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

Dates: 2000 – 2004

You searched for subject:( chromosome). Showing records 1 – 30 of 73 total matches.

[1] [2] [3]

Search Limiters

Last 2 Years | English Only

Levels

▼ Search Limiters


Central Connecticut State University

1. LaMonica, Kristi April. Re-derivation of the B6.C-H2d/bBy inbred mouse strain to remove an unwanted spontaneously arising new barrier to histocompatibility.

Degree: Department of Biological Sciences, 2003, Central Connecticut State University

 Minor histocompatibility (H) antigens are typically identified as barriers to transplantation in graft exchange experiments between major histocompatibility complex (MHC)-matched hosts (Bailey 1975; Snell and… (more)

Subjects/Keywords: Histocompatibility; X chromosome

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

LaMonica, K. A. (2003). Re-derivation of the B6.C-H2d/bBy inbred mouse strain to remove an unwanted spontaneously arising new barrier to histocompatibility. (Thesis). Central Connecticut State University. Retrieved from http://content.library.ccsu.edu/u?/ccsutheses,1094

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):

LaMonica, Kristi April. “Re-derivation of the B6.C-H2d/bBy inbred mouse strain to remove an unwanted spontaneously arising new barrier to histocompatibility.” 2003. Thesis, Central Connecticut State University. Accessed October 20, 2019. http://content.library.ccsu.edu/u?/ccsutheses,1094.

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

MLA Handbook (7th Edition):

LaMonica, Kristi April. “Re-derivation of the B6.C-H2d/bBy inbred mouse strain to remove an unwanted spontaneously arising new barrier to histocompatibility.” 2003. Web. 20 Oct 2019.

Vancouver:

LaMonica KA. Re-derivation of the B6.C-H2d/bBy inbred mouse strain to remove an unwanted spontaneously arising new barrier to histocompatibility. [Internet] [Thesis]. Central Connecticut State University; 2003. [cited 2019 Oct 20]. Available from: http://content.library.ccsu.edu/u?/ccsutheses,1094.

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

Council of Science Editors:

LaMonica KA. Re-derivation of the B6.C-H2d/bBy inbred mouse strain to remove an unwanted spontaneously arising new barrier to histocompatibility. [Thesis]. Central Connecticut State University; 2003. Available from: http://content.library.ccsu.edu/u?/ccsutheses,1094

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


NSYSU

2. Chang, Ching-Fen. Localization and comparative analysis of microsatellite repeats in human chromosome 20.

Degree: Master, Institute of Biomedical Sciences, 2003, NSYSU

 Abstract . A draft of the whole human genomic sequence has been completed and published in 2001. Researches on structural genomics, functional genomics, proteomics, evolutionary… (more)

Subjects/Keywords: human chromosome 14; human chromosome 20; microsatellite

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chang, C. (2003). Localization and comparative analysis of microsatellite repeats in human chromosome 20. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0717103-182723

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):

Chang, Ching-Fen. “Localization and comparative analysis of microsatellite repeats in human chromosome 20.” 2003. Thesis, NSYSU. Accessed October 20, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0717103-182723.

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

MLA Handbook (7th Edition):

Chang, Ching-Fen. “Localization and comparative analysis of microsatellite repeats in human chromosome 20.” 2003. Web. 20 Oct 2019.

Vancouver:

Chang C. Localization and comparative analysis of microsatellite repeats in human chromosome 20. [Internet] [Thesis]. NSYSU; 2003. [cited 2019 Oct 20]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0717103-182723.

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

Council of Science Editors:

Chang C. Localization and comparative analysis of microsatellite repeats in human chromosome 20. [Thesis]. NSYSU; 2003. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0717103-182723

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


University of Adelaide

3. Allen, Lillian Rose. Investigation of the role of the MID1 and MID2 genes in the Opitz syndrome.

Degree: 2003, University of Adelaide

 To determine whether or not the MID1 and MID2 genes contribute to the Optiz Syndrome (OS) phenotype, a mutation screen was undertaken. Fifteen Australasian and… (more)

Subjects/Keywords: Sex Chromosome Abnormalities  – familial & genetic

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Allen, L. R. (2003). Investigation of the role of the MID1 and MID2 genes in the Opitz syndrome. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/116371

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):

Allen, Lillian Rose. “Investigation of the role of the MID1 and MID2 genes in the Opitz syndrome.” 2003. Thesis, University of Adelaide. Accessed October 20, 2019. http://hdl.handle.net/2440/116371.

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

MLA Handbook (7th Edition):

Allen, Lillian Rose. “Investigation of the role of the MID1 and MID2 genes in the Opitz syndrome.” 2003. Web. 20 Oct 2019.

Vancouver:

Allen LR. Investigation of the role of the MID1 and MID2 genes in the Opitz syndrome. [Internet] [Thesis]. University of Adelaide; 2003. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2440/116371.

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

Council of Science Editors:

Allen LR. Investigation of the role of the MID1 and MID2 genes in the Opitz syndrome. [Thesis]. University of Adelaide; 2003. Available from: http://hdl.handle.net/2440/116371

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


University of Adelaide

4. Hu, Dong Gui. Development of a DNA microarray for detection of aneuploidy in single blastomeres / Dong Gui Hu.

Degree: 2004, University of Adelaide

Subjects/Keywords: Aneuploidy; Sex chromosome abnormalities

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hu, D. G. (2004). Development of a DNA microarray for detection of aneuploidy in single blastomeres / Dong Gui Hu. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/22076

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):

Hu, Dong Gui. “Development of a DNA microarray for detection of aneuploidy in single blastomeres / Dong Gui Hu.” 2004. Thesis, University of Adelaide. Accessed October 20, 2019. http://hdl.handle.net/2440/22076.

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

MLA Handbook (7th Edition):

Hu, Dong Gui. “Development of a DNA microarray for detection of aneuploidy in single blastomeres / Dong Gui Hu.” 2004. Web. 20 Oct 2019.

Vancouver:

Hu DG. Development of a DNA microarray for detection of aneuploidy in single blastomeres / Dong Gui Hu. [Internet] [Thesis]. University of Adelaide; 2004. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2440/22076.

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

Council of Science Editors:

Hu DG. Development of a DNA microarray for detection of aneuploidy in single blastomeres / Dong Gui Hu. [Thesis]. University of Adelaide; 2004. Available from: http://hdl.handle.net/2440/22076

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


Michigan State University

5. Jones, Nicole M. Apolipoprotein E as an hereditary risk factor for nondisjunction : a feasibility study.

Degree: MS, 2002, Michigan State University

Subjects/Keywords: Trisomy; Chromosome disorders; Genetic disorders

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Jones, N. M. (2002). Apolipoprotein E as an hereditary risk factor for nondisjunction : a feasibility study. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:31607

Chicago Manual of Style (16th Edition):

Jones, Nicole M. “Apolipoprotein E as an hereditary risk factor for nondisjunction : a feasibility study.” 2002. Masters Thesis, Michigan State University. Accessed October 20, 2019. http://etd.lib.msu.edu/islandora/object/etd:31607.

