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:(Membrane Proteins genetics). Showing records 1 – 27 of 27 total matches.

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters


University of California – Riverside

1. Qureshi, Nadia Naeem. Characterization of Beta-lactam Resistance in the Gastric Pathogen Helicobacter pylori.

Degree: Genetics, Genomics and Bioinformatics, 2010, University of California – Riverside

 Helicobacter pylori is a major cause of peptic ulcer disease and potentially stomach cancer. Treatment of patients with gastritis is warranted and normally done with… (more)

Subjects/Keywords: Biology, Microbiology; Biology, Molecular; Biology, Genetics; Amoxicillin resistance; Beta-lactam; Helicobacter pylori; Homology Modeling; Outer membrane proteins; Penicillin Binding Proteins

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Qureshi, N. N. (2010). Characterization of Beta-lactam Resistance in the Gastric Pathogen Helicobacter pylori. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/6s43c7qv

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):

Qureshi, Nadia Naeem. “Characterization of Beta-lactam Resistance in the Gastric Pathogen Helicobacter pylori.” 2010. Thesis, University of California – Riverside. Accessed December 08, 2019. http://www.escholarship.org/uc/item/6s43c7qv.

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

MLA Handbook (7th Edition):

Qureshi, Nadia Naeem. “Characterization of Beta-lactam Resistance in the Gastric Pathogen Helicobacter pylori.” 2010. Web. 08 Dec 2019.

Vancouver:

Qureshi NN. Characterization of Beta-lactam Resistance in the Gastric Pathogen Helicobacter pylori. [Internet] [Thesis]. University of California – Riverside; 2010. [cited 2019 Dec 08]. Available from: http://www.escholarship.org/uc/item/6s43c7qv.

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

Council of Science Editors:

Qureshi NN. Characterization of Beta-lactam Resistance in the Gastric Pathogen Helicobacter pylori. [Thesis]. University of California – Riverside; 2010. Available from: http://www.escholarship.org/uc/item/6s43c7qv

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

2. Spencer, Emily. Expanding Genetic Analysis Of Patients With A Neurofibromatosis Type 1-Like Phenotype.

Degree: 2011, University of Alabama – Birmingham

Neurofibromatosis Type 1, a common autosomal dominant disorder with neuro-cardio- facio-cutaneous presentation, is caused by mutations in the NF1 gene, a negative regulator of RAS-MAPK… (more)

Subjects/Keywords: Cafe-au-Lait Spots – genetics.<; br>; Gene Dosage – genetics.<; br>; Intracellular Signaling Peptides and Proteins – genetics.<; br>; Membrane Proteins – genetics<; br>; Neurofibromatosis 1 – diagnosis.<; br>; Neurofibromatosis 1 – genetics<; br>; Sequence Deletion – genetics.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Spencer, E. (2011). Expanding Genetic Analysis Of Patients With A Neurofibromatosis Type 1-Like Phenotype. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1638

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):

Spencer, Emily. “Expanding Genetic Analysis Of Patients With A Neurofibromatosis Type 1-Like Phenotype.” 2011. Thesis, University of Alabama – Birmingham. Accessed December 08, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1638.

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

MLA Handbook (7th Edition):

Spencer, Emily. “Expanding Genetic Analysis Of Patients With A Neurofibromatosis Type 1-Like Phenotype.” 2011. Web. 08 Dec 2019.

Vancouver:

Spencer E. Expanding Genetic Analysis Of Patients With A Neurofibromatosis Type 1-Like Phenotype. [Internet] [Thesis]. University of Alabama – Birmingham; 2011. [cited 2019 Dec 08]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1638.

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

Council of Science Editors:

Spencer E. Expanding Genetic Analysis Of Patients With A Neurofibromatosis Type 1-Like Phenotype. [Thesis]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1638

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


University of Hong Kong

3. 楊新海; Yang, Xinhai. Latent membrane protein 1 of Epstein-barr virus induces cell proliferation and participates in the inhibition of replicativesenescence.

Degree: PhD, 2000, University of Hong Kong

published_or_final_version

Microbiology

Doctoral

Doctor of Philosophy

Subjects/Keywords: Membrane proteins - Genetics.; Epstein-barr virus.; Cell proliferation.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

楊新海; Yang, X. (2000). Latent membrane protein 1 of Epstein-barr virus induces cell proliferation and participates in the inhibition of replicativesenescence. (Doctoral Dissertation). University of Hong Kong. Retrieved from Yang, X. [楊新海]. (2000). Latent membrane protein 1 of Epstein-barr virus induces cell proliferation and participates in the inhibition of replicative senescence. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124125 ; http://dx.doi.org/10.5353/th_b3124125 ; http://hdl.handle.net/10722/35999

Chicago Manual of Style (16th Edition):

楊新海; Yang, Xinhai. “Latent membrane protein 1 of Epstein-barr virus induces cell proliferation and participates in the inhibition of replicativesenescence.” 2000. Doctoral Dissertation, University of Hong Kong. Accessed December 08, 2019. Yang, X. [楊新海]. (2000). Latent membrane protein 1 of Epstein-barr virus induces cell proliferation and participates in the inhibition of replicative senescence. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124125 ; http://dx.doi.org/10.5353/th_b3124125 ; http://hdl.handle.net/10722/35999.

MLA Handbook (7th Edition):

楊新海; Yang, Xinhai. “Latent membrane protein 1 of Epstein-barr virus induces cell proliferation and participates in the inhibition of replicativesenescence.” 2000. Web. 08 Dec 2019.

Vancouver:

楊新海; Yang X. Latent membrane protein 1 of Epstein-barr virus induces cell proliferation and participates in the inhibition of replicativesenescence. [Internet] [Doctoral dissertation]. University of Hong Kong; 2000. [cited 2019 Dec 08]. Available from: Yang, X. [楊新海]. (2000). Latent membrane protein 1 of Epstein-barr virus induces cell proliferation and participates in the inhibition of replicative senescence. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124125 ; http://dx.doi.org/10.5353/th_b3124125 ; http://hdl.handle.net/10722/35999.

Council of Science Editors:

楊新海; Yang X. Latent membrane protein 1 of Epstein-barr virus induces cell proliferation and participates in the inhibition of replicativesenescence. [Doctoral Dissertation]. University of Hong Kong; 2000. Available from: Yang, X. [楊新海]. (2000). Latent membrane protein 1 of Epstein-barr virus induces cell proliferation and participates in the inhibition of replicative senescence. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3124125 ; http://dx.doi.org/10.5353/th_b3124125 ; http://hdl.handle.net/10722/35999


University of Hong Kong

4. Chen, Qinfang. Expression of acyl-coenzyme A binding proteins ACBP6, ACBP1 and ACBP2 in Arabidopsis.

Degree: PhD, 2010, University of Hong Kong

published_or_final_version

Biological Sciences

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Chye, ML.

