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C&W Library Catalogue

Browse and borrow resources that support the learning needs and professional development of C&W staff, clinicians, students and faculty.

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19 records – page 1 of 1.

American journal of human genetics

https://cwslc.andornot.com/en/permalink/catalog114382

Behavior Genetics: An International Journal Devoted to Research in the Inheritance of Behavior

https://cwslc.andornot.com/en/permalink/catalog114441

Canadian journal of diabetes

https://cwslc.andornot.com/en/permalink/catalog114593
Canadian Diabetes Association. [Toronto, ON]: Elsevier , 2001 - Present.
Website
UBC Users:
http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_B&C=canadian+journal+of+diabetes
Material Type
Serial
Website
UBC Users:
http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_B&C=canadian+journal+of+diabetes
Continues / Continued By
Canadian journal of diabetes care
Corporate Author
Canadian Diabetes Association.
Place of Publication
[Toronto, ON]
Publisher
Elsevier
Publication Date
2001 - Present
ISSN
1499-2671
Language
English
Material Type
Serial
Frequency
Bimonthly
Holdings
CFRI/Study & Learning Commons - Print: v.21:3-v.23:4 (1997-1999); 25:1-v.37:1 (2001-2013.
Missing: v.22:3 (1998); v.26:2 (2002); 27:3 (2003); v.29:1-2 (2005).
Online: 2001 to present.
Websites
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Canadian Medical Association Journal

https://cwslc.andornot.com/en/permalink/catalog114598
Website
PHSA Users:
http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp15402&site=pfi-live
UBC Users:
http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_B&C=+Canadian+Medical+Association+journal
Alternate Title
CMAJ
Canadian Medical Association journal = Journal de l'Association Medicale Canadienne
Corporate Author
Canadian Medical Association
Place of Publication
[Ottawa, ON]
Publisher
Canadian Medical Association
Publication Date
1911 - Present
ISSN
0820-3946
Language
English
Material Type
Serial
Frequency
Biweekly
Holdings
CFRI/Study & Learning Commons - Print: v.150:1-v.186:9 (1994-2014).
Missing: v.154:1 (1996); v.156:3 (1997); v.157:5-7,9 (1997).
Online: 1911 to present.
Websites
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Characterizations of a tumor-associated antigen COX-1

https://cwslc.andornot.com/en/permalink/catalog113988
Sheu, Fong-Shyong. [Vancouver, BC?]: University of British Columbia , 1991.
Website
http://hdl.handle.net/2429/30332
Material Type
Thesis
Call Number
Thesis Shelf
By using modified hybridoma technology, monoclonal antibodies against an ovarian tumor cell line, OC-3-VGH, were generated in Dr. Lee's laboratory. Among these antibodies, RP 215 was shown to react specifically with a tumor-associated antigen, COX-1. On SDS gel, COX-1 has a molecular weight of 60 K…
Website
http://hdl.handle.net/2429/30332
Author
Sheu, Fong-Shyong
Place of Publication
[Vancouver, BC?]
Publisher
University of British Columbia
Publication Date
1991
Subject
Faculty of Medicine
Theses
Abstract
By using modified hybridoma technology, monoclonal antibodies against an ovarian tumor cell line, OC-3-VGH, were generated in Dr. Lee's laboratory. Among these antibodies, RP 215 was shown to react specifically with a tumor-associated antigen, COX-1. On SDS gel, COX-1 has a molecular weight of 60 KD and exists as an aggregate in the natural- state. A highly purified COX-1 was obtained mainly by immunoaffirtity chromatography, with RP 215 as the affinity ligand, from the shed medium of cultured tumor cells.
Language
English
Material Type
Thesis
Call Number
Thesis Shelf
Websites
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Clinical Genetics: An International Journal of Genetics, Molecular and Personalized Medicine

https://cwslc.andornot.com/en/permalink/catalog114754
Website
PHSA Users:
http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp18084&site=pfi-live
UBC Users:
http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_B&C=clinical+genetics
Place of Publication
Malden, Ma.
Publisher
John Wiley & Sons, Inc.
Publication Date
1970 - Present.
ISSN
0009-9163
Language
English
Material Type
Serial
Frequency
Monthly
Holdings
CFRI/Study & Learning Commons - Print: v.45:6-v.57:4+special issue (1994-2000); v.61:1 (2002); v.69:3-v.76:3 (2006-2009).
Missing: v.51:3, v.52:4 (1997); v.53:2 (1998); v.55:4, v.56:1,3 (1999); v.57:1-3, v.58:1-6 (2000); v.59:1-6, v.60:1-6 (2001); v.61:2-6, v.62:1-6 (2002); 2003-2005; v.69:1-2 (2006); v.73:3-5 (2008); v.75:1,3,4, v.76:2,4-6 (2009).
Online: 1970 to present.
Websites
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Diabetes: A Journal of the American Diabetes Association