MLA Handbook (7th Edition):

Jones, Nicole M. “Apolipoprotein E as an hereditary risk factor for nondisjunction : a feasibility study.” 2002. Web. 20 Oct 2019.

Vancouver:

Jones NM. Apolipoprotein E as an hereditary risk factor for nondisjunction : a feasibility study. [Internet] [Masters thesis]. Michigan State University; 2002. [cited 2019 Oct 20]. Available from: http://etd.lib.msu.edu/islandora/object/etd:31607.

Council of Science Editors:

Jones NM. Apolipoprotein E as an hereditary risk factor for nondisjunction : a feasibility study. [Masters Thesis]. Michigan State University; 2002. Available from: http://etd.lib.msu.edu/islandora/object/etd:31607


University of Hong Kong

6. 鍾文健.; Chung, Man-kin. A study on the prevalence of AZFd Y-chromosome microdeletion in Hong Kong Chinese men with severe male factor infertility.

Degree: Master of Medical Sciences, 2004, University of Hong Kong

published_or_final_version

Medical Sciences

Master

Master of Medical Sciences

Subjects/Keywords: Chromosome polymorphism; Polymerase chain reaction.; Infertility, Male.; Oligospermia.; Y chromosome.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

鍾文健.; Chung, M. (2004). A study on the prevalence of AZFd Y-chromosome microdeletion in Hong Kong Chinese men with severe male factor infertility. (Masters Thesis). University of Hong Kong. Retrieved from Chung, M. [鍾文健]. (2004). A study on the prevalence of AZFd Y-chromosome microdeletion in Hong Kong Chinese men with severe male factor infertility. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197169 ; http://dx.doi.org/10.5353/th_b3197169 ; http://hdl.handle.net/10722/30017

Chicago Manual of Style (16th Edition):

鍾文健.; Chung, Man-kin. “A study on the prevalence of AZFd Y-chromosome microdeletion in Hong Kong Chinese men with severe male factor infertility.” 2004. Masters Thesis, University of Hong Kong. Accessed October 20, 2019. Chung, M. [鍾文健]. (2004). A study on the prevalence of AZFd Y-chromosome microdeletion in Hong Kong Chinese men with severe male factor infertility. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197169 ; http://dx.doi.org/10.5353/th_b3197169 ; http://hdl.handle.net/10722/30017.

MLA Handbook (7th Edition):

鍾文健.; Chung, Man-kin. “A study on the prevalence of AZFd Y-chromosome microdeletion in Hong Kong Chinese men with severe male factor infertility.” 2004. Web. 20 Oct 2019.

Vancouver:

鍾文健.; Chung M. A study on the prevalence of AZFd Y-chromosome microdeletion in Hong Kong Chinese men with severe male factor infertility. [Internet] [Masters thesis]. University of Hong Kong; 2004. [cited 2019 Oct 20]. Available from: Chung, M. [鍾文健]. (2004). A study on the prevalence of AZFd Y-chromosome microdeletion in Hong Kong Chinese men with severe male factor infertility. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197169 ; http://dx.doi.org/10.5353/th_b3197169 ; http://hdl.handle.net/10722/30017.

Council of Science Editors:

鍾文健.; Chung M. A study on the prevalence of AZFd Y-chromosome microdeletion in Hong Kong Chinese men with severe male factor infertility. [Masters Thesis]. University of Hong Kong; 2004. Available from: Chung, M. [鍾文健]. (2004). A study on the prevalence of AZFd Y-chromosome microdeletion in Hong Kong Chinese men with severe male factor infertility. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197169 ; http://dx.doi.org/10.5353/th_b3197169 ; http://hdl.handle.net/10722/30017


University of Kentucky

7. Myka, Jennifer Leigh. COMPARATIVE GENE MAPPING FOR EQUUS PRZEWALSKII AND E. HEMIONUS ONAGER WITH INVESTIGATION OF A HOMOLOGOUS CHROMOSOME POLYMORPHISM IN EQUIDAE.

Degree: 2003, University of Kentucky

 The ten extant species in the genus Equus are separated by less than 3.7 million years of evolution. Three lines of investigation were pursued to… (more)

Subjects/Keywords: Comparative Gene Map; Chromosome Number Polymorphism; Equus; Chromosome Rearrangement; Robertsonian Translocation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Myka, J. L. (2003). COMPARATIVE GENE MAPPING FOR EQUUS PRZEWALSKII AND E. HEMIONUS ONAGER WITH INVESTIGATION OF A HOMOLOGOUS CHROMOSOME POLYMORPHISM IN EQUIDAE. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/gradschool_diss/476

Chicago Manual of Style (16th Edition):

Myka, Jennifer Leigh. “COMPARATIVE GENE MAPPING FOR EQUUS PRZEWALSKII AND E. HEMIONUS ONAGER WITH INVESTIGATION OF A HOMOLOGOUS CHROMOSOME POLYMORPHISM IN EQUIDAE.” 2003. Doctoral Dissertation, University of Kentucky. Accessed October 20, 2019. https://uknowledge.uky.edu/gradschool_diss/476.

MLA Handbook (7th Edition):

Myka, Jennifer Leigh. “COMPARATIVE GENE MAPPING FOR EQUUS PRZEWALSKII AND E. HEMIONUS ONAGER WITH INVESTIGATION OF A HOMOLOGOUS CHROMOSOME POLYMORPHISM IN EQUIDAE.” 2003. Web. 20 Oct 2019.

Vancouver:

Myka JL. COMPARATIVE GENE MAPPING FOR EQUUS PRZEWALSKII AND E. HEMIONUS ONAGER WITH INVESTIGATION OF A HOMOLOGOUS CHROMOSOME POLYMORPHISM IN EQUIDAE. [Internet] [Doctoral dissertation]. University of Kentucky; 2003. [cited 2019 Oct 20]. Available from: https://uknowledge.uky.edu/gradschool_diss/476.

Council of Science Editors:

Myka JL. COMPARATIVE GENE MAPPING FOR EQUUS PRZEWALSKII AND E. HEMIONUS ONAGER WITH INVESTIGATION OF A HOMOLOGOUS CHROMOSOME POLYMORPHISM IN EQUIDAE. [Doctoral Dissertation]. University of Kentucky; 2003. Available from: https://uknowledge.uky.edu/gradschool_diss/476


University of Oxford

8. Neville, Matt J. Characterisation of the genomic region around the TNF locus within the human major histocompatibility complex in the chromosome band 6p21.3.

