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Search life-sciences literature (45,103,589 articles, preprints and more)

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Current insights and future directions of Li-Fraumeni syndrome.
Hosseini MS
Discov Oncol, 15(1):561, 15 Oct 2024
Cited by: 0 articles | PMID: 39404911 | PMCID: PMC11480288
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Osteosarcoma patient with Li-Fraumeni syndrome: the first case report in Vietnam.
Le TT, Ha TS, To LM, Dang QM, Bui HTP, Tran TD, Vu PT, Giang HB, Tran DT, Nguyen XH
Front Oncol, 14:1458232, 08 Oct 2024
Cited by: 0 articles | PMID: 39439949 | PMCID: PMC11493536
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Cancer Risk Factors in Southern Brazil: Report of a Comprehensive, Matched Case-Control Study.
Giacomazzi J, Ziegelmann PK, da Costa S, Bittar CM, Obst FM, Rosset C, Macedo GS, Bock H, Canal T, Paese MI, Benvenuti JL, Buj MC, Ashton-Prolla P, Goldim JR, Pozza R
JCO Glob Oncol, 9:e2300006, 01 Sep 2023
Cited by: 0 articles | PMID: 38060977 | PMCID: PMC10723862
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Retrospective Analysis of Prognostic Factors in Pediatric Patients with Adrenocortical Tumor from Unique Tertiary Center with Long-Term Follow-Up.
Bachega FS, Suartz CV, Almeida MQ, Brondani VB, Charchar HLS, Lacombe AMF, Martins-Filho SN, Soares IC, Zerbini MCN, Dénes FT, Mendonca B, Lopes RI, Latronico AC, Fragoso MCBV
J Clin Med, 11(22):6641, 09 Nov 2022
Cited by: 0 articles | PMID: 36431124 | PMCID: PMC9692695
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Choroid Plexus Carcinomas With TP53 Germline Mutations: Management and Outcome.
Li Y, Liu H, Li T, Feng J, He Y, Chen L, Li C, Qiu X
Front Oncol, 11:751784, 30 Sep 2021
Cited by: 8 articles | PMID: 34660315 | PMCID: PMC8514937
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Prevalence of the Brazilian TP53 Founder c.1010G>A (p.Arg337His) in Lung Adenocarcinoma: Is Genotyping Warranted in All Brazilian Patients?
Vieira IA, Andreis TF, Fernandes BV, Achatz MI, Macedo GS, Schramek D, Ashton-Prolla P
Front Genet, 12:606537, 02 Feb 2021
Cited by: 3 articles | PMID: 33603772 | PMCID: PMC7885268
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What 20 years of research has taught us about the TP53 p.R337H mutation.
Pinto EM, Zambetti GP
Cancer, 126(21):4678-4686, 17 Aug 2020
Cited by: 26 articles | PMID: 32875577 | PMCID: PMC7589304
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Active DNA demethylation-The epigenetic gatekeeper of development, immunity, and cancer.
Prasad R, Yen TJ, Bellacosa A
Adv Genet (Hoboken), 2(1):e10033, 27 Nov 2020
Cited by: 8 articles | PMID: 36618446 | PMCID: PMC9744510
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TP53 p.Arg337His geographic distribution correlates with adrenocortical tumor occurrence.
Seidinger AL, Caminha IP, Mastellaro MJ, Gabetta CS, Nowill AE, Pinheiro VRP, Yunes JA
Mol Genet Genomic Med, 8(9):e1168, 27 Jun 2020
Cited by: 7 articles | PMID: 32592449 | PMCID: PMC7503091
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Germline genetic landscape of pediatric central nervous system tumors.
Muskens IS, Zhang C, de Smith AJ, Biegel JA, Walsh KM, Wiemels JL
Neuro Oncol, 21(11):1376-1388, 01 Nov 2019
Cited by: 17 articles | PMID: 31247102 | PMCID: PMC6827836
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p53 signaling pathway polymorphisms, cancer risk and tumor phenotype in TP53 R337H mutation carriers.
Macedo GS, Vieira IA, Vianna FSL, Alemar B, Giacomazzi J, Brandalize APC, Caleffi M, Volc SM, de Campos Reis Galvão H, Palmero EI, Achatz MI, Ashton-Prolla P
Fam Cancer, 17(2):269-274, 01 Apr 2018
Cited by: 7 articles | PMID: 28756477
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Detailed genomic characterization identifies high heterogeneity and histotype-specific genomic profiles in adrenocortical carcinomas.
Vatrano S, Volante M, Duregon E, Giorcelli J, Izzo S, Rapa I, Votta A, Germano A, Scagliotti G, Berruti A, Terzolo M, Papotti AM
Mod Pathol, 31(8):1257-1269, 26 Mar 2018
Cited by: 14 articles | PMID: 29581542
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Androgen production in pediatric adrenocortical tumors may occur via both the classic and/or the alternative backdoor pathway.