https://cwslc.andornot.com/en/permalink/catalog114772
Website
PHSA Users:
http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp23385&site=pfi-live
UBC Users:
http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_B&C=Diabetes
Corporate Author
American Diabetes Association
Place of Publication
Alexandria, Va.
Publisher
American Diabetes Association
Publication Date
1952- Present.
ISSN
0012-1797
Language
English
Material Type
Serial
Frequency
Monthly
Holdings
CFRI/Study & Learning Commons - Print: v.44:1-v.61:9 (1995-2012).
Missing: v.46:3 (1997); v.47:9,10 (1998); v.53:1 (2004); v.54:9 (2005); v.55:12 (2006); v.56:4,7 (2007).
Online: 1952 to present.
Websites
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Human molecular genetics

https://cwslc.andornot.com/en/permalink/catalog119692
Website
PHSA Users:
http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp33596&site=pfi-live
UBC Users:
http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_M&C=human+molecular+genetics
Place of Publication
Oxford, England
Publisher
Oxford University Press
Publication Date
1992 - Present
ISSN
0964-6906
Language
English
Material Type
Serial
Frequency
Bimonthly
Holdings
CFRI/Study & Learning Commons - Print: v.3:1-v.8:13 (1994-1999); v.9:15-16 (2000); v.10:1-16,19,20,22-25 (2001); v.11:17,20 (2002); v.12:13 (2003).
Missing: v.4:8 (1995); v.5:8 (1996); v.6:8,10 (1997).
Online: 1992 to present.
Websites
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Journal of medical genetics

https://cwslc.andornot.com/en/permalink/catalog119703
Website
PHSA Users:
http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp41514&site=pfi-live
UBC Users:
http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_M&C=Journal+of+Medical+Genetics
Alternate Title
J. Med. Genet.
Place of Publication
London, United Kingdom of Great Britain & Northern Ireland
Publisher
BMJ Publishing Group
Publication Date
1964 - Present
ISSN
0022-2593
Language
English
Material Type
Serial
Frequency
Monthly
Holdings
CFRI/Study & Learning Commons - Print: v.30:12-v.40:1+suppls. (1993-2003).
Missing: v.31:12 (1994); v.37:4 (2000).
Online: 1964 to present.
Websites
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Mendelian inheritance in man: A catalog of human genes and genetic disorders: Vol 1

https://cwslc.andornot.com/en/permalink/catalog112687
McKusiak, Victor A (Ed). Baltimore, MD: Johns Hopkins University Press , 1998. 12th Ed.
Website
http://www.ncbi.nlm.nih.gov/omim
Material Type
Book
Call Number
REF GI 20 MCK 1998 VOL 1
Availability
2 copies, 2 available
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
Website
http://www.ncbi.nlm.nih.gov/omim
Website Notes
The database corresponds to the print publication.
Author
McKusiak, Victor A (Ed).
Edition
12th Ed.
Place of Publication
Baltimore, MD
Publisher
Johns Hopkins University Press
Publication Date
1998
Physical Description
Hardcover
Subject
Genetics
Genetic Disorders
Genetics/Genetic Disorders-Encyclopedias
Abstract
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
ISBN
0801857422
Language
English
Material Type
Book
Call Number
REF GI 20 MCK 1998 VOL 1

Copies

Copy 1 BC Children's and Women's Study and Learning Commons REF Available
Copy 2 BC Children's and Women's Study and Learning Commons REF Available
Websites
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Mendelian inheritance in man: A catalog of human genes and genetic disorders: Vol 2

https://cwslc.andornot.com/en/permalink/catalog112688
McKusiak, Victor A (Ed). Baltimore, MD: Johns Hopkins University Press , 1998. 12th Ed.
Website
http://www.ncbi.nlm.nih.gov/omim
Material Type
Book
Call Number
REF GI 20 MCK 1998 VOL 2
Availability
2 copies, 2 available
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
Website
http://www.ncbi.nlm.nih.gov/omim
Website Notes
The database corresponds to the print publication.
Author
McKusiak, Victor A (Ed).
Edition
12th Ed.
Place of Publication
Baltimore, MD
Publisher
Johns Hopkins University Press
Publication Date
1998
Physical Description
Hardcover
Subject
Genetics
Genetics/Genetic Disorders-Encyclopedias
Genetic Disorders
Abstract
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
ISBN
0801857422
Language
English
Material Type
Book
Call Number
REF GI 20 MCK 1998 VOL 2

