Genetics

Displaying 201 - 250 of 316

Kidney Volume, Blood Pressure, and Albuminuria: Findings in an Australian Aboriginal Community

Articles » Scholarly, peer reviewed
Author/Creator
Gurmeet R. Singh
Wendy E. Hoy
American Journal of Kidney Diseases, vol. 43, no. 2, February 2004, pp. 254-259
Description
Found an association between lower kidney volumes and higher blood pressures and albuminuria in an Australian Aboriginal community from a remote coastal island. Data suggests that higher blood pressures linked with low birth weight may be mediated by a lower number of nephrons in addition to other theoretical factors.
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LCO Community Wrestles With Bio-tech Issues

Articles » General
Tribal College Journal of American Indian Higher Education, vol. 17, no. 2, Sustainability, Winter, 2005
Description
Instructors from Lac Courte Oreilles Ojibwa Community Colleges attend conferences, develop materials for specific tribal issues through use of a Tribal Learning Community model.
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Lessons From Genetic Studies in Native Canadian Populations / Discussion

Articles » Scholarly, peer reviewed
Author/Creator
Robert A. Hegele
Nutrition Reviews, vol. 57, no. 5, Part 2, May 1999, pp. S43-S49
Description
Study compares genetic and environmental attributes of the Sandy Lake Oji-Cree and the Keeewatin Inuit in an attempt to explain disease prevalence in the two communities.
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Linkage Analysis of X-linked Cleft Palate and Ankyloglossia in Manitoba Mennonite and British Columbia Native Kindreds

Articles » Scholarly, peer reviewed
Author/Creator
Sharon M. Gorski
Karen J. Adams
Patricia H. Birch
Bernard N. Chodirker
Cheryl R. Greenberg
Paul J. Goodfellow
Human Genetics, vol. 94, no. 2, August 1994, pp. 141-148
Description
Studies additional linkage analyses on a B.C. family and in a newly identified Manitoba Mennonite family with X-linked cleft palate and ankyloglossia.
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Linkage of Tuberculosis to Chromosome 2q35 Loci, Including NRAMP1 in a Large Aboriginal Canadian Family

Articles » Scholarly, peer reviewed
Author/Creator
Celia M.T. Greenwood
T. Mary Fujiwara
Lucy J. Boothroyd
Mark A. Miller
Danielle Frappier
E. Anne Fanning
Erwin Schurr
Kenneth Morgan
American Journal of Human Genetics, vol. 67, no. 2, August 2000, pp. 405-416
Description
Study findings indicate significant linkage was present to support a role for NRAMP1 or genes closely linked to it in susceptibility to active tuberculosis disease.
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Localization of a Recessive Gene for North America Indian Childhood Cirrhosis to Chromosome Region 16q22 - and Identification of a Shared Haplotype

Articles » Scholarly, peer reviewed
Author/Creator
Christine Bétard
Andrée Rasquin-Weber
Carl Brewer
Eric Drouin
Suzanne Clark
et al.
American Journal of Human Genetics, vol. 67, no. 1, July 2000, pp. 222-228
Description
Results from a genome wide scan on three DNA pools of samples from 13 patients, 16 unaffected siblings, and 22 parents from five families of Ojibway-Cree in northwestern Quebec.
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Low levels of STRP Variability Are Not Universal in American Indians

Articles » Scholarly, peer reviewed
Author/Creator
Mara H. Hutz
Sidia M. Callegari-Jacques
Sabrina E. M. Almeida ... et al.
Human Biology, vol. 74, no. 6, December 2002, pp. 791-806
Description
Study confirms that short tandem repeat polymorphisms (STRP) are good markers for the distinction of continental groups.
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Man's Best Friend: Implications of Tuberculosis in a 16th Century Neutral Iroquois Dog From Canada

Alternate Title
Multiplying and Dividing: Tuberculosis in Canada and Aotearoa New Zealand
RAL-e ; no.3, 2008
Research in Anthropology & Linguistics-e ; no. 3, 2008
E-Books » Chapters
Author/Creator
Jodi Lynn Barta
Description
Chapter 2 from: Multiplying and Dividing: Tuberculosis in Canada and Aotearoa New Zealand edited by Judith Littleton, Julie Park, Ann Herring and Tracy Farmer. Scroll down to page 22 to read chapter.
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Manitoba Aboriginal Kindred with Original Cerebro-Oculo-Facio-Skeletal (COFS) Syndrome Has a Mutation in the Cockayne Syndrome Group B (CSB) Gene

Articles » Scholarly, peer reviewed
Author/Creator
Lisiane B. Meira
John M. Graham
Cheryl R. Greenberg
David B. Busch
Ana T. B. Doughty
Deborah W. Ziffer
Donna M. Coleman
Isabelle Savre-Train
Errol C. Friedberg
American Journal of Human Genetics, vol. 66, no. 4, April 2000, pp. 1221-1228
Description
Evidence that two probands within COFS syndrome which was originally reported have cellular phenotypes indistinguishable from those in cockayne syndrome (CS) cells, which suggests that CS and COFS syndrome share a common pathogenesis.
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Metabolic Syndrome in Aboriginal Canadians: Prevalence and Genetic Associations

