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Academic Journal

Acute myeloid leukemia: from NGS, through scRNA-seq, to CAR-T. dissect cancer heterogeneity and tailor the treatment.

Authors : Peroni, Edoardo¹ (AUTHOR) ; Randi, Maria Luigia² (AUTHOR); Rosato, Antonio^1,3 (AUTHOR)

Source: Journal of Experimental & Clinical Cancer Research (17569966). 11/21/2023, Vol. 42 Issue 1, p1-22. 22p.

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The analysis of the genotype of Sapovirus outbreaks in Zhejiang Province.

Authors : Su, Lingxuan^1,2 (AUTHOR); Mao, Haiyan^1,2 (AUTHOR); Sun, Yi^1,2 (AUTHOR)

Source: Virology Journal. 11/16/2023, Vol. 20 Issue 1, p1-9. 9p.

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Diagnosis of leptospira by metagenomics next-generation sequencing with extracorporeal membrane oxygenation support: a case report.

Authors : Ji, Jianyu^1,2,3 (AUTHOR); Wang, Wei^1,2,3 (AUTHOR); Xiang, Shulin^1,2,3 (AUTHOR)

Source: BMC Infectious Diseases. 11/13/2023, Vol. 23 Issue 1, p1-7. 7p.

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Rapid profiling of Plasmodium parasites from genome sequences to assist malaria control.

Authors : Phelan, Jody E.¹ (AUTHOR) ; Turkiewicz, Anna¹ (AUTHOR); Manko, Emilia¹ (AUTHOR)

Source: Genome Medicine. 11/10/2023, Vol. 15 Issue 1, p1-11. 11p.

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Crizotinib combined with bronchoscopic interventional treatment in ALK-positive inflammatory myofibroblastic tumor of left main stem bronchus: a case report.

Authors : Zhang, Peng¹ (AUTHOR); Wang, Chenchen² (AUTHOR); Lv, Zechao³ (AUTHOR)

Source: Journal of Cardiothoracic Surgery. 11/10/2023, Vol. 18 Issue 1, p1-6. 6p.

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IRE1-mediated degradation of pre-miR-301a promotes apoptosis through upregulation of GADD45A.

Authors : Gebert, Magdalena¹ (AUTHOR); Bartoszewska, Sylwia² (AUTHOR); Opalinski, Lukasz³ (AUTHOR)

Source: Cell Communication & Signaling. 11/9/2023, Vol. 21 Issue 1, p1-20. 20p.

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Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases.

Authors : Pagnamenta, Alistair T.^1,2 (AUTHOR); Camps, Carme^1,2 (AUTHOR); Giacopuzzi, Edoardo^1,2,3 (AUTHOR)

Source: Genome Medicine. 11/9/2023, Vol. 15 Issue 1, p1-25. 25p.

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Magnetic resonance imaging and next-generation sequencing for the diagnosis of cystic echinococcosis in the intradural spine: a case report.

Authors : Lao, Xiaojie¹ (AUTHOR); Hu, Diefei² (AUTHOR); Ji, Lei³ (AUTHOR)

Source: Journal of Medical Case Reports. 11/10/2023, Vol. 17 Issue 1, p1-4. 4p.

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International Undiagnosed Diseases Programs (UDPs): components and outcomes.

Authors : Curic, Ela¹ (AUTHOR); Ewans, Lisa^1,2,3 (AUTHOR); Pysar, Ryan^1,2,4 (AUTHOR)

Source: Orphanet Journal of Rare Diseases. 11/9/2023, Vol. 18 Issue 1, p1-15. 15p.

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Variant allelic frequencies of driver mutations can identify gliomas with potentially false-negative MGMT promoter methylation results.

Authors : McCord, Matthew¹ (AUTHOR); Jamshidi, Pouya¹ (AUTHOR); Thirunavu, Vineeth² (AUTHOR)

Source: Acta Neuropathologica Communications. 11/2/2023, Vol. 11 Issue 1, p1-15. 15p.

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