Copies

Copy 1 BC Children's and Women's Study and Learning Commons REF Available
Copy 2 BC Children's and Women's Study and Learning Commons REF Available
Websites
Show Less

Mendelian inheritance in man: A catalog of human genes and genetic disorders: Vol 3

https://cwslc.andornot.com/en/permalink/catalog112689
McKusiak, Victor A (Ed). Baltimore, MD: Johns Hopkins University Press , 1998.
Website
http://www.ncbi.nlm.nih.gov/omim
Material Type
Book
Call Number
REF GI 20 MCK 1998 VOL 3
Availability
2 copies, 2 available
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
Website
http://www.ncbi.nlm.nih.gov/omim
Website Notes
The database corresponds to the print publication.
Author
McKusiak, Victor A (Ed).
Place of Publication
Baltimore, MD
Publisher
Johns Hopkins University Press
Publication Date
1998
Physical Description
Hardcover
Subject
Genetic Disorders
Genetics
Genetics/Genetic Disorders-Encyclopedias
Abstract
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
ISBN
0801857422
Language
English
Material Type
Book
Call Number
REF GI 20 MCK 1998 VOL 3

Copies

Copy 1 BC Children's and Women's Study and Learning Commons REF Available
Copy 2 BC Children's and Women's Study and Learning Commons REF Available
Websites
Show Less

Nature genetics

https://cwslc.andornot.com/en/permalink/catalog119777
Website
PHSA Users:
http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp50993&site=pfi-live
UBC Users:
http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_M&C=nature+genetics
Alternate Title
Nat. Genet.
Place of Publication
New York, NY
Publisher
Nature Publishing Group
Publication Date
1992 - Present.
ISSN
1061-4036
Language
English
Material Type
Serial
Frequency
Monthly
Holdings
CFRI/Study & Learning Commons - Print: v.6:1-v.46:6+suppls. (1994-2012).
Missing: v.11:1(1995); v.12:1 (1996); v.21:4; v.23:3 (1999); v.27:2; v.28:3 (2001); v.31:2; v.32:4 (2002); v.35:4 (2003).
Online: 1992 to present.
Websites
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Physical and functional interaction of p53 and p110a and implications in ovarian carcinogenesis

https://cwslc.andornot.com/en/permalink/catalog113967
Astanehe, Arezoo. [Vancouver, BC?]: University of British Columbia , 2005.
Website
http://hdl.handle.net/2429/16421
Material Type
Thesis
Call Number
Thesis Shelf
n approximately 40% of ovarian cancers, PIK3CA, which encodes the p110α catalytic subunit of phosphatidylinositol 3-kinase (PI3K) is amplified. This amplification correlates with increased PIK3CA transcription, p110α protein expression, and PI3K activity. Moreover, PIK3CA is implicated as…
Website
http://hdl.handle.net/2429/16421
Author
Astanehe, Arezoo
Place of Publication
[Vancouver, BC?]
Publisher
University of British Columbia
Publication Date
2005
Subject
Faculty of Medicine
Theses
Abstract
n approximately 40% of ovarian cancers, PIK3CA, which encodes the p110α catalytic subunit of phosphatidylinositol 3-kinase (PI3K) is amplified. This amplification correlates with increased PIK3CA transcription, p110α protein expression, and PI3K activity. Moreover, PIK3CA is implicated as an oncogene in ovarian cancers. Another common mutation in ovarian cancer leads to loss of p53 function. Alterations to p53 are known to be involved in tumour development and progression.
Language
English
Material Type
Thesis
Call Number
Thesis Shelf
Websites
Show Less

The PIERS (Pre-eclampsia Integrated Estimate of RiSk) model : development of a valid outcome prediction model for pre-eclampsia.