Marti N, Malikova J, Galván JA, Aebischer M, Janner M, Sumnik Z, Obermannova B, Escher G, Perren A, Flück CE
Mol Cell Endocrinol, 452:64-73, 10 May 2017
Cited by: 3 articles | PMID: 28501574
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Spectrum of germline mutations in smokers and non-smokers in Brazilian non-small-cell lung cancer (NSCLC) patients.
Couto PP, Bastos-Rodrigues L, Schayek H, Melo FM, Lisboa RGC, Miranda DM, Vilhena A, Bale AE, Friedman E, De Marco L
Carcinogenesis, 38(11):1112-1118, 01 Oct 2017
Cited by: 15 articles | PMID: 28968711
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Full-length mutation search of the TP53 gene in acute myeloid leukemia has increased significance as a prognostic factor.
Terada K, Yamaguchi H, Ueki T, Usuki K, Kobayashi Y, Tajika K, Gomi S, Kurosawa S, Miyadera K, Tokura T, Omori I, Marumo A, Fujiwara Y, Yui S, Ryotokuji T, Osaki Y, Arai K, Kitano T, Kosaka F, [...] Inokuchi K
Ann Hematol, 97(1):51-61, 04 Oct 2017
Cited by: 6 articles | PMID: 28980058
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Characterization of potential driver mutations involved in human breast cancer by computational approaches.
Rajendran BK, Deng CX
Oncotarget, 8(30):50252-50272, 01 Jul 2017
Cited by: 37 articles | PMID: 28477017 | PMCID: PMC5564847
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Recommended Guidelines for Validation, Quality Control, and Reporting of TP53 Variants in Clinical Practice.
Leroy B, Ballinger ML, Baran-Marszak F, Bond GL, Braithwaite A, Concin N, Donehower LA, El-Deiry WS, Fenaux P, Gaidano G, Langerød A, Hellstrom-Lindberg E, Iggo R, Lehmann-Che J, Mai PL, Malkin D, Moll UM, Myers JN, Nichols KE, [...] Soussi T
Cancer Res, 77(6):1250-1260, 01 Mar 2017
Cited by: 48 articles | PMID: 28254861 | PMCID: PMC7457206
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Pediatric adrenal cortical carcinomas: Histopathological criteria and clinical trials. A systematic review.
Xu X, Sergi C
Contemp Clin Trials, 50:37-44, 14 Jul 2016
Cited by: 6 articles | PMID: 27424218
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Li-Fraumeni syndrome: a paradigm for the understanding of hereditary cancer predisposition.
Valdez JM, Nichols KE, Kesserwan C
Br J Haematol, 176(4):539-552, 16 Dec 2016
Cited by: 43 articles | PMID: 27984644
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Time to incorporate germline multigene panel testing into breast and ovarian cancer patient care.
Graffeo R, Livraghi L, Pagani O, Goldhirsch A, Partridge AH, Garber JE
Breast Cancer Res Treat, 160(3):393-410, 12 Oct 2016
Cited by: 32 articles | PMID: 27734215
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Brain tumors in Li-Fraumeni syndrome: a commentary and a case of a gliosarcoma patient.
Guidi M, Giunti L, Lucchesi M, Scoccianti S, Giglio S, Favre C, Oliveri G, Sardi I
Future Oncol, 13(1):9-12, 15 Aug 2016
Cited by: 1 article | PMID: 27523101
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Ancestry of the Brazilian TP53 c.1010G>A (p.Arg337His, R337H) Founder Mutation: Clues from Haplotyping of Short Tandem Repeats on Chromosome 17p.
Paskulin DD, Giacomazzi J, Achatz MI, Costa S, Reis RM, Hainaut P, dos Santos SE, Ashton-Prolla P
PLoS One, 10(11):e0143262, 30 Nov 2015
Cited by: 8 articles | PMID: 26618902 | PMCID: PMC4664269
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Self-reported cancer family history is a useful tool for identification of individuals at risk of hereditary cancer predisposition syndrome at primary care centers in middle-income settings: a longitudinal study.
Flória-Santos M, Lopes-Júnior LC, Alvarenga Lde M, Ribeiro MS, Ferraz VE, Nascimento LC, Pereira-da-Silva G
Genet Mol Biol, 39(2):178-183, 01 Jun 2016
Cited by: 13 articles | PMID: 27275666 | PMCID: PMC4910551
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Surveillance recommendations for patients with germline TP53 mutations.
Ballinger ML, Mitchell G, Thomas DM
Curr Opin Oncol, 27(4):332-337, 01 Jul 2015
Cited by: 23 articles | PMID: 26049273
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Genotype Versus Phenotype: The Yin and Yang of Germline TP53 Mutations in Li-Fraumeni Syndrome.
Nichols KE, Malkin D
J Clin Oncol, 33(21):2331-2333, 22 Jun 2015
Cited by: 15 articles | PMID: 26101242
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1-25 of 29 results

