Apolipoprotein B genetic variability in Brazilian Indians.

Abstract:

:Three apolipoprotein B restriction fragment length polymorphism (RFLPs) (XbaI, MspI, and EcoRI) and the signal peptide insertion-deletion polymorphism were investigated using the polymerase chain reaction in 140 individuals from 5 Brazilian Indian tribes. All studied markers were polymorphic in this ethnic group. The insertion allele 5' beta SP*29 at the signal peptide previously observed in Mexican Americans was detected in about 8% of the chromosomes of 2 tribes (Gavião and Zoró), therefore confirming the Amerindian origin of this allele. Negative linkage disequilibrium was observed between alleles at the signal peptide and the EcoRI polymorphism in all tribes. In 3 populations (Gavião, Suruí, and Zoró) a negative disequilibrium was also detected between the insertion-deletion signal peptide markers and the XbaI polymorphism. In the whole sample of Amerindians 14 of the 24 (58%) possible 4-marker extended haplotypes were identified, but only haplotype 2 (5' beta SP*24/*X+/*M+/*E+) and haplotype 5 (5' beta SP*27/*X-/*M+/*E+) were shared by all tribes. No associations between plasma lipid levels or body mass index and these polymorphisms were observed in this sample.

journal_name

Hum Biol

journal_title

Human biology

authors

Kaufman L,Vargas AF,Coimbra Júnior CE,Santos RV,Salzano FM,Hutz MH

subject

Has Abstract

pub_date

1999-02-01 00:00:00

pages

87-98

issue

1

eissn

0018-7143

issn

1534-6617

journal_volume

71

pub_type

杂志文章
  • Mountain pygmies of Western New Guinea: a morphological and molecular approach.

    abstract::The presence of "pygmy" or pygmoid groups among New Guinea populations has been the object of scientific interest since the end of the nineteenth century. Morphological and molecular data are used here to study western New Guinea population variability, focusing in particular on two pygmoid groups living in the easter...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.3378/027.085.0314

    authors: Tommaseo-Ponzetta M,Mona S,Calabrese F,Konrad G,Vacca E,Attimonelli M

    更新日期:2013-02-01 00:00:00

  • Finding Rare, Disease-Associated Variants in Isolated Groups: Potential Advantages of Mennonite Populations.

    abstract::Large-scale genotyping and next-generation sequencing techniques have allowed great advances in the field of molecular genetics. Numerous common variants of low impact have been associated with many complex human traits and diseases, such as bipolar disorder and schizophrenia. Although they may exert a greater impact ...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.13110/humanbiology.88.2.0109

    authors: Lopes FL,Hou L,Boldt AB,Kassem L,Alves VM,Nardi AE,McMahon FJ

    更新日期:2016-04-01 00:00:00

  • How the Atacama Skeleton Might Advance Discussion of Responsible Conduct of Research Responsibilities.

    abstract::Controversies resulting from genetic testing on skeletal remains of disputed stewardship raise important questions about obligations inherent on genetic researchers to assure ethical chain of custody. In this article, we analyze and evaluate several proposed positions on whether such research should be published. Foll...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.13110/humanbiology.91.1.01

    authors: May T,Nakano-Okuno M

    更新日期:2019-02-17 00:00:00

  • The genetic position of the autochthonous subpopulation of Northern Navarre (Spain) in relation to other basque subpopulations. A study based on GM and KM immunoglobulin allotypes.

    abstract::GM and KM immunoglobulin (Ig) allotypes were tested in 118 autochthonous Basques from northern Navarre. The results are compared to those obtained for the same genetic markers in 6 other Basque subpopulations, 3 from Spain (Guipúzcoa, Vizcaya, and Alava) and 3 from France: Macaye, Saint-Jean Pied de Port, and Mauleon....

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Calderón R,Perez-Miranda A,Peña JA,Vidales C,Aresti U,Dugoujon JM

    更新日期:2000-08-01 00:00:00

  • Possible migration routes into South America deduced from mitochondrial DNA studies in Colombian Amerindian populations.

    abstract::Mitochondrial DNA haplotype studies have been useful in unraveling the origins of Native Americans. Such studies are based on restriction site and intergenic deletion/insertion polymorphisms, which define four main haplotype groups common to Asian and American populations. Several studies have characterized these line...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.1353/hub.2002.0022

    authors: Keyeux G,Rodas C,Gelvez N,Carter D

    更新日期:2002-04-01 00:00:00

  • Sex ratio at reproductive age: changes over the last century in the Italian population.

