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News
Your best photos of National Parks - The Globe and Mail
www.theglobeandmail.com
Rachel Wevrick photo: Teenage bighorn sheep makes a decision - A young bighorn sheep scampers down a vertical rock wall in Jasper ...
Scoliosis Research Society Newsletter
www.srs.org
Research Grant Committee Report. By Dilip K. Sengupta, MD ... Rachel Wevrick, PhD Etiology of Scoliosis in a Mouse Model of Prader-Willi Syndrome $100, Years;
News :: Cambridge Neuroscience
www.neuroscience.cam.ac.uk
Professor Dick Swaab ♢ Professor Maite Tauber ♢ Professor Rachel Wevrick. The distinguished guest lecture will be given by Professor ...
Researchers Find how Caffeine Kills Cancer Cells | Nature World News
www.natureworldnews.com
Cancer cells are highly sensitive to caffeine. However, the stimulant can't really be used to treat cancers, because the body can't tolerate high doses of...
Telephone & Addresses
Rachel Wevrick, Menlo Park, US, Menalto Ave, Unit B
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WhitePages: Rachel Wevrick | 2 records found | Whitepages
View phone numbers, addresses, public records, background check reports and possible arrest records for Rachel Wevrick. Whitepages people search is the ...
Network Profiles
LinkedIn: Rachel Wevrick - Professor - University of Alberta | LinkedIn
View Rachel Wevrick's profile on LinkedIn, the world's largest professional community. Rachel has 1 job listed on their profile. See the complete profile on ...
Rachel Wevrick | SFARI
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Rachel Wevrick - University of Alberta: Find a Person
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Interests
Identification of Novel Imprinted Transcripts in the Prader-Willi Cell
www.cell.com
... Syndrome Deletion Region: Further Evidence for Regional Imprinting Control. Syann Lee. x. Syann Lee. Search for articles by this author. ,. Rachel Wevrick.
Business Profiles
Researchgate: Rachel Wevrick
Edmonton, Alberta, Canada
patentbuddy: Rachel Wevrick
THE UNITED MEDICAL AND DENTAL SCHOOLS OF GUY'S AND ST. THOMAS'S HOSPITALS, Menlo Park, CA, US
Rachel Wevrick, University of Alberta • Expertise Finder Network
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Rachel Wevrick at University of Alberta is an expert in Genetic disease, Human genetic disorders, Pediatric obesity, Prader-Willi syndrome, Psychiatric...
Private Homepages
PWSA USA Annual Report FINAL.pub - Web Control Center
www103.ssldomain.com
Rachel Wevrick, Ph.D., University of Alberta, Edmonton, Alberta, Canada. Barbara Y. Whitman, Ph.D., St. Louis University School of Medicine, St. Louis, MO.
Employees
Scientific Advisory Board - Prader-Willi Syndrome Association (USA)
www.pwsausa.org
Rachel Wevrick, Ph.D. Department of Medical Genetics University of Alberta Edmonton, Alberta, Canada. Barbara Y. Whitman, Ph.D. Department of Pediatrics
Education
Genetic basis for respiratory control disorders [electronic resource ...
catalog.princeton.edu
Respiratory control abnormalities in necdin-null mice: implications for the pathogenesis of Prader-Willi syndrome / John J. Greer and Rachel Wevrick
Books & Literature
Ghent University Academic Bibliography
biblio.ugent.be
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The Prader-Willi syndrome proteins MAGEL2 and necdin regulate leptin...
biblio.ugent.be
... UGent, Matthea R Sanderson, Karin Vanessa Carias, Jan Tavernier UGent and Rachel Wevrick (2017) HUMAN MOLECULAR GENETICS.
Genetic Basis for Respiratory Control Disorders - Google Books
books.google.hu
Bringing together top-level contributions on all aspects of the subject, this book provides an overview of the recent advances in the genetics of respiratory...
Genomic Disorders: The Genomic Basis of Disease - Google Books
books.google.hu
A grand summary and synthesis of the tremendous amount of data now available in the post genomic era on the structural features, architecture, and evolution of...
