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Items: 1 to 50 of 108

1.

Hsa-miR-210-3p expression in breast cancer and its putative association with worse outcome in patients treated with Docetaxel.

Pasculli B, Barbano R, Rendina M, Fontana A, Copetti M, Mazza T, Valori VM, Morritti M, Maiello E, Graziano P, Murgo R, Fazio VM, Esteller M, Parrella P.

Sci Rep. 2019 Oct 17;9(1):14913. doi: 10.1038/s41598-019-51581-3.

PMID:
31624308
2.

A Multi-Layered Study on Harmonic Oscillations in Mammalian Genomics and Proteomics.

Genov N, Castellana S, Scholkmann F, Capocefalo D, Truglio M, Rosati J, Turco EM, Biagini T, Carbone A, Mazza T, Relógio A, Mazzoccoli G.

Int J Mol Sci. 2019 Sep 17;20(18). pii: E4585. doi: 10.3390/ijms20184585.

3.

Double missense mutations in cardiac myosin-binding protein C and myopalladin genes: A case report with diffuse coronary disease, complete atrioventricular block, and progression to dilated cardiomyopathy.

Mastroianno S, Palumbo P, Castellana S, Leone MP, Massaro R, Potenza DR, Mazza T, Russo A, Castori M, Carella M, Di Stolfo G.

Ann Noninvasive Electrocardiol. 2019 Sep 16:e12687. doi: 10.1111/anec.12687. [Epub ahead of print]

PMID:
31524317
4.

Concurrent chromothripsis events in a case of TP53 depleted acute myeloid leukemia with myelodysplasia-related changes.

Tolomeo D, L'Abbate A, Lonoce A, D'Addabbo P, Miccoli MF, Lo Cunsolo C, Iuzzolino P, Palumbo O, Carella M, Racanelli V, Mazza T, Ottaviani E, Martinelli G, Macchia G, Storlazzi CT.

Cancer Genet. 2019 Sep;237:63-68. doi: 10.1016/j.cancergen.2019.06.009. Epub 2019 Jun 12.

PMID:
31447067
5.

Deficiency and haploinsufficiency of histone macroH2A1.1 in mice recapitulate hematopoietic defects of human myelodysplastic syndrome.

Bereshchenko O, Lo Re O, Nikulenkov F, Flamini S, Kotaskova J, Mazza T, Le Pannérer MM, Buschbeck M, Giallongo C, Palumbo G, Li Volti G, Pazienza V, Cervinek L, Riccardi C, Krejci L, Pospisilova S, Stewart AF, Vinciguerra M.

Clin Epigenetics. 2019 Aug 22;11(1):121. doi: 10.1186/s13148-019-0724-z.

6.

Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2.

De Mori R, Severino M, Mancardi MM, Anello D, Tardivo S, Biagini T, Capra V, Casella A, Cereda C, Copeland BR, Gagliardi S, Gamucci A, Ginevrino M, Illi B, Lorefice E, Musaev D, Stanley V, Micalizzi A, Gleeson JG, Mazza T, Rossi A, Valente EM.

Brain. 2019 Oct 1;142(10):2965-2978. doi: 10.1093/brain/awz247.

7.

Molecular diagnostic workflow, clinical interpretation of sequence variants and data repository procedures in 140 individuals with familial cerebral cavernous malformations.

Fusco C, Copetti M, Mazza T, Amoruso L, Mastoianno S, Nardella G, Guarnieri V, Micale L, D'Agruma L, Castori M.

Hum Mutat. 2019 Jun 29. doi: 10.1002/humu.23851. [Epub ahead of print]

PMID:
31254430
8.

Are Gaming-Enabled Graphic Processing Unit Cards Convenient for Molecular Dynamics Simulation?

Biagini T, Petrizzelli F, Truglio M, Cespa R, Barbieri A, Capocefalo D, Castellana S, Tevy MF, Carella M, Mazza T.

Evol Bioinform Online. 2019 May 22;15:1176934319850144. doi: 10.1177/1176934319850144. eCollection 2019.

9.

Association of a homozygous GCK missense mutation with mild diabetes.

Marucci A, Biagini T, Di Paola R, Menzaghi C, Fini G, Castellana S, Cardinale GM, Mazza T, Trischitta V.

