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Cancers
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March 29, 2023
Novel Generation of FAP Inhibitor-Based Homodimers for Improved Application in Radiotheranostics
Marcel Martin, Sanjana Ballal, Madhav Prasad Yadav, et al.
International Journal of Cancer
|
August 22, 2012
Next-generation RNA sequencing reveals differential expression of MYCN target genes and suggests the mTOR pathway as a promising therapy target in MYCN-amplified neuroblastoma
Alexander Schramm, Johannes Köster, Tobias Marschall, et al.
Nature Genetics
|
June 25, 2013
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3
Marcel Martin, Lars Maßhöfer, Petra Temming, et al.
F1000Research
|
September 15, 2020
Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants
Maxime Garcia, Szilveszter Juhos, Malin Larsson, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
August 29, 2023
Head-to-head comparison of [<sup>68</sup>Ga]Ga-DOTA.SA.FAPi with [<sup>18</sup>F]F-FDG PET/CT in radioiodine-resistant follicular-cell derived thyroid cancers
Sanjana Ballal, Madhav P Yadav, Frank Roesch, et al.
Nature Communications
|
August 4, 2025
Precise mapping of single-stranded DNA breaks by sequence-templated erroneous DNA polymerase end-labelling
Leonie Wenson, Johan Heldin, Marcel Martin, et al.
Cell Systems
|
February 10, 2024
Clonally heritable gene expression imparts a layer of diversity within cell types
Jeff E Mold, Martin H Weissman, Michael Ratz, et al.
Cell Systems
|
January 15, 2026
A combinatorial transcription factor screening platform for immune cell reprogramming
Ilia Kurochkin, Abigail R Altman, Inês Caiado, et al.
The Journal of Experimental Medicine
|
November 10, 2019
Extensive dissemination and intraclonal maturation of HIV Env vaccine-induced B cell responses
Ganesh E Phad, Pradeepa Pushparaj, Karen Tran, et al.
Orphanet Journal of Rare Diseases
|
July 25, 2013
Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations
Claudia Voigt, André Mégarbané, Kornelia Neveling, et al.
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of 6
Search research articles
Search
Showing results (41-50 of 56) with videos related to
Sort By:
Page
of 6
Cancers
|
March 29, 2023
Novel Generation of FAP Inhibitor-Based Homodimers for Improved Application in Radiotheranostics
Marcel Martin, Sanjana Ballal, Madhav Prasad Yadav, et al.
International Journal of Cancer
|
August 22, 2012
Next-generation RNA sequencing reveals differential expression of MYCN target genes and suggests the mTOR pathway as a promising therapy target in MYCN-amplified neuroblastoma
Alexander Schramm, Johannes Köster, Tobias Marschall, et al.
Nature Genetics
|
June 25, 2013
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3
Marcel Martin, Lars Maßhöfer, Petra Temming, et al.
F1000Research
|
September 15, 2020
Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants
Maxime Garcia, Szilveszter Juhos, Malin Larsson, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
August 29, 2023
Head-to-head comparison of [<sup>68</sup>Ga]Ga-DOTA.SA.FAPi with [<sup>18</sup>F]F-FDG PET/CT in radioiodine-resistant follicular-cell derived thyroid cancers
Sanjana Ballal, Madhav P Yadav, Frank Roesch, et al.
Nature Communications
|
August 4, 2025
Precise mapping of single-stranded DNA breaks by sequence-templated erroneous DNA polymerase end-labelling
Leonie Wenson, Johan Heldin, Marcel Martin, et al.
Cell Systems
|
February 10, 2024
Clonally heritable gene expression imparts a layer of diversity within cell types
Jeff E Mold, Martin H Weissman, Michael Ratz, et al.
Cell Systems
|
January 15, 2026
A combinatorial transcription factor screening platform for immune cell reprogramming
Ilia Kurochkin, Abigail R Altman, Inês Caiado, et al.
The Journal of Experimental Medicine
|
November 10, 2019
Extensive dissemination and intraclonal maturation of HIV Env vaccine-induced B cell responses
Ganesh E Phad, Pradeepa Pushparaj, Karen Tran, et al.
Orphanet Journal of Rare Diseases
|
July 25, 2013
Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations
Claudia Voigt, André Mégarbané, Kornelia Neveling, et al.
Page
of 6