chen WJ, Chen WQ, Chen W, Chen X, Chen YH, Chen YG, Chen Y, Chen Y, Chen Y, Chen YJ, Chen YQ, Chen Y, Chen Z, Chen Z, Cheng A, Cheng CH, Cheng H, Cheong H, Cherry S, Chesney J, Cheung CH, Chevet E, Chi HC, Chi SG, Chiacchiera F, Chiang HL, Chiarelli R, Chiariello M, Chieppa M, Chin LS, Chiong M, Chiu GN, Cho DH, Cho SG, Cho WC, Cho YY, Cho YS, Choi AM, Choi EJ, Choi EK, Choi J, Choi ME, Choi SI, Chou TF, Chouaib S, Choubey D, Choubey V, Chow KC, Chowdhury K, Chu CT, Chuang TH, Chun T, Chung H, Chung T, Chung YL, Chwae YJ, Cianfanelli V, Ciarcia R, Ciechomska IA, Ciriolo MR, Cirone M, Claerhout S, Clague MJ, Clària J, Clarke PG, Clarke R, Clementi E, Cleyrat C, Cnop M, Coccia EM, Cocco T, Codogno P, Coers J, Cohen EE, Colecchia D, Coletto L, Coll NS, Colucci-Guyon E, Comincini S, Condello M, Cook KL, Coombs GH, Cooper CD, Cooper JM, Coppens I, Corasaniti MT, Corazzari M, Corbalan R, Corcelle-Termeau E, Cordero MD, Corral-Ramos C, Corti O, Cossarizza A, Costelli P, Costes S, Cotman SL, Coto-Montes A, Cottet S, Couve E, Covey LR, Cowart LA, Cox JS, Coxon FP, Coyne CB, Cragg MS, Craven RJ, Crepaldi T, Crespo JL, Criollo A, Crippa V, Cruz MT, Cuervo AM, Cuezva JM, Cui T, Cutillas PR, Czaja MJ, Czyzyk-Krzeska MF, Dagda RK, Dahmen U, Dai C, Dai W, Dai Y, Dalby KN, Dalla Valle L, Dalmasso G, D'Amelio M, Damme M, Darfeuille-Michaud A, Dargemont C, Darley-Usmar VM, Dasarathy S, Dasgupta B, Dash S, Dass CR, Davey HM, Davids LM, Dávila D, Davis RJ, Dawson TM, Dawson VL, Daza P, de Belleroche J, de Figueiredo P, de Figueiredo RC, de la Fuente J, De Martino L, De Matteis A, De Meyer GR, De Milito A, De Santi M, de Souza W, De Tata V, De Zio D, Debnath J, Dechant R, Decuypere JP, Deegan S, Dehay B, Del Bello B, Del Re DP, Delage-Mourroux R, Delbridge LM, Deldicque L, Delorme-Axford E, Deng Y, Dengjel J, Denizot M, Dent P, Der CJ, Deretic V, Derrien B, Deutsch E, Devarenne TP, Devenish RJ, Di Bartolomeo S, Di Daniele N, Di Domenico F, Di Nardo A, Di Paola S, Di Pietro A, Di Renzo L, DiAntonio A, Díaz-Araya G, Díaz-Laviada I, Diaz-Meco MT, Diaz-Nido J, Dickey CA, Dickson RC, Diederich M, Digard P, Dikic I, Dinesh-Kumar SP, Ding C, Ding WX, Ding Z, Dini L, Distler JH, Diwan A, Djavaheri-Mergny M, Dmytruk K, Dobson RC, Doetsch V, Dokladny K, Dokudovskaya S, Donadelli M, Dong XC, Dong X, Dong Z, Donohue TM Jr, Doran KS, D'Orazi G, Dorn GW 2nd, Dosenko V, Dridi S, Drucker L, Du J, Du LL, Du L, du Toit A, Dua P, Duan L, Duann P, Dubey VK, Duchen MR, Duchosal MA, Duez H, Dugail I, Dumit VI, Duncan MC, 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JT, Yu J, Yu L, Yu WH, Yu XF, Yu Z, Yuan J, Yuan ZM, Yue BY, Yue J, Yue Z, Zacks DN, Zacksenhaus E, Zaffaroni N, Zaglia T, Zakeri Z, Zecchini V, Zeng J, Zeng M, Zeng Q, Zervos AS, Zhang DD, Zhang F, Zhang G, Zhang GC, Zhang H, Zhang H, Zhang H, Zhang H, Zhang J, Zhang J, Zhang J, Zhang J, Zhang JP, Zhang L, Zhang L, Zhang L, Zhang L, Zhang MY, Zhang X, Zhang XD, Zhang Y, Zhang Y, Zhang Y, Zhang Y, Zhang Y, Zhao M, Zhao WL, Zhao X, Zhao YG, Zhao Y, Zhao Y, Zhao YX, Zhao Z, Zhao ZJ, Zheng D, Zheng XL, Zheng X, Zhivotovsky B, Zhong Q, Zhou GZ, Zhou G, Zhou H, Zhou SF, Zhou XJ, Zhu H, Zhu H, Zhu WG, Zhu W, Zhu XF, Zhu Y, Zhuang SM, Zhuang X, Ziparo E, Zois CE, Zoladek T, Zong WX, Zorzano A, Zughaier SM.

