Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:( mutaatio ). Showing records 1 – 21 of 21 total matches.

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters


Tampere University

1. Visto, Anni-Laura. Rauta-aineenvaihduntaan liittyvien geenipolymorfioiden yhteys verenpainetautiin .

Degree: 2017, Tampere University

 Työn tavoitteena oli perehtyä rauta-aineenvaihdunnan proteiineihin sekä niiden polymorfioihin, joilla on yhteys verenpainetautiin. Työhön kuului tilastoanalyysien laatimista sekä osallistuminen lehdessä julkaistavan tieteellisen artikkelin kirjoittamiseen. Tutkimuskohteeksi… (more)

Subjects/Keywords: hypertensio ; hepsidiini ; hemojuveliini ; mutaatio

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Visto, A. (2017). Rauta-aineenvaihduntaan liittyvien geenipolymorfioiden yhteys verenpainetautiin . (Masters Thesis). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/102227

Chicago Manual of Style (16th Edition):

Visto, Anni-Laura. “Rauta-aineenvaihduntaan liittyvien geenipolymorfioiden yhteys verenpainetautiin .” 2017. Masters Thesis, Tampere University. Accessed March 03, 2021. https://trepo.tuni.fi/handle/10024/102227.

MLA Handbook (7th Edition):

Visto, Anni-Laura. “Rauta-aineenvaihduntaan liittyvien geenipolymorfioiden yhteys verenpainetautiin .” 2017. Web. 03 Mar 2021.

Vancouver:

Visto A. Rauta-aineenvaihduntaan liittyvien geenipolymorfioiden yhteys verenpainetautiin . [Internet] [Masters thesis]. Tampere University; 2017. [cited 2021 Mar 03]. Available from: https://trepo.tuni.fi/handle/10024/102227.

Council of Science Editors:

Visto A. Rauta-aineenvaihduntaan liittyvien geenipolymorfioiden yhteys verenpainetautiin . [Masters Thesis]. Tampere University; 2017. Available from: https://trepo.tuni.fi/handle/10024/102227


Tampere University

2. Pakkanen, Pihla. Akuutille alkoholihaimatulehdukselle altistavat geenit .

Degree: 2016, Tampere University

 Akuutin haimatulehduksen ilmaantuvuus on Suomessa suurempi kuin monissa muissa Euroopan maissa ja alkoholi aiheuttaa Suomessa 70 % haimatulehdustapauksista. 2-3 % alkoholin suurkuluttajista sairastuu elämänsä aikana… (more)

Subjects/Keywords: akuutti pankreatiitti; geenipolymorfia; mutaatio; patogeneesi

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Pakkanen, P. (2016). Akuutille alkoholihaimatulehdukselle altistavat geenit . (Masters Thesis). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/99137

Chicago Manual of Style (16th Edition):

Pakkanen, Pihla. “Akuutille alkoholihaimatulehdukselle altistavat geenit .” 2016. Masters Thesis, Tampere University. Accessed March 03, 2021. https://trepo.tuni.fi/handle/10024/99137.

MLA Handbook (7th Edition):

Pakkanen, Pihla. “Akuutille alkoholihaimatulehdukselle altistavat geenit .” 2016. Web. 03 Mar 2021.

Vancouver:

Pakkanen P. Akuutille alkoholihaimatulehdukselle altistavat geenit . [Internet] [Masters thesis]. Tampere University; 2016. [cited 2021 Mar 03]. Available from: https://trepo.tuni.fi/handle/10024/99137.

Council of Science Editors:

Pakkanen P. Akuutille alkoholihaimatulehdukselle altistavat geenit . [Masters Thesis]. Tampere University; 2016. Available from: https://trepo.tuni.fi/handle/10024/99137


Tampere University

3. AHO, AUNE. RAD50:n merkitys perinnöllisessä rintasyöpäalttiudessa .

Degree: 2014, Tampere University

 Rintasyöpä on suomalaisten naisten yleisin syöpä. Noin 75 % syövistä on satunnaisesti ilmaantuvia eli ei-perinnöllisiä ja noin 25 % perinnöllisiä. Vain osa perinnölliseen rintasyöpäalttiuteen liittyvistä… (more)

Subjects/Keywords: karsinogeneesi; geeni; mutaatio; MRN-kompleksi; BRCA1/2

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

AHO, A. (2014). RAD50:n merkitys perinnöllisessä rintasyöpäalttiudessa . (Masters Thesis). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/94949

Chicago Manual of Style (16th Edition):

AHO, AUNE. “RAD50:n merkitys perinnöllisessä rintasyöpäalttiudessa .” 2014. Masters Thesis, Tampere University. Accessed March 03, 2021. https://trepo.tuni.fi/handle/10024/94949.

