日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Seasonal Phenology and Climate Associated Feeding Activity of Introduced Marchalina hellenica in Southeast Australia

澳大利亚东南部引入的墨西哥地鼠(Marchalina hellenica)的季节性物候和气候相关摄食活动

Jaroslow, Duncan D; Cunningham, John P; Smith, David I; Steinbauer, Martin J

Whole genome sequencing reveals complexity in both HPV sequences present and HPV integrations in HPV-positive oropharyngeal squamous cell carcinomas

全基因组测序揭示了HPV阳性口咽鳞状细胞癌中HPV序列和HPV整合的复杂性

Gao, Ge; Wang, Jintu; Kasperbauer, Jan L; Tombers, Nicole M; Teng, Fei; Gou, Honglan; Zhao, Yonggang; Bao, Zhenhong; Smith, David I

Mate-Pair Sequencing as a Powerful Clinical Tool for the Characterization of Cancers with a DNA Viral Etiology

配对末端测序作为一种强大的临床工具,可用于表征具有DNA病毒病因的癌症

Gao, Ge; Smith, David I

WWOX, large common fragile site genes, and cancer

WWOX、大型常见脆性位点基因和癌症

Gao, Ge; Smith, David I

Very large common fragile site genes and their potential role in cancer development

非常大的常见脆性位点基因及其在癌症发展中的潜在作用

Gao, Ge; Smith, David I

Prognostic significance of decreased expression of six large common fragile site genes in oropharyngeal squamous cell carcinomas

口咽鳞状细胞癌中六个大型常见脆性位点基因表达降低的预后意义

Gao, Ge; Kasperbauer, Jan L; Tombers, Nicole M; Cornell, Melissa D; Smith, David I

Genome-wide analysis reveals recurrent structural abnormalities of TP63 and other p53-related genes in peripheral T-cell lymphomas

全基因组分析揭示外周T细胞淋巴瘤中TP63和其他p53相关基因的复发性结构异常

Vasmatzis, George; Johnson, Sarah H; Knudson, Ryan A; Ketterling, Rhett P; Braggio, Esteban; Fonseca, Rafael; Viswanatha, David S; Law, Mark E; Kip, N Sertac; Ozsan, Nazan; Grebe, Stefan K; Frederick, Lori A; Eckloff, Bruce W; Thompson, E Aubrey; Kadin, Marshall E; Milosevic, Dragana; Porcher, Julie C; Asmann, Yan W; Smith, David I; Kovtun, Irina V; Ansell, Stephen M; Dogan, Ahmet; Feldman, Andrew L

Transcriptional profiling by sequencing of oropharyngeal cancer

通过测序进行口咽癌转录组分析

Laborde, Rebecca R; Wang, Vivian W; Smith, Todd M; Olson, N Eric; Olsen, Steven M; García, Joaquín J; Olsen, Kerry D; Moore, Eric J; Kasperbauer, Jan L; Tombers, Nicole M; Smith, David I

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss.

DNMT1基因突变会导致遗传性感觉神经病,并伴有痴呆和听力丧失

Klein Christopher J, Botuyan Maria-Victoria, Wu Yanhong, Ward Christopher J, Nicholson Garth A, Hammans Simon, Hojo Kaori, Yamanishi Hiromitch, Karpf Adam R, Wallace Douglas C, Simon Mariella, Lander Cecilie, Boardman Lisa A, Cunningham Julie M, Smith Glenn E, Litchy William J, Boes Benjamin, Atkinson Elizabeth J, Middha Sumit, B Dyck P James, Parisi Joseph E, Mer Georges, Smith David I, Dyck Peter J

Discovery of recurrent t(6;7)(p25.3;q32.3) translocations in ALK-negative anaplastic large cell lymphomas by massively parallel genomic sequencing

通过大规模平行基因组测序发现ALK阴性间变性大细胞淋巴瘤中存在复发性t(6;7)(p25.3;q32.3)易位

Feldman, Andrew L; Dogan, Ahmet; Smith, David I; Law, Mark E; Ansell, Stephen M; Johnson, Sarah H; Porcher, Julie C; Ozsan, Nazan; Wieben, Eric D; Eckloff, Bruce W; Vasmatzis, George