Autophagy. 2016;12(1):1-222. doi: 10.1080/15548627.2015.1100356. No abstract available. Erratum in: Autophagy. 2016;12(2):443. Selliez, Iban [corrected to Seiliez, Iban].

37.

Microfluidic White Organic Light-Emitting Diode Based on Integrated Patterns of Greenish-Blue and Yellow Solvent-Free Liquid Emitters.

Kobayashi N, Kasahara T, Edura T, Oshima J, Ishimatsu R, Tsuwaki M, Imato T, Shoji S, Mizuno J.

Sci Rep. 2015 Oct 6;5:14822. doi: 10.1038/srep14822.

38.

POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome.

Lessel D, Hisama FM, Szakszon K, Saha B, Sanjuanelo AB, Salbert BA, Steele PD, Baldwin J, Brown WT, Piussan C, Plauchu H, Szilvássy J, Horkay E, Högel J, Martin GM, Herr AJ, Oshima J, Kubisch C.

Hum Mutat. 2015 Nov;36(11):1070-9. doi: 10.1002/humu.22833. Epub 2015 Aug 6.

39.

[A Case Report of Right Atrial Tumor Thrombus from Renal Cell Carcinoma].

Oshima J, Fujita K, Nakai Y, Kainuma T, Nishi H, Nonomura N.

Hinyokika Kiyo. 2015 May;61(5):207-10. Japanese.

40.

Truncated prelamin A expression in HGPS-like patients: a transcriptional study.

Barthélémy F, Navarro C, Fayek R, Da Silva N, Roll P, Sigaudy S, Oshima J, Bonne G, Papadopoulou-Legbelou K, Evangeliou AE, Spilioti M, Lemerrer M, Wevers RA, Morava E, Robaglia-Schlupp A, Lévy N, Bartoli M, De Sandre-Giovannoli A.

Eur J Hum Genet. 2015 Aug;23(8):1051-61. doi: 10.1038/ejhg.2014.239. Epub 2015 Feb 4.

41.

Genetic diversity is a predictor of mortality in humans.

Bihlmeyer NA, Brody JA, Smith AV, Lunetta KL, Nalls M, Smith JA, Tanaka T, Davies G, Yu L, Mirza SS, Teumer A, Coresh J, Pankow JS, Franceschini N, Scaria A, Oshima J, Psaty BM, Gudnason V, Eiriksdottir G, Harris TB, Li H, Karasik D, Kiel DP, Garcia M, Liu Y, Faul JD, Kardia SL, Zhao W, Ferrucci L, Allerhand M, Liewald DC, Redmond P, Starr JM, De Jager PL, Evans DA, Direk N, Ikram MA, Uitterlinden A, Homuth G, Lorbeer R, Grabe HJ, Launer L, Murabito JM, Singleton AB, Weir DR, Bandinelli S, Deary IJ, Bennett DA, Tiemeier H, Kocher T, Lumley T, Arking DE.