MLA Handbook (7th Edition):

AHO, AUNE. “RAD50:n merkitys perinnöllisessä rintasyöpäalttiudessa .” 2014. Web. 03 Mar 2021.

Vancouver:

AHO A. RAD50:n merkitys perinnöllisessä rintasyöpäalttiudessa . [Internet] [Masters thesis]. Tampere University; 2014. [cited 2021 Mar 03]. Available from: https://trepo.tuni.fi/handle/10024/94949.

Council of Science Editors:

AHO A. RAD50:n merkitys perinnöllisessä rintasyöpäalttiudessa . [Masters Thesis]. Tampere University; 2014. Available from: https://trepo.tuni.fi/handle/10024/94949


Tampere University

4. Peltola, Niina. Fabryn tauti ja perinnölliseen amyloidoosiin liittyvä polyneuropatia idiopaattisen ohutsäieneuropatian aiheuttajina .

Degree: 2017, Tampere University

 Tässä työssä tarkasteltiin potilaita, joilla oli idiopaattinen eli syyltään tuntematon ohutsäieneuropatia. Tutkimuksessa määritettiin, kuinka monella on Fabryn tautiin tai perinnölliseen amyloidoosiin (transtyretiiniamyloidoosi) liittyvä geenimutaatio ohutsäieneuropatian… (more)

Subjects/Keywords: transtyretiiniamyloidoosi; mutaatio; geeni; etiologia; ihobiopsia; tuntokynnysmittaus

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Peltola, N. (2017). Fabryn tauti ja perinnölliseen amyloidoosiin liittyvä polyneuropatia idiopaattisen ohutsäieneuropatian aiheuttajina . (Masters Thesis). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/100590

Chicago Manual of Style (16th Edition):

Peltola, Niina. “Fabryn tauti ja perinnölliseen amyloidoosiin liittyvä polyneuropatia idiopaattisen ohutsäieneuropatian aiheuttajina .” 2017. Masters Thesis, Tampere University. Accessed March 03, 2021. https://trepo.tuni.fi/handle/10024/100590.

MLA Handbook (7th Edition):

Peltola, Niina. “Fabryn tauti ja perinnölliseen amyloidoosiin liittyvä polyneuropatia idiopaattisen ohutsäieneuropatian aiheuttajina .” 2017. Web. 03 Mar 2021.

Vancouver:

Peltola N. Fabryn tauti ja perinnölliseen amyloidoosiin liittyvä polyneuropatia idiopaattisen ohutsäieneuropatian aiheuttajina . [Internet] [Masters thesis]. Tampere University; 2017. [cited 2021 Mar 03]. Available from: https://trepo.tuni.fi/handle/10024/100590.

Council of Science Editors:

Peltola N. Fabryn tauti ja perinnölliseen amyloidoosiin liittyvä polyneuropatia idiopaattisen ohutsäieneuropatian aiheuttajina . [Masters Thesis]. Tampere University; 2017. Available from: https://trepo.tuni.fi/handle/10024/100590


Tampere University

5. Parhiala, Mikael. Analysis of the effects of mitochondrial mutator system in Drosophila melanogaster .

Degree: 2015, Tampere University

Subjects/Keywords: Mitokondrio; banaanikärpänen; mutaatio; restriktioentsyymi; EcoBI

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Parhiala, M. (2015). Analysis of the effects of mitochondrial mutator system in Drosophila melanogaster . (Masters Thesis). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/98200

Chicago Manual of Style (16th Edition):

Parhiala, Mikael. “Analysis of the effects of mitochondrial mutator system in Drosophila melanogaster .” 2015. Masters Thesis, Tampere University. Accessed March 03, 2021. https://trepo.tuni.fi/handle/10024/98200.

MLA Handbook (7th Edition):

Parhiala, Mikael. “Analysis of the effects of mitochondrial mutator system in Drosophila melanogaster .” 2015. Web. 03 Mar 2021.

Vancouver:

Parhiala M. Analysis of the effects of mitochondrial mutator system in Drosophila melanogaster . [Internet] [Masters thesis]. Tampere University; 2015. [cited 2021 Mar 03]. Available from: https://trepo.tuni.fi/handle/10024/98200.