Articles » Scholarly, peer reviewed
Author/Creator
Rebecca L. Pollexa
Anthony J.G. Hanley
Bernard Zinman
Stewart B. Harris
Hafiz M.R. Khand
Robert A. Hegele
Atherosclerosis, vol. 184, January 2006, pp. 121-129
Description
Presents metabolic syndrome which increases the risk of type 2 diabetes and coronary heart disease. The study examines prevalence and genetic aspects of the syndrome in the Oji-Cree.
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Microsatellites Provide Evidence for Y Chromosome Diversity among the Founders of the New World

Articles » Scholarly, peer reviewed
Author/Creator
Andres Ruiz-Linares
Daniel Ortiz-Barrientos
Mauricio Figueroa
Natalia Mesa
Juan G. Munera
Gabriel Bedoya
Ivan D. Velez
Luis F. Garcia
Anna Perez-Lezaun
Jaume Bertranpetit
Marcus W. Feldman
David B. Goldstein
Proceedings of the National Academy of Sciences of the United States of America, vol. 96, no. 11, May 25, 1999, pp. 6312-6317
Description
Discussion of Y chromosome markers that are mainly restricted to North American Aboriginal males.
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A Missense Mutation (R565W) in Cirhin (FLJ14728) in North American Indian Childhood Cirrhosis

Articles » Scholarly, peer reviewed
Author/Creator
Pierre Chagnon
Jacques Michaud
Grant Mitchell
Jocelyne Mercier
Marion Jean-Francois
et al.
American Journal of Human Genetics, vol. 71, no. 6, December 2002, pp. 1443-1449
Description
Study concludes that a single gene mutation causes North American Indian Childhood Cirrhosis, a distinct and severe form of familial cholestasis, which occurs in aboriginal children in the Abitibi region of northwestern Quebec.
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Mitochondrial DNA and Y Chromosome Diversity and the Peopling of the Americas: Evolutionary and Demographic Evidence

Articles » Scholarly, peer reviewed
Author/Creator
Theodore G. Schurr
Stephen T. Sherry
American Journal of Human Biology, vol. 16, no. 4, 2004, pp. 420-439
Description
Discussion of the mitrochondrial DNA (mtDNA) specific locations on the chromosome of A-D, NRY and P-M45a and Q-242/Q-M3, with the observation that these were dispersed throughout the entire Americas.
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Mitochondrial DNA of Protohistoric Remains of an Arikara Population from South Dakota: Implications for the Macro-Siouan Language Hypothesis

Articles » Scholarly, peer reviewed
Author/Creator
Diana M. Lawrence
Brian M. Kemp
Jason Eshleman
Richard L. Jantz
Meradeth Snow
Debra George
David Glenn Smith
Human Biology, vol. 82, no. 2, April 2010, pp. 157-178
Description
Looks at data collected on Macro-Siouan hypothesis and the relationship of the language spoken by the Sahnish to other languages.
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Mitochondrial Genome Diversity of Native Americans Supports a Single Early Entry of Founder Populations into America

Articles » Scholarly, peer reviewed
Author/Creator
Wilson A. Silva
Sandro L. Bonatto
Adriano J. Holanda
Andrea K. Ribeiro-dos-Santos
Beatriz M. Paixão
et al.
American Journal of Human Genetics, vol. 71, no. 1, July 2002, pp. 187-192
Description
Argues that through their research they have determined there is a common origin among peoples who migrated to the Americas.
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Mitochondrial Haplogroup M Discovered in Prehistoric North Americans

Articles » Scholarly, peer reviewed
Author/Creator
Ripan S. Malhi
Brian M. Kemp
Jason A. Eshleman
Jerome Cybulski
David Glenn Smith
Scott Cousins
Harold Harry
Journal of Archaeological Science , vol. 34, no. 4, April 2007, pp. 642-648
Description
Presents evidence of mitrochrondrial DNA of the haplogroup M, a group that is common in East Asia, but had never before been reported for Indigenous populations in North American. Estimates put the time frame at about five thousand years before present.
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Molecular Epidemiology of Serotype 19A Streptococcus Pneumoniae among Invasive Isolates from Alaska, 1986-2010