Mol Genet Genomic Med. 2019 Jul;7(7):e00728. doi: 10.1002/mgg3.728. Epub 2019 Jun 14.

10.

Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathy.

Motta M, Giancotti A, Mastromoro G, Chandramouli B, Pinna V, Pantaleoni F, Di Giosaffatte N, Petrini S, Mazza T, D'Ambrosio V, Versacci P, Ventriglia F, Chillemi G, Pizzuti A, Tartaglia M, De Luca A.

Hum Mutat. 2019 Aug;40(8):1046-1056. doi: 10.1002/humu.23767. Epub 2019 May 6.

PMID:
31059601
11.

Cardiac valvular Ehlers-Danlos syndrome is a well-defined condition due to recessive null variants in COL1A2.

Guarnieri V, Morlino S, Di Stolfo G, Mastroianno S, Mazza T, Castori M.

Am J Med Genet A. 2019 May;179(5):846-851. doi: 10.1002/ajmg.a.61100. Epub 2019 Mar 1.

PMID:
30821104
12.

Sudden death in mild hypertrophic cardiomyopathy with compound DSG2/DSC2/MYH6 mutations: Revisiting phenotype after genetic assessment in a master runner athlete.

Castellana S, Mastroianno S, Palumbo P, Palumbo O, Biagini T, Leone MP, De Luca G, Potenza DR, Amico CM, Mazza T, Russo A, Di Stolfo G, Carella M.

J Electrocardiol. 2019 Mar - Apr;53:95-99. doi: 10.1016/j.jelectrocard.2019.01.002. Epub 2019 Jan 2.

PMID:
30716529
13.

Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing.

Dallali H, Pezzilli S, Hechmi M, Sallem OK, Elouej S, Jmel H, Ben Halima Y, Chargui M, Gharbi M, Mercuri L, Alberico F, Mazza T, Bahlous A, Ben Ahmed M, Jamoussi H, Abid A, Trischitta V, Abdelhak S, Prudente S, Kefi R.

Acta Diabetol. 2019 May;56(5):515-523. doi: 10.1007/s00592-018-01283-5. Epub 2019 Jan 17.

PMID:
30656436
14.

Mono-ADP-Ribosylhydrolase MACROD2 Is Dispensable for Murine Responses to Metabolic and Genotoxic Insults.

Lo Re O, Mazza T, Vinciguerra M.

Front Genet. 2018 Dec 12;9:654. doi: 10.3389/fgene.2018.00654. eCollection 2018.

15.

TRIM8-driven transcriptomic profile of neural stem cells identified glioma-related nodal genes and pathways.

Venuto S, Castellana S, Monti M, Appolloni I, Fusilli C, Fusco C, Pucci P, Malatesta P, Mazza T, Merla G, Micale L.

Biochim Biophys Acta Gen Subj. 2019 Feb;1863(2):491-501. doi: 10.1016/j.bbagen.2018.12.001. Epub 2018 Dec 5.

PMID:
30528352
16.

EphB2 stem-related and EphA2 progression-related miRNA-based networks in progressive stages of CRC evolution: clinical significance and potential miRNA drivers.

De Robertis M, Mazza T, Fusilli C, Loiacono L, Poeta ML, Sanchez M, Massi E, Lamorte G, Diodoro MG, Pescarmona E, Signori E, Pesole G, Vescovi AL, Garcia-Foncillas J, Fazio VM.

Mol Cancer. 2018 Nov 30;17(1):169. doi: 10.1186/s12943-018-0912-z.

17.

Symmetry breakdown of electron emission in extreme ultraviolet photoionization of argon.

Ilchen M, Hartmann G, Gryzlova EV, Achner A, Allaria E, Beckmann A, Braune M, Buck J, Callegari C, Coffee RN, Cucini R, Danailov M, De Fanis A, Demidovich A, Ferrari E, Finetti P, Glaser L, Knie A, Lindahl AO, Plekan O, Mahne N, Mazza T, Raimondi L, Roussel E, Scholz F, Seltmann J, Shevchuk I, Svetina C, Walter P, Zangrando M, Viefhaus J, Grum-Grzhimailo AN, Meyer M.

Nat Commun. 2018 Nov 7;9(1):4659. doi: 10.1038/s41467-018-07152-7.

