Zobrazeno 1 - 10
of 107
pro vyhledávání: '"C P, Kratz"'
Publikováno v:
Der Pathologe. 40:592-599
Das Li-Fraumeni-Syndrom (LFS; „Online Mendelian Inheritance in Man“, OMIM #151623) gilt als eines der aggressivsten derzeit bekannten Krebspradispositionssyndrome. Das heterogene Tumorspektrum wird dominiert von Knochen- und Weichteilsarkomen, ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa25a7219f2e4e69a606041ce6761353
https://doi.org/10.1007/s00292-019-00657-y
https://doi.org/10.1007/s00292-019-00657-y
Publikováno v:
Der Pathologe. 40(6)
The Li-Fraumeni syndrome (LFS, online Mendelian inheritance in man, OMIM #151623) is considered to be one of the currently known most aggressive cancer predisposition syndromes. The heterogeneous spectrum of tumors is dominated by bone and soft tissu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2091afdbeb80a002f8bf8786dd6c41bc
https://pubmed.ncbi.nlm.nih.gov/31511974
https://pubmed.ncbi.nlm.nih.gov/31511974
Publikováno v:
WHO/IARC Classification of Tumours; 2021, Vol. 6, p429-433, 5p
Autor:
Huang, Guanyu1,2 (AUTHOR), Zhang, Jiajun1,2 (AUTHOR), Xu, Yu1,2 (AUTHOR), Wu, Fei1,2 (AUTHOR), Fu, Yiwei1,2 (AUTHOR), Zhang, Xuelin1,2 (AUTHOR), Yin, Hanxiao1,2 (AUTHOR), You, Yuanyuan3 (AUTHOR), Zhao, Peng3 (AUTHOR), Liu, Weihai1,2 (AUTHOR) liuwh25@mail.sysu.edu.cn, Shen, Jingnan1,2 (AUTHOR) shenjn@mail.sysu.edu.cn, Yin, Junqiang1,2 (AUTHOR) yinjunq@mail.sysu.edu.cn
Publikováno v:
Advanced Science. 11/20/2024, Vol. 11 Issue 43, p1-15. 15p.
Autor:
Dokhanchi, Maryam1 (AUTHOR), Javaherdehi, Atefe Panahipoor2 (AUTHOR), Raad, Mohammad3 (AUTHOR), Khalilollah, Shayan4 (AUTHOR), Mahdavi, Pooya5 (AUTHOR), Razizadeh, Mohammad Hossein6,7 (AUTHOR) Razizadeh.mh@gmail.com, Zafarani, Alireza8,9 (AUTHOR)
Publikováno v:
Immunity, Inflammation & Disease. Nov2024, Vol. 12 Issue 11, p1-18. 18p.
Autor:
D. A., Solomon, C. P., Kratz
Publikováno v:
WHO/IARC Classification of Tumours; 2021, Vol. 6, p478-480, 3p
Publikováno v:
WHO/IARC Classification of Tumours; 2021, Vol. 6, p446-448, 3p
Autor:
Gao, Xiaoyue1,2 (AUTHOR), Zhuang, Qiyuan3,4 (AUTHOR), Li, Yun1,2 (AUTHOR), Li, Guochao1,2 (AUTHOR), Huang, Zheng1,2 (AUTHOR), Chen, Shenzhi1,5 (AUTHOR), Sun, Shaoxing1,2 (AUTHOR), Yang, Hui3,4,6 (AUTHOR) hui_yang@fudan.edu.cn, Jiang, Lan1,2,5,7 (AUTHOR) jiangl@big.ac.cn, Mao, Ying3,4 (AUTHOR) maoying@fudan.edu.cn
Publikováno v:
Advanced Science. 8/14/2024, Vol. 11 Issue 30, p1-17. 17p.
Publikováno v:
International journal of andrology. 34(4 Pt 2)
Three genome-wide association studies of testicular cancer have uncovered predisposition alleles in or near KITLG, BAK1, SPRY4, TERT, ATF7IP and DMRT1. We investigated whether testicular cancer-risk alleles can be utilized in the clinical setting. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3de4abfe78d05d75ac10e4a55987550c
https://pubmed.ncbi.nlm.nih.gov/21564132
https://pubmed.ncbi.nlm.nih.gov/21564132
Autor:
Dominik Schneider, Peter Vorwerk, C. P. Kratz, Norbert Graf, R. E. Schultze-Florey, E. Koscielniak
Publikováno v:
Klinische Pädiatrie. 225:177-178
Recently, germline mutations of DICER1 have been identified in patients with rare neoplasms suggesting the existence of a newly discovered cancer prone syndrome. Initially, DICER1 mutations were identified in patients with familial pleuropulmonary bl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07cc6a472b00122610c1f6789536202b
https://doi.org/10.1055/s-0033-1337976
https://doi.org/10.1055/s-0033-1337976