主页文献库搜索
PARP Inhibitor Sensitivity in Tumors Harboring Non-BRCA Homologous Recombinat...

Dos Santos(ES),Cicilini(AL),Simões(MFE),Ba... Int J Mol Sci 2026-07-28

Poly(ADP-ribose) polymerase inhibitors (PARPis) have demonstrated remarkable efficacy in tumors carrying BRCA1/2 pathoge...

Mechanisms of PARP Inhibitor Resistance: From Replication Gap Biology and Tra...

Abinawanto,Sophian(A) Environ Mol Mutagen 2026-06-00

...BRCA1/2-mutant tumors. Despite initial efficacy, resistance inevitably emerges, limiting long-term clinical benefit. Thi...

Landscape of germline genetic alterations among non-western young male patien...

Abdel-Razeq(H),Bani Hani(H),Alafeef(S),Tam... Front Oncol None

...BRCA1 P/LP variants were identified. Germline P/LP variants are common in young male patients with cancer, particularly ...

Severe radiodermatitis and implant loss associated with pembrolizumab and ola...

Gao(J),Wang(S),Huang(A),Wang(H),Xiao(Z) AME Case Rep None

...BRCA1 mutation. After completion of multidisciplinary neoadjuvant systemic therapy, the patient underwent E-NSM with imm...

How Often are druggable mutations detectable in Metastatic Castration Resista...

Steenbock(O),Rieger(C),Heidenreich(J),Paff... Urol Int 2026-08-13

...BRCA1/2, CDK12, CTNNB1, DLL3, ETS family, FOXA1, FOXO1, MED12, PIK3CA, PTEN, RAD51C, TP53, Wnt-Pathway). Since 2023, we ...

Uncovering Hereditary Risk: Germline Homologous Recombination Repair Variant ...

Kapoor(A),Uthale(S),Chain(A),Rungta(A),Ano... JCO Glob Oncol 2026-08-00

...BRCA1/2, potentially underidentifying patients with other HRR gene variants who could benefit from targeted therapies. A...

Incidence of Germline Genetic Variants in Patients with a Urinary Tract Cance...

Kamau(K),Byrne(L),Goradia(R),Sundi(D),Meng... Eur Urol Oncol 2026-08-13

...BRCA1, BRCA2, and ATM. Very small cohorts of patients with UC and LS or a DDR variant responded well to immune checkpoin...

Germline BRCA1 pathogenic variants and T cell dysfunction.

Kay(J),Harris(MA),Lara Gonzalez(LE),van Ge... Immunooncol Technol 2026-09-00

...BRCA1 (gBRCA1) pathogenic variants (PVs) are the most common cause of inherited breast cancer. Preclinical studies have ...

Interpreting homologous recombination deficiency in rare gynecological cancer...

Kabeer(F),Cochrane(D),Grisdale(C),Lynch(BJ... Gynecol Oncol Rep 2026-08-00

...BRCA1 mutation with somatic loss of heterozygosity (LOH), resulting in biallelic BRCA1 loss. A high HRDetect score (0.96...

Ionizing Radiation and Ultraviolet Light Irradiation-Associated DNA Damage In...

Yoshioka(KI),Matsuno(Y),Kusumoto-Matsuo(R) Cancer Sci 2026-08-14

...BRCA1/2 mutations. However, many cancers exhibiting genomic instability occur without detectable defects in canonical re...

上一页 70 71 72 73 74 75 76 77 78 下一页 74 / 共 1000

联系地址

山东省济南市章丘区文博路2号

齐鲁师范学院 genelibs生信实验室

山东省济南市高新区舜华路750号

大学科技园北区F座4单元2楼

电话: 0531-88819269

微信公众号

关注微信订阅号,实时查看信息,关注医学生物学动态。


商务邮箱

E-mail: product@genelibs.com