Subjects/Keywords: Arabidopsis thaliana - Genetics.; Acetylcoenzyme A.; Membrane proteins.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chen, Q. (2010). Expression of acyl-coenzyme A binding proteins ACBP6, ACBP1 and ACBP2 in Arabidopsis. (Doctoral Dissertation). University of Hong Kong. Retrieved from Chen, Q. [陈琴芳]. (2010). Expression of acyl-coenzyme A binding proteins ACBP6, ACBP1 and ACBP2 in Arabidopsis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4381367 ; http://dx.doi.org/10.5353/th_b4381367 ; http://hdl.handle.net/10722/182384

Chicago Manual of Style (16th Edition):

Chen, Qinfang. “Expression of acyl-coenzyme A binding proteins ACBP6, ACBP1 and ACBP2 in Arabidopsis.” 2010. Doctoral Dissertation, University of Hong Kong. Accessed December 08, 2019. Chen, Q. [陈琴芳]. (2010). Expression of acyl-coenzyme A binding proteins ACBP6, ACBP1 and ACBP2 in Arabidopsis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4381367 ; http://dx.doi.org/10.5353/th_b4381367 ; http://hdl.handle.net/10722/182384.

MLA Handbook (7th Edition):

Chen, Qinfang. “Expression of acyl-coenzyme A binding proteins ACBP6, ACBP1 and ACBP2 in Arabidopsis.” 2010. Web. 08 Dec 2019.

Vancouver:

Chen Q. Expression of acyl-coenzyme A binding proteins ACBP6, ACBP1 and ACBP2 in Arabidopsis. [Internet] [Doctoral dissertation]. University of Hong Kong; 2010. [cited 2019 Dec 08]. Available from: Chen, Q. [陈琴芳]. (2010). Expression of acyl-coenzyme A binding proteins ACBP6, ACBP1 and ACBP2 in Arabidopsis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4381367 ; http://dx.doi.org/10.5353/th_b4381367 ; http://hdl.handle.net/10722/182384.

Council of Science Editors:

Chen Q. Expression of acyl-coenzyme A binding proteins ACBP6, ACBP1 and ACBP2 in Arabidopsis. [Doctoral Dissertation]. University of Hong Kong; 2010. Available from: Chen, Q. [陈琴芳]. (2010). Expression of acyl-coenzyme A binding proteins ACBP6, ACBP1 and ACBP2 in Arabidopsis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4381367 ; http://dx.doi.org/10.5353/th_b4381367 ; http://hdl.handle.net/10722/182384


University of Oxford

5. Hill, Jamie Richard. Fold recognition and alignment in the 'twilight zone'.

Degree: PhD, 2013, University of Oxford

 At present, the most accurate approach to predicting protein structure, comparative modelling, builds a model of a target sequence using known protein structures as templates.… (more)

Subjects/Keywords: 572; Bioinformatics (biochemistry); Bioinformatics (life sciences); Membrane proteins; Protein folding; Mathematical genetics and bioinformatics (statistics); Membrane protein; protein; twilight zone; fold recognition; comparative modelling; homology; alignment; correlated substitution

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hill, J. R. (2013). Fold recognition and alignment in the 'twilight zone'. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:353a9832-b2a4-41fb-a9f2-f3cae1a30039 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595946

Chicago Manual of Style (16th Edition):

Hill, Jamie Richard. “Fold recognition and alignment in the 'twilight zone'.” 2013. Doctoral Dissertation, University of Oxford. Accessed December 08, 2019. http://ora.ox.ac.uk/objects/uuid:353a9832-b2a4-41fb-a9f2-f3cae1a30039 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595946.

MLA Handbook (7th Edition):

Hill, Jamie Richard. “Fold recognition and alignment in the 'twilight zone'.” 2013. Web. 08 Dec 2019.

Vancouver:

Hill JR. Fold recognition and alignment in the 'twilight zone'. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Dec 08]. Available from: http://ora.ox.ac.uk/objects/uuid:353a9832-b2a4-41fb-a9f2-f3cae1a30039 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595946.

Council of Science Editors:

Hill JR. Fold recognition and alignment in the 'twilight zone'. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:353a9832-b2a4-41fb-a9f2-f3cae1a30039 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595946

6. Yu, Wei Hong. Cloning and subcellular localization of human VDAC isoforms.

Degree: PhD, 1995, Oregon Health Sciences University

Subjects/Keywords: Ion Channels  – genetics; Membrane Proteins  – genetics; DNA, Complementary; Intracellular Membranes; Subcellular Fractions

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Yu, W. H. (1995). Cloning and subcellular localization of human VDAC isoforms. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M48C9TH5 ; http://digitalcommons.ohsu.edu/etd/2761

Chicago Manual of Style (16th Edition):

Yu, Wei Hong. “Cloning and subcellular localization of human VDAC isoforms.” 1995. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 08, 2019. doi:10.6083/M48C9TH5 ; http://digitalcommons.ohsu.edu/etd/2761.

MLA Handbook (7th Edition):

Yu, Wei Hong. “Cloning and subcellular localization of human VDAC isoforms.” 1995. Web. 08 Dec 2019.

Vancouver:

Yu WH. Cloning and subcellular localization of human VDAC isoforms. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1995. [cited 2019 Dec 08]. Available from: doi:10.6083/M48C9TH5 ; http://digitalcommons.ohsu.edu/etd/2761.

Council of Science Editors:

Yu WH. Cloning and subcellular localization of human VDAC isoforms. [Doctoral Dissertation]. Oregon Health Sciences University; 1995. Available from: doi:10.6083/M48C9TH5 ; http://digitalcommons.ohsu.edu/etd/2761


University of Hong Kong

7. Cheung, Kai-wing. Generation of recombinant influenza A virus without M2 ion channel protein by introducing a point mutation at the 5' end of viral intron.

Degree: M. Phil., 2004, University of Hong Kong

published_or_final_version

abstract

Microbiology

Master

Master of Philosophy

Subjects/Keywords: Introns.; Viral genetics.; Membrane proteins - Genetics.; Influenza viruses.; Ion channels.; Mutation (Biology)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cheung, K. (2004). Generation of recombinant influenza A virus without M2 ion channel protein by introducing a point mutation at the 5' end of viral intron. (Masters Thesis). University of Hong Kong. Retrieved from Cheung, K.. (2004). Generation of recombinant influenza A virus without M2 ion channel protein by introducing a point mutation at the 5' end of viral intron. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3147723 ; http://dx.doi.org/10.5353/th_b3147723 ; http://hdl.handle.net/10722/40041

Chicago Manual of Style (16th Edition):

Cheung, Kai-wing. “Generation of recombinant influenza A virus without M2 ion channel protein by introducing a point mutation at the 5' end of viral intron.” 2004. Masters Thesis, University of Hong Kong. Accessed December 08, 2019. Cheung, K.. (2004). Generation of recombinant influenza A virus without M2 ion channel protein by introducing a point mutation at the 5' end of viral intron. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3147723 ; http://dx.doi.org/10.5353/th_b3147723 ; http://hdl.handle.net/10722/40041.

