المؤلفون: Yan, Ran, Murakami, Wakana, Mortazavi, Shabnam, Yu, Tiffany, Chu, Fang-I, Lee-Felker, Stephanie, Sung, Kyunghyun

مصطلحات موضوعية: Biomedical and Clinical Sciences, Oncology and Carcinogenesis, Cancer, Breast Cancer, Clinical Research, Aging, Background parenchymal enhancement, Breast cancer, Quantitative background parenchymal enhancement, Lifetime risk, BRCA germline mutation, Clinical Sciences, Nuclear Medicine & Medical Imaging, Clinical sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/4q04z9wz

المؤلفون: Laws, Alison^{Aff1, Aff2, Aff3}, Leonard, Saskia^{Aff1, Aff4}, Hershey, Emma, Stokes, Samantha, Vincuilla, Julie, Sharma, Eshita, Milliron, Kara, Garber, Judy E.^{Aff2, Aff3, Aff6}, Merajver, Sofia D., King, Tari A.^{Aff1, Aff2, Aff3}, Pilewskie, Melissa L.^{Aff5, IDs10434024149470_cor11}

المصدر: Annals of Surgical Oncology. 31(5):3120-3127

المؤلفون: Yang M, Bai L, Ma Y, Cao X, Cui Q, Wu D, Tang X

المصدر: OncoTargets and Therapy, Vol Volume 17, Pp 733-738 (2024)

مصطلحات موضوعية: familial, acute promyelocytic leukemia, apl differentiation syndrome, hereditary predisposition, germline mutation, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://www.dovepress.com/familial-acute-promyelocytic-leukemia-a-case-report-and-review-of-the--peer-reviewed-fulltext-article-OTT; https://doaj.org/toc/1178-6930

URL الوصول: https://doaj.org/article/6d1c3a0ce41a44c1a96f20d2544d7150

المؤلفون: Farrah Bakr, Anjana Kulkarni, Stephen Mounsey, Tracey Mitchell, Sean Whittaker, Katie Lacy

المصدر: JEADV Clinical Practice, Vol 3, Iss 4, Pp 1236-1239 (2024)

مصطلحات موضوعية: familial melanoma, germline mutation, germline variant, melanoma, melanoma‐susceptibility genes, POT1, Dermatology, RL1-803, Diseases of the genitourinary system. Urology, RC870-923

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2768-6566

URL الوصول: https://doaj.org/article/145699f5d19947daae9d90f496fb4d28

المؤلفون: Ortiz-Urda, Susana^Aff4, Ho, Wilson^Aff4, Lee, Albert^Aff4

المساهمون: Ortiz-Urda, Susana^Aff1, Ho, Wilson^Aff2, Lee, Albert^Aff3

المصدر: Melanoma : From Diagnosis to Therapy. :17-21

المؤلفون: Feng, Zheng^{Aff1, Aff2}, Wen, Hao^{Aff1, Aff2}, Chen, Yaqiong^{Aff2, Aff3}, Chen, Xiaojun^{Aff1, Aff2}, Bi, Rui^{Aff2, Aff4}, Wu, Xiaohua^{Aff1, Aff2, IDs1267202401344y_cor6}, Li, Jin^{Aff1, Aff2, IDs1267202401344y_cor7}, Ju, Xingzhu^{Aff1, Aff2, IDs1267202401344y_cor8}

المصدر: Discover Oncology. 15(1)

المؤلفون: Abdel-Razeq, Hikmat^{Aff1, Aff2, IDs41598024633008_cor1}, Tamimi, Faris, Iweir, Sereen^{Aff1, Aff3}, Sharaf, Baha, Abdel-Razeq, Sarah, Salama, Osama, Edaily, Sarah, Bani Hani, Hira, Azzam, Khansa, Abaza, Haneen

المصدر: Scientific Reports. 14(1)

المؤلفون: Wu, Zhiyuan, Zhang, Qingyun, Jin, Yiting, Zhang, Xinju, Chen, Yanli, Yang, Can, Tang, Xuemei, Jiang, Haowen, Wang, Xiaoyi, Zhou, Xinli, Yu, Feng, Wang, Bing^{Aff7, IDs1288502412089w_cor12}, Guan, Ming^{Aff1, Aff2, IDs1288502412089w_cor13}

المصدر: BMC Cancer. 24(1)

المؤلفون: Bataba, Eudoxie, Babcock, Kevin, Isensee, Kathryn A., Eldhose, Binil^{Aff3, Aff4}, Kohaar, Indu^{Aff3, Aff4, Aff5}, Chesnut, Gregory T.^{Aff1, Aff3}, Dobi, Albert^{Aff3, Aff4, IDs1191202401493x_cor7}

المصدر: Current Oncology Reports. 26(2):175-180

المؤلفون: Jain, S., Niroula, A., Vihinen, M., Zook, J.M.

المصدر: Genome Biology StemTherapy: National Initiative on Stem Cells for Regenerative Therapy. 25(1)

مصطلحات موضوعية: nucleotide, area under the curve, art, Article, biochemistry, cancer risk, CDKN2A gene, cell growth, CHEK2 gene, clinical practice, complex trait disease risk, computational genetic variant interpretation method, computer model, correlation coefficient, Critical Assessment of Genome Interpretation, Crohn disease, diagnostic accuracy, diagnostic test accuracy study, diseases, DNA repair, DNA splicing, effect size, environmental risk, enzyme activity, FXN gene, gene deletion, gene expression, gene insertion, gene linkage disequilibrium, genetic analysis, genetic database, genetic identification, genetic information, genetic trait, genetic transcription, genetic variability, genetic variation, genome, genome-wide association study, genomic scale, germline mutation, human, intellectual impairment, interpretation bias, malignant neoplasm, medical research, missense mutation, monogenic disorder, MRE11 gene, multiomics, NBS1 gene, NPMALK gene, NSMCE2 gene, pathogenicity, phenotype, practice guideline, prediction, protein function, protein stability, PTEN gene, RAD50 gene, receiver operating characteristic, regulatory mechanism, social aspect, structure analysis, TP53 gene, TPMT gene, tumor suppressor gene, whole organism fitness, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics

URL الوصول: https://lup.lub.lu.se/record/14622294-f25a-471f-8a14-a043cac87a6e
http://dx.doi.org/10.1186/s13059-023-03113-6