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microphthalmia
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Microphthalmia in Mammals as a Sensory Adaptation: A Case Study
2001 |
Faculty of Science
publication
Microphthalmia and cataract in rats with a novel point mutation in connexin 50-L7Q
2008 |
First Faculty of Medicine
publication
Histone acetyltransferases PCAF and hGCN5 inhibit activity of the melanocyte-specific microphthalmia-associated transcription factor independent of their acetyltransferase activity
Publication without faculty affiliation
publication
Microphthalmia-associated transcription factor expression levels in melanoma cells contribute to cell invasion and proliferation
2015 |
First Faculty of Medicine
publication
Histone acetyltransferases p-300/CBP-associated factor and human general control nonrepresible-related 5 inhibit activity of the melanocyte-specific microphthalmia-associated transcription factor.
Publication without faculty affiliation
publication
Microphthalmia in Mammals as a Sensory Adaptation: A Case Study
2001 |
First Faculty of Medicine, Faculty of Mathematics and Physics
publication
SWI/SNF chromatin remodeling complex is critical for the expression of microphthalmia-associated transcription factor in melanoma cells
2010 |
First Faculty of Medicine, Central Library of Charles University
publication
Microphthalmia Transcription Factor: A Specific Marker for Malignant Melanoma
2004 |
First Faculty of Medicine
publication
X-linked Microcephaly, Microphthalmia, Microcornea, Congenital Catarct, Hypogenitalism, Mental Deficiency Growth Retardation, Spasticity: Possible New Syndrome
1996 |
Second Faculty of Medicine
publication
Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap
2009 |
Second Faculty of Medicine
publication
Chapter 4: MITF: A Critical Transcription Factor in Melanoma Transcriptional Regulatory Network
2013 |
First Faculty of Medicine
publication
The visual system in subterranean African mole-rats (Rodentia, Bathyergidae): Retina, subcortical visual nuclei and primary visual cortex
2008 |
Faculty of Science
publication
Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders
2021 |
First Faculty of Medicine
publication
Transcription physiology of pigment formation in melanocytes: central role of MITF
2010 |
First Faculty of Medicine
publication
MITF meets chromatin in melanoma
2012 |
First Faculty of Medicine
publication
FMR1 Gene Expansion, Large Deletion of Xp, and Skewed X-Inactivation in a Girl With Mental Retardation and Autism
2010 |
First Faculty of Medicine
publication
FMR1 Gene Expansion, Large Deletion of Xp, and Skewed X-Inactivation in a Girl With Mental Retardation and Autism
2010 |
Second Faculty of Medicine
publication
The many roles of MITF in melanoma
2017 |
First Faculty of Medicine
publication
Integrative analysis of transcriptomics and clinical data uncovers the tumor- suppressive activity of MITF in prostate cancer
2018 |
Second Faculty of Medicine
publication
Eosinophilic solid and cystic renal cell carcinoma with melanin pigment - expanding the morphological spectrum
2022 |
Faculty of Medicine in Pilsen
publication
Ectopic Activation of Wnt/beta-Catenin Signaling in Lens Fiber Cells Results in Cataract Formation and Aberrant Fiber Cell Differentiation
2013 |
Faculty of Science
publication
Embryotoxicity of cisplatin and a cisplatin-procaine complex (DPR) studied in chick embryo
2002 |
Third Faculty of Medicine
publication
Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies
2011 |
Second Faculty of Medicine
publication
Inducibly decreased MITF levels do not affect proliferation and phenotype switching but reduce differentiation of melanoma cells
2018 |
First Faculty of Medicine
publication
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities
2021 |
First Faculty of Medicine, Second Faculty of Medicine
publication
MITF-Independent Pro-Survival Role of BRG1-Containing SWI/SNF Complex in Melanoma Cells
2013 |
First Faculty of Medicine
publication
Dominant variants in the splicing factor PUF60 cause a recognizable syndrome with intellectual disability, heart defects and short stature
2017 |
Second Faculty of Medicine
publication
Rare heterozygous GDF6 variants in patients with renal anomalies
2020 |
Second Faculty of Medicine
publication
Advantages of nanofibrous membranes for culturing of primary RPE cells compared to commercial scaffolds
2022 |
Faculty of Science, Third Faculty of Medicine