MLA Handbook (7th Edition):

Cheung, Kai-wing. “Generation of recombinant influenza A virus without M2 ion channel protein by introducing a point mutation at the 5' end of viral intron.” 2004. Web. 08 Dec 2019.

Vancouver:

Cheung K. Generation of recombinant influenza A virus without M2 ion channel protein by introducing a point mutation at the 5' end of viral intron. [Internet] [Masters thesis]. University of Hong Kong; 2004. [cited 2019 Dec 08]. Available from: Cheung, K.. (2004). Generation of recombinant influenza A virus without M2 ion channel protein by introducing a point mutation at the 5' end of viral intron. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3147723 ; http://dx.doi.org/10.5353/th_b3147723 ; http://hdl.handle.net/10722/40041.

Council of Science Editors:

Cheung K. Generation of recombinant influenza A virus without M2 ion channel protein by introducing a point mutation at the 5' end of viral intron. [Masters Thesis]. University of Hong Kong; 2004. Available from: Cheung, K.. (2004). Generation of recombinant influenza A virus without M2 ion channel protein by introducing a point mutation at the 5' end of viral intron. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3147723 ; http://dx.doi.org/10.5353/th_b3147723 ; http://hdl.handle.net/10722/40041


University of Oxford

8. Hoon, A. C. The effect of manipulating the expression of the NR2B subunit of the NMDA receptor on learning and memory.

Degree: PhD, 2011, University of Oxford

 Overexpression of the NR2B subunit of the NMDA receptor in the forebrain has been shown to improve learning and memory in mice (Tang et al… (more)

Subjects/Keywords: 612.8233; Neuroscience; Cognitive Neuroscience; Memory; Learning; Behavioural Neuroscience; Cognition; Transgenics; Molecular genetics; Membrane proteins; Experimental psychology; Neurology; Neurogenetics; Physiology; Genetics (life sciences); learning; memory; neuroscience; mice; NMDA receptor

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hoon, A. C. (2011). The effect of manipulating the expression of the NR2B subunit of the NMDA receptor on learning and memory. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:eae324a3-873f-4b50-9bcc-8c43b72866a3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558439

Chicago Manual of Style (16th Edition):

Hoon, A C. “The effect of manipulating the expression of the NR2B subunit of the NMDA receptor on learning and memory.” 2011. Doctoral Dissertation, University of Oxford. Accessed December 08, 2019. http://ora.ox.ac.uk/objects/uuid:eae324a3-873f-4b50-9bcc-8c43b72866a3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558439.

MLA Handbook (7th Edition):

Hoon, A C. “The effect of manipulating the expression of the NR2B subunit of the NMDA receptor on learning and memory.” 2011. Web. 08 Dec 2019.

Vancouver:

Hoon AC. The effect of manipulating the expression of the NR2B subunit of the NMDA receptor on learning and memory. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Dec 08]. Available from: http://ora.ox.ac.uk/objects/uuid:eae324a3-873f-4b50-9bcc-8c43b72866a3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558439.

Council of Science Editors:

Hoon AC. The effect of manipulating the expression of the NR2B subunit of the NMDA receptor on learning and memory. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:eae324a3-873f-4b50-9bcc-8c43b72866a3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558439

9. Masyukova, Svetlana V. Analysis of NPHP complex genetic interactions associated with human cilia disorders.

Degree: PhD, 2011, University of Alabama – Birmingham

Primary cilia are antenna-like organelles that extend from the surface of almost all mammalian cell types. They regulate many signaling pathways and sense physical and… (more)

Subjects/Keywords: Caenorhabditis elegans Proteins – metabolism.<; br>; Cilia – metabolism.<; br>; Membrane Proteins – metabolism<; br>; Mutation, Missense – physiology.<; br>; Proteins – genetics<; br>; Proteins – metabolism

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Masyukova, S. V. (2011). Analysis of NPHP complex genetic interactions associated with human cilia disorders. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1352

Chicago Manual of Style (16th Edition):

Masyukova, Svetlana V. “Analysis of NPHP complex genetic interactions associated with human cilia disorders.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 08, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1352.

MLA Handbook (7th Edition):

Masyukova, Svetlana V. “Analysis of NPHP complex genetic interactions associated with human cilia disorders.” 2011. Web. 08 Dec 2019.

Vancouver:

Masyukova SV. Analysis of NPHP complex genetic interactions associated with human cilia disorders. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Dec 08]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1352.

Council of Science Editors:

Masyukova SV. Analysis of NPHP complex genetic interactions associated with human cilia disorders. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1352

10. Rupp, Paul A. Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome.

Degree: PhD, 1999, Oregon Health Sciences University

Subjects/Keywords: Base Sequence; Blotting, Western; Heart Defects, Congenital; Chromosome Deletion; Membrane Proteins  – genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rupp, P. A. (1999). Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341

Chicago Manual of Style (16th Edition):

Rupp, Paul A. “Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome.” 1999. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 08, 2019. doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341.

MLA Handbook (7th Edition):

Rupp, Paul A. “Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome.” 1999. Web. 08 Dec 2019.

Vancouver:

Rupp PA. Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1999. [cited 2019 Dec 08]. Available from: doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341.

Council of Science Editors:

Rupp PA. Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome. [Doctoral Dissertation]. Oregon Health Sciences University; 1999. Available from: doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341

11. Deng, Vivianne Wei. Deregulated gene expression in the brain of Rett syndrome patients and MeCP2-null mice.

Degree: PhD, 2005, Oregon Health Sciences University

Subjects/Keywords: Methyl-CpG-Binding Protein 2  – genetics; Rett Syndrome  – genetics; Membrane Proteins  – genetics; Gene Expression Regulation, Developmental; Sodium-Potassium-Exchanging ATPase  – physiology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Deng, V. W. (2005). Deregulated gene expression in the brain of Rett syndrome patients and MeCP2-null mice. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4959FTW ; http://digitalcommons.ohsu.edu/etd/2993

Chicago Manual of Style (16th Edition):

Deng, Vivianne Wei. “Deregulated gene expression in the brain of Rett syndrome patients and MeCP2-null mice.” 2005. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 08, 2019. doi:10.6083/M4959FTW ; http://digitalcommons.ohsu.edu/etd/2993.

MLA Handbook (7th Edition):

Deng, Vivianne Wei. “Deregulated gene expression in the brain of Rett syndrome patients and MeCP2-null mice.” 2005. Web. 08 Dec 2019.