18.

Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis.

Fusilli C, Migliore S, Mazza T, Consoli F, De Luca A, Barbagallo G, Ciammola A, Gatto EM, Cesarini M, Etcheverry JL, Parisi V, Al-Oraimi M, Al-Harrasi S, Al-Salmi Q, Marano M, Vonsattel JG, Sabatini U, Landwehrmeyer GB, Squitieri F.

Lancet Neurol. 2018 Nov;17(11):986-993. doi: 10.1016/S1474-4422(18)30294-1. Epub 2018 Sep 19.

PMID:
30243861
19.

Establishment of stable iPS-derived human neural stem cell lines suitable for cell therapies.

Rosati J, Ferrari D, Altieri F, Tardivo S, Ricciolini C, Fusilli C, Zalfa C, Profico DC, Pinos F, Bernardini L, Torres B, Manni I, Piaggio G, Binda E, Copetti M, Lamorte G, Mazza T, Carella M, Gelati M, Valente EM, Simeone A, Vescovi AL.

Cell Death Dis. 2018 Sep 17;9(10):937. doi: 10.1038/s41419-018-0990-2.

20.

A novel mutation in CDH11, encoding cadherin-11, cause Branchioskeletogenital (Elsahy-Waters) syndrome.

Castori M, Ott CE, Bisceglia L, Leone MP, Mazza T, Castellana S, Tomassi J, Lanciotti S, Mundlos S, Hennekam RC, Kornak U, Brancati F.

Am J Med Genet A. 2018 Sep;176(9):2028-2033. doi: 10.1002/ajmg.a.40379. Epub 2018 Sep 8.

PMID:
30194892
21.

Systematic Analysis of Mouse Genome Reveals Distinct Evolutionary and Functional Properties Among Circadian and Ultradian Genes.

Castellana S, Mazza T, Capocefalo D, Genov N, Biagini T, Fusilli C, Scholkmann F, Relógio A, Hogenesch JB, Mazzoccoli G.

Front Physiol. 2018 Aug 23;9:1178. doi: 10.3389/fphys.2018.01178. eCollection 2018.

22.

Sudden cardiac death in J wave syndrome with short QT associated to a novel mutation in Nav 1.8 coding gene SCN10A: First case report for a possible pharmacogenomic role.

Di Stolfo G, Palumbo P, Castellana S, Mastroianno S, Biagini T, Palumbo O, Leone MP, De Luca G, Potenza DR, Mazza T, Russo AA, Carella M.

J Electrocardiol. 2018 Sep - Oct;51(5):809-813. doi: 10.1016/j.jelectrocard.2018.06.005. Epub 2018 Jun 9.

PMID:
30177317
23.

Histone variant macroH2A1 rewires carbohydrate and lipid metabolism of hepatocellular carcinoma cells towards cancer stem cells.

Lo Re O, Douet J, Buschbeck M, Fusilli C, Pazienza V, Panebianco C, Castracani CC, Mazza T, Li Volti G, Vinciguerra M.

Epigenetics. 2018;13(8):829-845. doi: 10.1080/15592294.2018.1514239. Epub 2018 Sep 29.

24.

A single-center study on 140 patients with cerebral cavernous malformations: 28 new pathogenic variants and functional characterization of a PDCD10 large deletion.

Nardella G, Visci G, Guarnieri V, Castellana S, Biagini T, Bisceglia L, Palumbo O, Trivisano M, Vaira C, Scerrati M, Debrasi D, D'Angelo V, Carella M, Merla G, Mazza T, Castori M, D'Agruma L, Fusco C.

Hum Mutat. 2018 Dec;39(12):1885-1900. doi: 10.1002/humu.23629. Epub 2018 Sep 24.

PMID:
30161288
25.

Time-resolved electron spectroscopy for chemical analysis of photodissociation: Photoelectron spectra of Fe(CO)5, Fe(CO)4, and Fe(CO)3.

Leitner T, Josefsson I, Mazza T, Miedema PS, Schröder H, Beye M, Kunnus K, Schreck S, Düsterer S, Föhlisch A, Meyer M, Odelius M, Wernet P.

J Chem Phys. 2018 Jul 28;149(4):044307. doi: 10.1063/1.5035149.

