408 research outputs found

    36 Months Survivability And Its Predictors In Patients With Chronic Heart Failure And Decreased Fraction Of Left Ventricular Ejection Depending On Sex

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    Aim of the work: to compare survivability parameters during 36 months and their predictors among men and women with chronic heart failure and decreased fraction of left ventricular ejection.Materials and methods: the research included 356 patients with CHF (NYHA Π†Π† –ІV) with decreased LVEF<40 %, 18–75 years old. Using Kaplan-Meier method, there was analyzed the survivability in men and women during 36 months, then there were analyzed independent factors that influenced survivability terms depending on sex using the multiple logistic regression.Results. Our analysis of the survivability of patients with CHF with decreased LVEF demonstrated that the cumulative survival after 3 years of observation was 49 and 51 % for men and women, respectively. The curves of 36 months survivability didn\u27t reliably differ. At the analysis of factors, associated with the bad prognosis, there were observed differences between groups of men and women with CHF. Thus, in men the predictors of 36 month survival were: the thickness of the right ventricle wall, size of the right atrium, end-diastolic volume and end-systolic volume of LV, indices of EDV and ESV of LV, urinary acid level, value of LVEF. In women the predictors of survivability during 3 years were the following parameters: BMI, DM type 2 in an anamnesis, end-diastolic size of LV, end-systolic size of LV, blood glucose level, LVEF.Conclusion. The survivability of men and women with CHF with decreased LVEF during 36 months didn\u27t reliably differ and was 49 and 51 % respectively. But predictors of the lethal outcome in men and women essentially differed during 36 months, and their number is essentially higher in men

    Climate variation influences host specificity in avian malaria parasites

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    Parasites with low host specificity (e.g. infecting a large diversity of host species) are of special interest in disease ecology, as they are likely more capable of circumventing ecological or evolutionary barriers to infect new hosts than are specialist parasites. Yet for many parasites, host specificity is not fixed and can vary in response to environmental conditions. Using data on host associations for avian malaria parasites (Apicomplexa: Haemosporida), we develop a hierarchical model that quantifies this environmental dependency by partitioning host specificity variation into region- and parasite-level effects. Parasites were generally phylogenetic host specialists, infecting phylogenetically clustered subsets of available avian hosts. However, the magnitude of this specialization varied biogeographically, with parasites exhibiting higher host specificity in regions with more pronounced rainfall seasonality and wetter dry seasons. Recognizing the environmental dependency of parasite specialization can provide useful leverage for improving predictions of infection risk in response to global climate change

    Comparing the mitochondrial genomes of Wolbachia-dependent and independent filarial nematode species

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    BACKGROUND: Many species of filarial nematodes depend on Wolbachia endobacteria to carry out their life cycle. Other species are naturally Wolbachia-free. The biological mechanisms underpinning Wolbachia-dependence and independence in filarial nematodes are not known. Previous studies have indicated that Wolbachia have an impact on mitochondrial gene expression, which may suggest a role in energy metabolism. If Wolbachia can supplement host energy metabolism, reduced mitochondrial function in infected filarial species may account for Wolbachia-dependence. Wolbachia also have a strong influence on mitochondrial evolution due to vertical co-transmission. This could drive alterations in mitochondrial genome sequence in infected species. Comparisons between the mitochondrial genome sequences of Wolbachia-dependent and independent filarial worms may reveal differences indicative of altered mitochondrial function. RESULTS: The mitochondrial genomes of 5 species of filarial nematodes, Acanthocheilonema viteae, Chandlerella quiscali, Loa loa, Onchocerca flexuosa, and Wuchereria bancrofti, were sequenced, annotated and compared with available mitochondrial genome sequences from Brugia malayi, Dirofilaria immitis, Onchocerca volvulus and Setaria digitata. B. malayi, D. immitis, O. volvulus and W. bancrofti are Wolbachia-dependent while A. viteae, C. quiscali, L. loa, O. flexuosa and S. digitata are Wolbachia-free. The 9 mitochondrial genomes were similar in size and AT content and encoded the same 12 protein-coding genes, 22 tRNAs and 2 rRNAs. Synteny was perfectly preserved in all species except C. quiscali, which had a different order for 5 tRNA genes. Protein-coding genes were expressed at the RNA level in all examined species. In phylogenetic trees based on mitochondrial protein-coding sequences, species did not cluster according to Wolbachia dependence. CONCLUSIONS: Thus far, no discernable differences were detected between the mitochondrial genome sequences of Wolbachia-dependent and independent species. Additional research will be needed to determine whether mitochondria from Wolbachia-dependent filarial species show reduced function in comparison to the mitochondria of Wolbachia-independent species despite their sequence-level similarities