Degree: 2000, University of Oxford

 It is becoming increasingly apparent that many of the genes in the class III region of the human Major Histocompatibility Complex encode proteins involved in… (more)

Subjects/Keywords: 572.8; Chromosome banding : Tumor necrosis factor

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Neville, M. J. (2000). Characterisation of the genomic region around the TNF locus within the human major histocompatibility complex in the chromosome band 6p21.3. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:1fcb0019-0b54-418a-a44c-b1b4a7d5a51e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325981

Chicago Manual of Style (16th Edition):

Neville, Matt J. “Characterisation of the genomic region around the TNF locus within the human major histocompatibility complex in the chromosome band 6p21.3.” 2000. Doctoral Dissertation, University of Oxford. Accessed October 20, 2019. http://ora.ox.ac.uk/objects/uuid:1fcb0019-0b54-418a-a44c-b1b4a7d5a51e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325981.

MLA Handbook (7th Edition):

Neville, Matt J. “Characterisation of the genomic region around the TNF locus within the human major histocompatibility complex in the chromosome band 6p21.3.” 2000. Web. 20 Oct 2019.

Vancouver:

Neville MJ. Characterisation of the genomic region around the TNF locus within the human major histocompatibility complex in the chromosome band 6p21.3. [Internet] [Doctoral dissertation]. University of Oxford; 2000. [cited 2019 Oct 20]. Available from: http://ora.ox.ac.uk/objects/uuid:1fcb0019-0b54-418a-a44c-b1b4a7d5a51e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325981.

Council of Science Editors:

Neville MJ. Characterisation of the genomic region around the TNF locus within the human major histocompatibility complex in the chromosome band 6p21.3. [Doctoral Dissertation]. University of Oxford; 2000. Available from: http://ora.ox.ac.uk/objects/uuid:1fcb0019-0b54-418a-a44c-b1b4a7d5a51e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325981


Johannes Gutenberg Universität Mainz

9. Niketeghad, Fataneh. Analyse genomischer Imbalancen in hepatozellulären Karzinomen und präneoplastischen Leberläsionen.

Degree: 2004, Johannes Gutenberg Universität Mainz

Das hepatozelluläre Karzinom (HCC) ist mit ungefähr 1,000,000 neuen Fällen pro Jahr einer der häufigsten malignen Tumore weltweit. Es ist hauptsächlich in Südost-Asien und im… (more)

Subjects/Keywords: chromosomale Imbalancen; chromosome imbalances; Life sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Niketeghad, F. (2004). Analyse genomischer Imbalancen in hepatozellulären Karzinomen und präneoplastischen Leberläsionen. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2005/687/

Chicago Manual of Style (16th Edition):

Niketeghad, Fataneh. “Analyse genomischer Imbalancen in hepatozellulären Karzinomen und präneoplastischen Leberläsionen.” 2004. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed October 20, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2005/687/.

MLA Handbook (7th Edition):

Niketeghad, Fataneh. “Analyse genomischer Imbalancen in hepatozellulären Karzinomen und präneoplastischen Leberläsionen.” 2004. Web. 20 Oct 2019.

Vancouver:

Niketeghad F. Analyse genomischer Imbalancen in hepatozellulären Karzinomen und präneoplastischen Leberläsionen. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2004. [cited 2019 Oct 20]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2005/687/.

Council of Science Editors:

Niketeghad F. Analyse genomischer Imbalancen in hepatozellulären Karzinomen und präneoplastischen Leberläsionen. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2004. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2005/687/


University of Hong Kong

10. Wong, Yee-man, Elaine. Identification and characterization of VCY2 interacting proteins.

Degree: M. Phil., 2002, University of Hong Kong

published_or_final_version

Obstetrics and Gynaecology

Master

Master of Philosophy

Advisors/Committee Members: Yeung, WSB.

Subjects/Keywords: Infertility, Male - Genetic aspects.; Y chromosome.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wong, Yee-man, E. (2002). Identification and characterization of VCY2 interacting proteins. (Masters Thesis). University of Hong Kong. Retrieved from Wong, Y. E. [王怡雯]. (2002). Identification and characterization of VCY2 interacting proteins. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122800 ; http://dx.doi.org/10.5353/th_b3122800 ; http://hdl.handle.net/10722/39503

Chicago Manual of Style (16th Edition):

Wong, Yee-man, Elaine. “Identification and characterization of VCY2 interacting proteins.” 2002. Masters Thesis, University of Hong Kong. Accessed October 20, 2019. Wong, Y. E. [王怡雯]. (2002). Identification and characterization of VCY2 interacting proteins. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122800 ; http://dx.doi.org/10.5353/th_b3122800 ; http://hdl.handle.net/10722/39503.

MLA Handbook (7th Edition):

Wong, Yee-man, Elaine. “Identification and characterization of VCY2 interacting proteins.” 2002. Web. 20 Oct 2019.

Vancouver:

Wong, Yee-man E. Identification and characterization of VCY2 interacting proteins. [Internet] [Masters thesis]. University of Hong Kong; 2002. [cited 2019 Oct 20]. Available from: Wong, Y. E. [王怡雯]. (2002). Identification and characterization of VCY2 interacting proteins. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122800 ; http://dx.doi.org/10.5353/th_b3122800 ; http://hdl.handle.net/10722/39503.

Council of Science Editors:

Wong, Yee-man E. Identification and characterization of VCY2 interacting proteins. [Masters Thesis]. University of Hong Kong; 2002. Available from: Wong, Y. E. [王怡雯]. (2002). Identification and characterization of VCY2 interacting proteins. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122800 ; http://dx.doi.org/10.5353/th_b3122800 ; http://hdl.handle.net/10722/39503


University of Bath

11. Charalambous, M. Characterisation of a putative control element which lies between the imprinted IGF2 and H19 genes in the mouse.

Degree: PhD, 2000, University of Bath

Subjects/Keywords: 572.8; Chromosome 7; Beckwith Wiedemann syndrome

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Charalambous, M. (2000). Characterisation of a putative control element which lies between the imprinted IGF2 and H19 genes in the mouse. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/characterisation-of-a-putative-control-element-which-lies-between-the-imprinted-igf2-and-h19-genes-in-the-mouse(d0c1d19d-6329-4ac8-ba19-2e5b5cf01a41).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341145

Chicago Manual of Style (16th Edition):

Charalambous, M. “Characterisation of a putative control element which lies between the imprinted IGF2 and H19 genes in the mouse.” 2000. Doctoral Dissertation, University of Bath. Accessed October 20, 2019. https://researchportal.bath.ac.uk/en/studentthesis/characterisation-of-a-putative-control-element-which-lies-between-the-imprinted-igf2-and-h19-genes-in-the-mouse(d0c1d19d-6329-4ac8-ba19-2e5b5cf01a41).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341145.