    abstract::The radical improvement in living conditions experienced in Italy during the last century caused a reduction in male extra-mortality during the prereproductive years. As a consequence, a progressive increase in the sex ratio at the beginning of the reproductive age (15-19 years) occurred, so that in recent times the s...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.1353/hub.2001.0014

    authors: Ulizzi L,Astolfi P,Zonta LA

    更新日期:2001-02-01 00:00:00

  • Evolutionary relationships between black South American and African populations.

    abstract::Data related to ten protein genetic loci expressed in blood obtained from four South American black populations were compared with data from seven African countries. Estimates of admixture among South American blacks were revised, and several indexes of gene diversity and genetic distances between the 11 populations w...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Bortolini MC,Weimer Tde A,Salzano FM,Callegari-Jacques SM,Schneider H,Layrisse Z,Bonatto SL

    更新日期:1995-08-01 00:00:00

  • Genetic diversity of serum proteins in some muslim populations of India.

    abstract::The Muslim population of India is known for its historical and socioreligious significance. Literature on the genetic structure of this segment of India's population is scanty. Therefore we have investigated the allele frequency distribution of haptoglobin (HP) and transferrin (TF) phenotypes among the Muslims to expl...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.3378/1534-6617-80.5.501

    authors: Ahmad R,Alam A,Fatima F,Hasnain AU

    更新日期:2008-10-01 00:00:00

  • Temporal changes and rural-urban differences in cardiovascular disease risk factors and mortality in China.

    abstract::We summarize several studies, from the last 10 years, of temporal changes and rural-urban differences in the risk factors of cardiovascular disease (CVD) in China to indicate the influences of economic modernization. Two national blood pressure surveys have shown that the prevalence of hypertension increased from 5.1%...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Zhai S,McGarvey ST

    更新日期:1992-12-01 00:00:00

  • Genetic studies of human apolipoproteins. XVIII. Apolipoprotein polymorphisms in Australian Aborigines.

    abstract::A tribal aboriginal community, the Mowanjum, from the Kimberley region in Western Australia has been screened to determine the extent of genetic variation in the products of genes coding for apolipoproteins, which are intimately involved in lipid metabolism. Of the seven systems tested, APOE and APOH revealed common s...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Kamboh MI,Serjeantson SW,Ferrell RE

    更新日期:1991-04-01 00:00:00

  • Studies of human sex ratios at birth may lead to the understanding of several forms of pathology.

    abstract::This article deals with the problem of the causes of the variation of sex ratio (proportion male) at birth. This problem is common to a number of areas in biology and medicine, for example, obstetrics, neurology/psychiatry, parasitology, virology, oncology, and teratology. It is established that there are signifi cant...

    journal_title:Human biology

    pub_type: 杂志文章,评审

    doi:10.3378/027.085.0513

    authors: James WH

    更新日期:2013-10-01 00:00:00

  • Age structure and sex-biased mortality among Herero pastoralists.

    abstract::Details of the population pyramid of living Herero and Mbanderu of Botswana suggest that infant and childhood mortality of males has been substantially greater than that of females. Direct tests from reproductive histories show that the hazard ratio is approximately 3 to 1 in favor of female survival in infancy and 2 ...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Harpending HC,Pennington R

    更新日期:1991-06-01 00:00:00

  • Haplotype analysis of the apolipoprotein E and apolipoprotein C1 loci in Portugal and São Tomé e Príncipe (Gulf of Guinea): linkage disequilibrium evidence that APOE*4 is the ancestral APOE allele.

    abstract::The joint distributions of phenotypes from the apolipoprotein E gene (APOE) and from a closely linked restriction site polymorphism at the apolipoprotein C1 locus (APOC1) were studied in population samples from Portugal and São Tomé e Príncipe (Gulf of Guinea), a former Portuguese colony that was originally populated ...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Seixas S,Trovoada MJ,Rocha J

    更新日期:1999-12-01 00:00:00

  • Genetic Evidence for Modifying Oceanic Boundaries Relative to Fiji.

    abstract::We present the most comprehensive genetic characterization to date of five Fijian island populations: Viti Levu, Vanua Levu, Kadavu, the Lau Islands, and Rotuma, including nonrecombinant Y (NRY) chromosome and mitochondrial DNA (mtDNA) haplotypes and haplogroups. As a whole, Fijians are genetically intermediate betwee...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.13110/humanbiology.88.3.0232

    authors: Shipley GP,Taylor DA,N'Yeurt ADR,Tyagi A,Tiwari G,Redd AJ

    更新日期:2016-07-01 00:00:00

  • Genetic structure of Mennonite populations of Kansas and Nebraska.