    Treatment and prevention of arresive bleeding in patients with pancreonecrosis.

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    The article is devoted to the study of acute necrotizing pancreatitis, which leads to the development of various fluid pathologies different in pathogenesis and time, which in turn can lead to an arrosive bleeding. Diagnostic-treatment ispresented algorithm with the active use of modern methods of hemostasis in patients with arrosive bleeding developed against the background of pancreatonecrosis

    Treatment and prevention of arresive bleeding in patients with pancreonecrosis.

    Get PDF
    The article is devoted to the study of acute necrotizing pancreatitis, which leads to the development of various fluid pathologies different in pathogenesis and time, which in turn can lead to an arrosive bleeding. Diagnostic-treatment ispresented algorithm with the active use of modern methods of hemostasis in patients with arrosive bleeding developed against the background of pancreatonecrosis

    ΠœΠΎΠ΄Π΅Π»ΠΈΡ€ΠΎΠ²Π°Π½ΠΈΠ΅ двиТСния Π°Π½Ρ‚Ρ€ΠΎΠΏΠΎΠΌΠΎΡ€Ρ„Π½ΠΎΠ³ΠΎ ΡˆΠ°Π³Π°ΡŽΡ‰Π΅Π³ΠΎ Π°ΠΏΠΏΠ°Ρ€Π°Ρ‚Π° Π½Π° ΠΏΡ€ΠΎΠΈΠ·Π²ΠΎΠ»ΡŒΠ½ΠΎΠΉ Ρ‚Π²Π΅Ρ€Π΄ΠΎΠΉ повСрхности

