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1
Frequency of Thyroid Carcinoma in Brazilian TP53 p.R337H Carriers With Li Fraumeni Syndrome.
JAMA Oncol. 2017 Oct 1;3(10):1400-1402. doi: 10.1001/jamaoncol.2016.6389.
2
Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation.
J Steroid Biochem Mol Biol. 2019 Jun;190:250-255. doi: 10.1016/j.jsbmb.2019.04.011. Epub 2019 Apr 8.
3
Li-Fraumeni and Li-Fraumeni-like syndrome among children diagnosed with pediatric cancer in Southern Brazil.
Cancer. 2013 Dec 15;119(24):4341-9. doi: 10.1002/cncr.28346. Epub 2013 Oct 7.
4
The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families.
Cancer Lett. 2007 Jan 8;245(1-2):96-102. doi: 10.1016/j.canlet.2005.12.039. Epub 2006 Feb 21.
7
Clinical and molecular characterization of patients fulfilling Chompret criteria for Li-Fraumeni syndrome in Southern Brazil.
PLoS One. 2021 Sep 16;16(9):e0251639. doi: 10.1371/journal.pone.0251639. eCollection 2021.
9
Breast Cancer Phenotype Associated With Li-Fraumeni Syndrome: A Brazilian Cohort Enriched by p.R337H Carriers.
Front Oncol. 2022 Mar 16;12:836937. doi: 10.3389/fonc.2022.836937. eCollection 2022.
10
The Brazilian founder mutation TP53 p.R337H is uncommon in Portuguese women diagnosed with breast cancer.
Breast J. 2014 Sep-Oct;20(5):534-6. doi: 10.1111/tbj.12308. Epub 2014 Jul 23.

引用本文的文献

1
Allele frequency in thyroid cancer: mechanisms, challenges, and applications in cancer therapy.
Thyroid Res. 2025 May 6;18(1):19. doi: 10.1186/s13044-025-00237-8.
2
Personalized screening strategies for R337H carriers: a retrospective cohort study of tumor spectrum in Li-Fraumeni syndrome adult carriers.
Lancet Reg Health Am. 2025 Jan 18;42:100982. doi: 10.1016/j.lana.2024.100982. eCollection 2025 Feb.
3
Papillary Thyroid Carcinoma, Cushing Disease, and Adrenocortical Carcinoma in a Patient with Li-Fraumeni Syndrome.
AACE Clin Case Rep. 2024 Mar 28;10(4):127-131. doi: 10.1016/j.aace.2024.03.007. eCollection 2024 Jul-Aug.
4
Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way Street.
Biomedicines. 2023 Jul 29;11(8):2143. doi: 10.3390/biomedicines11082143.
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Genetic susceptibility to hereditary non-medullary thyroid cancer.
Hered Cancer Clin Pract. 2022 Mar 7;20(1):9. doi: 10.1186/s13053-022-00215-3.
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The Enigmatic Role of TP53 in Germ Cell Tumours: Are We Missing Something?
Int J Mol Sci. 2021 Jul 2;22(13):7160. doi: 10.3390/ijms22137160.
9
Genetic Mutations and Variants in the Susceptibility of Familial Non-Medullary Thyroid Cancer.
Genes (Basel). 2020 Nov 18;11(11):1364. doi: 10.3390/genes11111364.
10

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Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
J Clin Oncol. 2015 Jul 20;33(21):2345-52. doi: 10.1200/JCO.2014.59.5728. Epub 2015 May 26.
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Germline TP53 mutations and the changing landscape of Li-Fraumeni syndrome.
Hum Mutat. 2014 Jun;35(6):654-62. doi: 10.1002/humu.22559.
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Li-fraumeni syndrome.
Genes Cancer. 2011 Apr;2(4):475-84. doi: 10.1177/1947601911413466.
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The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families.
Cancer Lett. 2007 Jan 8;245(1-2):96-102. doi: 10.1016/j.canlet.2005.12.039. Epub 2006 Feb 21.
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The concise handbook of family cancer syndromes. Mayo Familial Cancer Program.
J Natl Cancer Inst. 1998 Jul 15;90(14):1039-71. doi: 10.1093/jnci/90.14.1039.
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Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms.
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