1 2

Search life-sciences literature (45,103,589 articles, preprints and more)

Search results

Current insights and future directions of Li-Fraumeni syndrome.

Osteosarcoma patient with Li-Fraumeni syndrome: the first case report in Vietnam.

Cancer Risk Factors in Southern Brazil: Report of a Comprehensive, Matched Case-Control Study.

Retrospective Analysis of Prognostic Factors in Pediatric Patients with Adrenocortical Tumor from Unique Tertiary Center with Long-Term Follow-Up.

Choroid Plexus Carcinomas With TP53 Germline Mutations: Management and Outcome.

Prevalence of the Brazilian TP53 Founder c.1010G>A (p.Arg337His) in Lung Adenocarcinoma: Is Genotyping Warranted in All Brazilian Patients?

What 20 years of research has taught us about the TP53 p.R337H mutation.

Active DNA demethylation-The epigenetic gatekeeper of development, immunity, and cancer.

TP53 p.Arg337His geographic distribution correlates with adrenocortical tumor occurrence.

Germline genetic landscape of pediatric central nervous system tumors.

p53 signaling pathway polymorphisms, cancer risk and tumor phenotype in TP53 R337H mutation carriers.

Detailed genomic characterization identifies high heterogeneity and histotype-specific genomic profiles in adrenocortical carcinomas.

Androgen production in pediatric adrenocortical tumors may occur via both the classic and/or the alternative backdoor pathway.

Spectrum of germline mutations in smokers and non-smokers in Brazilian non-small-cell lung cancer (NSCLC) patients.

Full-length mutation search of the TP53 gene in acute myeloid leukemia has increased significance as a prognostic factor.

Characterization of potential driver mutations involved in human breast cancer by computational approaches.

Recommended Guidelines for Validation, Quality Control, and Reporting of TP53 Variants in Clinical Practice.

Pediatric adrenal cortical carcinomas: Histopathological criteria and clinical trials. A systematic review.

Li-Fraumeni syndrome: a paradigm for the understanding of hereditary cancer predisposition.

Time to incorporate germline multigene panel testing into breast and ovarian cancer patient care.

Brain tumors in Li-Fraumeni syndrome: a commentary and a case of a gliosarcoma patient.

Ancestry of the Brazilian TP53 c.1010G>A (p.Arg337His, R337H) Founder Mutation: Clues from Haplotyping of Short Tandem Repeats on Chromosome 17p.

Self-reported cancer family history is a useful tool for identification of individuals at risk of hereditary cancer predisposition syndrome at primary care centers in middle-income settings: a longitudinal study.

Surveillance recommendations for patients with germline TP53 mutations.

Genotype Versus Phenotype: The Yin and Yang of Germline TP53 Mutations in Li-Fraumeni Syndrome.

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