Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Manuel Torres Diz"'
Autor:
Mariela Cortés-López, Laura Schulz, Mihaela Enculescu, Claudia Paret, Bea Spiekermann, Mathieu Quesnel-Vallières, Manuel Torres-Diz, Sebastian Unic, Anke Busch, Anna Orekhova, Monika Kuban, Mikhail Mesitov, Miriam M. Mulorz, Rawan Shraim, Fridolin Kielisch, Jörg Faber, Yoseph Barash, Andrei Thomas-Tikhonenko, Kathi Zarnack, Stefan Legewie, Julian König
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-17 (2022)
Multiple alternative splicing events in CD19 mRNA have been associated with resistance/relapse to CD19 CAR-T therapy in patients with B cell malignancies. Here, by combining patient data and a high-throughput mutagenesis screen, the authors identify
Externí odkaz:
https://doaj.org/article/c08d347a8dc943b8ab905da6ad76b36d
Autor:
Laura Schulz, Manuel Torres-Diz, Mariela Cortés-López, Katharina E. Hayer, Mukta Asnani, Sarah K. Tasian, Yoseph Barash, Elena Sotillo, Kathi Zarnack, Julian König, Andrei Thomas-Tikhonenko
Publikováno v:
Genome Biology, Vol 22, Iss 1, Pp 1-12 (2021)
Abstract Resistance to CD19-directed immunotherapies in lymphoblastic leukemia has been attributed, among other factors, to several aberrant CD19 pre-mRNA splicing events, including recently reported excision of a cryptic intron embedded within CD19
Externí odkaz:
https://doaj.org/article/7a025226aeea4eeeb954f32ea7752bb3
Autor:
Andrei Thomas-Tikhonenko, Sarah K. Tasian, Yoseph Barash, Marco Ruella, Kristen W. Lynch, Nathan Singh, Maureen M. O'Brien, Susan R. Rheingold, Deanne M. Taylor, Rawan Shraim, Mukta Asnani, Carolin Schmidt, John Chukinas, Asen Bagashev, David A. Hottman, Mathieu Quesnel-Vallières, Manuel Torres-Diz, Zhiwei Ang, Katharina E. Hayer, Ammar S. Naqvi, Elisabeth Gillespie, Sisi Zheng
Supplementary Data from Modulation of CD22 Protein Expression in Childhood Leukemia by Pervasive Splicing Aberrations: Implications for CD22-Directed Immunotherapies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ab6aeb24bca7462aba4fb3d2d8eb381
https://doi.org/10.1158/2643-3230.22544534.v1
https://doi.org/10.1158/2643-3230.22544534.v1
Autor:
Montse Sanchez-Cespedes, Jun Yokota, Takashi Kohno, Luis M. Montuenga, Alberto Villanueva, Reika Iwakawa, Carmen Saez, Sebastian Moran, Antonio Gomez, Suvi Savola, Eva Pros, Manuel Torres-Diz, Octavio A. Romero
PDF file 422K, Fig. S1. Radio charts of the multiplex ligation-dependent probe amplification (MLPA), depicting intragenic deletions at the indicated lung cancer cell lines and lung primary tumor. The five exons of the MAX gene and the names and the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03082b626618899b3c9bf09e8daba03d
https://doi.org/10.1158/2159-8290.22530671
https://doi.org/10.1158/2159-8290.22530671
Autor:
Montse Sanchez-Cespedes, Jun Yokota, Takashi Kohno, Luis M. Montuenga, Alberto Villanueva, Reika Iwakawa, Carmen Saez, Sebastian Moran, Antonio Gomez, Suvi Savola, Eva Pros, Manuel Torres-Diz, Octavio A. Romero
PDF file 48K, Description of the methodology for: -Lung tumor specimens and cancer cell lines. -Screening for MAX gene alterations: Sanger direct sequencing and Multiplex ligation dependent probe amplification (MLPA). -Expression vectors and lentivir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97901dcb4b92069096cb143833847074
https://doi.org/10.1158/2159-8290.22530668
https://doi.org/10.1158/2159-8290.22530668
Autor:
Andrei Thomas-Tikhonenko, Struan F.A. Grant, James A. Pippin, Manuel Torres-Diz, Katharina Hayer, Priyanka Sehgal, Claudia B. Lanauze
About 10% to 30% of patients with colorectal cancer harbor either loss of or missense mutations in SMAD4, a critical component of the TGFβ signaling pathway. The pathophysiologic function of missense mutations in Smad4 is not fully understood. They
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98265ca73ce1e4a48df2705e6b56cac5
https://doi.org/10.1158/1541-7786.c.6545193.v1
https://doi.org/10.1158/1541-7786.c.6545193.v1
Autor:
Andrei Thomas-Tikhonenko, Christopher J. Lengner, Ben Z. Stanger, Yogev Sela, N. Adrian Leu, Manuel Torres-Diz, Katharina E. Hayer, Xin Wang, Claudia Lanauze, Priyanka Sehgal
S1. DKK3 and Wnt signaling in CRC cells. S2. Derivation of murine colorectal tumoroids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a55d0c97bb65b4a4927a9c6eabb62c9
https://doi.org/10.1158/1541-7786.22526006
https://doi.org/10.1158/1541-7786.22526006
Autor:
Andrei Thomas-Tikhonenko, Christopher J. Lengner, Ben Z. Stanger, Yogev Sela, N. Adrian Leu, Manuel Torres-Diz, Katharina E. Hayer, Xin Wang, Claudia Lanauze, Priyanka Sehgal
Activation of Wnt signaling is among the earliest events in colon cancer development. It is achieved either via activating mutations in the CTNNB1 gene encoding β-catenin, the key transcription factor in the Wnt pathway, or most commonly by inactiva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9c4527f515cf88cde97282be383efb3
https://doi.org/10.1158/1541-7786.c.6544982.v1
https://doi.org/10.1158/1541-7786.c.6544982.v1
Autor:
Montse Sanchez-Cespedes, Jun Yokota, Takashi Kohno, Luis M. Montuenga, Alberto Villanueva, Reika Iwakawa, Carmen Saez, Sebastian Moran, Antonio Gomez, Suvi Savola, Eva Pros, Manuel Torres-Diz, Octavio A. Romero
PDF file 236K, Table S1. List of the 121 lung cancer cell lines screened for MAX alterations. Information about the histopathology of each cell line, and the presence of alterations at MYC and BRG1 is also included. Grey boxes indicate that no inform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::305648071ad88fcb65873ac1ec7b85b0
https://doi.org/10.1158/2159-8290.22530665
https://doi.org/10.1158/2159-8290.22530665
Autor:
Andrei Thomas-Tikhonenko, Struan F.A. Grant, James A. Pippin, Manuel Torres-Diz, Katharina Hayer, Priyanka Sehgal, Claudia B. Lanauze
S1. Wnt signaling in CRC cell lines with Smad4 R361 mutations. S2. Wnt signaling in CRC cell lines with Smad4 R361 mutations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::345ca818af4f5cd876c0091d8c8514b3
https://doi.org/10.1158/1541-7786.22526730.v1
https://doi.org/10.1158/1541-7786.22526730.v1