Alternate Title
Proceedings of the 15th International Congress on Circumpolar Health
Articles » Scholarly, peer reviewed
Author/Creator
Karen Rudolph
M.G. Bruce
L. Bulkow
T. Zulz
A. Reasonover
M. Harker-Jones
D. Hurlburt
T.W. Hennessy
International Journal of Circumpolar Health, vol. 72, Supplement 1, 2013, p. article no. 20854
Description
Findings emphasize need for continual monitoring of invasive pneumococcal disease (IPD) to determine the effects of vaccination.
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mtDNA Diversity in Chukchi and Siberian Eskimos: Implications for the Genetic History of the Ancient Beringia and the Peopling of the New World

Articles » Scholarly, peer reviewed
Author/Creator
Yelena B. Starikovskaya
Rem I. Sukernik
Theodore G. Schurr
Andreas M. Kogelnik
Douglas C. Wallace
American Journal of Human Genetics, vol. 63, no. 5, November 1998, pp. 1473-1491
Description
Concludes that about 34,000 years before present (YBP) ancient Beringia had Haplogroups A, C, and D and that a second migration brought haplogroup B, probably from Siberia.
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The Nagoya Protocol and Indigenous Peoples

Articles » Scholarly, peer reviewed
Author/Creator
Maria Yoland Teran
International Indigenous Policy Journal, vol. 7, no. 2, April 2016, pp. 1-32
Description
Explores involvement with the Nagoya Protocol which governs access to genetic resources and the equitable sharing of the benefits.
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Navigating the Cultural Geography of Indigenous Peoples' Attitude toward Genetic Research: The Ohana (Family) Heart Project

Alternate Title
Proceedings of the 15th International Congress on Circumpolar Health
Articles » Scholarly, peer reviewed
Author/Creator
May Vawer
Patsy Kaina
Ann Leonard
Michael Ogata
Beth Blackburn
Malia Young
Todd B. Seto
International Journal of Circumpolar Health, vol. 72, Supplement 1, 2013, p. article no. 21346
Description
Study confirms that priorities for both researchers and Indigenous populations needs to be taken into account to ensure a mutually satisfying outcome.
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The Non-Thrifty Genotype

Articles » Scholarly, peer reviewed
Author/Creator
John S. Allen
Susan M. Cheer
Current Anthropology, vol. 37, no. 5, December 1996, pp. 831-842
Description
Argues that the thrifty genotype hypothesis for diabetes presupposes the presence of a non-thrifty genotype.
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Nonencapsulated Haemophilus Influenzae in Aboriginal Infants with Otitis Media: Prolonged Carriage of P2 Porin Variants and Evidence for Horizontal P2 Gene Transfer

Articles » Scholarly, peer reviewed
Author/Creator
H. C. Smith-Vaughan
K. S. Sriprakash
J. D. Mathews
D. J. Kemp
Infection and Immunity, vol. 65, no. 4, April 1997, pp. 1468-1474
Description
Study sequenced loops 4, 5, and 6 of nonencapsulated Haemophilus influenza P2 porin gene, characterizing several strains that had prolonged carriage times. The authors suggest that there has been transfer of the P2 gene between strains.
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The North-Western Tribes of Canada: Eleventh Report of the Committee, Consisting of Professor E.B. Tylor (Chairman), Mr. Cuthbert E. Peek (Secretary), Dr. G.M. Dawson, Mr. R.G. Haliburton, and Mr. Horatio Hale ...

Alternate Title
Sixth Report on the Indians of British Columbia
E-Books
Author/Creator
Franz Boas
Description
"Appointed to investigate the physical characteristics, languages, and industrial and social conditions of the people of British Columbia."
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A Novel Missense RAG-1 Mutation Results In T¯B¯NK + SCID in Athabascan-Speaking Dine Indians From The Canadian Northwest Territories

Articles » Scholarly, peer reviewed
Author/Creator
Zheng Xiao
Steven M. Yanonne
Elizabeth Dunn
Morton J. Cowan
European Journal of Human Genetics, vol. 17, no. 2, February 2009, pp. 205-212
Description
Study identified a third immunological mutation in this isolated population, which points to the need for newborn screenings in this high-risk population.
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Obesity and Type 2 Diabetes in Northern Canada's Remote First Nations Communities: The Dietary Dilemma

Articles » Scholarly, peer reviewed
Author/Creator
F. Haman
B. Fontaine-Bisson
M. Batal
P. Imbeault
J. M. Blais ... [et al.]
International Journal of Obesity, vol. 34, no. S2, Supplement 2, December 2010, pp. [S24]-S31
Description
Explores the biological predispositions and potential environmental factors that contribute to the high incidence of obesity and type 2 diabetes.
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Osteogenesis Imperfecta Type VII Maps to the Short Arm of Chromosome 3

Articles » Scholarly, peer reviewed
Author/Creator
M. Labuda
J. Morrisette
L. M. Ward
F. Rauch
L. Lalic
P. J. Roughley
F. H. Glorieux
Bone, vol. 31, no. 1, July 2002, pp. 19-25
Description
Report on research to identify the gene responsible for a novel form of this debilitating condition in a small First Nations community in Quebec.
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