0000000000319232

AUTHOR

M. Bajatzadeh

showing 8 related works from this author

Hp, Gc, Cp, Tf, Bg and Pi phenotypes in leprosy patients and healthy controls from West Bengal (India)

1972

On a sample of n=601 leprous individuals and n=386 healthy controls from West Bengal (India) the question is discussed, if there are existing any associations between leprosy and several serum protein groups like haptoglobin, Gc, ceruloplasmin, transferrin, β2 I and Pi. No associations were found concerning the haptoglobins and transferrins. Certain associations came out respecting ceruloplasmin, β2 I and Pi phenotypes. However, these associations, which were found in connection with the different types and clinical courses of leprosy, should be reexamined by further research. The most striking results were obtained concerning the Gc proteins. In accordance with previously performed investi…

Serum proteinIndiaGene FrequencyLeprosyGeneticsmedicineHumansMetabolic diseaseGenetics (clinical)Glycoproteinschemistry.chemical_classificationPolymorphism GeneticHaptoglobinsbiologyHaptoglobinTransferrinCeruloplasminPi phenotypesmedicine.diseasePhenotypechemistryTransferrinImmunologybiology.proteinSerum GlobulinsWest bengalLeprosyFactor Analysis StatisticalCeruloplasminHuman Genetics
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Associations between leprosy and serum protein groups

1970

Serum protein group typings were done on a sample of n=173 adult healthy Negroes from the Macua tribe in Mozambique and on n=129 leprous individuals from the same tribe. Unfortunately, the type of leprosy is not known. Whilst between leprosy and haptoglobins, transferrins and Pi proteins no associations could be observed, statistically significant associations between leprosy and ceruloplasmin resp. β2 I were found. It is pointed out that these associations should be confirmed by further research on other populations and with respect to type and process of leprosy, until biological and population genetical interpretations will be possible.

AdultMalePopulationSerum proteinBlack PeopleTribe (biology)LeprosyGeneticsmedicineHumansAlleleMetabolic diseaseeducationAllelesMozambiqueGenetics (clinical)Glycoproteinseducation.field_of_studyHaptoglobinsbiologyHaptoglobinTransferrinCeruloplasminfood and beveragesmedicine.diseaseBlack or African AmericanGenetics PopulationPhenotypeImmunologyBlood Group Antigensbiology.proteinFemaleLeprosyTrypsin InhibitorsCeruloplasminHuman Genetics
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Phosphoglucomutase (EC 2.7.5.1.) and adenylate kinase (EC 2.7.4.3.) typings in Koreans and Irish.

1969

PGM1 and AK phenotypes were determined in samples from Korea and Ireland. the frequencies of PGM 1 1 genes amount to 0.916 in Koreans and 0.864 in Irish. AK1 frequencies come to 0.933 in Koreans and 0.873 in Irish.

GeneticsAdultMaleKoreaPolymorphism GeneticPhosphotransferasesAdenylate kinaseBiologyPhenotypeMolecular medicinelanguage.human_languageHuman geneticsIrishPhosphoglucomutasePGM1GeneticslanguageHumansPhosphoglucomutaseFemaleGeneIrelandGenetics (clinical)Humangenetik
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Untersuchungen �ber die Verteilung der Hp-, Gc- und Gm-Gruppen in Pakistan

1966

Evolutionary biologyGeneticsDistribution (pharmacology)BiologyGenetics (clinical)Human geneticsHuman Genetics
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Pseudocholinesterases and human red cell acid phosphatases in Koreans.

1969

The authors reveal the results of pseudocholinesterase and human red cell acid phosphatase typings in a sample of 115 unrelated female Koreans aged from 20–30. No atypical pseudocholinesterase variants could be demonstrated. The frequencies of human red cell acid phosphatase alleles run up to: phA=0.231, phB=0.769, phC=0.000.

AdultErythrocytesKoreaRed CellRed cell acid phosphatasePhosphataseAcid PhosphataseAcid phosphataseBiologyIsozymeMolecular medicineIsoenzymesGenetics PopulationBiochemistryGene FrequencyGeneticsbiology.proteinCholinesterasesHumansFemaleAlleleAllele frequencyGenetics (clinical)Humangenetik
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Investigations on the geographical variability of the human transferrins.

1971

On the basis of own and from the widely scattered literature compiled materials the geographical distribution of the transferrin alleles is discussed. They reveal a characteristic distribution pattern, as the slow Tf variants produced by TfD alleles are obviously more frequent in tropical than in non-tropical populations. Considering similar results in cattle and its interpretation by Ashton (1958, 1965), it is hypothesized, that the relatively high TfΓ frequencies in tropical biotops might be a selective adaptation to their special climatic conditions. In this connection an association between slowly moving transferrin proteins in man and tolerance to hotter climates — as could be found in…

chemistry.chemical_classificationGeneticsPhysiological functionTropical ClimateNative Hawaiian or Other Pacific IslanderGeographyRacial GroupsTransferrinBlack PeopleGenetic VariationBiologyWhite PeopleGenetics PopulationCharacteristic distributionchemistryAsian PeopleEvolutionary biologyTransferrinInuitGeneticsHumansAlleleAdaptationGenetics (clinical)AllelesHumangenetik
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Investigations on the genetics and population genetics of the ?2 polymorphism

1970

The results of studies on 49 families with 107 children and various populations of Caucasoid, Negroid and Mongoloid origin concerning the genetics and population genetics of the β2-glycoprotein I polymorphism are reported. In general the genetical model proposed by Cleve (1968) is confirmed: two autosomal alleles BgN and BgD controlling the phenotypes Bg N-N, Bg N-D and Bg D-D. However, divergences from this model were found in two families. They indicate the assumption of non-genetic factors influencing the phenotype expression rather than more complicated genetical control mechanisms. Within Caucasoid populations phenotype and gene frequencies show almost a homogeneous distribution. This …

GeneticsEvolutionary biologyGeneticsBeta 2-Glycoprotein IPopulation geneticsMongoloidAlleleBiologyGeneAllele frequencyPhenotypeGenetics (clinical)Human geneticsHuman Genetics
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Studies on the population genetics of the ceruloplasmin polymorphism

1969

Phenotype and gene frequencies of the ceruloplasmin polymorphism are reported. In all populations considered here (Germans, Icelanders, Iranians, Pakistani, and Koreans) high frequencies of the allele CpB (0.978–0.996) could be observed, whilst the frequencies of the alleles CpA (0.003–0.013) and CpC (0.000–0.013) are very low.

GeneticsPolymorphism GeneticCeruloplasminPopulation geneticsBiologyPhenotypeHuman geneticsPolymorphism (computer science)otorhinolaryngologic diseasesGeneticsbiology.proteinHumanspopulation characteristicsAlleleCeruloplasminAllele frequencyGeneGenetics (clinical)Human Genetics
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