    abstract::We describe the gene frequency distributions for 29 different blood group, serum, and erythrocytic proteins for three Mennonite communities from Kansas and Nebraska and compare their gene frequencies with those of Amish, Hutterite, and Mennonite populations using the topological method of Harpending and Jenkins (1973)...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Crawford MH,Dykes DD,Polesky HF

    更新日期:1989-08-01 00:00:00

  • Complement components C2, C3, and C4 (C4A and C4B) and BF polymorphisms in populations of the Indian subcontinent.

    abstract::Genetic polymorphisms of the complement components (five loci: C2, C3, C4A, C4B, and BF) have been investigated in the Telugu-speaking Hindu population of Hyderabad, Andhra Pradesh, India, and the Bangali-speaking Muslim population of Dacca, Bangladesh. The available data are compared to understand the genetic variati...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Ad'hiah AH,Papiha SS

    更新日期:1996-10-01 00:00:00

  • Distribution of hemoglobin E in several Mongoloid populations of northeast India.

    abstract::Nine-hundred seventy-eight subjects from eight Mongoloid tribes of northeastern India were investigated for the distribution of hemoglobin phenotypes by starch-gel electrophoresis. The sample included 157 Khasi and 24 Bodo from Cherrapunji (Meghalaya), 148, Rengma Naga and 81 Hmar of the Cachar district of Assam, 215 ...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Saha N

    更新日期:1990-08-01 00:00:00

  • Misclassification, correlation, and cause of death studies.

    abstract::Relatives may tend to die of the same cause. A model is proposed specifying the degree of this association, simultaneously allowing for misclassification of cause of death. These mistakes usually degrade any existing correlation structure, the effects being marked when error rates reach between 20% to 30%. It is then ...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.1353/hub.2002.0013

    authors: Tallis GM

    更新日期:2002-02-01 00:00:00

  • Identification of Whole Mitochondrial Genomes from Venezuela and Implications on Regional Phylogenies in South America.

    abstract::Recent studies have expanded and refined the founding haplogroups of the Americas using whole mitochondrial (mtDNA) genome analysis. In addition to pan-American lineages, specific variants have been identified in a number of studies that show higher frequencies in restricted geographical areas. To further characterize...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.13110/humanbiology.87.1.0029

    authors: Lee EJ,Merriwether DA

    更新日期:2015-01-01 00:00:00

  • Association of PPARG2 Pro12Ala variant with larger body mass index in Mestizo and Amerindian populations of Mexico.

    abstract::Previous studies have sought to associate the Pro12Ala variant of the peroxisome proliferator-activated receptor gamma2 (PPARG2) gene with type 2 diabetes, insulin resistance, and obesity, with controversial results. We have determined the Pro12Ala variant frequency in 370 nondiabetic Mexican Mestizo subjects and in f...

    journal_title:Human biology

    pub_type: 杂志文章,多中心研究

    doi:10.1353/hub.2007.0022

    authors: Canizales-Quinteros S,Aguilar-Salinas CA,Ortiz-López MG,Rodríguez-Cruz M,Villarreal-Molina MT,Coral-Vázquez R,Huertas-Vázquez A,Hernández-Caballero A,López-Alarcón M,Brito-Zurita OR,Domínguez-Banda A,Martinez-Sánchez LR,Canto-de

    更新日期:2007-02-01 00:00:00

  • Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African Brazilians.

    abstract::Mutations in the GJB2 gene are a major cause of congenital deafness. One specific mutation, the 35delG mutation, has accounted for most of the GJB2 mutations detected in European populations and is one of the most frequent disease mutations identified so far. We evaluated the frequency of the 35delG mutation in DNA sa...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.1353/hub.2004.0035

    authors: Oliveira CA,Alexandrino F,Abe-Sandes K,Silva WA Jr,Maciel-Guerra AT,Magna LA,Sartorato EL

    更新日期:2004-04-01 00:00:00

  • Optimizing utilization of DNA from rare or archival anthropological samples.

    abstract::There is widespread interest in obtaining genetic samples from human populations worldwide for various studies of human genetic diversity. Many samples exist today only in the form of small, rare, irreplaceable, or archival samples, such as material from ancient bone, hair bulbs, or remnants of samples collected in th...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Weiss KM,Buchanan AV,Daniel C,Stoneking M