MLA Handbook (7th Edition):

Charalambous, M. “Characterisation of a putative control element which lies between the imprinted IGF2 and H19 genes in the mouse.” 2000. Web. 20 Oct 2019.

Vancouver:

Charalambous M. Characterisation of a putative control element which lies between the imprinted IGF2 and H19 genes in the mouse. [Internet] [Doctoral dissertation]. University of Bath; 2000. [cited 2019 Oct 20]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/characterisation-of-a-putative-control-element-which-lies-between-the-imprinted-igf2-and-h19-genes-in-the-mouse(d0c1d19d-6329-4ac8-ba19-2e5b5cf01a41).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341145.

Council of Science Editors:

Charalambous M. Characterisation of a putative control element which lies between the imprinted IGF2 and H19 genes in the mouse. [Doctoral Dissertation]. University of Bath; 2000. Available from: https://researchportal.bath.ac.uk/en/studentthesis/characterisation-of-a-putative-control-element-which-lies-between-the-imprinted-igf2-and-h19-genes-in-the-mouse(d0c1d19d-6329-4ac8-ba19-2e5b5cf01a41).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341145


The Ohio State University

12. Maybruck, Julie Lauren. The identification and characterization of new y-chromosome short tandem repeat LOCI and a closer look at the YpXq 3-4mb homology block.

Degree: PhD, Molecular Genetics, 2004, The Ohio State University

 The ability to discriminate between individuals is the basis of DNA forensics. Variable autosomal short tandem repeat (STR) loci are currently the markers used in… (more)

Subjects/Keywords: Biology, Genetics; Y-chromosome; Y-chromosome short tandem repeats; Y-STRs; Y-chromosome microsatellites

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Maybruck, J. L. (2004). The identification and characterization of new y-chromosome short tandem repeat LOCI and a closer look at the YpXq 3-4mb homology block. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1085600591

Chicago Manual of Style (16th Edition):

Maybruck, Julie Lauren. “The identification and characterization of new y-chromosome short tandem repeat LOCI and a closer look at the YpXq 3-4mb homology block.” 2004. Doctoral Dissertation, The Ohio State University. Accessed October 20, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1085600591.

MLA Handbook (7th Edition):

Maybruck, Julie Lauren. “The identification and characterization of new y-chromosome short tandem repeat LOCI and a closer look at the YpXq 3-4mb homology block.” 2004. Web. 20 Oct 2019.

Vancouver:

Maybruck JL. The identification and characterization of new y-chromosome short tandem repeat LOCI and a closer look at the YpXq 3-4mb homology block. [Internet] [Doctoral dissertation]. The Ohio State University; 2004. [cited 2019 Oct 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1085600591.

Council of Science Editors:

Maybruck JL. The identification and characterization of new y-chromosome short tandem repeat LOCI and a closer look at the YpXq 3-4mb homology block. [Doctoral Dissertation]. The Ohio State University; 2004. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1085600591


University of Kentucky

13. Mains, Christine Marie. COMPARATIVE MAPPING: HOMOLOGY WITHIN THE ORDER PERISSODACTYLA OF FOUR GENES LOCATED ON EQUUS CABALLUS CHROMOSOME 20.

Degree: 2004, University of Kentucky

 Since changes in chromosome morphology contribute to the knowledge of evolution as well as to chromosome dynamics, this study looks specifically at one chromosome compared… (more)

Subjects/Keywords: Chromosome Mapping; FISH; Equus caballus; Equidae; Major Histocompatibility Complex

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mains, C. M. (2004). COMPARATIVE MAPPING: HOMOLOGY WITHIN THE ORDER PERISSODACTYLA OF FOUR GENES LOCATED ON EQUUS CABALLUS CHROMOSOME 20. (Masters Thesis). University of Kentucky. Retrieved from http://uknowledge.uky.edu/gradschool_theses/418

Chicago Manual of Style (16th Edition):

Mains, Christine Marie. “COMPARATIVE MAPPING: HOMOLOGY WITHIN THE ORDER PERISSODACTYLA OF FOUR GENES LOCATED ON EQUUS CABALLUS CHROMOSOME 20.” 2004. Masters Thesis, University of Kentucky. Accessed October 20, 2019. http://uknowledge.uky.edu/gradschool_theses/418.

MLA Handbook (7th Edition):

Mains, Christine Marie. “COMPARATIVE MAPPING: HOMOLOGY WITHIN THE ORDER PERISSODACTYLA OF FOUR GENES LOCATED ON EQUUS CABALLUS CHROMOSOME 20.” 2004. Web. 20 Oct 2019.

Vancouver:

Mains CM. COMPARATIVE MAPPING: HOMOLOGY WITHIN THE ORDER PERISSODACTYLA OF FOUR GENES LOCATED ON EQUUS CABALLUS CHROMOSOME 20. [Internet] [Masters thesis]. University of Kentucky; 2004. [cited 2019 Oct 20]. Available from: http://uknowledge.uky.edu/gradschool_theses/418.

Council of Science Editors:

Mains CM. COMPARATIVE MAPPING: HOMOLOGY WITHIN THE ORDER PERISSODACTYLA OF FOUR GENES LOCATED ON EQUUS CABALLUS CHROMOSOME 20. [Masters Thesis]. University of Kentucky; 2004. Available from: http://uknowledge.uky.edu/gradschool_theses/418


Texas A&M University

14. Kim, Jeong-Soon. Genomic analysis of sorghum by fluorescence in situ hybridization.

Degree: 2004, Texas A&M University

 The reliability of genome analysis and proficiency of genetic manipulation in vivo and in vitro are increased by assignment of linkage groups to specific chromosomes,… (more)

Subjects/Keywords: FISH; sorghum; chromosome; DNA; gene; cytogenetic map; physical map

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kim, J. (2004). Genomic analysis of sorghum by fluorescence in situ hybridization. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/1184

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):

Kim, Jeong-Soon. “Genomic analysis of sorghum by fluorescence in situ hybridization.” 2004. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/1184.

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

MLA Handbook (7th Edition):

Kim, Jeong-Soon. “Genomic analysis of sorghum by fluorescence in situ hybridization.” 2004. Web. 20 Oct 2019.

Vancouver:

Kim J. Genomic analysis of sorghum by fluorescence in situ hybridization. [Internet] [Thesis]. Texas A&M University; 2004. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/1184.