https://cwslc.andornot.com/en/permalink/catalog113957
Menzies, Jennifer Marie. [Vancouver, BC?]: University of British Columbia , 2009.
Website
http://hdl.handle.net/2429/6844
Material Type
Thesis
Call Number
Thesis Shelf
Availability
1 copy, 1 available
This research responded to the need to define evidence-based criteria of maternal risk by developing a model - the Pre-eclampsia Integrated Estimate of RiSk (or PIERS) model ? that predicts a combined adverse maternal outcome (mortality and/or significant morbidities) within 48 hour of, and up to s…
Website
http://hdl.handle.net/2429/6844
Author
Menzies, Jennifer Marie
Place of Publication
[Vancouver, BC?]
Publisher
University of British Columbia
Publication Date
2009
Subject
Faculty of Medicine
Theses
Abstract
This research responded to the need to define evidence-based criteria of maternal risk by developing a model - the Pre-eclampsia Integrated Estimate of RiSk (or PIERS) model ? that predicts a combined adverse maternal outcome (mortality and/or significant morbidities) within 48 hour of, and up to seven days after, admission with pre-eclampsia (study eligibility)
Language
English
Material Type
Thesis
Call Number
Thesis Shelf

Copies

Copy 1 BC Children's and Women's Study and Learning Commons Thesis Shelf Available
Websites
Show Less

The prediction of adverse maternal outcomes in pre-eclampsia

https://cwslc.andornot.com/en/permalink/catalog113966
Devarakonda, Rajashree M. [Vancouver, BC?]: University of British Columbia , 2005.
Website
http://hdl.handle.net/2429/16403
Material Type
Thesis
Call Number
Thesis Shelf
Pre-eclampsia (PET) continues to contribute to maternal and perinatal morbidity and mortality. Management decisions include an evaluation of maternal risk, which is assisted by expert opinion-based guidelines, while not accounting for gestational age (GA) at diagnosis. We evaluated the feasibility …
Website
http://hdl.handle.net/2429/16403
Author
Devarakonda, Rajashree M.
Place of Publication
[Vancouver, BC?]
Publisher
University of British Columbia
Publication Date
2005
Subject
Faculty of Medicine
Theses
Abstract
Pre-eclampsia (PET) continues to contribute to maternal and perinatal morbidity and mortality. Management decisions include an evaluation of maternal risk, which is assisted by expert opinion-based guidelines, while not accounting for gestational age (GA) at diagnosis. We evaluated the feasibility of developing a severity score that can predict adverse maternal outcome.
Language
English
Material Type
Thesis
Call Number
Thesis Shelf
Websites
Show Less

Trends in genetics

https://cwslc.andornot.com/en/permalink/catalog119854
Website
PHSA Users:
Not available online:
UBC Users:
http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_B&C=trends+in+genetics
Place of Publication
Cambridge, Ma.
Publisher
Elsevier Inc.
Publication Date
1985 - Present.
ISSN
0168-9525
Language
English
Material Type
Serial
Frequency
Monthly
Holdings
CFRI/Study & Learning Commons - Print: v.13:1-v.14:12 (1997-1998); v.15:1,10 (1999); v.16:4.10 (2000); v.17:1-11 (2001); v.18:2-4,6 (2002); v.22:5-9,11,12+suppls. (2006).
Missing: v.13:8 (1997); v.15:2-9,11,12 (1999); v.16:1-3,5-9,11,12 (2000); v.17:12 (2001); v.18:1,5,7-12 (2002); v.119-v.21 (2003-2005); v.22:1-4,10 (2006).
Online: 1985 to present.
Websites
Show Less

Trends in genetics

https://cwslc.andornot.com/en/permalink/catalog119855
Website
PHSA Users:
Not available online:
UBC Users:
http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_B&C=trends+in+genetics
Place of Publication
Cambridge, Ma.
Publisher
Elsevier Inc.
Publication Date
1985 - Present.
ISSN
0168-9525
Language
English
Material Type
Serial
Frequency
Monthly
Holdings
CFRI/Study & Learning Commons - Print: v.13:1-v.14:12 (1997-1998); v.15:1,10 (1999); v.16:4.10 (2000); v.17:1-11 (2001); v.18:2-4,6 (2002); v.22:5-9,11,12+suppls. (2006).
Missing: v.13:8 (1997); v.15:2-9,11,12 (1999); v.16:1-3,5-9,11,12 (2000); v.17:12 (2001); v.18:1,5,7-12 (2002); v.119-v.21 (2003-2005); v.22:1-4,10 (2006).
Online: 1985 to present.
Websites
Show Less

19 records – page 1 of 1.