PMID:
30068152
26.

Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect.

Ferese R, Bonetti M, Consoli F, Guida V, Sarkozy A, Lepri FR, Versacci P, Gambardella S, Calcagni G, Margiotti K, Piceci Sparascio F, Hozhabri H, Mazza T, Digilio MC, Dallapiccola B, Tartaglia M, Marino B, Hertog JD, De Luca A.

Hum Mutat. 2018 Oct;39(10):1428-1441. doi: 10.1002/humu.23593. Epub 2018 Jul 30.

PMID:
30007050
27.

Between SCA5 and SCAR14: delineation of the SPTBN2 p.R480W-associated phenotype.

Nuovo S, Micalizzi A, D'Arrigo S, Ginevrino M, Biagini T, Mazza T, Valente EM.

Eur J Hum Genet. 2018 Jul;26(7):928-929. doi: 10.1038/s41431-018-0158-7. Epub 2018 May 25. No abstract available.

28.

The Biological Clock: A Pivotal Hub in Non-alcoholic Fatty Liver Disease Pathogenesis.

Mazzoccoli G, De Cosmo S, Mazza T.

Front Physiol. 2018 Mar 15;9:193. doi: 10.3389/fphys.2018.00193. eCollection 2018. Review.

29.

Association Between MICA Gene Variants and the Risk of Hepatitis C Virus-Induced Hepatocellular Cancer in a Sicilian Population Sample.

Augello G, Balasus D, Fusilli C, Mazza T, Emma MR, Giannitrapani L, Agliastro R, Cervello M, Montalto G.

OMICS. 2018 Apr;22(4):274-282. doi: 10.1089/omi.2017.0215. Epub 2018 Mar 27.

PMID:
29584564
30.

Novel α-Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical-Pathologic Correlation.

Frustaci A, De Luca A, Guida V, Biagini T, Mazza T, Gaudio C, Letizia C, Russo MA, Galea N, Chimenti C.

J Am Heart Assoc. 2018 Feb 10;7(4). pii: e008068. doi: 10.1161/JAHA.117.008068.

31.

MicroRNA co-expression networks exhibit increased complexity in pancreatic ductal compared to Vater's papilla adenocarcinoma.

Mazza T, Copetti M, Capocefalo D, Fusilli C, Biagini T, Carella M, De Bonis A, Mastrodonato N, Piepoli A, Pazienza V, Maiello E, di Mola FF, di Sebastiano P, Andriulli A, Tavano F.

Oncotarget. 2017 Oct 31;8(62):105320-105339. doi: 10.18632/oncotarget.22184. eCollection 2017 Dec 1.

32.

A primary tumor gene expression signature identifies a crucial role played by tumor stroma myofibroblasts in lymph node involvement in oral squamous cell carcinoma.

Mazzoccoli G, Castellana S, Carella M, Palumbo O, Tiberio C, Fusilli C, Capocefalo D, Biagini T, Mazza T, Lo Muzio L.

Oncotarget. 2017 Sep 5;8(62):104913-104927. doi: 10.18632/oncotarget.20645. eCollection 2017 Dec 1.

33.

Insights From Molecular Characterization of Adult Patients of Families With Multigenerational Diabetes.

Pezzilli S, Ludovico O, Biagini T, Mercuri L, Alberico F, Lauricella E, Dallali H, Capocefalo D, Carella M, Miccinilli E, Piscitelli P, Scarale MG, Mazza T, Trischitta V, Prudente S.

Diabetes. 2018 Jan;67(1):137-145. doi: 10.2337/db17-0867. Epub 2017 Oct 9.

34.

Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal Defects.

De Mori R, Romani M, D'Arrigo S, Zaki MS, Lorefice E, Tardivo S, Biagini T, Stanley V, Musaev D, Fluss J, Micalizzi A, Nuovo S, Illi B, Chiapparini L, Di Marcotullio L, Issa MY, Anello D, Casella A, Ginevrino M, Leggins AS, Roosing S, Alfonsi R, Rosati J, Schot R, Mancini GMS, Bertini E, Dobyns WB, Mazza T, Gleeson JG, Valente EM.

Am J Hum Genet. 2017 Oct 5;101(4):552-563. doi: 10.1016/j.ajhg.2017.08.017. Epub 2017 Sep 28.