Vancouver:

Deng VW. Deregulated gene expression in the brain of Rett syndrome patients and MeCP2-null mice. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2005. [cited 2019 Dec 08]. Available from: doi:10.6083/M4959FTW ; http://digitalcommons.ohsu.edu/etd/2993.

Council of Science Editors:

Deng VW. Deregulated gene expression in the brain of Rett syndrome patients and MeCP2-null mice. [Doctoral Dissertation]. Oregon Health Sciences University; 2005. Available from: doi:10.6083/M4959FTW ; http://digitalcommons.ohsu.edu/etd/2993

12. Ling, Shiyun. Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation.

Degree: PhD, 2010, University of Alabama – Birmingham

Unrestricted cell proliferation and suppression of cell death are two essential events for tumor development. My dissertation research involves two proteins, 14-3-3 &tau and EDD… (more)

Subjects/Keywords: 14-3-3 Proteins – metabolism.<; br>; Breast Neoplasms<; br>; Down-Regulation<; br>; Membrane Proteins – genetics<; br>; Ovarian Neoplasms<; br>; Protein Processing, Post-Translational<; br>; Transcriptional Activation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ling, S. (2010). Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1419

Chicago Manual of Style (16th Edition):

Ling, Shiyun. “Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 08, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1419.

MLA Handbook (7th Edition):

Ling, Shiyun. “Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation.” 2010. Web. 08 Dec 2019.

Vancouver:

Ling S. Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 08]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1419.

Council of Science Editors:

Ling S. Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1419


University of Florida

13. Hines, Stephen Alan, 1955-. Identification, characterization, and molecular cloning of the immunodominant Babesia bovis merozoite surface protein Bv42.

Degree: 1989, University of Florida

Subjects/Keywords: Antibodies; Antigens; Babesiosis; Cattle; Erythrocytes; Membrane proteins; Merozoites; Monoclonal antibodies; Parasites; Vaccinations; Babesia  – genetics ( mesh ); Cloning, Molecular ( mesh ); Membrane Proteins ( mesh ); Pathology thesis Ph.D ( mesh )

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hines, Stephen Alan, 1. (1989). Identification, characterization, and molecular cloning of the immunodominant Babesia bovis merozoite surface protein Bv42. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00009079

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):

Hines, Stephen Alan, 1955-. “Identification, characterization, and molecular cloning of the immunodominant Babesia bovis merozoite surface protein Bv42.” 1989. Thesis, University of Florida. Accessed December 08, 2019. http://ufdc.ufl.edu/AA00009079.

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

MLA Handbook (7th Edition):

Hines, Stephen Alan, 1955-. “Identification, characterization, and molecular cloning of the immunodominant Babesia bovis merozoite surface protein Bv42.” 1989. Web. 08 Dec 2019.

Vancouver:

Hines, Stephen Alan 1. Identification, characterization, and molecular cloning of the immunodominant Babesia bovis merozoite surface protein Bv42. [Internet] [Thesis]. University of Florida; 1989. [cited 2019 Dec 08]. Available from: http://ufdc.ufl.edu/AA00009079.

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

Council of Science Editors:

Hines, Stephen Alan 1. Identification, characterization, and molecular cloning of the immunodominant Babesia bovis merozoite surface protein Bv42. [Thesis]. University of Florida; 1989. Available from: http://ufdc.ufl.edu/AA00009079

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


University of Oxford

14. Wilman, Henry R. Computational studies of protein helix kinks.

Degree: PhD, 2014, University of Oxford

 Kinks are functionally important structural features found in the alpha-helices of many proteins, particularly membrane proteins. Structurally, they are points at which a helix abruptly… (more)

Subjects/Keywords: 572; Bioinformatics (biochemistry); Life Sciences; Bioinformatics (life sciences); Computational chemistry; Membrane proteins; Protein chemistry; Mathematical genetics and bioinformatics (statistics); Physical Sciences; Polymers Amino acid and peptide chemistry; Bioinformatics (technology); Technology and Applied Sciences; Protein; Helix; Kink; Secondary structure; Structural biology; protein structure prediction; crowdsourcing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wilman, H. R. (2014). Computational studies of protein helix kinks. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:21225f0e-efed-49c6-af27-5d3fe78fa731 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655081

Chicago Manual of Style (16th Edition):

Wilman, Henry R. “Computational studies of protein helix kinks.” 2014. Doctoral Dissertation, University of Oxford. Accessed December 08, 2019. http://ora.ox.ac.uk/objects/uuid:21225f0e-efed-49c6-af27-5d3fe78fa731 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655081.

MLA Handbook (7th Edition):

Wilman, Henry R. “Computational studies of protein helix kinks.” 2014. Web. 08 Dec 2019.

Vancouver:

Wilman HR. Computational studies of protein helix kinks. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2019 Dec 08]. Available from: http://ora.ox.ac.uk/objects/uuid:21225f0e-efed-49c6-af27-5d3fe78fa731 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655081.

Council of Science Editors:

Wilman HR. Computational studies of protein helix kinks. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:21225f0e-efed-49c6-af27-5d3fe78fa731 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655081


University of Oxford

15. Fu, Josephine K. Y. Functional characterization of the teleost multiple tissue (tmt) opsin family and their role in light detection.

Degree: PhD, 2013, University of Oxford

 In addition to a central circadian clock in the suprachiasmatic nucleus (SCN), zebrafish (Danio rerio) have local clock systems in their peripheral tissues. These peripheral… (more)

Subjects/Keywords: 573.8; Life Sciences; Biochemistry; Bioinformatics (biochemistry); Molecular biophysics (biochemistry); Bioinformatics (life sciences); Biology; Cell Biology; Genetics (life sciences); Medical sciences; Biology (medical sciences); DNA damage signalling; Genetics (medical sciences); Ophthamology; Physiology; Physical Sciences; Biophysics; Membrane proteins; Molecular genetics; Photochemistry and reaction dynamics; Protein chemistry; Protein folding; Spectroscopy and molecular structure; Opsin; G protein-coupled receptor; Photopigment; Multiple Tissue expression; Transduction; Photosensory; Biological rhythms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fu, J. K. Y. (2013). Functional characterization of the teleost multiple tissue (tmt) opsin family and their role in light detection. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:39bc18bb-16cb-4549-94cd-5f872daafe7e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595930

Chicago Manual of Style (16th Edition):

Fu, Josephine K Y. “Functional characterization of the teleost multiple tissue (tmt) opsin family and their role in light detection.” 2013. Doctoral Dissertation, University of Oxford. Accessed December 08, 2019. http://ora.ox.ac.uk/objects/uuid:39bc18bb-16cb-4549-94cd-5f872daafe7e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595930.