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

Council of Science Editors:

Kim J. Genomic analysis of sorghum by fluorescence in situ hybridization. [Thesis]. Texas A&M University; 2004. Available from: http://hdl.handle.net/1969.1/1184

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


University of Cincinnati

15. STUABACH, AMY ELIZABETH. THE REGULATION OF BubR1 EXPRESSION BY p53: A ROLE FOR p53 IN THE MITOTIC SPINDLE CHECKPOINT AND CHROMOSOME INSTABILITY.

Degree: MS, Medicine : Cell and Molecular Biology, 2004, University of Cincinnati

 During mitosis, chromosomes must segregate equally to daughter cells thus ensuring genomic stability. The tumor suppressor protein, p53, plays a key role in maintaining a… (more)

Subjects/Keywords: BubR1; p53; mitotic spindle checkpoint; chromosome instability; aneuploidy; cancer

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

STUABACH, A. E. (2004). THE REGULATION OF BubR1 EXPRESSION BY p53: A ROLE FOR p53 IN THE MITOTIC SPINDLE CHECKPOINT AND CHROMOSOME INSTABILITY. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1100831777

Chicago Manual of Style (16th Edition):

STUABACH, AMY ELIZABETH. “THE REGULATION OF BubR1 EXPRESSION BY p53: A ROLE FOR p53 IN THE MITOTIC SPINDLE CHECKPOINT AND CHROMOSOME INSTABILITY.” 2004. Masters Thesis, University of Cincinnati. Accessed October 20, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1100831777.

MLA Handbook (7th Edition):

STUABACH, AMY ELIZABETH. “THE REGULATION OF BubR1 EXPRESSION BY p53: A ROLE FOR p53 IN THE MITOTIC SPINDLE CHECKPOINT AND CHROMOSOME INSTABILITY.” 2004. Web. 20 Oct 2019.

Vancouver:

STUABACH AE. THE REGULATION OF BubR1 EXPRESSION BY p53: A ROLE FOR p53 IN THE MITOTIC SPINDLE CHECKPOINT AND CHROMOSOME INSTABILITY. [Internet] [Masters thesis]. University of Cincinnati; 2004. [cited 2019 Oct 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1100831777.

Council of Science Editors:

STUABACH AE. THE REGULATION OF BubR1 EXPRESSION BY p53: A ROLE FOR p53 IN THE MITOTIC SPINDLE CHECKPOINT AND CHROMOSOME INSTABILITY. [Masters Thesis]. University of Cincinnati; 2004. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1100831777


University of Edinburgh

16. Petruti-Mot, Anca. Genetic and functional analysis of topoisomerase II in vertebrates.

Degree: PhD, 2000, University of Edinburgh

 The degree of DNA supercoiling in the cell is carefully controlled by DNA topoisomerases. These enzymes catalyze the passage of individual DNA strands (Type I… (more)

Subjects/Keywords: DNA topoisomerases; Chromatin condensation; Chromosome segregation; Mitosis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Petruti-Mot, A. (2000). Genetic and functional analysis of topoisomerase II in vertebrates. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8985

Chicago Manual of Style (16th Edition):

Petruti-Mot, Anca. “Genetic and functional analysis of topoisomerase II in vertebrates.” 2000. Doctoral Dissertation, University of Edinburgh. Accessed October 20, 2019. http://hdl.handle.net/1842/8985.

MLA Handbook (7th Edition):

Petruti-Mot, Anca. “Genetic and functional analysis of topoisomerase II in vertebrates.” 2000. Web. 20 Oct 2019.

Vancouver:

Petruti-Mot A. Genetic and functional analysis of topoisomerase II in vertebrates. [Internet] [Doctoral dissertation]. University of Edinburgh; 2000. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1842/8985.

Council of Science Editors:

Petruti-Mot A. Genetic and functional analysis of topoisomerase II in vertebrates. [Doctoral Dissertation]. University of Edinburgh; 2000. Available from: http://hdl.handle.net/1842/8985


McGill University

17. Lemmens, Trudo. Genetic information and insurance : a contextual analysis of legal and regulatory means of promoting just distributions.

Degree: Doctor of Civil Law, Institute of Comparative Law., 2003, McGill University

This thesis analyzes the rationale, appropriateness and value of the available legal and regulatory means to deal with genetic discrimination in the context of insurance.… (more)

Subjects/Keywords: Insurance law; Human chromosome abnormalities  – Diagnosis; Privacy, Right of

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lemmens, T. (2003). Genetic information and insurance : a contextual analysis of legal and regulatory means of promoting just distributions. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile84213.pdf

Chicago Manual of Style (16th Edition):

Lemmens, Trudo. “Genetic information and insurance : a contextual analysis of legal and regulatory means of promoting just distributions.” 2003. Doctoral Dissertation, McGill University. Accessed October 20, 2019. http://digitool.library.mcgill.ca/thesisfile84213.pdf.

MLA Handbook (7th Edition):

Lemmens, Trudo. “Genetic information and insurance : a contextual analysis of legal and regulatory means of promoting just distributions.” 2003. Web. 20 Oct 2019.

Vancouver:

Lemmens T. Genetic information and insurance : a contextual analysis of legal and regulatory means of promoting just distributions. [Internet] [Doctoral dissertation]. McGill University; 2003. [cited 2019 Oct 20]. Available from: http://digitool.library.mcgill.ca/thesisfile84213.pdf.

Council of Science Editors:

Lemmens T. Genetic information and insurance : a contextual analysis of legal and regulatory means of promoting just distributions. [Doctoral Dissertation]. McGill University; 2003. Available from: http://digitool.library.mcgill.ca/thesisfile84213.pdf

18. SRIVIDYA RAJAGOPALAN. An analysis of the role of the Schizosaccharomyces pombe homolog of survivin, Bir1p, in mitosis.

Degree: 2004, National University of Singapore

Subjects/Keywords: S. pombe; Mitosis; IAPs; BIR domain; Microtubules; chromosome passengers

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

RAJAGOPALAN, S. (2004). An analysis of the role of the Schizosaccharomyces pombe homolog of survivin, Bir1p, in mitosis. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/14022

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):

RAJAGOPALAN, SRIVIDYA. “An analysis of the role of the Schizosaccharomyces pombe homolog of survivin, Bir1p, in mitosis.” 2004. Thesis, National University of Singapore. Accessed October 20, 2019. http://scholarbank.nus.edu.sg/handle/10635/14022.

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

MLA Handbook (7th Edition):

RAJAGOPALAN, SRIVIDYA. “An analysis of the role of the Schizosaccharomyces pombe homolog of survivin, Bir1p, in mitosis.” 2004. Web. 20 Oct 2019.

Vancouver:

RAJAGOPALAN S. An analysis of the role of the Schizosaccharomyces pombe homolog of survivin, Bir1p, in mitosis. [Internet] [Thesis]. National University of Singapore; 2004. [cited 2019 Oct 20]. Available from: http://scholarbank.nus.edu.sg/handle/10635/14022.