Council of Science Editors:

Parhiala M. Analysis of the effects of mitochondrial mutator system in Drosophila melanogaster . [Masters Thesis]. Tampere University; 2015. Available from: https://trepo.tuni.fi/handle/10024/98200


University of Helsinki

6. Andersson, Birgitta. Dynaamisten mutaatioiden aiheuttamia ihmisen perinnöllisiä sairauksia.

Degree: 1995, University of Helsinki

Subjects/Keywords: epästabiili DNA; dynaaminen mutaatio; antisipaatio; Perinnöllisyystiede; epästabiili DNA; dynaaminen mutaatio; antisipaatio

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Andersson, B. (1995). Dynaamisten mutaatioiden aiheuttamia ihmisen perinnöllisiä sairauksia. (Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/157640

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Andersson, Birgitta. “Dynaamisten mutaatioiden aiheuttamia ihmisen perinnöllisiä sairauksia.” 1995. Thesis, University of Helsinki. Accessed March 03, 2021. http://hdl.handle.net/10138/157640.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Andersson, Birgitta. “Dynaamisten mutaatioiden aiheuttamia ihmisen perinnöllisiä sairauksia.” 1995. Web. 03 Mar 2021.

Vancouver:

Andersson B. Dynaamisten mutaatioiden aiheuttamia ihmisen perinnöllisiä sairauksia. [Internet] [Thesis]. University of Helsinki; 1995. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10138/157640.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Andersson B. Dynaamisten mutaatioiden aiheuttamia ihmisen perinnöllisiä sairauksia. [Thesis]. University of Helsinki; 1995. Available from: http://hdl.handle.net/10138/157640

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Tampere University

7. Nurminen, Anssi. A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma .

Degree: 2018, Tampere University

 Geneettisen testauksen kustannusten laskiessa, pullonkaulaksi saatavilla olevan tiedon hyödyntämiseen on muodostumassa tietämyksemme eri geneettisten variaatioiden ja mutaatioden merkityksestä. Jokaisella henkilöllä on satoja, yksilöllisiä variaatioita perimässään… (more)

Subjects/Keywords: DNA polymeraasi gamma ; POLG ; mutaatio ; proteiinirakenne ; patogeenisyys ; DNA polymerase gamma ; mutation ; protein structure ; pathogenicity

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Nurminen, A. (2018). A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/102657

Chicago Manual of Style (16th Edition):

Nurminen, Anssi. “A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma .” 2018. Doctoral Dissertation, Tampere University. Accessed March 03, 2021. https://trepo.tuni.fi/handle/10024/102657.

MLA Handbook (7th Edition):

Nurminen, Anssi. “A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma .” 2018. Web. 03 Mar 2021.

Vancouver:

Nurminen A. A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma . [Internet] [Doctoral dissertation]. Tampere University; 2018. [cited 2021 Mar 03]. Available from: https://trepo.tuni.fi/handle/10024/102657.

Council of Science Editors:

Nurminen A. A Bioinformatics Approach to Analyzing the Pathogenicity of Mutations by Using Protein Structure Information : A Study on DNA Polymerase Gamma . [Doctoral Dissertation]. Tampere University; 2018. Available from: https://trepo.tuni.fi/handle/10024/102657


University of Helsinki

8. Saarela, Olli. Perunan Y-viruksen rekombinanttikantojen kyky infektoida kolmea eri Solanaceae-heimon kasvilajia.

Degree: Department of Agricultural Sciences; Helsingfors universitet, Agrikultur- och forstvetenskapliga fakulteten, Institutionen för lantsbruksvetenskaper, 2016, University of Helsinki

 Perunan Y-virus (PVY) kuuluu potyviruksiin, joka on suurin kasvivirusten suku. PVY on yksi taloudellisesti tärkeimpiä koisokasvien (Solanaceae) taudinaiheuttajia. Perunalla PVY on tärkeä ongelma varsinkin siemenperunaviljelyssä.… (more)

Subjects/Keywords: PVY; PTNRD; virus; rekombinantti; mutaatio; peruna; tomaatti; paprika; Växtproduktionsvetenskap; Plant Production Science; Kasvintuotantotieteet

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Saarela, O. (2016). Perunan Y-viruksen rekombinanttikantojen kyky infektoida kolmea eri Solanaceae-heimon kasvilajia. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/161662

Chicago Manual of Style (16th Edition):

Saarela, Olli. “Perunan Y-viruksen rekombinanttikantojen kyky infektoida kolmea eri Solanaceae-heimon kasvilajia.” 2016. Masters Thesis, University of Helsinki. Accessed March 03, 2021. http://hdl.handle.net/10138/161662.

MLA Handbook (7th Edition):

Saarela, Olli. “Perunan Y-viruksen rekombinanttikantojen kyky infektoida kolmea eri Solanaceae-heimon kasvilajia.” 2016. Web. 03 Mar 2021.

Vancouver:

Saarela O. Perunan Y-viruksen rekombinanttikantojen kyky infektoida kolmea eri Solanaceae-heimon kasvilajia. [Internet] [Masters thesis]. University of Helsinki; 2016. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10138/161662.

