Cancer Prevention Research最新文献

筛选
英文 中文
Evaluating the Reach of a Patient Navigation Program for Follow-up Colonoscopy in a Large Federally Qualified Health Center 评估大型联邦合格医疗中心结肠镜检查随访患者导航计划的覆盖范围
IF 3.3 3区 医学
Cancer Prevention Research Pub Date : 2024-04-20 DOI: 10.1158/1940-6207.capr-23-0498
Priyanka Gautom, A. Gabriela Rosales, Amanda F. Petrik, Jamie H. Thompson, Matthew T. Slaughter, Leslie Mosso, Syed Akmal. Hussain, Ricardo Jimenez, Gloria D. Coronado
{"title":"Evaluating the Reach of a Patient Navigation Program for Follow-up Colonoscopy in a Large Federally Qualified Health Center","authors":"Priyanka Gautom, A. Gabriela Rosales, Amanda F. Petrik, Jamie H. Thompson, Matthew T. Slaughter, Leslie Mosso, Syed Akmal. Hussain, Ricardo Jimenez, Gloria D. Coronado","doi":"10.1158/1940-6207.capr-23-0498","DOIUrl":"https://doi.org/10.1158/1940-6207.capr-23-0498","url":null,"abstract":"Patient navigation (PN) has been shown to improve participation in cancer screening, including colorectal cancer screening, and the Community Preventive Services Task Force now recommends the practice. Despite the effectiveness of PN programs, little is known about the number of contacts needed to successfully reach patients or about the demographic and healthcare utilization factors associated with reach. PRECISE was an individual randomized study of PN vs. usual care conducted as a partnership between two large health systems in the Pacific Northwest. The navigation program was a six topic-area telephonic program designed to support patients with an abnormal fecal test result to obtain a follow-up colonoscopy. We report the number of contact attempts needed to successfully reach navigated patients. We used logistic regression to report the demographic and healthcare utilization characteristics associated with patients allocated to PN who were successfully reached. We identified 1200 patients with an abnormal FIT result, among whom 970 were randomized into the study (45.7% were female, 17.5% were Spanish-speaking, mean age was 60.8). Of the 479 patients allocated to the PN intervention, 382 (79.7%) were reached within 18 call attempts and nearly all (n = 356; 93.2%) were reached within six contact attempts. Patient characteristics associated with reach were race, county of residence, and body mass index. Our findings can guide future efforts to optimize the reach of PN programs.","PeriodicalId":9373,"journal":{"name":"Cancer Prevention Research","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2024-04-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140629062","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Germline and Somatic Fumarate Hydratase Testing in Atypical Uterine Leiomyomata 非典型子宫纵隔肌瘤的种系和体细胞富马酸氢化酶检测
IF 3.3 3区 医学
Cancer Prevention Research Pub Date : 2024-04-18 DOI: 10.1158/1940-6207.capr-23-0535
Lindsay M. Kipnis, Katelyn M. Breen, Diane R. Koeller, Alison Schwartz Levine, Zelei Yang, Hyeji Jun, Nabihah Tayob, Samantha M. Stokes, Connor P. Hayes, Arezou A. Ghazani, Sarah J. Hill, Huma Q. Rana
{"title":"Germline and Somatic Fumarate Hydratase Testing in Atypical Uterine Leiomyomata","authors":"Lindsay M. Kipnis, Katelyn M. Breen, Diane R. Koeller, Alison Schwartz Levine, Zelei Yang, Hyeji Jun, Nabihah Tayob, Samantha M. Stokes, Connor P. Hayes, Arezou A. Ghazani, Sarah J. Hill, Huma Q. Rana","doi":"10.1158/1940-6207.capr-23-0535","DOIUrl":"https://doi.org/10.1158/1940-6207.capr-23-0535","url":null,"abstract":"Women with germline pathogenic variants (PV) in the fumarate hydratase (FH) gene develop cutaneous and uterine leiomyomata and have an increased risk of developing aggressive renal cell carcinomas. Many of these women are unaware of their cancer predisposition until an atypical uterine leiomyoma is diagnosed during a myomectomy or hysterectomy, making a streamlined genetic counseling process after a pathology-based atypical uterine leiomyoma diagnosis critical. However, the prevalence of germline pathogenic/likely PVs in FH among atypical