MLA Handbook (7th Edition):

Fu, Josephine K Y. “Functional characterization of the teleost multiple tissue (tmt) opsin family and their role in light detection.” 2013. Web. 08 Dec 2019.

Vancouver:

Fu JKY. Functional characterization of the teleost multiple tissue (tmt) opsin family and their role in light detection. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Dec 08]. Available from: http://ora.ox.ac.uk/objects/uuid:39bc18bb-16cb-4549-94cd-5f872daafe7e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595930.

Council of Science Editors:

Fu JKY. Functional characterization of the teleost multiple tissue (tmt) opsin family and their role in light detection. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:39bc18bb-16cb-4549-94cd-5f872daafe7e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595930


University of Oxford

16. Jain, Jayati. Engineering antibodies to study and improve immunomagnetic isolation of tumour cells.

Degree: PhD, 2013, University of Oxford

 Cell separation based on antibody-targeted magnetic beads has been widely used in a number of applications in immunology, microbiology, oncology and more recently, in the… (more)

Subjects/Keywords: 616.99; Biochemistry; Molecular biophysics (biochemistry); Bioinformatics (life sciences); Biology; Cell Biology (see also Plant sciences); Genetics (life sciences); Nano-biotechnology; Genetics (medical sciences); Immunology; Membrane proteins; Molecular genetics; Protein chemistry; Protein folding; antibodies; protein engineering; HER2; Herceptin; 4D5; microbiology; cancer; immunomagnetic; cell isolation; cholesterol; Fab; tumour cell; magnetic bead; circulating tumour cell; biotinylation; 9E10; BT474; clamping; periplasmic expression; cell sorting; myc peptide; streptavidin; flow cytometry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Jain, J. (2013). Engineering antibodies to study and improve immunomagnetic isolation of tumour cells. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:81355801-b331-4705-bfef-204a29ee0347 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629498

Chicago Manual of Style (16th Edition):

Jain, Jayati. “Engineering antibodies to study and improve immunomagnetic isolation of tumour cells.” 2013. Doctoral Dissertation, University of Oxford. Accessed December 08, 2019. http://ora.ox.ac.uk/objects/uuid:81355801-b331-4705-bfef-204a29ee0347 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629498.

MLA Handbook (7th Edition):

Jain, Jayati. “Engineering antibodies to study and improve immunomagnetic isolation of tumour cells.” 2013. Web. 08 Dec 2019.

Vancouver:

Jain J. Engineering antibodies to study and improve immunomagnetic isolation of tumour cells. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Dec 08]. Available from: http://ora.ox.ac.uk/objects/uuid:81355801-b331-4705-bfef-204a29ee0347 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629498.

Council of Science Editors:

Jain J. Engineering antibodies to study and improve immunomagnetic isolation of tumour cells. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:81355801-b331-4705-bfef-204a29ee0347 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.629498

17. Pyle, Louise Clare. Cystic fibrosis transmembrane conductance regulator (CFTR) modulators and their mechanistic basis: relevance to emerging therapies for cystic fibrosis.

Degree: PhD, 2009, University of Alabama – Birmingham

Cystic fibrosis (CF) is a lethal genetic disorder leading to pulmonary decline and premature death. The gene responsible for CF, the cystic fibrosis transmembrane conductance… (more)

Subjects/Keywords: Biological Markers  – metabolism<; br>; Cystic Fibrosis  – metabolism<; br>; Cystic Fibrosis Transmembrane Conductance Regulator<; br>; High-Throughput Screening Assays<; br>; Ion Channel Gating  – drug effects<; br>; Membrane Transport Modulators  – pharmacology<; br>; Mutant Proteins  – metabolism<; br>; Protein Structure, Tertiary  – genetics<; br>; Quercetin  – pharmacology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pyle, L. C. (2009). Cystic fibrosis transmembrane conductance regulator (CFTR) modulators and their mechanistic basis: relevance to emerging therapies for cystic fibrosis. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1106

Chicago Manual of Style (16th Edition):

Pyle, Louise Clare. “Cystic fibrosis transmembrane conductance regulator (CFTR) modulators and their mechanistic basis: relevance to emerging therapies for cystic fibrosis.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 08, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1106.

MLA Handbook (7th Edition):

Pyle, Louise Clare. “Cystic fibrosis transmembrane conductance regulator (CFTR) modulators and their mechanistic basis: relevance to emerging therapies for cystic fibrosis.” 2009. Web. 08 Dec 2019.

Vancouver:

Pyle LC. Cystic fibrosis transmembrane conductance regulator (CFTR) modulators and their mechanistic basis: relevance to emerging therapies for cystic fibrosis. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Dec 08]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1106.

Council of Science Editors:

Pyle LC. Cystic fibrosis transmembrane conductance regulator (CFTR) modulators and their mechanistic basis: relevance to emerging therapies for cystic fibrosis. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1106


University of Florida

18. Sturgeon, Joyce Anne, 1951-. Low-temperature conditional cell division mutants of Escherichia coli.

Degree: 1977, University of Florida

Subjects/Keywords: Antibiotics; Cell division; DNA; Escherichia coli; Genetics; Lesions; Lipoproteins; Membrane proteins; Phospholipids; RNA; Escherichia coli; Microbiology and Cell Science thesis Ph. D; Mutation (Biology)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sturgeon, Joyce Anne, 1. (1977). Low-temperature conditional cell division mutants of Escherichia coli. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00058785

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):

Sturgeon, Joyce Anne, 1951-. “Low-temperature conditional cell division mutants of Escherichia coli.” 1977. Thesis, University of Florida. Accessed December 08, 2019. http://ufdc.ufl.edu/AA00058785.

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

MLA Handbook (7th Edition):

Sturgeon, Joyce Anne, 1951-. “Low-temperature conditional cell division mutants of Escherichia coli.” 1977. Web. 08 Dec 2019.

Vancouver:

Sturgeon, Joyce Anne 1. Low-temperature conditional cell division mutants of Escherichia coli. [Internet] [Thesis]. University of Florida; 1977. [cited 2019 Dec 08]. Available from: http://ufdc.ufl.edu/AA00058785.