Council of Science Editors:

Saarela O. Perunan Y-viruksen rekombinanttikantojen kyky infektoida kolmea eri Solanaceae-heimon kasvilajia. [Masters Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/161662


University of Helsinki

9. Rämö, Joel. The Contribution of GWAS Loci in Familial Dyslipidemias.

Degree: Medicinska fakulteten, 2016, University of Helsinki

 Familial combined hyperlipidemia (FCH) is a complex and common familial dyslipidemia characterized by elevated total cholesterol and/or triglyceride levels with over five-fold risk of coronary… (more)

Subjects/Keywords: familiaalinen kombinoitu hyperlipidemia; kolesteroli; triglyseridi; dyslipidemia; genetiikka; perinnöllinen; polygeeninen; mutaatio; Public Health; Kansanterveystiede; Folkhälsovetenskap

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Rämö, J. (2016). The Contribution of GWAS Loci in Familial Dyslipidemias. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/169759

Chicago Manual of Style (16th Edition):

Rämö, Joel. “The Contribution of GWAS Loci in Familial Dyslipidemias.” 2016. Masters Thesis, University of Helsinki. Accessed March 03, 2021. http://hdl.handle.net/10138/169759.

MLA Handbook (7th Edition):

Rämö, Joel. “The Contribution of GWAS Loci in Familial Dyslipidemias.” 2016. Web. 03 Mar 2021.

Vancouver:

Rämö J. The Contribution of GWAS Loci in Familial Dyslipidemias. [Internet] [Masters thesis]. University of Helsinki; 2016. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10138/169759.

Council of Science Editors:

Rämö J. The Contribution of GWAS Loci in Familial Dyslipidemias. [Masters Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/169759


University of Oulu

10. Peltonen, J. (Jenni). TP53 as clinical marker in head and neck cancer.

Degree: 2011, University of Oulu

Abstract The prognosis of patients with head and neck squamous cell carcinoma has improved only little during the last decades. Clinical markers for the biological… (more)

Subjects/Keywords: TP53 mutation; head and neck cancer; prognostic marker; survival; TP53 -mutaatio; ennuste; merkkiaine; pään ja kaulan alueen syöpä

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Peltonen, J. (. (2011). TP53 as clinical marker in head and neck cancer. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514295409

Chicago Manual of Style (16th Edition):

Peltonen, J (Jenni). “TP53 as clinical marker in head and neck cancer.” 2011. Doctoral Dissertation, University of Oulu. Accessed March 03, 2021. http://urn.fi/urn:isbn:9789514295409.

MLA Handbook (7th Edition):

Peltonen, J (Jenni). “TP53 as clinical marker in head and neck cancer.” 2011. Web. 03 Mar 2021.

Vancouver:

Peltonen J(. TP53 as clinical marker in head and neck cancer. [Internet] [Doctoral dissertation]. University of Oulu; 2011. [cited 2021 Mar 03]. Available from: http://urn.fi/urn:isbn:9789514295409.

Council of Science Editors:

Peltonen J(. TP53 as clinical marker in head and neck cancer. [Doctoral Dissertation]. University of Oulu; 2011. Available from: http://urn.fi/urn:isbn:9789514295409


University of Helsinki

11. Mustjoki, Satu. Somatic mutations in clonally expanded cytotoxic T lymphocytes in patients with newly diagnosed rheumatoid arthritis.

Degree: Medicinska fakulteten, 2017, University of Helsinki

 Kaikissa jakautuvissa solutyypeissä tapahtuu niiden elinkaaren aikana perimän muutoksia eli somaattisia mutaatioita. Somaattiset mutaatiot aiheuttavat syöpää, mutta niiden esiintyvyyttä tai merkitystä muissa sairauksissa kuin syövässä… (more)

Subjects/Keywords: T-solu; CD8+ T-solu; lymfosyytti; Nivelreuma; DNA-mutaatioanalyysi; Mutaatio; CD8-solut; Internal Medicine; Sisätaudit; Inre medicin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Mustjoki, S. (2017). Somatic mutations in clonally expanded cytotoxic T lymphocytes in patients with newly diagnosed rheumatoid arthritis. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/228716

Chicago Manual of Style (16th Edition):

Mustjoki, Satu. “Somatic mutations in clonally expanded cytotoxic T lymphocytes in patients with newly diagnosed rheumatoid arthritis.” 2017. Masters Thesis, University of Helsinki. Accessed March 03, 2021. http://hdl.handle.net/10138/228716.

MLA Handbook (7th Edition):

Mustjoki, Satu. “Somatic mutations in clonally expanded cytotoxic T lymphocytes in patients with newly diagnosed rheumatoid arthritis.” 2017. Web. 03 Mar 2021.

Vancouver:

Mustjoki S. Somatic mutations in clonally expanded cytotoxic T lymphocytes in patients with newly diagnosed rheumatoid arthritis. [Internet] [Masters thesis]. University of Helsinki; 2017. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10138/228716.