35.

Observation and Control of Laser-Enabled Auger Decay.

Iablonskyi D, Ueda K, Ishikawa KL, Kheifets AS, Carpeggiani P, Reduzzi M, Ahmadi H, Comby A, Sansone G, Csizmadia T, Kuehn S, Ovcharenko E, Mazza T, Meyer M, Fischer A, Callegari C, Plekan O, Finetti P, Allaria E, Ferrari E, Roussel E, Gauthier D, Giannessi L, Prince KC.

Phys Rev Lett. 2017 Aug 18;119(7):073203. doi: 10.1103/PhysRevLett.119.073203. Epub 2017 Aug 14.

PMID:
28949652
36.

Induction of cancer cell stemness by depletion of macrohistone H2A1 in hepatocellular carcinoma.

Lo Re O, Fusilli C, Rappa F, Van Haele M, Douet J, Pindjakova J, Rocha SW, Pata I, Valčíková B, Uldrijan S, Yeung RS, Peixoto CA, Roskams T, Buschbeck M, Mazza T, Vinciguerra M.

Hepatology. 2018 Feb;67(2):636-650. doi: 10.1002/hep.29519. Epub 2018 Jan 2.

PMID:
28913935
37.

Analysis of MTNR1B gene polymorphisms in relationship with IRS2 gene variants, epicardial fat thickness, glucose homeostasis and cognitive performance in the elderly.

Mazzoccoli G, Dagostino MP, Paroni G, Seripa D, Ciccone F, Addante F, Favuzzi G, Grandone E, Avola R, Mazza T, Fusilli C, Greco A, De Cosmo S.

Chronobiol Int. 2017;34(8):1083-1093. doi: 10.1080/07420528.2017.1340894. Epub 2017 Jul 14.

PMID:
28708046
38.

High-confidence assessment of functional impact of human mitochondrial non-synonymous genome variations by APOGEE.

Castellana S, Fusilli C, Mazzoccoli G, Biagini T, Capocefalo D, Carella M, Vescovi AL, Mazza T.

PLoS Comput Biol. 2017 Jun 22;13(6):e1005628. doi: 10.1371/journal.pcbi.1005628. eCollection 2017 Jun.

39.

Communication: Direct evidence for sequential dissociation of gas-phase Fe(CO)5 via a singlet pathway upon excitation at 266 nm.

Wernet P, Leitner T, Josefsson I, Mazza T, Miedema PS, Schröder H, Beye M, Kunnus K, Schreck S, Radcliffe P, Düsterer S, Meyer M, Odelius M, Föhlisch A.

J Chem Phys. 2017 Jun 7;146(21):211103. doi: 10.1063/1.4984774.

40.

Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cells.

Daniele G, Simonetti G, Fusilli C, Iacobucci I, Lonoce A, Palazzo A, Lomiento M, Mammoli F, Marsano RM, Marasco E, Mantovani V, Quentmeier H, Drexler HG, Ding J, Palumbo O, Carella M, Nadarajah N, Perricone M, Ottaviani E, Baldazzi C, Testoni N, Papayannidis C, Ferrari S, Mazza T, Martinelli G, Storlazzi CT.

Haematologica. 2017 Jul;102(7):1204-1214. doi: 10.3324/haematol.2016.163022. Epub 2017 Apr 14.

41.

Stepwise analysis of MIR9 loci identifies miR-9-5p to be involved in Oestrogen regulated pathways in breast cancer patients.

Barbano R, Pasculli B, Rendina M, Fontana A, Fusilli C, Copetti M, Castellana S, Valori VM, Morritti M, Graziano P, Luigi C, Coco M, Picardo F, Mazza T, Evron E, Murgo R, Maiello E, Esteller M, Fazio VM, Parrella P.

Sci Rep. 2017 Mar 27;7:45283. doi: 10.1038/srep45283.

42.

Molecular dynamics recipes for genome research.

Biagini T, Chillemi G, Mazzoccoli G, Grottesi A, Fusilli C, Capocefalo D, Castellana S, Vescovi AL, Mazza T.

Brief Bioinform. 2018 Sep 28;19(5):853-862. doi: 10.1093/bib/bbx006.

PMID:
28334084
43.