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

Council of Science Editors:

Sturgeon, Joyce Anne 1. Low-temperature conditional cell division mutants of Escherichia coli. [Thesis]. University of Florida; 1977. Available from: http://ufdc.ufl.edu/AA00058785

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


University of Oxford

19. Ramraj, Varun. Exploiting whole-PDB analysis in novel bioinformatics applications.

Degree: PhD, 2014, University of Oxford

 The Protein Data Bank (PDB) is the definitive electronic repository for experimentally-derived protein structures, composed mainly of those determined by X-ray crystallography. Approximately 200 new… (more)

Subjects/Keywords: 572.80285; Medical Sciences; Computer science (mathematics); Bioinformatics (biochemistry); Life Sciences; Genetics (life sciences); Computational biochemistry; Bioinformatics (life sciences); Biology (medical sciences); Genetics (medical sciences); Structural genomics; Crystallography; Enzymes; Membrane proteins; Protein chemistry; Protein folding; Polymers Amino acid and peptide chemistry; NMR spectroscopy; Mass spectrometry; Chemistry & allied sciences; Physical Sciences; Mathematical genetics and bioinformatics (statistics); Computationally-intensive statistics; Bioinformatics (technology); Computing; Applications and algorithms; Program development and tools; Scalable systems; Software engineering; Theory and automated verification; Biomedical engineering; protein data bank; structural biology; bioinformatics; clustering; disorder prediction; unit cell; space group; OpenMP; parallelization; proteins; peptides; fragments; training; neural network; MoreRONN; nearest cell; nearest-cell

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ramraj, V. (2014). Exploiting whole-PDB analysis in novel bioinformatics applications. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:6c59c813-2a4c-440c-940b-d334c02dd075 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618510

Chicago Manual of Style (16th Edition):

Ramraj, Varun. “Exploiting whole-PDB analysis in novel bioinformatics applications.” 2014. Doctoral Dissertation, University of Oxford. Accessed December 08, 2019. http://ora.ox.ac.uk/objects/uuid:6c59c813-2a4c-440c-940b-d334c02dd075 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618510.

MLA Handbook (7th Edition):

Ramraj, Varun. “Exploiting whole-PDB analysis in novel bioinformatics applications.” 2014. Web. 08 Dec 2019.

Vancouver:

Ramraj V. Exploiting whole-PDB analysis in novel bioinformatics applications. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2019 Dec 08]. Available from: http://ora.ox.ac.uk/objects/uuid:6c59c813-2a4c-440c-940b-d334c02dd075 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618510.

Council of Science Editors:

Ramraj V. Exploiting whole-PDB analysis in novel bioinformatics applications. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:6c59c813-2a4c-440c-940b-d334c02dd075 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618510


University of Florida

20. McMahon, Robert Joseph, 1968-. Regulation of expression of the glucose transporter GLUT1 by glucose in 3T3-L1 adipocytes.

Degree: 1995, University of Florida

Subjects/Keywords: Adipocytes; Antibodies; Antiserum; Cell membranes; Cells; CHO cells; Glycogen; Membrane proteins; Molecular weight; Oligosaccharides; Adipocytes  – physiology ( mesh ); Cricetulus ( mesh ); Department of Biochemistry and Molecular Biology thesis Ph.D ( mesh ); Gene Expression Regulation ( mesh ); Glucose  – physiology ( mesh ); Glycosylation ( mesh ); Monosaccharide Transport Proteins  – genetics ( mesh ); Monosaccharide Transport Proteins  – isolation &; purification ( mesh ); Monosaccharide Transport Proteins  – metabolism ( mesh ); Research ( mesh )

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

McMahon, Robert Joseph, 1. (1995). Regulation of expression of the glucose transporter GLUT1 by glucose in 3T3-L1 adipocytes. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00011803

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):

McMahon, Robert Joseph, 1968-. “Regulation of expression of the glucose transporter GLUT1 by glucose in 3T3-L1 adipocytes.” 1995. Thesis, University of Florida. Accessed December 08, 2019. http://ufdc.ufl.edu/AA00011803.

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

MLA Handbook (7th Edition):

McMahon, Robert Joseph, 1968-. “Regulation of expression of the glucose transporter GLUT1 by glucose in 3T3-L1 adipocytes.” 1995. Web. 08 Dec 2019.

Vancouver:

McMahon, Robert Joseph 1. Regulation of expression of the glucose transporter GLUT1 by glucose in 3T3-L1 adipocytes. [Internet] [Thesis]. University of Florida; 1995. [cited 2019 Dec 08]. Available from: http://ufdc.ufl.edu/AA00011803.

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

Council of Science Editors:

McMahon, Robert Joseph 1. Regulation of expression of the glucose transporter GLUT1 by glucose in 3T3-L1 adipocytes. [Thesis]. University of Florida; 1995. Available from: http://ufdc.ufl.edu/AA00011803

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


ETH Zürich

21. Eichmann, Cédric. NMR studies of large biomolecular systems.

Degree: 2011, ETH Zürich

Subjects/Keywords: KERNRESONANZSPEKTROSKOPIE (BIOLOGISCHE TECHNIKEN); STRUKTURANALYSE VON PROTEINEN UND PEPTIDEN; FALTUNG DER POLYPEPTIDKETTE (PROTEINE, PEPTIDE); STRUKTURÄNDERUNGEN VON PROTEINEN UND PEPTIDEN; MEMBRANPROTEINSTRUKTUR; TRANSLATION (MOLEKULARE GENETIK); RIBOSOMALE PROTEINE (MOLEKULARBIOLOGIE); NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY (BIOLOGICAL TECHNIQUES); STRUCTURE ANALYSIS OF PROTEINS AND PEPTIDES; FOLDING OF POLYPEPTIDE CHAIN (PROTEINS, PEPTIDES); STRUCTURAL CHANGES OF PROTEINS AND PEPTIDES; MEMBRANE PROTEIN STRUCTURE; TRANSLATION (MOLECULAR GENETICS); RIBOSOMAL PROTEINS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/570; Life sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Eichmann, C. (2011). NMR studies of large biomolecular systems. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/152786

Chicago Manual of Style (16th Edition):

Eichmann, Cédric. “NMR studies of large biomolecular systems.” 2011. Doctoral Dissertation, ETH Zürich. Accessed December 08, 2019. http://hdl.handle.net/20.500.11850/152786.

MLA Handbook (7th Edition):

Eichmann, Cédric. “NMR studies of large biomolecular systems.” 2011. Web. 08 Dec 2019.

Vancouver:

Eichmann C. NMR studies of large biomolecular systems. [Internet] [Doctoral dissertation]. ETH Zürich; 2011. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/20.500.11850/152786.