Council of Science Editors:

Mustjoki S. Somatic mutations in clonally expanded cytotoxic T lymphocytes in patients with newly diagnosed rheumatoid arthritis. [Masters Thesis]. University of Helsinki; 2017. Available from: http://hdl.handle.net/10138/228716


Tampere University

12. Taskinen, Barbara. Protein Engineering of Avidin by Rational Design and DNA Family Shuffling .

Degree: 2014, Tampere University

 Parempia proteiineja laboratoriossa ohjatun evoluution avulla Eliöiden perimässä tapahtuvat muutokset mahdollistavat evoluution. Perimän muutokset, mutaatiot, muokkaavat perimän koodaamien proteiinien ominaisuuksia. Proteiinit ovat molekyylikoneita, jotka ovat… (more)

Subjects/Keywords: avidiini ; DNA:n sekoittaminen geeniperheen sisällä ; faagiesittely-menetelmä ; proteiini ; DNA mutaatio ; avidin ; DNA shuffling ; phage display ; proteins ; DNA mutagenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Taskinen, B. (2014). Protein Engineering of Avidin by Rational Design and DNA Family Shuffling . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/94865

Chicago Manual of Style (16th Edition):

Taskinen, Barbara. “Protein Engineering of Avidin by Rational Design and DNA Family Shuffling .” 2014. Doctoral Dissertation, Tampere University. Accessed March 03, 2021. https://trepo.tuni.fi/handle/10024/94865.

MLA Handbook (7th Edition):

Taskinen, Barbara. “Protein Engineering of Avidin by Rational Design and DNA Family Shuffling .” 2014. Web. 03 Mar 2021.

Vancouver:

Taskinen B. Protein Engineering of Avidin by Rational Design and DNA Family Shuffling . [Internet] [Doctoral dissertation]. Tampere University; 2014. [cited 2021 Mar 03]. Available from: https://trepo.tuni.fi/handle/10024/94865.

Council of Science Editors:

Taskinen B. Protein Engineering of Avidin by Rational Design and DNA Family Shuffling . [Doctoral Dissertation]. Tampere University; 2014. Available from: https://trepo.tuni.fi/handle/10024/94865


Tampere University

13. Niranjan, Yashavanthi. Functional Characterization of the Kinase and Pseudokinase Domains in the Janus Tyrosine Kinase (JAK) 2 .

Degree: 2014, Tampere University

 Hematopoieesin eli verenmuodostuksen aikana liukoiset sytokiinimolekyylit säätelevät tarkasti solujen kasvua ja erilaistumista. Sytokiinit aktivoivat JAK/STAT-signaalinvälitysreitin, jolla on merkittävä rooli verisolujen kehityksessä. Sytokiinit ja JAK/STAT-reitti vaikuttavat… (more)

Subjects/Keywords: JAK2-proteiini ; karakterisointi ; sääntely ; polysytemian mutaatio V617F ; JAK2 regulation ; ATP-binding ; polycythemia vera V617F mutation ; characterization

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Niranjan, Y. (2014). Functional Characterization of the Kinase and Pseudokinase Domains in the Janus Tyrosine Kinase (JAK) 2 . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/95184

Chicago Manual of Style (16th Edition):

Niranjan, Yashavanthi. “Functional Characterization of the Kinase and Pseudokinase Domains in the Janus Tyrosine Kinase (JAK) 2 .” 2014. Doctoral Dissertation, Tampere University. Accessed March 03, 2021. https://trepo.tuni.fi/handle/10024/95184.

MLA Handbook (7th Edition):

Niranjan, Yashavanthi. “Functional Characterization of the Kinase and Pseudokinase Domains in the Janus Tyrosine Kinase (JAK) 2 .” 2014. Web. 03 Mar 2021.

Vancouver:

Niranjan Y. Functional Characterization of the Kinase and Pseudokinase Domains in the Janus Tyrosine Kinase (JAK) 2 . [Internet] [Doctoral dissertation]. Tampere University; 2014. [cited 2021 Mar 03]. Available from: https://trepo.tuni.fi/handle/10024/95184.