Putative TMPRSS3/GJB2 digenic inheritance of hearing loss detected by targeted resequencing.

Leone MP, Palumbo P, Ortore R, Castellana S, Palumbo O, Melchionda S, Palladino T, Stallone R, Mazza T, Cocchi R, Carella M.

Mol Cell Probes. 2017 Jun;33:24-27. doi: 10.1016/j.mcp.2017.03.001. Epub 2017 Mar 3.

PMID:
28263784
44.

Circular Dichroism in Multiphoton Ionization of Resonantly Excited He^{+} Ions.

Ilchen M, Douguet N, Mazza T, Rafipoor AJ, Callegari C, Finetti P, Plekan O, Prince KC, Demidovich A, Grazioli C, Avaldi L, Bolognesi P, Coreno M, Di Fraia M, Devetta M, Ovcharenko Y, Düsterer S, Ueda K, Bartschat K, Grum-Grzhimailo AN, Bozhevolnov AV, Kazansky AK, Kabachnik NM, Meyer M.

Phys Rev Lett. 2017 Jan 6;118(1):013002. doi: 10.1103/PhysRevLett.118.013002. Epub 2017 Jan 5.

PMID:
28106422
45.

Wnt5a Drives an Invasive Phenotype in Human Glioblastoma Stem-like Cells.

Binda E, Visioli A, Giani F, Trivieri N, Palumbo O, Restelli S, Dezi F, Mazza T, Fusilli C, Legnani F, Carella M, Di Meco F, Duggal R, Vescovi AL.

Cancer Res. 2017 Feb 15;77(4):996-1007. doi: 10.1158/0008-5472.CAN-16-1693. Epub 2016 Dec 23. Erratum in: Cancer Res. 2017 Jul 15;77(14 ):3962.

46.

Inflammatory Bowel Disease Meets Systems Biology: A Multi-Omics Challenge and Frontier.

Palmieri O, Mazza T, Castellana S, Panza A, Latiano T, Corritore G, Andriulli A, Latiano A.

OMICS. 2016 Dec;20(12):692-698.

PMID:
27930092
47.

Chirped pulse amplification in an extreme-ultraviolet free-electron laser.

Gauthier D, Allaria E, Coreno M, Cudin I, Dacasa H, Danailov MB, Demidovich A, Di Mitri S, Diviacco B, Ferrari E, Finetti P, Frassetto F, Garzella D, Künzel S, Leroux V, Mahieu B, Mahne N, Meyer M, Mazza T, Miotti P, Penco G, Raimondi L, Ribič PR, Richter R, Roussel E, Schulz S, Sturari L, Svetina C, Trovò M, Walker PA, Zangrando M, Callegari C, Fajardo M, Poletto L, Zeitoun P, Giannessi L, De Ninno G.

Nat Commun. 2016 Dec 1;7:13688. doi: 10.1038/ncomms13688.

48.

The association of variants in PNPLA3 and GRP78 and the risk of developing hepatocellular carcinoma in an Italian population.

Balasus D, Way M, Fusilli C, Mazza T, Morgan MY, Cervello M, Giannitrapani L, Soresi M, Agliastro R, Vinciguerra M, Montalto G.

Oncotarget. 2016 Dec 27;7(52):86791-86802. doi: 10.18632/oncotarget.13558.

49.

Circular dichroism measurements at an x-ray free-electron laser with polarization control.

Hartmann G, Lindahl AO, Knie A, Hartmann N, Lutman AA, MacArthur JP, Shevchuk I, Buck J, Galler A, Glownia JM, Helml W, Huang Z, Kabachnik NM, Kazansky AK, Liu J, Marinelli A, Mazza T, Nuhn HD, Walter P, Viefhaus J, Meyer M, Moeller S, Coffee RN, Ilchen M.

Rev Sci Instrum. 2016 Aug;87(8):083113. doi: 10.1063/1.4961470.

PMID:
27587106
50.

Identification of p53-target genes in Danio rerio.

Mandriani B, Castellana S, Rinaldi C, Manzoni M, Venuto S, Rodriguez-Aznar E, Galceran J, Nieto MA, Borsani G, Monti E, Mazza T, Merla G, Micale L.

Sci Rep. 2016 Sep 1;6:32474. doi: 10.1038/srep32474.

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