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exon 7
Publication
Class
Person
Publication
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publication
Non-invasive fetal RHD exon 7 and exon 10 genotyping using real-time PCR testing of fetal DNA in maternal plasma
2005 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Somatic Mutations in Exon 7 of the TP53 Gene in Index Colorectal Lesions Are Associated with the Early Occurrence of Metachronous Adenoma
2022 |
First Faculty of Medicine, Faculty of Science, Central Library of Charles University
publication
Non-invasive fetal RHD exon 7 and exon 10 genotyping using real-time PCR testing of fetal DNA in maternal plasma
2005 |
Second Faculty of Medicine
publication
Non-invasive fetal RHD exon 7 and exon 10 genotyping using real-time PCR testing of fetal DNA in maternal plasma
2005 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
The influence of endothelial nitric oxide synthase gene polymorphism in exon 7 on the progression of autosomal dominant polycystic kidney disease
Publication without faculty affiliation
publication
Late diagnosis of complete androgen insensitivity syndrome and transmission/carriers of the condition in a family with mutation c.2495G. T p.(Arg832Leu) in exon 7 of the androgen receptor gene: genetic, clinical and ethical aspects
2019 |
Second Faculty of Medicine, Faculty of Medicine in Pilsen
publication
The influence of G-Protein beta 3-subunit gene and endothelial nitric oxide synthase gene in exon 7 polymorphisms on progression of autosomal dominant polycystic kidney disease
2004 |
First Faculty of Medicine
publication
The influence of G-Protein beta 3-subunit gene and endothelial nitric oxide synthase gene in exon 7 polymorphisms on progression of autosomal dominant polycystic kidney disease
2004 |
Faculty of Physical Education and Sport
publication
Non-invasive fetal RHD genotyping on DNA isolated from maternal plasma in RhD negative pregnancies
2003 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Molecular etiopathogenesis of spinal muscular atrophy
2002 |
Second Faculty of Medicine
publication
Absence of spermatozoal CD46 protein expression and associated rapid acrosome reaction rate in striped field mice (Apodemus agrarius)
2009 |
Faculty of Science
publication
Non-invasive foetal RHD, RHC and RHE genotyping from maternal plasma in RhD negative pregnancies
2004 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Low Prevalence and Variable Clinical Presentation of Troponin I and Troponin T Gene Mutations in Hypertrophic Cardiomyopathy
2009 |
Third Faculty of Medicine
publication
Low Prevalence and Variable Clinical Presentation of Troponin I and Troponin T Gene Mutations in Hypertrophic Cardiomyopathy
2009 |
Publication without faculty affiliation
publication
Pregnancy-Associated Plasma Protein A Polymorphisms in Patients with Risk Pregnancies
2011 |
First Faculty of Medicine
publication
Non-invasive fetal RHD and RHCE genotyping from maternal plasma in alloimmunized pregnancies
2005 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Role of intron 5 C/T polymorphism of the kalcium sensing receptor gene in the regulation of the serum FSH and LH in post-menopausal women.
2005 |
Faculty of Science
publication
Haplotype analysis of the endothelial nitric oxide synthase gene in asthma
2008 |
Second Faculty of Medicine
publication
Analysis of point mutations in the SMN1 gene in SMA patients bearing a single SMN1 copy
2007 |
Second Faculty of Medicine
publication
Non-invasive fetal RHD and RHCE genotyping using real-time PCR testing of maternal plasma in RhD-negative pregnancies
2005 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
High frequency of SLC22A12 variants causing renal hypouricemia 1 in the Czech and Slovak Roma population; simple and rapid detection method by allele-specific polymerase chain reaction
2015 |
First Faculty of Medicine
publication
Two Novel Variants Affecting CDKL5 Transcript Associated with Epileptic Encephalopathy
2017 |
Second Faculty of Medicine
publication
Atypical Teratoid/Rhabdoid Tumor (AT/RT) With Molecular Features of Pleomorphic Xanthoastrocytoma
2021 |
Second Faculty of Medicine
publication
Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study
2009 |
Second Faculty of Medicine
publication
RET Variants and Haplotype Analysis in a Cohort of Czech Patients with Hirschsprung Disease
2014 |
Second Faculty of Medicine
publication
RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease
2014 |
Central Library of Charles University
publication
Molecular Profiling of Salivary Gland Intraductal Carcinoma Revealed a Subset of Tumors Harboring NCOA4-RET and Novel TRIM27-RET Fusions A Report of 17 cases
2018 |
Faculty of Medicine in Pilsen, Faculty of Medicine in Hradec Králové
publication
Sarcomas Harboring EWSR1::PATZ1 Fusions: A Clinicopathologic Study of 17 Cases
2024 |
Faculty of Medicine in Pilsen
publication
NCOA4-RET and TRIM27-RET Are Characteristic Gene Fusions in Salivary Intraductal Carcinoma, Including Invasive and Metastatic Tumors: Is "Intraductal" Correct?
2019 |
Faculty of Medicine in Pilsen