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

Council of Science Editors:

RAJAGOPALAN S. An analysis of the role of the Schizosaccharomyces pombe homolog of survivin, Bir1p, in mitosis. [Thesis]. National University of Singapore; 2004. Available from: http://scholarbank.nus.edu.sg/handle/10635/14022

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

19. TAN MAY MAY, JEANNE. Isolation and characterization of the novel human gene, MOST-1.

Degree: 2004, National University of Singapore

Subjects/Keywords: MOST-1; breast; prostate; cancer; chromosome 8q24.2; HPV

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

TAN MAY MAY, J. (2004). Isolation and characterization of the novel human gene, MOST-1. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/16936

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):

TAN MAY MAY, JEANNE. “Isolation and characterization of the novel human gene, MOST-1.” 2004. Thesis, National University of Singapore. Accessed October 20, 2019. http://scholarbank.nus.edu.sg/handle/10635/16936.

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

MLA Handbook (7th Edition):

TAN MAY MAY, JEANNE. “Isolation and characterization of the novel human gene, MOST-1.” 2004. Web. 20 Oct 2019.

Vancouver:

TAN MAY MAY J. Isolation and characterization of the novel human gene, MOST-1. [Internet] [Thesis]. National University of Singapore; 2004. [cited 2019 Oct 20]. Available from: http://scholarbank.nus.edu.sg/handle/10635/16936.

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

Council of Science Editors:

TAN MAY MAY J. Isolation and characterization of the novel human gene, MOST-1. [Thesis]. National University of Singapore; 2004. Available from: http://scholarbank.nus.edu.sg/handle/10635/16936

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


Michigan State University

20. Kaplan, Evan L. Introduction of chromosome 15 into the immortalized human fibroblast cell strain MSU-1,1 prevents malignant transformation by the T24 H-RAS oncogene.

Degree: PhD, Department of Pharmacology and Toxicology, 2002, Michigan State University

Subjects/Keywords: Carcinogenesis; Cancer – Genetic aspects; Fibroblasts; Human chromosome 15; Oncogenes

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kaplan, E. L. (2002). Introduction of chromosome 15 into the immortalized human fibroblast cell strain MSU-1,1 prevents malignant transformation by the T24 H-RAS oncogene. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:31581

Chicago Manual of Style (16th Edition):

Kaplan, Evan L. “Introduction of chromosome 15 into the immortalized human fibroblast cell strain MSU-1,1 prevents malignant transformation by the T24 H-RAS oncogene.” 2002. Doctoral Dissertation, Michigan State University. Accessed October 20, 2019. http://etd.lib.msu.edu/islandora/object/etd:31581.

MLA Handbook (7th Edition):

Kaplan, Evan L. “Introduction of chromosome 15 into the immortalized human fibroblast cell strain MSU-1,1 prevents malignant transformation by the T24 H-RAS oncogene.” 2002. Web. 20 Oct 2019.

Vancouver:

Kaplan EL. Introduction of chromosome 15 into the immortalized human fibroblast cell strain MSU-1,1 prevents malignant transformation by the T24 H-RAS oncogene. [Internet] [Doctoral dissertation]. Michigan State University; 2002. [cited 2019 Oct 20]. Available from: http://etd.lib.msu.edu/islandora/object/etd:31581.

Council of Science Editors:

Kaplan EL. Introduction of chromosome 15 into the immortalized human fibroblast cell strain MSU-1,1 prevents malignant transformation by the T24 H-RAS oncogene. [Doctoral Dissertation]. Michigan State University; 2002. Available from: http://etd.lib.msu.edu/islandora/object/etd:31581


Université de Montréal

21. Moujahidine, Myriam. Localisation d'un locus pour trait quantitatif pour l'hypertension sur les chromosomes 16 et 17 du rat Dahl Salt-Sensitive .

Degree: 2004, Université de Montréal

Subjects/Keywords: Hypertension essentielle; Pression artérielle; Pression sanguine; Rat congénique; Liaison (génétique); Modèle animal; Génétique moléculaire; Chromosome 16; Chromosome 17

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Moujahidine, M. (2004). Localisation d'un locus pour trait quantitatif pour l'hypertension sur les chromosomes 16 et 17 du rat Dahl Salt-Sensitive . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/14652

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):

Moujahidine, Myriam. “Localisation d'un locus pour trait quantitatif pour l'hypertension sur les chromosomes 16 et 17 du rat Dahl Salt-Sensitive .” 2004. Thesis, Université de Montréal. Accessed October 20, 2019. http://hdl.handle.net/1866/14652.

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

MLA Handbook (7th Edition):

Moujahidine, Myriam. “Localisation d'un locus pour trait quantitatif pour l'hypertension sur les chromosomes 16 et 17 du rat Dahl Salt-Sensitive .” 2004. Web. 20 Oct 2019.

Vancouver:

Moujahidine M. Localisation d'un locus pour trait quantitatif pour l'hypertension sur les chromosomes 16 et 17 du rat Dahl Salt-Sensitive . [Internet] [Thesis]. Université de Montréal; 2004. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1866/14652.

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

Council of Science Editors:

Moujahidine M. Localisation d'un locus pour trait quantitatif pour l'hypertension sur les chromosomes 16 et 17 du rat Dahl Salt-Sensitive . [Thesis]. Université de Montréal; 2004. Available from: http://hdl.handle.net/1866/14652

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

22. Sergei Kalupniek. Diversidade genética e desempenho forense da análise de haplótipos de locos microssatélites no cromossomo Y em populações brasileiras.

Degree: 2002, Universidade Católica de Brasilia

 Polimorfismos de DNA no cromossomo Y em humanos têm sido utilizados de forma crescente para estudos evolucionários e na identificação individual. Locos microssatélites, também comumente… (more)

Subjects/Keywords: Ciências Biológicas; genética - análise; genética forense; cromossomo Y; microssatélites; chromosome; polymorphisms; Ciências Biológicas

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kalupniek, S. (2002). Diversidade genética e desempenho forense da análise de haplótipos de locos microssatélites no cromossomo Y em populações brasileiras. (Masters Thesis). Universidade Católica de Brasilia. Retrieved from http://www.bdtd.ucb.br/tede/tde_busca/arquivo.php?codArquivo=117

Chicago Manual of Style (16th Edition):

Kalupniek, Sergei. “Diversidade genética e desempenho forense da análise de haplótipos de locos microssatélites no cromossomo Y em populações brasileiras.” 2002. Masters Thesis, Universidade Católica de Brasilia. Accessed October 20, 2019. http://www.bdtd.ucb.br/tede/tde_busca/arquivo.php?codArquivo=117.