Council of Science Editors:

Eichmann C. NMR studies of large biomolecular systems. [Doctoral Dissertation]. ETH Zürich; 2011. Available from: http://hdl.handle.net/20.500.11850/152786


ETH Zürich

22. Bischof, Sylvain. Chloroplast proteome analysis: new insights into intracellular trafficking.

Degree: 2010, ETH Zürich

Subjects/Keywords: ARABIDOPSIS (BOTANIK); PLASTIDENGENOM + PLASTIDENGENE + PLASTIDEN-DNA (GENETIK); PROTEINTRANSPORT + PEPTIDTRANSPORT (MEMBRANBIOLOGIE); PERMEASEN + TRANSLOKATOREN + TRANSPORTER (MEMBRANTRANSPORT); ACETYLIERUNGSREAKTIONEN (CHEMISCHE REAKTIONEN); PLASTIDENPROTEINE (CYTOLOGIE); ARABIDOPSIS (BOTANY); PLASTID GENOME + PLASTID GENES + PLASTID DNA (GENETICS); PROTEIN TRANSPORT + PEPTIDE TRANSPORT (MEMBRANE BIOLOGY); PERMEASES + TRANSLOCATORS + TRANSPORTERS (MEMBRANE TRANSPORT); ACETYLATIONS (CHEMICAL REACTIONS); PLASTID PROTEINS (CYTOLOGY); info:eu-repo/classification/ddc/580; info:eu-repo/classification/ddc/570; Botanical sciences; Life sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bischof, S. (2010). Chloroplast proteome analysis: new insights into intracellular trafficking. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/152012

Chicago Manual of Style (16th Edition):

Bischof, Sylvain. “Chloroplast proteome analysis: new insights into intracellular trafficking.” 2010. Doctoral Dissertation, ETH Zürich. Accessed December 08, 2019. http://hdl.handle.net/20.500.11850/152012.

MLA Handbook (7th Edition):

Bischof, Sylvain. “Chloroplast proteome analysis: new insights into intracellular trafficking.” 2010. Web. 08 Dec 2019.

Vancouver:

Bischof S. Chloroplast proteome analysis: new insights into intracellular trafficking. [Internet] [Doctoral dissertation]. ETH Zürich; 2010. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/20.500.11850/152012.

Council of Science Editors:

Bischof S. Chloroplast proteome analysis: new insights into intracellular trafficking. [Doctoral Dissertation]. ETH Zürich; 2010. Available from: http://hdl.handle.net/20.500.11850/152012


University of Florida

23. Macauley, Shawn P., 1964-. Changes in extracellular matrix gene and protein expression in developing mouse submandibular glands.

Degree: 1996, University of Florida

Subjects/Keywords: Basement membrane; Cells; Collagens; Extracellular matrix; Messenger RNA; Molecules; Morphogenesis; Rats; RNA; Salivary glands; Amino Acid Sequence ( mesh ); Base Sequence ( mesh ); Department of Oral Biology thesis Ph.D ( mesh ); Extracellular Matrix Proteins  – genetics ( mesh ); Extracellular Matrix Proteins  – physiology ( mesh ); Gene Expression ( mesh ); Gene Expression Regulation, Developmental ( mesh ); Mice, Inbred BALB C ( mesh ); Molecular Sequence Data ( mesh ); Research ( mesh ); Submandibular Gland  – chemistry ( mesh ); Submandibular Gland  – embryology ( mesh )

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Macauley, Shawn P., 1. (1996). Changes in extracellular matrix gene and protein expression in developing mouse submandibular glands. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00022654

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):

Macauley, Shawn P., 1964-. “Changes in extracellular matrix gene and protein expression in developing mouse submandibular glands.” 1996. Thesis, University of Florida. Accessed December 08, 2019. http://ufdc.ufl.edu/AA00022654.

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

MLA Handbook (7th Edition):

Macauley, Shawn P., 1964-. “Changes in extracellular matrix gene and protein expression in developing mouse submandibular glands.” 1996. Web. 08 Dec 2019.

Vancouver:

Macauley, Shawn P. 1. Changes in extracellular matrix gene and protein expression in developing mouse submandibular glands. [Internet] [Thesis]. University of Florida; 1996. [cited 2019 Dec 08]. Available from: http://ufdc.ufl.edu/AA00022654.

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

Council of Science Editors:

Macauley, Shawn P. 1. Changes in extracellular matrix gene and protein expression in developing mouse submandibular glands. [Thesis]. University of Florida; 1996. Available from: http://ufdc.ufl.edu/AA00022654

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

24. Vânia Belintani Piatto. Análise molecular do gene da conexina 26 em pacientes com deficiênica auditiva sensorioneural não-sindrômica.

Degree: 2003, Faculdade de Medicina de São José do Rio Preto

 Mutações no gene que codifica a proteína conexina 26 têm contribuído para a maioria das deficiências auditivas pré-lingual, sensorioneural não-sindrômicas recessivas. Uma mutação específica, a… (more)

Subjects/Keywords: Ciências da Saúde; Deficiência Auditiva; Análise Molecular; Conexina 26; Conexinas; Surdez; Mapeamento Cromossômico; Proteínas de Membrana; Biologia Molecular; Perda Auditiva Neurossensorial; Transtornos da Audição; Variação (Genética); Sordera; Conexinas; Connexins; Deafness; Mapeo Cromosómico; Chromosome Mapping; Proteínas de la Membrana; Membrane Proteins; Biología Molecular; Molecular Biology; Pérdida Auditiva Sensorioneural; Sensorineural Hearing Loss; Trastornos de la Audición; Hearing Disorders; Variación (Genetica); Variation (Genetics)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Piatto, V. B. (2003). Análise molecular do gene da conexina 26 em pacientes com deficiênica auditiva sensorioneural não-sindrômica. (Thesis). Faculdade de Medicina de São José do Rio Preto. Retrieved from http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=23

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):

Piatto, Vânia Belintani. “Análise molecular do gene da conexina 26 em pacientes com deficiênica auditiva sensorioneural não-sindrômica.” 2003. Thesis, Faculdade de Medicina de São José do Rio Preto. Accessed December 08, 2019. http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=23.

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

MLA Handbook (7th Edition):

Piatto, Vânia Belintani. “Análise molecular do gene da conexina 26 em pacientes com deficiênica auditiva sensorioneural não-sindrômica.” 2003. Web. 08 Dec 2019.

Vancouver:

Piatto VB. Análise molecular do gene da conexina 26 em pacientes com deficiênica auditiva sensorioneural não-sindrômica. [Internet] [Thesis]. Faculdade de Medicina de São José do Rio Preto; 2003. [cited 2019 Dec 08]. Available from: http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=23.

