نتائج البحث - Inna Inashkina
- يعرض 1 - 7 نتائج من 7
-
1
Somatic polyploidy is associated with the upregulation of c-MYC interacting genes and EMT-like signature حسب Alejandro Vázquez‐Martín, Olga V. Anatskaya, Alessandro Giuliani, Jekaterina Ērenpreisa, Sui Huang, Kristīne Salmiņa, Inna Inashkina, Anda Huna, Nikolay Nikolsky, Alexander E. Vinogradov
منشور في 2016Artigo -
2
“Mitotic Slippage” and Extranuclear DNA in Cancer Chemoresistance: A Focus on Telomeres حسب Kristīne Salmiņa, Agnieszka Bojko, Inna Inashkina, Karolina Staniak, Magdalena Dudkowska, Petar Podlesniy, Fēlikss Rūmnieks, Ninel M. Vainshelbaum, Dace Pjanova, Ewa Sikora, Jekaterina Ērenpreisa
منشور في 2020Artigo -
3
DNA damage causes TP53-dependent coupling of self-renewal and senescence pathways in embryonal carcinoma cells حسب Thomas Jackson, Kristīne Salmiņa, Anda Huna, Inna Inashkina, Eriks Jankevics, Una Riekstiņa, Zane Kalniņa, Andrei A. Ivanov, Paul A. Townsend, Mark S. Cragg, Jekaterina Ērenpreisa
منشور في 2013Artigo -
4
Multiple NF-ATc Isoforms with Individual Transcriptional Properties Are Synthesized in T Lymphocytes حسب Sergei Chuvpilo, Andris Avots, Friederike Berberich‐Siebelt, Judith Glöckner, Christian Fischer, Andreas Kerstan, Cornelia Escher, Inna Inashkina, Falk Hlubek, Eriks Jankevics, Thomas Brabletz, Edgar Serfling
منشور في 1999Artigo -
5
Alternative Polyadenylation Events Contribute to the Induction of NF-ATc in Effector T Cells حسب Sergei Chuvpilo, Michael Zimmer, Andreas Kerstan, Judith Glöckner, Andris Avots, Cornelia Escher, Christian Fischer, Inna Inashkina, Eriks Jankevics, Friederike Berberich‐Siebelt, Edgar Schmitt, Edgar Serfling
منشور في 1999Artigo -
6
Novel mutations in <i>MYBPC1</i> are associated with myogenic tremor and mild myopathy حسب Janis Stavusis, Baiba Lāce, Jochen Schäfer, Janelle Geist, Inna Inashkina, Dita Kidere, Sander Pajusalu, Nathan T. Wright, Annika Saak, Manja Weinhold, Dietrich Haubenberger, Sandra L. Jackson, Aikaterini Kontrogianni‐Konstantopoulos, Carsten G. Bönnemann
منشور في 2019Artigo -
7
Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe Cases حسب Yoshiko Murakami, Thi Tuyet Mai Nguyen, Nissan Vida Baratang, Praveen K. Raju, Alexej Knaus, Sian Ellard, Gabriela Jones, Baiba Lāce, Justine Rousseau, Norbert Fonya Ajeawung, Atsushi Kamei, Gaku Minase, Manami Akasaka, Nami Araya, Eriko Koshimizu, Jenneke van den Ende, Florian Erger, Janine Altmüller, Zita Krūmiņa, Jurgis Strautmanis, Inna Inashkina, Janis Stavusis, Areeg El‐Gharbawy, Jessica Sebastian, Ratna Dua Puri, Samarth Kulshrestha, Ishwar C. Verma, Esther M. Maier, Tobias B. Haack, Anil Israni, Júlia Baptista, Adam C. Gunning, Jill A. Rosenfeld, Pengfei Liu, Marieke Joosten, María Eugenia Rocha, Mais Hashem, Hesham Aldhalaan, Fowzan S. Alkuraya, Satoko Miyatake, Naomichi Matsumoto, Peter Krawitz, Elsa Rossignol, Taroh Kinoshita, Philippe M. Campeau
منشور في 2019Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Cell biology
Genetics
Gene expression
Molecular biology
Phenotype
Cancer research
DNA
DNA damage
Effector
Gene isoform
Medicine
Mutation
Polyadenylation
Transcription factor
Alternative splicing
Biochemistry
Biopsy
Cancer
Cancer cell
Cell
Cell cycle
Cellular differentiation
Cellular senescence
Cleavage (geology)
Cleavage and polyadenylation specificity factor
DNA repair
Downregulation and upregulation
Embryonal carcinoma