Related Documents
Developmental Abnormalities of Neuronal Structure and Function in ...
ajp.amjpathol.org
Affiliations. Department of Physiology, University of Alberta, Edmonton, Alberta, Canada. ,. Rachel Wevrick. x. Rachel Wevrick. Search for articles by this author ...
A MAGE/NDN‐like gene in zebrafish, Developmental Dynamics |...
www.deepdyve.com
A MAGE/NDN‐like gene in zebrafish Bischof, Jocelyn M.; Ekker, Marc; Wevrick, Rachel The human necdin/MAGE gene family has over 50 members, but most of the ...
Loss of the Circadian Rhythm Gene Magel2 Leads to Metabolic ...
www.canadianjournalofdiabetes.com
Rachel Wevrick. x. Rachel Wevrick. Search for articles by this author. Department of Medical Genetics, University of Alberta, Edmonton, AB. Loss of the Circadian ...
Page th Annual Drosophila Research Conference Program Guide
www.dros-conf.org
Rachel Wevrick ). Department of. Medical Genetics, University of Alberta, Edmonton, Alberta,. Canada; 2) Department of Biological Sciences, University of.
Scientific Publications
Necdin Gene is Deleted in Prader-Willi Syndrome and is Imprinted in...
academic.oup.com
Heather R. MacDonald and Rachel Wevrick * Department of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada T6G 2S2
Magel2 , a Prader-Willi syndrome candidate gene, modulates the...
jcircadianrhythms.biomedcentral.com
The Magel2 gene is most highly expressed in the suprachiasmatic nucleus of the hypothalamus, where its expression cycles in a circadian pattern comparable to...
Publications
Respiratory control abnormalities in necdinnull mice: implications...
link.springer.com
264 John J. GREER and Rachel WEVRICK hormone (TRH), 5HT and noradrenaline. However, the fluctuations in the respira-tory frequency continued in the necdin-null …
Table of contents for The genetics of obesity syndromes
catdir.loc.gov
Table of Contents for The genetics of obesity syndromes / [edited by] Philip L. Beales, Sadaf Farooqi, Stephen O'Rahilly, available from the Library of...
Oalib search
www.oalib.com
Rebecca E. Mercer, Rachel Wevrick PLOS ONE , 2009, DOI: journal.pone Abstract: Background MAGEL2 is one of ...
Reports & Statements
Scientific Advisory Board Archives - Foundation for …
www.fpwr.org
Scientific Advisory Board Archives - Foundation for Prader-Willi Research Scientific Advisory Board Archives - Foundation for Prader-Willi Research ... Rachel Wevrick, Ph.D., Professor of Department of Medical Genetics, University of Alberta, received her BSc from Queen’s University and her PhD from the University of Toronto. She performed ...
A mouse model for Prader-Willi syndrome …
www.nature.com
Rachel Wevrick Department of Genetics and Howard Hughes Medical Institute, Beckman Center for Molecular and Genetic Medicine, Stanford University School of Medicine, Stanford, California,
2016 IPWSO conference: Building global community — …
praderwilli.org.au
Members of the Scientific Conference Organising Committee are Dr Rachel Wevrick ... Scientific Director of the Foundation for Prader-Willi Research, ...
Miscellaneous
Rachel Wevrick - Foundation for Prader-Willi Research
www.old.fpwr.org
Rachel Wevrick, Ph.D., Professor of Department of Medical Genetics, University of Alberta, received her BSc from Queen's University and her PhD from the ...
Rachel Wevrick - Alberta Diabetes Institute …
adi.ualberta.ca
Rachel Wevrick, PhD Office: 8-16A Medical Sciences Building Mail: University of Alberta, Edmonton AB T6G 2H7 Phone: (Office)
Obesity: Wevrick, Rachel - Expertscape.com
www.expertscape.com
The expertise of Rachel Wevrick ranks in the Top 1.8%... of 262,285 published authors worldwide on Obesity... from through based on contributions to 15 …
Rachel Wevrick | Define Feminine
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"Ready for anything" in the outdoors, Rachel loves outdoor adventure in all its forms
Rachel Wevrick - Department of Medical Genetics - University of...
