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Hledat publikace relevantní k dotazu "splicing factor"
splicing factor
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Publikace
Studium
publication
Formation of nuclear splicing factor compartments is independent of lamins A/C
Publikace bez příslušnosti k fakultě
publication
Formation of Nuclear Splicing Factor Compartments Is Independent of Lamins A/C
2004 |
1. lékařská fakulta
publication
Formation of Nuclear Splicing Factor Compartments Is Independent of Lamins A/C
2004 |
Fakulta tělesné výchovy a sportu
publication
Nuclear pre-mRNA compartmentalization: Trafficking of released transcripts to splicing factor reservoirs
2000 |
1. lékařská fakulta
publication
Expression of circular RNAs in myelodysplastic neoplasms and their association with mutations in the splicing factor gene SF3B1
2023 |
Přírodovědecká fakulta, Ústřední knihovna
publication
The SC-35 Splicing Factor Interacts with RNA Pol II and A-Type Lamin Depletion Weakens This Interaction
2021 |
1. lékařská fakulta
publication
Altered Expression of MBNL Family of Alternative Splicing Factors in Colorectal Cancer
2021 |
1. lékařská fakulta, Lékařská fakulta v Plzni
publication
The splicing factor U1-70K interacts with the SMN complex and is required for nuclear gem integrity
2014 |
Přírodovědecká fakulta
publication
Dominant variants in the splicing factor PUF60 cause a recognizable syndrome with intellectual disability, heart defects and short stature
2017 |
2. lékařská fakulta
publication
Human galectin-2: nuclear presence in vitro and its modulation by quiescence/stress factors
2008 |
Publikace bez příslušnosti k fakultě
publication
Significance of nuclear hTra2-beta 1 expression in cervical cancer
2009 |
Ústřední knihovna
publication
Prespliceosomal assembly on microinjected precursor mRNA takes place in nuclear speckles
2001 |
1. lékařská fakulta
publication
Intronová mutace c.903+469T>C v genu MTRR vytváří nový exon splicin enhancer vážící SF2/ASF, vede k aktivaci pseudoexonů a způsobuje homocystinurii typu cblE
2010 |
1. lékařská fakulta
publication
Retinitis pigmentosa-linked mutation in DHX38 modulates its splicing activity
2022 |
Přírodovědecká fakulta, Ústřední knihovna
publication
SKIP Is a Component of the Spliceosome Linking Alternative Splicing and the Circadian Clock in Arabidopsis
2012 |
Přírodovědecká fakulta
publication
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features
2024 |
2. lékařská fakulta
publication
Stress-induced expression of p53 target genes is insensitive to SNW1/SKIP downregulation
2011 |
Přírodovědecká fakulta
publication
Upregulation of ZEB1-Derived Circular RNAs Is Associated with SF3B1-Mutated Myelodysplastic Neoplasms
Publikace bez příslušnosti k fakultě
publication
In vivo kinetics of U4/U6.U5 tri-snRNP formation in Cajal bodies
2011 |
Matematicko-fyzikální fakulta
publication
Assembly of the U5 snRNP component PRPF8 is controlled by the HSP90/R2TP chaperones
2017 |
Přírodovědecká fakulta
publication
Antisense Therapy for a Common Corneal Dystrophy Ameliorates TCF4 Repeat Expansion-Mediated Toxicity
2018 |
1. lékařská fakulta
publication
Nineteen complex-related factor Prp45 is required for the early stages of cotranscriptional spliceosome assembly
2017 |
Přírodovědecká fakulta
publication
Azacitidine Switch to Lenalidomide Eradicated the TP53/ CDKN2A Co-Mutated Clone and Induced Long-Term Erythroid Response in Del(5q) MDS
2019 |
1. lékařská fakulta
publication
SF3B1 mutations and their impact on cellular bioenergetics in myelodysplastic syndromes
Publikace bez příslušnosti k fakultě
publication
Changes in otoacoustic emissions and high-frequency hearing thresholds in children and adolescents
2006 |
2. lékařská fakulta
publication
Intronic microduplications of RBFOX1 gene and their phenotypic consequences
Publikace bez příslušnosti k fakultě
publication
New aspects of galectin functionality in nuclei of cultured bone marrow stromal and epidermal cells: biotinylated galectins as tool to detect specific binding sites
2003 |
1. lékařská fakulta, Fakulta tělesné výchovy a sportu, 2. lékařská fakulta, 3. lékařská fakulta
publication
Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits
2022 |
Přírodovědecká fakulta