MLA Handbook (7th Edition):

Kalupniek, Sergei. “Diversidade genética e desempenho forense da análise de haplótipos de locos microssatélites no cromossomo Y em populações brasileiras.” 2002. Web. 20 Oct 2019.

Vancouver:

Kalupniek S. Diversidade genética e desempenho forense da análise de haplótipos de locos microssatélites no cromossomo Y em populações brasileiras. [Internet] [Masters thesis]. Universidade Católica de Brasilia; 2002. [cited 2019 Oct 20]. Available from: http://www.bdtd.ucb.br/tede/tde_busca/arquivo.php?codArquivo=117.

Council of Science Editors:

Kalupniek S. Diversidade genética e desempenho forense da análise de haplótipos de locos microssatélites no cromossomo Y em populações brasileiras. [Masters Thesis]. Universidade Católica de Brasilia; 2002. Available from: http://www.bdtd.ucb.br/tede/tde_busca/arquivo.php?codArquivo=117


Université de Montréal

23. Chalhoub, Nader. Identification par clonage positionnel du gène grey-lethal (gl) chez la souris .

Degree: 2004, Université de Montréal

Subjects/Keywords: Ostéopétrose; Ostéoclaste; Mélanocyte; OCL; Grey-lethal; YAC; BAC; Contig; Chromosome 10; 6q21

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chalhoub, N. (2004). Identification par clonage positionnel du gène grey-lethal (gl) chez la souris . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/14647

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):

Chalhoub, Nader. “Identification par clonage positionnel du gène grey-lethal (gl) chez la souris .” 2004. Thesis, Université de Montréal. Accessed October 20, 2019. http://hdl.handle.net/1866/14647.

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

MLA Handbook (7th Edition):

Chalhoub, Nader. “Identification par clonage positionnel du gène grey-lethal (gl) chez la souris .” 2004. Web. 20 Oct 2019.

Vancouver:

Chalhoub N. Identification par clonage positionnel du gène grey-lethal (gl) chez la souris . [Internet] [Thesis]. Université de Montréal; 2004. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1866/14647.

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

Council of Science Editors:

Chalhoub N. Identification par clonage positionnel du gène grey-lethal (gl) chez la souris . [Thesis]. Université de Montréal; 2004. Available from: http://hdl.handle.net/1866/14647

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

24. Nones, Kátia. Mapeamento de QTLS no cromossomo 1 de Gallus gallus que influenciam características de desempenho e carcaça.

Degree: PhD, Ciência Animal e Pastagens, 2004, University of São Paulo

Uma população experimental F2 foi desenvolvida a partir do cruzamento de uma linhagem macho de frangos de corte com uma linhagem de postura, com o… (more)

Subjects/Keywords: carcaça; carcass; chicken; chromosome mapping; galinha; mapeamento cromossômico; marcador molecular

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nones, K. (2004). Mapeamento de QTLS no cromossomo 1 de Gallus gallus que influenciam características de desempenho e carcaça. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/11/11139/tde-27102004-160256/ ;

Chicago Manual of Style (16th Edition):

Nones, Kátia. “Mapeamento de QTLS no cromossomo 1 de Gallus gallus que influenciam características de desempenho e carcaça.” 2004. Doctoral Dissertation, University of São Paulo. Accessed October 20, 2019. http://www.teses.usp.br/teses/disponiveis/11/11139/tde-27102004-160256/ ;.

MLA Handbook (7th Edition):

Nones, Kátia. “Mapeamento de QTLS no cromossomo 1 de Gallus gallus que influenciam características de desempenho e carcaça.” 2004. Web. 20 Oct 2019.

Vancouver:

Nones K. Mapeamento de QTLS no cromossomo 1 de Gallus gallus que influenciam características de desempenho e carcaça. [Internet] [Doctoral dissertation]. University of São Paulo; 2004. [cited 2019 Oct 20]. Available from: http://www.teses.usp.br/teses/disponiveis/11/11139/tde-27102004-160256/ ;.

Council of Science Editors:

Nones K. Mapeamento de QTLS no cromossomo 1 de Gallus gallus que influenciam características de desempenho e carcaça. [Doctoral Dissertation]. University of São Paulo; 2004. Available from: http://www.teses.usp.br/teses/disponiveis/11/11139/tde-27102004-160256/ ;

25. Παπανικολάου, Γεώργιος. Μελέτη της γενετικής βάσης της ιδιοπαθούς αιμοχρωμάτωσης στον ελληνικό πληθυσμό.

Degree: 2003, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Subjects/Keywords: Σίδηρος; Αιμοχρωμάτωση; Επσιδίνη; Χρωμόσωμα 19; HFE; HAMP; Iron; Hemochromatosis; Hepcidin; Chromosome 19

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Παπανικολάου, . . (2003). Μελέτη της γενετικής βάσης της ιδιοπαθούς αιμοχρωμάτωσης στον ελληνικό πληθυσμό. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/20291

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):

Παπανικολάου, Γεώργιος. “Μελέτη της γενετικής βάσης της ιδιοπαθούς αιμοχρωμάτωσης στον ελληνικό πληθυσμό.” 2003. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 20, 2019. http://hdl.handle.net/10442/hedi/20291.

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

MLA Handbook (7th Edition):

Παπανικολάου, Γεώργιος. “Μελέτη της γενετικής βάσης της ιδιοπαθούς αιμοχρωμάτωσης στον ελληνικό πληθυσμό.” 2003. Web. 20 Oct 2019.

Vancouver:

Παπανικολάου . Μελέτη της γενετικής βάσης της ιδιοπαθούς αιμοχρωμάτωσης στον ελληνικό πληθυσμό. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2003. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10442/hedi/20291.

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

Council of Science Editors:

Παπανικολάου . Μελέτη της γενετικής βάσης της ιδιοπαθούς αιμοχρωμάτωσης στον ελληνικό πληθυσμό. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2003. Available from: http://hdl.handle.net/10442/hedi/20291

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


Universiteit Utrecht

26. Verkaar, Edward Louis Christian. Structure and evolution of the Y-chromosomal and mitochondrial DNA of cattle.

Degree: 2003, Universiteit Utrecht

 The research described in this thesis is focused on the structure and evolution of the bovine Y-chromosome and the use of paternal markers in molecular… (more)

Subjects/Keywords: Diergeneeskunde; Y-chromosome; TSPY; transpatry; mitochondria; bovinii; SRY; polymorphism; phylogeny; concerted evolution

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Verkaar, E. L. C. (2003). Structure and evolution of the Y-chromosomal and mitochondrial DNA of cattle. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/316

Chicago Manual of Style (16th Edition):

Verkaar, Edward Louis Christian. “Structure and evolution of the Y-chromosomal and mitochondrial DNA of cattle.” 2003. Doctoral Dissertation, Universiteit Utrecht. Accessed October 20, 2019. http://dspace.library.uu.nl:8080/handle/1874/316.