uterine leiomyomata cases is unknown. To better understand FH germline PV prevalence and current patterns of genetic counseling and germline genetic testing, we undertook a retrospective review of atypical uterine leiomyomata cases at a single large center. We compared clinical characteristics between the FH PV, FH wild-type (WT), and unknown genetic testing cohorts. Of the 144 cases with atypical uterine leiomyomata with evaluable clinical data, only 49 (34%) had documented genetic test results, and 12 (8.3%) had a germline FH PV. There were 48 IHC-defined FH-deficient cases, of which 41 (85%) had FH testing and nine had a germline FH PV, representing 22% of the tested cohort and 18.8% of the FH-deficient cohort. Germline FH PVs were present in 8.3% of evaluable patients, representing 24.5% of the cohort that completed genetic testing. These data highlight the disconnect between pathology and genetic counseling, and help to refine risk estimates that can be used when counseling patients with atypical uterine leiomyomata. Prevention Relevance: Women diagnosed with fumarate hydratase (FH)-deficient uterine leiomyomata are at increased risk of renal cancer. This work suggests a more standardized pathology-genetic counseling referral pathway for these patients, and that research on underlying causes of FH-deficient uterine leiomyomata in the absence of germline FH pathogenic/likely pathogenic variants is needed.","PeriodicalId":9373,"journal":{"name":"Cancer Prevention Research","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2024-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140629069","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
High-Fat Diet Induced PPARδ Promotes Self-renewal of Preleukemic Progenitors in Development of Acute Promyelocytic Leukemia 高脂饮食诱导的 PPARδ 在急性早幼粒细胞白血病的发展过程中促进白血病前祖细胞的自我更新
IF 3.3 3区 医学
Cancer Prevention Research Pub Date : 2024-02-02 DOI: 10.1158/1940-6207.capr-23-0469
Hiroshi Y. Yamada, Chinthalapally V. Rao
{"title":"High-Fat Diet Induced PPARδ Promotes Self-renewal of Preleukemic Progenitors in Development of Acute Promyelocytic Leukemia","authors":"Hiroshi Y. Yamada, Chinthalapally V. Rao","doi":"10.1158/1940-6207.capr-23-0469","DOIUrl":"https://doi.org/10.1158/1940-6207.capr-23-0469","url":null,"abstract":"From risk association between acute promyelocytic leukemia (APL) and obese-overweight individuals, Mazzarella and colleagues hypothesized that a high-fat diet (HFD) promotes development of APL. Using mouse APL model (PML-RARα knock-in), the authors demonstrated that linoleic acid drives activation of PPARδ in hematopoietic progenitors, and that activation of PPARδ increases proliferation of progenitor cells with PML-RARA expression toward APL. Involvements of PPARδ on regulation of stem cell renewal and proliferation were shown in colorectal cancers earlier, but this study newly demonstrates in hematopoietic progenitors, while suggesting use of diet rich in linoleic acid with caution. See related article by Mazzarella et al., p. 59","PeriodicalId":9373,"journal":{"name":"Cancer Prevention Research","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2024-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139665717","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editors' Selections from Relevant Scientific Publications 编辑从相关科学出版物中选取的内容
IF 3.3 3区 医学
Cancer Prevention Research Pub Date : 2024-02-02 DOI: 10.1158/1940-6207.capr-17-2-hfl
{"title":"Editors' Selections from Relevant Scientific Publications","authors":"","doi":"10.1158/1940-6207.capr-17-2-hfl","DOIUrl":"https://doi.org/10.1158/1940-6207.capr-17-2-hfl","url":null,"abstract":"","PeriodicalId":9373,"journal":{"name":"Cancer Prevention Research","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2024-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139808891","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editors' Selections from Relevant Scientific Publications 编辑从相关科学出版物中选取的内容
IF 3.3 3区 医学