Council of Science Editors:

Niranjan Y. Functional Characterization of the Kinase and Pseudokinase Domains in the Janus Tyrosine Kinase (JAK) 2 . [Doctoral Dissertation]. Tampere University; 2014. Available from: https://trepo.tuni.fi/handle/10024/95184


University of Helsinki

14. Laitinen, Päivi. Pitkä QT - oireyhtymälle altistavat HERG-geenin mutaatiot suomalaisissa suvuissa.

Degree: 2000, University of Helsinki

Subjects/Keywords: HERG; pitkä QT -oireyhtymä; ionikanavat; sekvensointi; mutaatio; Perinnöllisyystiede; HERG; pitkä QT -oireyhtymä; ionikanavat; sekvensointi; mutaatio

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Laitinen, P. (2000). Pitkä QT - oireyhtymälle altistavat HERG-geenin mutaatiot suomalaisissa suvuissa. (Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/156974

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Laitinen, Päivi. “Pitkä QT - oireyhtymälle altistavat HERG-geenin mutaatiot suomalaisissa suvuissa.” 2000. Thesis, University of Helsinki. Accessed March 03, 2021. http://hdl.handle.net/10138/156974.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Laitinen, Päivi. “Pitkä QT - oireyhtymälle altistavat HERG-geenin mutaatiot suomalaisissa suvuissa.” 2000. Web. 03 Mar 2021.

Vancouver:

Laitinen P. Pitkä QT - oireyhtymälle altistavat HERG-geenin mutaatiot suomalaisissa suvuissa. [Internet] [Thesis]. University of Helsinki; 2000. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10138/156974.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Laitinen P. Pitkä QT - oireyhtymälle altistavat HERG-geenin mutaatiot suomalaisissa suvuissa. [Thesis]. University of Helsinki; 2000. Available from: http://hdl.handle.net/10138/156974

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Helsinki

15. Outola, Mika. SSO1- ja SSO2-geenien kopioluvun noston vaikutus Saccharomyces cerevisiae-hiivan heterologisen proteiinin erityskykyyn.

Degree: 1993, University of Helsinki

Subjects/Keywords: SSO1- ja SSO2-geeni; heterologinen proteiinien tuotto; Sec1-mutaatio; Perinnöllisyystiede; SSO1- ja SSO2-geeni; heterologinen proteiinien tuotto; Sec1-mutaatio

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Outola, M. (1993). SSO1- ja SSO2-geenien kopioluvun noston vaikutus Saccharomyces cerevisiae-hiivan heterologisen proteiinin erityskykyyn. (Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/158040

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Outola, Mika. “SSO1- ja SSO2-geenien kopioluvun noston vaikutus Saccharomyces cerevisiae-hiivan heterologisen proteiinin erityskykyyn.” 1993. Thesis, University of Helsinki. Accessed March 03, 2021. http://hdl.handle.net/10138/158040.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Outola, Mika. “SSO1- ja SSO2-geenien kopioluvun noston vaikutus Saccharomyces cerevisiae-hiivan heterologisen proteiinin erityskykyyn.” 1993. Web. 03 Mar 2021.

Vancouver:

Outola M. SSO1- ja SSO2-geenien kopioluvun noston vaikutus Saccharomyces cerevisiae-hiivan heterologisen proteiinin erityskykyyn. [Internet] [Thesis]. University of Helsinki; 1993. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10138/158040.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Outola M. SSO1- ja SSO2-geenien kopioluvun noston vaikutus Saccharomyces cerevisiae-hiivan heterologisen proteiinin erityskykyyn. [Thesis]. University of Helsinki; 1993. Available from: http://hdl.handle.net/10138/158040

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Oulu

16. Stefanius, K. (Karoliina). Colorectal carcinogenesis via serrated route.

Degree: 2011, University of Oulu

Abstract Colorectal cancer is the third most common cancer in the developed countries. Originally, development of CRC was thought to proceed by a sequence of… (more)

Subjects/Keywords: DNA methylation; DNA mismatch repair; adenocarcinoma; adenoma; colorectal cancer; epigenetic; histopathology; immunohistochemistry; microsatellite instability; mutation; serrated; DNA metylaatio; DNA mismatch-korjaus; adenokarsinooma; adenooma; histopatologia; immunohistokemia; kolorektaalisyöpä; mikrosatelliitti-instabiliteetti; mutaatio; sahalaitainen

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Stefanius, K. (. (2011). Colorectal carcinogenesis via serrated route. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514293993

Chicago Manual of Style (16th Edition):

Stefanius, K (Karoliina). “Colorectal carcinogenesis via serrated route.” 2011. Doctoral Dissertation, University of Oulu. Accessed March 03, 2021. http://urn.fi/urn:isbn:9789514293993.

MLA Handbook (7th Edition):

Stefanius, K (Karoliina). “Colorectal carcinogenesis via serrated route.” 2011. Web. 03 Mar 2021.

Vancouver:

Stefanius K(. Colorectal carcinogenesis via serrated route. [Internet] [Doctoral dissertation]. University of Oulu; 2011. [cited 2021 Mar 03]. Available from: http://urn.fi/urn:isbn:9789514293993.