MLA Handbook (7th Edition):

Verkaar, Edward Louis Christian. “Structure and evolution of the Y-chromosomal and mitochondrial DNA of cattle.” 2003. Web. 20 Oct 2019.

Vancouver:

Verkaar ELC. Structure and evolution of the Y-chromosomal and mitochondrial DNA of cattle. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2003. [cited 2019 Oct 20]. Available from: http://dspace.library.uu.nl:8080/handle/1874/316.

Council of Science Editors:

Verkaar ELC. Structure and evolution of the Y-chromosomal and mitochondrial DNA of cattle. [Doctoral Dissertation]. Universiteit Utrecht; 2003. Available from: http://dspace.library.uu.nl:8080/handle/1874/316

27. Lensch, Mathew William. Clonal selection : the leukemic process in Fanconi anemia.

Degree: PhD, 2002, Oregon Health Sciences University

Subjects/Keywords: Fanconi Anemia; Hematopoietic Stem Cells; Clone Cells; Leukemia, Myeloid; Chromosome Aberrations

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lensch, M. W. (2002). Clonal selection : the leukemic process in Fanconi anemia. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4S46Q7F ; http://digitalcommons.ohsu.edu/etd/3207

Chicago Manual of Style (16th Edition):

Lensch, Mathew William. “Clonal selection : the leukemic process in Fanconi anemia.” 2002. Doctoral Dissertation, Oregon Health Sciences University. Accessed October 20, 2019. doi:10.6083/M4S46Q7F ; http://digitalcommons.ohsu.edu/etd/3207.

MLA Handbook (7th Edition):

Lensch, Mathew William. “Clonal selection : the leukemic process in Fanconi anemia.” 2002. Web. 20 Oct 2019.

Vancouver:

Lensch MW. Clonal selection : the leukemic process in Fanconi anemia. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2002. [cited 2019 Oct 20]. Available from: doi:10.6083/M4S46Q7F ; http://digitalcommons.ohsu.edu/etd/3207.

Council of Science Editors:

Lensch MW. Clonal selection : the leukemic process in Fanconi anemia. [Doctoral Dissertation]. Oregon Health Sciences University; 2002. Available from: doi:10.6083/M4S46Q7F ; http://digitalcommons.ohsu.edu/etd/3207


University of Gothenburg / Göteborgs Universitet

28. Enlund, Fredrik 1968-. Genetic susceptibility to psoriasis in Sweden.

Degree: 2000, University of Gothenburg / Göteborgs Universitet

 A common skin disease affecting about 2-3% of the population, psoriasis has an inheritance pattern that is unclear, but most probably many genes are involved… (more)

Subjects/Keywords: CD80; CD86; joint complaints; linkage analysis; NPL; psoriasis; TDT; chromosome region 3q21

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Enlund, F. 1. (2000). Genetic susceptibility to psoriasis in Sweden. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/10834

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):

Enlund, Fredrik 1968-. “Genetic susceptibility to psoriasis in Sweden.” 2000. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed October 20, 2019. http://hdl.handle.net/2077/10834.

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

MLA Handbook (7th Edition):

Enlund, Fredrik 1968-. “Genetic susceptibility to psoriasis in Sweden.” 2000. Web. 20 Oct 2019.

Vancouver:

Enlund F1. Genetic susceptibility to psoriasis in Sweden. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2000. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2077/10834.

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

Council of Science Editors:

Enlund F1. Genetic susceptibility to psoriasis in Sweden. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2000. Available from: http://hdl.handle.net/2077/10834

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


University of Gothenburg / Göteborgs Universitet

29. Bjursell, Cecilia 1971-. Genetics of the carbohydrate-deficient glycoprotein syndrome type Ia.

Degree: 2000, University of Gothenburg / Göteborgs Universitet

 In recent years, a revolution in the development of new techniques have made it possible to perform genetic studies of inherited disorders without prior knowledge… (more)

Subjects/Keywords: CDG Ia; PMM2; chromosome 16; linkage; linkage disequilibrium; prenatal diagnosis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bjursell, C. 1. (2000). Genetics of the carbohydrate-deficient glycoprotein syndrome type Ia. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/15171

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):

Bjursell, Cecilia 1971-. “Genetics of the carbohydrate-deficient glycoprotein syndrome type Ia.” 2000. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed October 20, 2019. http://hdl.handle.net/2077/15171.

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

MLA Handbook (7th Edition):

Bjursell, Cecilia 1971-. “Genetics of the carbohydrate-deficient glycoprotein syndrome type Ia.” 2000. Web. 20 Oct 2019.

Vancouver:

Bjursell C1. Genetics of the carbohydrate-deficient glycoprotein syndrome type Ia. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2000. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2077/15171.

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

Council of Science Editors:

Bjursell C1. Genetics of the carbohydrate-deficient glycoprotein syndrome type Ia. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2000. Available from: http://hdl.handle.net/2077/15171

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


Hong Kong University of Science and Technology

30. Liu, Shuk Ming. Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer.

Degree: 2003, Hong Kong University of Science and Technology

 GST is a big family of isoezymes, and based on their locations they can be divided into cytosolic and microsomal GST. The major role of… (more)

Subjects/Keywords: Glutathione transferase; Colon (Anatomy)  – Cancer; Rectum  – Cancer; Genetic polymorphisms; Human genetics; Chromosome polymorphism

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Liu, S. M. (2003). Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b802027 ; http://repository.ust.hk/ir/bitstream/1783.1-3899/1/th_redirect.html

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):

Liu, Shuk Ming. “Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer.” 2003. Thesis, Hong Kong University of Science and Technology. Accessed October 20, 2019. https://doi.org/10.14711/thesis-b802027 ; http://repository.ust.hk/ir/bitstream/1783.1-3899/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Liu, Shuk Ming. “Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer.” 2003. Web. 20 Oct 2019.

Vancouver:

Liu SM. Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2003. [cited 2019 Oct 20]. Available from: https://doi.org/10.14711/thesis-b802027 ; http://repository.ust.hk/ir/bitstream/1783.1-3899/1/th_redirect.html.

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

Council of Science Editors:

Liu SM. Single nucleotide polymorphism in human microsomal glutathione s-transferase gene and colorectal cancer. [Thesis]. Hong Kong University of Science and Technology; 2003. Available from: https://doi.org/10.14711/thesis-b802027 ; http://repository.ust.hk/ir/bitstream/1783.1-3899/1/th_redirect.html

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

[1] [2] [3]

.