Cancer Prevention Research Pub Date : 2024-02-02 DOI: 10.1158/1940-6207.capr-17-2-hfl
{"title":"Editors' Selections from Relevant Scientific Publications","authors":"","doi":"10.1158/1940-6207.capr-17-2-hfl","DOIUrl":"https://doi.org/10.1158/1940-6207.capr-17-2-hfl","url":null,"abstract":"","PeriodicalId":9373,"journal":{"name":"Cancer Prevention Research","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2024-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139868787","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editors' Selections from Relevant Scientific Publications 编辑对相关科学出版物的选择
3区 医学
Cancer Prevention Research Pub Date : 2023-10-02 DOI: 10.1158/1940-6207.capr-16-10-hfl
{"title":"Editors' Selections from Relevant Scientific Publications","authors":"","doi":"10.1158/1940-6207.capr-16-10-hfl","DOIUrl":"https://doi.org/10.1158/1940-6207.capr-16-10-hfl","url":null,"abstract":"Highlights from the Literature| October 02 2023 Editors' Selections from Relevant Scientific Publications Author & Article Information Online ISSN: 1940-6215 Print ISSN: 1940-6207 ©2023 American Association for Cancer Research2023American Association for Cancer Research Cancer Prev Res (Phila) (2023) 16 (10): 539. https://doi.org/10.1158/1940-6207.CAPR-16-10-HFL Views Icon Views Article contents Figures & tables Video Audio Supplementary Data Peer Review Share Icon Share Facebook Twitter LinkedIn Email Tools Icon Tools Get Permissions Cite Icon Cite Search Site Article Versions Icon Versions Version of Record October 2 2023 Citation Editors' Selections from Relevant Scientific Publications. Cancer Prev Res (Phila) 1 October 2023; 16 (10): 539. https://doi.org/10.1158/1940-6207.CAPR-16-10-HFL Download citation file: Ris (Zotero) Reference Manager EasyBib Bookends Mendeley Papers EndNote RefWorks BibTex toolbar search Search Dropdown Menu toolbar search search input Search input auto suggest Search Advanced Search Breast cancer cells (by Annie Cavanagh via Flickr) Using phylogenetic of microdissected samples of cancer and non-cancer proliferative lesions, Nishimura et al. explored the genetic evolution of breast cancer, revealing a unique evolutionary pattern harboring der(1;16), a common driver alteration in 20% of all breast cancers and one-third of Luminal A breast cancers. In der(1;16)(+) cancers, the derivative chromosome was acquired from early puberty to late adolescence, followed by the emergence of a common ancestor by the patient's early 30s, leading to both cancerous and non-cancerous clones. These clones expanded significantly within the premenopausal breast before cancer diagnosis. Interestingly, multiple cancer clones originated from noncancer ancestors and there was no correlation between histology and the number of driver events, suggesting the involvement of epigenetic or microenvironmental factors in cancer development. These findings contribute to a better understanding of breast carcinogenesis and may improve early detection and prevention strategies. Nishimura... You do not currently have access to this content.","PeriodicalId":9373,"journal":{"name":"Cancer Prevention Research","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135833465","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editors' Selections from Relevant Scientific Publications 编辑对相关科学出版物的选择
3区 医学
Cancer Prevention Research Pub Date : 2023-08-01 DOI: 10.1158/1940-6207.capr-16-8-hfl
{"title":"Editors' Selections from Relevant Scientific Publications","authors":"","doi":"10.1158/1940-6207.capr-16-8-hfl","DOIUrl":"https://doi.org/10.1158/1940-6207.capr-16-8-hfl","url":null,"abstract":"Highlights from the Literature| August 01 2023 Editors' Selections from Relevant Scientific Publications Author & Article Information Online ISSN: 1940-6215 Print ISSN: 1940-6207 ©2023 American Association for Cancer Research2023American Association for Cancer Research Cancer Prev Res (Phila) (2023) 16 (8): 419. https://doi.org/10.1158/1940-6207.CAPR-16-8-HFL Views Icon Views Article contents Figures & tables Video Audio Supplementary Data Peer Review Share Icon Share Facebook Twitter LinkedIn Email Tools Icon Tools Get Permissions Cite Icon Cite Search Site Article Versions Icon Versions Version of Record August 1 2023 Citation Editors' Selections from Relevant Scientific Publications. Cancer Prev Res (Phila) 1 August 2023; 16 (8): 419. https://doi.org/10.1158/1940-6207.CAPR-16-8-HFL Download citation file: Ris (Zotero) Reference Manager EasyBib Bookends Mendeley Papers EndNote RefWorks BibTex toolbar search Search Dropdown Menu toolbar search search input Search input auto suggest Search Advanced Search Polygenic risk scores for screening (from Centers for Disease Control and Prevention) Using UK metrics, Huntley et al. conducted a modeling analysis on the performance of polygenic risk score (PRS) tools and PRS-stratified cancer screening. They estimated the potential annual numbers of cancer cases detected and deaths averted for eight different cancers. The results suggested that, under favorable assumptions, hypothetical PRS-stratified screening programs could modestly improve efficiency for three cancer types. Specifically, they could reduce maximum number of annual deaths from 102 to 80 for breast cancer, 188 to 155 for prostate cancer, and 158 to 95 for colorectal cancer. However, UK-specific cluster-randomized trials are required to evaluate the real-world clinical impact, costs, and potential harm of PRS stratification. Huntley C, … Turnbull C. Lancet Oncol. 2023 Jun;24(6): 658-668. Illustration of deep learning (by OpenClipart via FreeSVG) Pancreatic cancer is often diagnosed too late to achieve good clinical outcomes,... You do not currently have access to this content.","PeriodicalId":9373,"journal":{"name":"Cancer Prevention Research","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135970943","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editors' Selections from Relevant Scientific Publications 编辑对相关科学出版物的选择
3区 医学
Cancer Prevention Research Pub Date : 2023-06-01 DOI: 10.1158/1940-6207.capr-16-6-hfl
{"title":"Editors' Selections from Relevant Scientific Publications","authors":"","doi":"10.1158/1940-6207.capr-16-6-hfl","DOIUrl":"https://doi.org/10.1158/1940-6207.capr-16-6-hfl","url":null,"abstract":"Highlights from the Literature| June 01 2023 Editors' Selections from Relevant Scientific Publications Author & Article Information Online ISSN: 1940-6215 Print ISSN: 1940-6207 ©2023 American Association for Cancer Research2023American Association for Cancer Research Cancer Prev Res (Phila) (2023) 16 (6): 303. https://doi.org/10.1158/1940-6207.CAPR-16-6-HFL Views Icon Views Article contents Figures & tables Video Audio Supplementary Data Peer Review Share Icon Share Facebook Twitter LinkedIn Email Tools Icon Tools Get Permissions Cite Icon Cite Search Site Article Versions Icon Versions Version of Record June 1 2023 Citation Editors' Selections from Relevant Scientific Publications. Cancer Prev Res (Phila) 1 June 2023; 16 (6): 303. https://doi.org/10.1158/1940-6207.CAPR-16-6-HFL Download citation file: Ris (Zotero) Reference Manager EasyBib Bookends Mendeley Papers EndNote RefWorks BibTex toolbar search Search Dropdown Menu toolbar search search input Search input auto suggest Search Advanced Search Obese adipose tissue in the mammary gland (by Arendt et al. via Cancer Research Bhardwaj et al. investigated whether high body mass index (BMI) increases breast cancer risks for women carrying BRCA 1 or BRCA2 mutations. They examined noncancerous breast tissue from 69 such women and found that BMI and biomarkers of metabolic dysfunction were positively correlated with DNA damage in epithelia. RNA sequencing data revealed that obesity altered breast adipose microenvironment and activated estrogen biosynthesis. Blocking signaling pathways mediated by either estrogen or obesity-associated factors leptin or insulin, reduced DNA damage. Additionally, a high-fat diet increased DNA damage and mammary tumors in Brca1+/−mice. These results provide mechanistic insight linking obesity and breast cancer in BRCA mutation carriers, and suggest that reducing risk may involve maintaining a lower body weight, addressing metabolic problems and targeting estrogen. Bhardwaj P, … Brown KA. Sci Transl Med. 2023 Feb 22;15(684):eade1857.... You do not currently have access to this content.","PeriodicalId":9373,"journal":{"name":"Cancer Prevention Research","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135727769","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acknowledgment to Reviewers 对审稿人的感谢