    更新日期:1994-10-01 00:00:00

  • Diabetic pregnancy: evidence of selection on the Rh blood group system.

    abstract::The blood glucose levels of pregnant women with insulin-dependent diabetes mellitus and the blood glucose levels of newborns during the first few hours of life show an association with maternal Rh genotype. Distortions of joint maternal-fetal Rh phenotype distribution have also been observed. Because a cluster of gene...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Gloria-Bottini F,Gerlini G,Amante A,Pascone R,Bottini E

    更新日期:1992-02-01 00:00:00

  • CYP2A6 polymorphism reveals differences in Japan and the existence of a specific variant in Ovambo and Turk populations.

    abstract::CYP2A6 is a polymorphic enzyme, and CYP2A6 genotype has been shown to be associated with smoking habits and lung cancer. We investigated CYP2A6 polymorphism in Japanese from four different geographic areas of Japan and in the Ovambo and Turk populations. Using two polymerase chain reaction restriction fragment length ...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.1353/hub.2006.0037

    authors: Takeshita H,Hieda Y,Fujihara J,Xue Y,Nakagami N,Takayama K,Imamura S,Kataoka K

    更新日期:2006-04-01 00:00:00

  • Craniometric variation in the Americas.

    abstract::Craniofacial variation is investigated in Latin America and the Caribbean. The samples included in this study are two historic and one prehistoric sample from Ecuador; prehistoric and modern Cuban samples; a prehistoric Peruvian sample; two prehistoric Mexican samples and one contemporary admixed Mexican sample; a 16t...

    journal_title:Human biology

    pub_type: 历史文章,杂志文章

    doi:10.1353/hub.2003.0010

    authors: Ross AH,Ubelaker DH,Falsetti AB

    更新日期:2002-12-01 00:00:00

  • Presentation, heritability, and genome-wide linkage analysis of the midchildhood growth spurt in healthy children from the Fels Longitudinal Study.

    abstract::Growth is a complex process composed of distinct phases over the course of childhood. Although the pubertal growth spurt has received the most attention from auxologists and pediatricians, the midchildhood growth spurt has been less well studied. The midchildhood growth spurt refers to a relatively small increase in g...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:10.3378/1534-6617-80.6.623

    authors: Towne B,Williams KD,Blangero J,Czerwinski SA,Demerath EW,Nahhas RW,Dyer TD,Cole SA,Lee M,Choh AC,Duren DL,Sherwood RJ,Chumlea WC,Siervogel RM

    更新日期:2008-12-01 00:00:00

  • Detection of differential gene flow from patterns of quantitative variation.

    abstract::A major goal in anthropological genetics is the assessment of the effects of different microevolutionary forces. Harpending and Ward (1982) developed a model that aids in this effort by comparing observed and expected heterozygosity within populations in a local region. The expected heterozygosity within a population ...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Relethford JH,Blangero J

    更新日期:1990-02-01 00:00:00

  • Some atypical and rare sickle cell gene haplotypes in populations of Andhra Pradesh, India.

    abstract::We have investigated the clinical, hematological, and molecular genetic characteristics of sickle cell anemia patients from 6 populations of Andhra Pradesh, South India. Of 72 sickle cell chromosomes (HBB*S) 60 belong to characteristic Arab-Indian haplotypes, 6 to variant Arab-Indian haplotypes, 1 to a Bantu haplotype...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Niranjan Y,Chandak GR,Veerraju P,Singh L

    更新日期:1999-06-01 00:00:00

  • Polymorphisms of the gene coding for the cholesteryl ester transfer protein and plasma lipid levels in Italian and Greek migrants to Australia.

    abstract::The relation between TaqI restriction fragment length polymorphisms (RFLPs) of the cholesteryl ester transfer protein (CETP) gene and plasma lipid and lipoprotein phenotypes was investigated in a sample of Italian and Greek migrants of both sexes, age 40-69 years. Italians display significantly higher mean triglycerid...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Mitchell RJ,Earl L,Williams J,Bisucci T,Gasiamis H

    更新日期:1994-02-01 00:00:00

  • Signature of ancient population growth in a low-resolution mitochondrial DNA mismatch distribution.

    abstract::A mismatch distribution is a tabulation of the number of pairwise differences among all DNA sequences in a sample. In a population that has been stationary for a long time these distributions from nonrecombinant DNA sequences become ragged and erratic, whereas a population that has been growing generates mismatch dist...

    journal_title:Human biology

    pub_type: 杂志文章

    doi:

    authors: Harpending HC

    更新日期:1994-08-01 00:00:00