BMC Genet. 2014 Dec 29;15:159. doi: 10.1186/s12863-014-0159-7.

42.

Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features.

Lessel D, Vaz B, Halder S, Lockhart PJ, Marinovic-Terzic I, Lopez-Mosqueda J, Philipp M, Sim JC, Smith KR, Oehler J, Cabrera E, Freire R, Pope K, Nahid A, Norris F, Leventer RJ, Delatycki MB, Barbi G, von Ameln S, Högel J, Degoricija M, Fertig R, Burkhalter MD, Hofmann K, Thiele H, Altmüller J, Nürnberg G, Nürnberg P, Bahlo M, Martin GM, Aalfs CM, Oshima J, Terzic J, Amor DJ, Dikic I, Ramadan K, Kubisch C.

Nat Genet. 2014 Nov;46(11):1239-44. doi: 10.1038/ng.3103. Epub 2014 Sep 28.

43.

Clinical utility gene card for: Werner Syndrome--Update 2014.

Hisama FM, Kubisch C, Martin GM, Oshima J.

Eur J Hum Genet. 2015 Jun;23(6). doi: 10.1038/ejhg.2014.171. Epub 2014 Sep 3. No abstract available.

44.

Atypical Aicardi-Goutieres syndrome: is the WRN locus a modifier?

Lessel D, Saha B, Hisama F, Kaymakamzade B, Nurlu G, Gursoy-Özdemir Y, Thiele H, Nürnberg P, Martin GM, Kubisch C, Oshima J.

Am J Med Genet A. 2014 Oct;164A(10):2510-3. doi: 10.1002/ajmg.a.36664. Epub 2014 Jul 2.

45.

[Modified BEP regimen leads to abatement of choriocarcinoma syndrome in a patient with extra gonadal germ cell tumor : a case report].

Oshima J, Uemura M, Kato T, Nagahara A, Kiuchi H, Tsujimura A, Nonomura N.

Hinyokika Kiyo. 2014 Apr;60(4):183-7. Japanese.

46.

An encouraging progress report on the treatment of progeria and its implications for atherogenesis.

Oshima J, Hisama FM, Martin GM.

Circulation. 2014 Jul 1;130(1):4-6. doi: 10.1161/CIRCULATIONAHA.114.010648. Epub 2014 May 2. No abstract available.

47.

Rectal perforation caused by mesalazine enema in a patient with ulcerative colitis.

Kume K, Watanabe T, Oshima J, Yoshikawa I, Harada M.

Endoscopy. 2014;46 Suppl 1 UCTN:E190. doi: 10.1055/s-0034-1365148. Epub 2014 Apr 22. No abstract available.

PMID:
24756289
48.

Search and insights into novel genetic alterations leading to classical and atypical Werner syndrome.

Oshima J, Hisama FM.

Gerontology. 2014;60(3):239-46. doi: 10.1159/000356030. Epub 2014 Jan 3. Review.

49.

Rapamycin decreases DNA damage accumulation and enhances cell growth of WRN-deficient human fibroblasts.

Saha B, Cypro A, Martin GM, Oshima J.

Aging Cell. 2014 Jun;13(3):573-5. doi: 10.1111/acel.12190. Epub 2014 Feb 5.

50.

Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry.

Saha B, Lessel D, Nampoothiri S, Rao AS, Hisama FM, Peter D, Bennett C, Nürnberg G, Nürnberg P, Martin GM, Kubisch C, Oshima J.

Mol Genet Genomic Med. 2013 May 1;1(1):7-14.

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