3区 医学
Cancer Prevention Research Pub Date : 2023-01-04 DOI: 10.1158/1940-6207.capr-16-1-ar
{"title":"Acknowledgment to Reviewers","authors":"","doi":"10.1158/1940-6207.capr-16-1-ar","DOIUrl":"https://doi.org/10.1158/1940-6207.capr-16-1-ar","url":null,"abstract":"The Cancer Prevention Research editors wish to acknowledge with sincere appreciation the assistance of the following reviewers who have generously contributed their time and effort during the past year1 in the appraisal of manuscripts. These reviewers have been enormously helpful in assessing the merit of original articles: their careful analysis and critique and their constructive recommendations have greatly enhanced the value of manuscripts they have handled. The quality of the journal can be attributed in large measure to the quality of their effort. We are sincerely grateful.Abdelwadoud, M.Agarwal, R.Alexeeff, S.Allanson, E.Alshalalfa, M.Amos, C.Anderson, K.Arayici, M.Arendt, L.Arthur, R.Aslam, M.Ballester, V.Bansal, A.Barry, K.Beane, J.Behrens, G.Benedetti, I.Benjaminsen Borch, K.Beretta, L.Bergan, R.Boland, R.Bosland, M.Bossuyt, P.Bouras, E.Bowers, L.Bresalier, R.Brooks, J.Brown, K.Brown, R.Burris, J.Butsch Kovacic, M.Butt, J.Carchman, E.Carlo, M.Chan, A.Chan, C.Chang, G.Charvat, H.Chen, H.Chen, J.Chen, M.Chen, W.Cho, H.Choi, J.Clapper, M.Colditz, G.Coronado, G.Cronin-Fenton, D.Croy, R.Cummings, K.D'Angelo, H.Daly, M.DeCensi, A.DeStephano, C.Djuric, Z.Dmitrovsky, E.Dooley, W.Dossus, L.Dubinett, S.Dwivedi, C.El-Bayoumy, K.Ellaithi, M.Eltoum, I.Eshak, E.Esserman, L.Evans, D.Falk, D.Fang, C.Figueroa, J.Ford, M.Fournier, A.Fowke, J.Franco, E.Freedland, S.Freisling, H.Friedenreich, C.Gail, M.Genkinger, J.George, S.Gershenwald, J.Giorgi-Rossi, P.Giovannucci, E.Gleber-Netto, F.Goetz, L.Goodwin, P.Gowans, E.Grant, E.Groopman, J.Grossman, D.Gu, J.Guerrero-Preston, R.Gümüş, Z.Han, Y.Hanash, S.Harper, D.Hecht, S.Heckman-Stoddard, B.Henry, K.Hilakivi-Clarke, L.Hodge, A.Hong, C.Hong, Y.Huang, Y.Hung, M.Huo, D.Hur, J.Imperiale, T.Inadomi, J.Iwasaki, M.Janakiram, N.Kadara, H.Kassie, F.Kensler, K.Khairan, P.Khan, S.Kim, J.Kim, R.Kingham, T.Kinney, A.Kong, A.Kratz, C.Kühn, T.Kypriotakis, G.La Vecchia, C.Lam, S.Land, S.Lazcano-Ponce, E.Lebwohl, B.Lee, H.Lee, J.Liby, K.Lipkin, S.Longatto-Filho, A.Lopez, D.Lu, J.Lu, Q.Lundberg, A.Luu, H.Lynch, P.MacInnis, R.Mandle, H.Manne, S.Mao, J.Mariosa, D.Marshall, J.Matthews, C.Mayrand, M.Mehta, A.Melkonian, S.Michail, G.Miller, M.Milne, R.Mitzner, W.Mix, J.Mohammed, A.Molokwu, J.Montuenga, L.Mousavi Seresht, L.Muller, D.Müller, M.Mulshine, J.Murphy, G.Murphy, N.Narayanapillai, S.Nash, S.Nasrollahzadeh, D.Neale, R.Nelson, K.Noh, H.Nounu, A.O'Dwyer, P.O'Mara, T.Ogunsina, K.Oh, H.Ondrey, F.Ortiz, A.Ose, J.Park, H.Parker, B.Paskett, E.Pass, H.Passarelli, M.Pepper, J.Perkins, R.Permuth, J.Petrick, J.Phillips, K.Piazza, G.Playdon, M.Porter, W.Qiao, Y.Quaife, S.Rachocki, C.Ramsey, A.Rao, C.Rauh-Hain, J.Robbins, H.Robson, M.Rosenberg, D.Sawada, N.Sboner, A.Scalbert, A.Schmeler, K.Schnoll, R.Seno, H.Sethi, S.Shahid, A.Shaukat, A.Shen, Q.Shen, Z.Sherman, M.Shibata, D.Shu, X.Shureiqi, I.Singh, S.Smith, S.Sporn, M.Srivastava, S.Stanton, S.Stevens, V.Stewart, S.Stoffel, E.Stoner, G.Sturgeon, S.Sukumar, S.Sun, C.Sun, Y.Surh, Y.Tabun","PeriodicalId":9373,"journal":{"name":"Cancer Prevention Research","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135500361","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信