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Magel2 Is Required for Leptin-Mediated Depolarization of POMC Neurons...
journals.plos.org
We then found that we could bypass this leptin insensitivity by administering a drug that compensates for the lack of ... Rachel Wevrick, William F ...
C57BL/6-Magel2/J
www.jax.org
Rachel Wevrick, University of Alberta. Disease/Phenotype. Disease Terms. Model with phenotypic similarity to human disease where etiologies involve orthologs. Human genes are associated with this disease. Orthologs of those genes appear in the mouse genotype(s). Prader-Willi syndrome;
Deconstructing Mendel: new paradigms in genetic mechanisms [CIM -...
collectionscanada.ca
Deconstructing Mendel: new paradigms in genetic mechanisms. Dawna Gilchrist, MD D. Moira Glerum, PhD Rachel Wevrick, PhD. Clin Invest Med 2000;23(3):
AnGenMap: Animal Genome Databases
animalgenome.org
Rachel Wevrick, Ph.D. Assistant Professor CIHR New Investigator and AHFMR Scholar Department of Medical Genetics 842 Medical Sciences ...
CSC Labs — Canadian Society for Chronobiology
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Rachel Wevrick's Laboratory (Rachel Wevrick), Department of Medical Genetics, University of Alberta, Edmonton, AB. We focus on genetic disorders that affect ...
Leptin resistance in mouse models of hyperphagia
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Leptin resistance in mouse models of hyperphagia. By: Rachel Wevrick, Ph.D. Department of Medical Genetics, University of Alberta . Hypothesis: They …
Collection Finding Aid | Duke Medical Center Archives
archives.mc.duke.edu
Rachel Wevrick, [Untitled], Box 29. Brian, Brian Primate alph sat (southerns), Box 29. PCR sequence cloning (screen davies library for specific ...
SFARI | MAGEL2, a candidate gene for autism and Prader-Willi syndrome
www.sfari.org
Rachel Wevrick, Ph.D. University of Alberta Children with the rare genetic disorder Prader-Willi syndrome have a high rate of autism spectrum disorders…
Necdin and MAGEL2
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Necdin and MAGEL2: Candidate Genes for Prader-Willi Syndrome . Rachel Wevrick, Jason R. Bush, Megan A. O’Neill, Alysa A. Tennese, Sharee L. Kuny, Christine L. Walker
Dopamine pathway imbalance in mice lacking Magel2, a Prader-Willi...
www.scholars.northwestern.edu
... pathway imbalance in mice lacking Magel2, a Prader-Willi syndrome candidate gene. Chloe Luck, Martha H. Vitaterna, Rachel Wevrick.
Prader-Willi Syndrome - Oxford Medicine
oxfordmedicine.com
Rachel Wevrick DOI: med Page of . PRINTED FROM OXFORD MEDICINE ONLINE (www.oxfordmedicine.com).
Isolation of a Novel Iris-Specific and Leucine-Rich Repeat Protein...
iovs.arvojournals.org
The authors thank members of the Ocular Genetics Laboratory, Rachel Wevrick, Roseline Godbout, and Fiona Punter, for their critical comments. 1. Collins FC.
Magel2-null mice have abnormal weight recovery and ...
figshare.com
Magel2 Is Required for Leptin-Mediated Depolarization of POMC Neurons in the Hypothalamic Arcuate Nucleus in Mice
Perinatal Imprintings and Neurodevelopmental Disorders | Inmed
www.inmed.fr
Institut de neurobiologie de la méditerranée
Prader - Willi syndrome transcripts are expressed in phenotypically...
utsouthwestern.pure.elsevier.com
... Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain. Syann Lee, Christine L. Walker, Rachel Wevrick.
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