Council of Science Editors:

Stefanius K(. Colorectal carcinogenesis via serrated route. [Doctoral Dissertation]. University of Oulu; 2011. Available from: http://urn.fi/urn:isbn:9789514293993


University of Oulu

17. Haanpää, M. (Maria). Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes.

Degree: 2014, University of Oulu

Abstract Around 5−10% of all breast cancer cases are estimated to result from a strong hereditary predisposition to the disease. However, mutations in the currently… (more)

Subjects/Keywords: DNA damage response; DNA repair; Fanconi anaemia; breast cancer; genetic predisposition to disease; germline mutation; DNA-korjaus; DNA-vauriovaste; Fanconin anemia; ituradan mutaatio; perinnöllinen rintasyöpäalttius; rintasyöpä; AATF; MRG15; PALB2

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Haanpää, M. (. (2014). Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789526204581

Chicago Manual of Style (16th Edition):

Haanpää, M (Maria). “Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes.” 2014. Doctoral Dissertation, University of Oulu. Accessed March 03, 2021. http://urn.fi/urn:isbn:9789526204581.

MLA Handbook (7th Edition):

Haanpää, M (Maria). “Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes.” 2014. Web. 03 Mar 2021.

Vancouver:

Haanpää M(. Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes. [Internet] [Doctoral dissertation]. University of Oulu; 2014. [cited 2021 Mar 03]. Available from: http://urn.fi/urn:isbn:9789526204581.

Council of Science Editors:

Haanpää M(. Hereditary predisposition to breast cancer – with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes. [Doctoral Dissertation]. University of Oulu; 2014. Available from: http://urn.fi/urn:isbn:9789526204581


Tampere University

18. Khan, Sofia. Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models .

Degree: Lääketieteellisen teknologian instituutti - Institute of Medical Technology, 2010, Tampere University

 Valkuaisaineet eli proteiinit ovat välttämättömiä elämää ylläpitäviä molekyylejä. Kaikkien proteiinien rakennusohjeet ovat perimässä ja ne rakentuvat 20 erilaisesta aminohaposta, joiden ominaisuudet ja järjestys määrittelevät proteiinin… (more)

Subjects/Keywords: mutaatio ; proteiini ; proteiinirakenne ; stabiilisuus ; homologiamallinnus ; missense mutation ; protein structure ; stability ; homology modeling

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Khan, S. (2010). Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/66579

Chicago Manual of Style (16th Edition):

Khan, Sofia. “Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models .” 2010. Doctoral Dissertation, Tampere University. Accessed March 03, 2021. https://trepo.tuni.fi/handle/10024/66579.

MLA Handbook (7th Edition):

Khan, Sofia. “Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models .” 2010. Web. 03 Mar 2021.

Vancouver:

Khan S. Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models . [Internet] [Doctoral dissertation]. Tampere University; 2010. [cited 2021 Mar 03]. Available from: https://trepo.tuni.fi/handle/10024/66579.

Council of Science Editors:

Khan S. Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models . [Doctoral Dissertation]. Tampere University; 2010. Available from: https://trepo.tuni.fi/handle/10024/66579


Tampere University

19. Thusberg, Janita. Molecular effects of missense mutations - Bioinformatics analysis of genetic defects .

Degree: Lääketieteellisen teknologian instituutti - Institute of Medical Technology, 2010, Tampere University

 Tietoa ihmisen geneettisistä eroista saadaan nykyaikaisilla menetelmillä nopeasti, mutta niiden mahdollisista yhteyksistä sairauksiin ja geneettisten sairauksien molekyylitason mekanismeista ei ymmärretä vielä riittävästi. Tämä johtuu siitä,… (more)

Subjects/Keywords: bioinformatiikka ; mutaatio ; variaatio ; perinnölliset sairaudet ; bioinformatics ; mutation ; SNP ; hereditary disease

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Thusberg, J. (2010). Molecular effects of missense mutations - Bioinformatics analysis of genetic defects . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/66629

Chicago Manual of Style (16th Edition):

Thusberg, Janita. “Molecular effects of missense mutations - Bioinformatics analysis of genetic defects .” 2010. Doctoral Dissertation, Tampere University. Accessed March 03, 2021. https://trepo.tuni.fi/handle/10024/66629.

MLA Handbook (7th Edition):

Thusberg, Janita. “Molecular effects of missense mutations - Bioinformatics analysis of genetic defects .” 2010. Web. 03 Mar 2021.

Vancouver:

Thusberg J. Molecular effects of missense mutations - Bioinformatics analysis of genetic defects . [Internet] [Doctoral dissertation]. Tampere University; 2010. [cited 2021 Mar 03]. Available from: https://trepo.tuni.fi/handle/10024/66629.

Council of Science Editors:

Thusberg J. Molecular effects of missense mutations - Bioinformatics analysis of genetic defects . [Doctoral Dissertation]. Tampere University; 2010. Available from: https://trepo.tuni.fi/handle/10024/66629


University of Oulu

20. Vuorela, M. (Mikko). Role of the RNF8, UBC13, MMS2 and RAD51C DNA damage response genes and rare copy number variants in hereditary predisposition to breast cancer.

Degree: 2013, University of Oulu

Abstract Mutations in the currently known breast cancer susceptibility genes account for only 25–30% of all familial cases. Novel susceptibility genes can be identified by… (more)

Subjects/Keywords: DNA copy number variations; DNA mutational analysis; DNA-binding proteins; Fanconi anemia; breast neoplasms; estrogens; genetics; germ-line mutation; tumor suppressor protein p53; ubiquitin-conjugating enzymes; DNA-kopiomäärän vaihtelut; DNA-mutaatioanalyysi; DNA:n sitojaproteiinit; Fanconin anemia; estrogeenit; ituradan mutaatio; kasvainsalpaajaproteiini p53; perinnöllisyystiede; rinnan kasvaimet; ubikitiini-konjugaatioentsyymit

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Vuorela, M. (. (2013). Role of the RNF8, UBC13, MMS2 and RAD51C DNA damage response genes and rare copy number variants in hereditary predisposition to breast cancer. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789526203096

Chicago Manual of Style (16th Edition):

Vuorela, M (Mikko). “Role of the RNF8, UBC13, MMS2 and RAD51C DNA damage response genes and rare copy number variants in hereditary predisposition to breast cancer.” 2013. Doctoral Dissertation, University of Oulu. Accessed March 03, 2021. http://urn.fi/urn:isbn:9789526203096.

MLA Handbook (7th Edition):

Vuorela, M (Mikko). “Role of the RNF8, UBC13, MMS2 and RAD51C DNA damage response genes and rare copy number variants in hereditary predisposition to breast cancer.” 2013. Web. 03 Mar 2021.

Vancouver:

Vuorela M(. Role of the RNF8, UBC13, MMS2 and RAD51C DNA damage response genes and rare copy number variants in hereditary predisposition to breast cancer. [Internet] [Doctoral dissertation]. University of Oulu; 2013. [cited 2021 Mar 03]. Available from: http://urn.fi/urn:isbn:9789526203096.

Council of Science Editors:

Vuorela M(. Role of the RNF8, UBC13, MMS2 and RAD51C DNA damage response genes and rare copy number variants in hereditary predisposition to breast cancer. [Doctoral Dissertation]. University of Oulu; 2013. Available from: http://urn.fi/urn:isbn:9789526203096


University of Oulu

21. Bose, M. (Muthiah). Molecular and functional characterization of ABRAXAS and PALB2 genes in hereditary breast cancer predisposition.

Degree: 2019, University of Oulu

Abstract Hereditary mutations in DNA damage response (DDR) genes often lead to genomic instability and ultimately tumor development. However, the molecular mechanism of how these… (more)

Subjects/Keywords: DNA damage response; DNA double-strand break repair; G2-M checkpoint; breast cancer; cancer genetics; cancer predisposition; heterozygous germline mutation; replication stress; tumorigenesis; DNA-korjaus; DNA-vauriovaste; G2/M-tarkastuspiste; heterotsygoottinen ituradan mutaatio; replikaatiostressi; rintasyöpä; syöpäalttius; syöpägenetiikka; syövän kehitys; ABRAXAS; BRCA1; CtIP; PALB2

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bose, M. (. (2019). Molecular and functional characterization of ABRAXAS and PALB2 genes in hereditary breast cancer predisposition. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789526218656

Chicago Manual of Style (16th Edition):

Bose, M (Muthiah). “Molecular and functional characterization of ABRAXAS and PALB2 genes in hereditary breast cancer predisposition.” 2019. Doctoral Dissertation, University of Oulu. Accessed March 03, 2021. http://urn.fi/urn:isbn:9789526218656.

MLA Handbook (7th Edition):

Bose, M (Muthiah). “Molecular and functional characterization of ABRAXAS and PALB2 genes in hereditary breast cancer predisposition.” 2019. Web. 03 Mar 2021.

Vancouver:

Bose M(. Molecular and functional characterization of ABRAXAS and PALB2 genes in hereditary breast cancer predisposition. [Internet] [Doctoral dissertation]. University of Oulu; 2019. [cited 2021 Mar 03]. Available from: http://urn.fi/urn:isbn:9789526218656.

Council of Science Editors:

Bose M(. Molecular and functional characterization of ABRAXAS and PALB2 genes in hereditary breast cancer predisposition. [Doctoral Dissertation]. University of Oulu; 2019. Available from: http://urn.fi/urn:isbn:9789526218656

.