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

Council of Science Editors:

Piatto VB. Análise molecular do gene da conexina 26 em pacientes com deficiênica auditiva sensorioneural não-sindrômica. [Thesis]. Faculdade de Medicina de São José do Rio Preto; 2003. Available from: http://bdtd.famerp.br//tde_busca/arquivo.php?codArquivo=23

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


ETH Zürich

25. Singhal, Ankita. Structural insights in the molecular causes of congenital stationary night blindness.

Degree: 2014, ETH Zürich

Subjects/Keywords: G-PROTEIN-GEKOPPELTE REZEPTOREN (MEMBRANBIOLOGIE); GENMUTATIONEN + PUNKTMUTATIONEN (GENETIK); RHODOPSINE (PHOTOREZEPTOREN); SEHSTÖRUNGEN (AUGENHEILKUNDE); KRISTALLSTRUKTUREN VON PROTEINEN UND PEPTIDEN; BINDUNGSSTELLEN VON REZEPTOREN (MOLEKULARBIOLOGIE); G PROTEIN COUPLED RECEPTORS (MEMBRANE BIOLOGY); GENE MUTATIONS + POINT MUTATIONS (GENETICS); RHODOPSINS (PHOTORECEPTORS); VISUAL DISORDERS (OPHTHALMOLOGY); CRYSTAL STRUCTURES OF PROTEINS AND PEPTIDES; BINDING SITES OF RECEPTORS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/610; info:eu-repo/classification/ddc/570; Medical sciences, medicine; Life sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Singhal, A. (2014). Structural insights in the molecular causes of congenital stationary night blindness. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/154592

Chicago Manual of Style (16th Edition):

Singhal, Ankita. “Structural insights in the molecular causes of congenital stationary night blindness.” 2014. Doctoral Dissertation, ETH Zürich. Accessed December 08, 2019. http://hdl.handle.net/20.500.11850/154592.

MLA Handbook (7th Edition):

Singhal, Ankita. “Structural insights in the molecular causes of congenital stationary night blindness.” 2014. Web. 08 Dec 2019.

Vancouver:

Singhal A. Structural insights in the molecular causes of congenital stationary night blindness. [Internet] [Doctoral dissertation]. ETH Zürich; 2014. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/20.500.11850/154592.

Council of Science Editors:

Singhal A. Structural insights in the molecular causes of congenital stationary night blindness. [Doctoral Dissertation]. ETH Zürich; 2014. Available from: http://hdl.handle.net/20.500.11850/154592


ETH Zürich

26. Szathmary, Reka. Identification of novel mechanisms in ERAD: Genetic and biochemical characterization of the YOS9 protein and Genetic screens to identify novel genes in ERAD.

Degree: 2005, ETH Zürich

Subjects/Keywords: ENDOPLASMATISCHES RETICULUM + VAKUOLENSYSTEME DES CYTOPLASMAS + MEMBRANSYSTEME DES CYTOPLASMAS (CYTOLOGIE); PROTEINKATABOLISMUS + PEPTIDKATABOLISMUS (METABOLISMUS); FALTUNG DER POLYPEPTIDKETTE (PROTEINE, PEPTIDE); SACCHAROMYCES (MYKOLOGIE); PILZGENETIK (MYKOLOGIE); ENDOPLASMIC RETICULUM + VACUOLAR SYSTEMS OF CYTOPLASM + MEMBRANE SYSTEMS OF THE CYTOPLASM (CYTOLOGY); PROTEIN CATABOLISM + PEPTIDE CATABOLISM (METABOLISM); FOLDING OF POLYPEPTIDE CHAIN (PROTEINS, PEPTIDES); SACCHAROMYCES (MYCOLOGY); FUNGAL GENETICS (MYCOLOGY); info:eu-repo/classification/ddc/570; Life sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Szathmary, R. (2005). Identification of novel mechanisms in ERAD: Genetic and biochemical characterization of the YOS9 protein and Genetic screens to identify novel genes in ERAD. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/149080

Chicago Manual of Style (16th Edition):

Szathmary, Reka. “Identification of novel mechanisms in ERAD: Genetic and biochemical characterization of the YOS9 protein and Genetic screens to identify novel genes in ERAD.” 2005. Doctoral Dissertation, ETH Zürich. Accessed December 08, 2019. http://hdl.handle.net/20.500.11850/149080.

MLA Handbook (7th Edition):

Szathmary, Reka. “Identification of novel mechanisms in ERAD: Genetic and biochemical characterization of the YOS9 protein and Genetic screens to identify novel genes in ERAD.” 2005. Web. 08 Dec 2019.

Vancouver:

Szathmary R. Identification of novel mechanisms in ERAD: Genetic and biochemical characterization of the YOS9 protein and Genetic screens to identify novel genes in ERAD. [Internet] [Doctoral dissertation]. ETH Zürich; 2005. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/20.500.11850/149080.

Council of Science Editors:

Szathmary R. Identification of novel mechanisms in ERAD: Genetic and biochemical characterization of the YOS9 protein and Genetic screens to identify novel genes in ERAD. [Doctoral Dissertation]. ETH Zürich; 2005. Available from: http://hdl.handle.net/20.500.11850/149080

27. Menezes, Luis Fernando Carvalho de. "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva".

Degree: PhD, Fisiopatologia Experimental, 2004, University of São Paulo

O gene PKHD1, mutado na doença renal policística autossômica recessiva, apresenta um padrão de splicing complexo associado a múltiplos transcritos alternativos. Neste trabalho estudamos o… (more)

Subjects/Keywords: BLOTTING WESTERN/methods; CÍLIOS/patologia; IMMUNOHISTOCHEMISTRY/methods; IMUNOHISTOQUÍMICA/métodos; ISOFORMAS DE PROTEÍNAS/análise; KIDNEY TUBULES COLLECTING/pathology; KIDNEY TUBULES COLLECTING/physiopathology; MEMBRANE PROTEINS/analysis; MICROSCOPIA IMUNOELETRÔNICA/métodos/ MICROSCOPIA DE FLUORESCÊNCIA/méto; MICROSCOPY FLUORESCENCE/methods; MICROSCOPY IMMUNOELECTRON/methods; POLYCYSTIC KIDNEY AUTOSOMAL RECESSIVE/etiology; POLYCYSTIC KIDNEY AUTOSOMAL RECESSIVE/genetics; POLYCYSTIC KIDNEY AUTOSOMAL RECESSIVE/physiopathology; PROTEIN ISOFORMS/analysis; PROTEÍNAS DE MEMBRANA/análise; RIM POLICÍSTICO AUTOSSÔMICO RECESSIVO/etiologia; RIM POLICÍSTICO AUTOSSÔMICO RECESSIVO/fisiopatologia; RIM POLICÍSTICO AUTOSSÔMICO RECESSIVO/genética; TÚBULOS COLETORES RENAIS/fisiopatologia; TÚBULOS COLETORES RENAIS/patologia; WESTERN BLOTTING/métodos

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Menezes, L. F. C. d. (2004). "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva". (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;

Chicago Manual of Style (16th Edition):

Menezes, Luis Fernando Carvalho de. “"Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva".” 2004. Doctoral Dissertation, University of São Paulo. Accessed December 08, 2019. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;.

MLA Handbook (7th Edition):

Menezes, Luis Fernando Carvalho de. “"Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva".” 2004. Web. 08 Dec 2019.

Vancouver:

Menezes LFCd. "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva". [Internet] [Doctoral dissertation]. University of São Paulo; 2004. [cited 2019 Dec 08]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;.

Council of Science Editors:

Menezes LFCd. "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva". [Doctoral Dissertation]. University of São Paulo; 2004. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;

.