NDLTD Global ETD Search
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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.

Search results

Showing 1 to 7 of 7 (0.039 seconds)
1

Construction expression and preliminary biological analysis of HCV and HCV-dengue chimeric virus genomes

Tuthill, Tobias J. January 2001 (has links)
No description available.
579
Liver disease; Genotype; RNA; DNA
2

SNP based strategies to study candidate genes for Alzheimer's disease /

Feuk, Lars, January 2002 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst., 2002. / Härtill 5 uppsatser.
3

Fibrinogen and susceptibility to myocardial infarction : role of gene-gene and gene-environment interactions /

Nastase Mannila, Maria, January 2006 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst., 2006. / Härtill 5 uppsatser.
4

Memory, genes, and brain imaging : relating the APOE gene to brain function and structure /

Lind, Johanna, January 2007 (has links)
Diss. (sammanfattning) Stockholm : Karolinska institutet, 2007. / Härtill 4 uppsatser.
5

SNP technology and Alzheimer's disease /

Howell, Walter Mathias, January 2003 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst., 2003. / Härtill 5 uppsatser.
6

On the genetic variation of interleukin-6 in health and coronary heart disesase /

Björnstedt Bennermo, Marie, January 2005 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst., 2005. / Härtill 4 uppsatser.
7

Sekvenční varianty genu HNF1B u autozomálně recesivní polycystické choroby ledvin / Sequence variety of HNF1B gene in autosomal recessive polycystic kidney disease

Kavec, Miriam January 2017 (has links)
Autosomal recessive polycystic kidney disease (ARPKD) is a rare severe inherited disease manifested by cystic renal disease, congenital hepatic fibrosis and dilatatation of bile ducts. The spectrum of clinical manifestations is very wide and variable, depends on the age at which the disease was manifested. In severe forms of the disease, it is possible to detect the first symptoms prenatally around the 20th week of pregnancy due to increased echogenic kidneys and the presence of oligohydramnios. The causal gene of this disease is thePKHD1 gene with protein product fibrocystin that is most likely contributing on maintaining the intracellular concentration of Ca2+ cations. The exact phatophysiology mechanism of ARPKD remains unknown. Phenotypic manifestations of this disease may overlap with mutations associated with other genes. One of the genes mimicking the ARPKD phenotype is the HNF1B gene. Mutations associated with HNF1B gene are the most common monogenic cause of developmental kidney abnormalities. HNF1B is a tissue-specific transcription factor that regulates the expression of PKHD1. In experimental part I worked on genetic analysis of the HNF1B gene in 28 patients who have not been confirmed ARPKD diagnosis by detection of 2 PKHD1 mutations. For the purposes of mutational screening, I used...

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