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    Π£ Ρ€ΠΎΠ±ΠΎΡ‚Ρ– основну ΡƒΠ²Π°Π³Ρƒ ΠΏΡ€ΠΈΠ΄Ρ–Π»Π΅Π½ΠΎ модСлюванню Ρ…ΠΎΠ΄ΠΈ АКА Π±Π΅Π· зіткнСння Π· ΠΏΠΎΠ²Π΅Ρ€Ρ…Π½Π΅ΡŽ ΠΏΡ–Π΄ час пСрСміщСння схилом Ρ‡ΠΈ ΠΏΡ–Π΄ΠΉΠΎΠΌΠΎΠΌ, Ρ‰ΠΎ Π°ΠΊΡ‚ΡƒΠ°Π»ΡŒΠ½ΠΎ для Π·Π°Π΄Π°Ρ‡Ρ– ΠΏΠΎΠ±ΡƒΠ΄ΠΎΠ²ΠΈ ΠΊΡ€ΠΎΠΊΡƒΡŽΡ‡ΠΈΡ… систСми Π½Π° основі Π°Π½Ρ‚Ρ€ΠΎΠΏΠ½ΠΎΠ³ΠΎ ΠΏΡ€ΠΈΠ½Ρ†ΠΈΠΏΡƒ. Для Ρ€Π΅Π°Π»Ρ–Π·Π°Ρ†Ρ–Ρ— Π°Π½Ρ‚Ρ€ΠΎΠΏΠΎΠΌΠΎΡ€Ρ„Π½ΠΎΠ³ΠΎ пСрСміщСння, Ρƒ дослідТСнні застосовувалися ΠΏΡ€ΠΈΠ½Ρ†ΠΈΠΏΠΈ Π·Π²ΠΎΡ€ΠΎΡ‚Π½ΡŒΠΎΡ— Π΄ΠΈΠ½Π°ΠΌΡ–ΠΊΠΈ Ρ‚Π° ΠΊΡ–Π½Π΅ΠΌΠ°Ρ‚ΠΈΠΊΠΈ Ρ€ΡƒΡ…Ρƒ Π±Π°Π³Π°Ρ‚ΠΎΠ»Π°Π½ΠΊΠΎΠ²ΠΎΡ— систСми. Розгляд СнСргоСфСктивності Π·Π΄Ρ–ΠΉΡΠ½ΡŽΠ²Π°Π²ΡΡ порівнянням СнСргозатратності Π΄ΠΎ продуктивності пСрСміщСння.This paper focuses on the modeling approaches AKA without contact with the surface when moving or lifting the hill, which is important for the task of building a walking system based on the anthropic principle. To implement an anthropomorphic moving, the study applied the principles of inverse dynamics and kinematics multi-tier system. Consideration of energy efficiency are compared to the performance of energy-consuming travel.Π’ Ρ€Π°Π±ΠΎΡ‚Π΅ основноС Π²Π½ΠΈΠΌΠ°Π½ΠΈΠ΅ ΡƒΠ΄Π΅Π»Π΅Π½ΠΎ ΠΌΠΎΠ΄Π΅Π»ΠΈΡ€ΠΎΠ²Π°Π½ΠΈΡŽ Ρ…ΠΎΠ΄Ρ‹ АКА Π±Π΅Π· соприкосновСния с ΠΏΠΎΠ²Π΅Ρ€Ρ…Π½ΠΎΡΡ‚ΡŒΡŽ ΠΏΡ€ΠΈ ΠΏΠ΅Ρ€Π΅ΠΌΠ΅Ρ‰Π΅Π½ΠΈΠΈ ΠΏΠΎ склону ΠΈΠ»ΠΈ подъСмом, Ρ‡Ρ‚ΠΎ Π°ΠΊΡ‚ΡƒΠ°Π»ΡŒΠ½ΠΎ для Π·Π°Π΄Π°Ρ‡ΠΈ построСния ΡˆΠ°Π³Π°ΡŽΡ‰ΠΈΡ… систСмы Π½Π° основС Π°Π½Ρ‚Ρ€ΠΎΠΏΠ½ΠΎΠ³ΠΎ ΠΏΡ€ΠΈΠ½Ρ†ΠΈΠΏΠ°. Для Ρ€Π΅Π°Π»ΠΈΠ·Π°Ρ†ΠΈΠΈ Π°Π½Ρ‚Ρ€ΠΎΠΏΠΎΠΌΠΎΡ€Ρ„Π½ΠΎΠ³ΠΎ пСрСмСщСния, Π² исслСдовании ΠΏΡ€ΠΈΠΌΠ΅Π½ΡΠ»ΠΈΡΡŒ ΠΏΡ€ΠΈΠ½Ρ†ΠΈΠΏΡ‹ ΠΎΠ±Ρ€Π°Ρ‚Π½ΠΎΠΉ Π΄ΠΈΠ½Π°ΠΌΠΈΠΊΠΈ ΠΈ ΠΊΠΈΠ½Π΅ΠΌΠ°Ρ‚ΠΈΠΊΠΈ двиТСния ΠΌΠ½ΠΎΠ³ΠΎΠ·Π²Π΅Π½Π½ΠΎΠΉ систСмы. РассмотрСниС энСргоэффСктивности осущСствлялся сравнСниСм энСргозатратности ΠΊ ΠΏΡ€ΠΎΠΈΠ·Π²ΠΎΠ΄ΠΈΡ‚Π΅Π»ΡŒΠ½ΠΎΡΡ‚ΠΈ пСрСмСщСния

    Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses

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    Aim. The determination of chromosomal abnormalities in samples from early pregnancy losses and allelic polymorphism of HLA–DRB1 and DQA1 genes in couples with recurrent miscarriage. Methods. Banding cytogenetic and interphase mFISH analysis, DNA extraction by salting method, PCR, agarose gel electrophoresis. Results. Cytogenetic and molecular-cytogenetic investigations of SA material identified karyotype anomalies in 32.4 % of cases with prevalence of autosomal trisomy – 42.65 %, triploidy – 30.38 % and monosomy X – 19.11 %. Complex analysis of frequency and distribution of allelic variants of genes HLA-DRB1 and HLA-DQA1 allowed establishing the alleles DRB1*0301, DRB1*1101-1104 and DQA1*0501 to be aggressor alleles in women with recurrent pregnancy loss (RPL). The cumulative homology of allelic polymorphism of more than 50 % of HLA-DRB1 and HLA-DQA1 loci between partners increases the risk of RPL by almost four times. Conclusion. The detected chromosome aneuploidies in the samples from products of conception and the changes in the major histocompatibility complex genes can cause the failure of a couples reproductive function and can lead to an early fetal loss.ΠœΠ΅Ρ‚Π°. Встановити хромосомні Π°Π½ΠΎΠΌΠ°Π»Ρ–Ρ— Ρƒ ΠΌΠ°Ρ‚Π΅Ρ€Ρ–Π°Π»Ρ– Ρ€Π°Π½Π½Ρ–Ρ… Ρ€Π΅ΠΏΡ€ΠΎΠ΄ΡƒΠΊΡ‚ΠΈΠ²Π½ΠΈΡ… Π²Ρ‚Ρ€Π°Ρ‚ Ρ– алСльний ΠΏΠΎΠ»Ρ–ΠΌΠΎΡ€Ρ„Ρ–Π·ΠΌ Π³Π΅Π½Ρ–Π² HLA – DRB1 Ρ– DQA1 Ρƒ ΠΏΠΎΠ΄Ρ€ΡƒΠΆΠ½Ρ–Ρ… ΠΏΠ°Ρ€ Ρ–Π· Π½Π°Π²ΠΈΠΊΠΎΠ²ΠΈΠΌ Π½Π΅Π²ΠΈΠ½ΠΎΡˆΡƒΠ²Π°Π½Π½ΡΠΌ вагітності. ΠœΠ΅Ρ‚ΠΎΠ΄ΠΈ. Π‘Ρ‚Π°Π½Π΄Π°Ρ€Ρ‚Π½ΠΈΠΉ Ρ†ΠΈΡ‚ΠΎΠ³Π΅Π½Π΅Ρ‚ΠΈΡ‡Π½ΠΈΠΉ Ρ‚Π° Ρ–Π½Ρ‚Π΅Ρ€Ρ„Π°Π·Π½ΠΈΠΉ mFISH ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΈ, виділСння Π”ΠΠš ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠΌ висолювання, ΠŸΠ›Π , Π΅Π»Π΅ΠΊΡ‚Ρ€ΠΎΡ„ΠΎΡ€Π΅Π· Π² Π°Π³Π°Ρ€ΠΎΠ·Π½ΠΎΠΌΡƒ Π³Π΅Π»Ρ–. Π Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚ΠΈ. Π¦ΠΈΡ‚ΠΎΠ³Π΅Π½Π΅Ρ‚ΠΈΡ‡Π½Ρ– Ρ‚Π° молСку­лярно-Ρ†ΠΈΡ‚ΠΎΠ³Π΅Π½Π΅Ρ‚ΠΈΡ‡Π½Ρ– дослідТСня ΠΌΠ°Ρ‚Π΅Ρ€Ρ–Π°Π»Ρƒ Π²Ρ‚Ρ€Π°Ρ‡Π΅Π½ΠΈΡ… вагітностСй ΠΏΠΎΠΊΠ°Π·Π°Π»ΠΈ Π°Π½ΠΎΠΌΠ°Π»Ρ–Ρ— ΠΊΠ°Ρ€Ρ–ΠΎΡ‚ΠΈΠΏΡƒ Π² 32.4 % Π²ΠΈΠΏΠ°Π΄ΠΊΠ°Ρ… Π· пСрСваТанням аутосомних трисомій – 42.65 %, Ρ‚Ρ€ΠΈΠΏΠ»ΠΎΡ—Π΄Ρ–ΠΉ – 30.38 % Ρ– моносомії X – 19.11 %. КомплСксний Π°Π½Π°Π»Ρ–Π· частоти Ρ– Ρ€ΠΎΠ·ΠΏΠΎΠ΄Ρ–Π»Ρƒ Π°Π»Π΅Π»ΡŒΠ½ΠΈΡ… Π²Π°Ρ€Ρ–Π°Π½Ρ‚Ρ–Π² Π³Π΅Π½Ρ–Π² HLA-DRB1 Ρ– HLA-DQA1 Π΄ΠΎΠ·Π²ΠΎΠ»ΠΈΠ² встановити, Ρ‰ΠΎ DRB1*0301, DRB1*1101-1104 Ρ– DQA1*0501 Ρ” алСлями-агрСсорами Ρƒ ΠΆΡ–Π½ΠΎΠΊ Ρ–Π· Ρ€Π°Π½Π½Ρ–ΠΌΠΈ Ρ€Π΅ΠΏΡ€ΠΎΠ΄ΡƒΠΊΡ‚ΠΈΠ²Π½ΠΈΠΌΠΈ Π²Ρ‚Ρ€Π°Ρ‚Π°ΠΌΠΈ (Π Π Π’). Π‘ΡƒΠΊΡƒΠΏΠ½Π° гомологія алСльного ΠΏΠΎΠ»Ρ–ΠΌΠΎΡ€Ρ„Ρ–Π·ΠΌΡƒ локусів HLA-DRB1 Ρ– HLA-DQA1 Π±Ρ–Π»ΡŒΡˆΠ΅ 50 % ΠΌΡ–ΠΆ ΠΏΠ°Ρ€Ρ‚Π½Π΅Ρ€Π°ΠΌΠΈ Π·Π±Ρ–Π»ΡŒΡˆΡƒΡ” Ρ€ΠΈΠ·ΠΈΠΊ Π Π Π’ ΠΌΠ°ΠΉΠΆΠ΅ Π² Ρ‡ΠΎΡ‚ΠΈΡ€ΠΈ Ρ€Π°Π·ΠΈ. Висновки. ВстановлСні хромосомні Π°Π½Π΅ΡƒΠΏΠ»ΠΎΡ—Π΄Ρ–Ρ— Π² ΠΌΠ°Ρ‚Π΅Ρ€Ρ–Π°Π»Ρ– Π²Ρ‚Ρ€Π°Ρ‡Π΅Π½ΠΈΡ… вагітностСй Ρ‚Π° Π·ΠΌΡ–Π½ΠΈ Π² Π³Π΅Π½Π°Ρ… Π³ΠΎΠ»ΠΎΠ²Π½ΠΎΠ³ΠΎ комплСкса гістосумістності Ρƒ ΠΏΠΎΠ΄Ρ€ΡƒΠΆΠ½Ρ–Ρ… ΠΏΠ°Ρ€ ΠΌΠΎΠΆΡƒΡ‚ΡŒ Π²ΠΈΠΊΠ»ΠΈΠΊΠ°Ρ‚ΠΈ ΠΏΠΎΡ€ΡƒΡˆΠ΅Π½Π½Ρ Ρ€Π΅ΠΏΡ€ΠΎΠ΄ΡƒΠΊΡ‚ΠΈΠ²Π½ΠΎΡ— Ρ„ΡƒΠ½ΠΊΡ†Ρ–Ρ— Ρ‚Π° Ρ€Π°Π½Π½ΡŽ Π΅Π»Ρ–ΠΌΡ–Π½Π°Ρ†Ρ–ΡŽ ΠΏΠ»ΠΎΠ΄Π°.ЦСль. ΠΈΠ·ΡƒΡ‡ΠΈΡ‚ΡŒ хромосомныС Π°Π½ΠΎΠΌΠ°Π»ΠΈΠΈ Π² биологичСском ΠΌΠ°Ρ‚Π΅Ρ€ΠΈΠ°Π»Π΅ Ρ€Π°Π½Π½ΠΈΡ… Ρ€Π΅ΠΏΡ€ΠΎΠ΄ΡƒΠΊΡ‚ΠΈΠ²Π½Ρ‹Ρ… ΠΏΠΎΡ‚Π΅Ρ€ΡŒ ΠΈ Π°Π»Π»Π΅Π»ΡŒΠ½Ρ‹ΠΉ ΠΏΠΎΠ»ΠΈΠΌΠΎΡ€Ρ„ΠΈΠ·ΠΌ Π³Π΅Π½ΠΎΠ² HLA – DRB1 ΠΈ DQA1 Ρƒ супруТСских ΠΏΠ°Ρ€ с ΠΏΡ€ΠΈΠ²Ρ‹Ρ‡Π½Ρ‹ΠΌ Π½Π΅Π²Ρ‹Π½Π°ΡˆΠΈΠ²Π°Π½ΠΈΠ΅ΠΌ бСрСмСнности. ΠœΠ΅Ρ‚ΠΎΠ΄Ρ‹. стан­дартный цитогСнСтичСский ΠΈ ΠΈΠ½Ρ‚Π΅Ρ€Ρ„Π°Π·Π½Ρ‹ΠΉ mFISH ΠΌΠ΅Ρ‚ΠΎΠ΄Ρ‹, Π²Ρ‹Π΄Π΅Π»Π΅Π½ΠΈΠ΅ Π”ΠΠš ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠΌ высаливания, ПЦР, элСктрофорСз Π² Π°Π³Π°Ρ€ΠΎΠ·Π½ΠΎΠΌ Π³Π΅Π»Π΅. Π Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Ρ‹. ΠŸΡ€ΠΎΠ²Π΅Π΄Π΅Π½Π½Ρ‹Π΅ цитогСнСтичСскиС ΠΈ молСкулярно-цитогСнСтичСскиС исслСдований ΠΌΠ°Ρ‚Π΅Ρ€ΠΈΠ°Π»Π° Ρ€Π°Π½Π½ΠΈΡ… Ρ€Π΅ΠΏΡ€ΠΎΠ΄ΡƒΠΊΡ‚ΠΈΠ²Π½Ρ‹Ρ… ΠΏΠΎΡ‚Π΅Ρ€ΡŒ ΠΏΠΎΠΊΠ°Π·Π°Π»ΠΈ Π°Π½ΠΎΠΌΠ°Π»ΠΈΠΈ ΠΊΠ°Ρ€ΠΈΠΎΡ‚ΠΈΠΏΠ° Π² 32.4 % случаСв с ΠΏΡ€Π΅ΠΎΠ±Π»Π°Β­Π΄Π°Π½ΠΈΠ΅ΠΌ аутосомных трисомий – 42.65 %, Ρ‚Ρ€ΠΈΠΏΠ»ΠΎΠΈΠ΄ΠΈΠΉ – 30.38 % ΠΈ моносомии Π₯ – 19.11 %. ΠšΠΎΠΌΠΏΠ»Π΅ΠΊΡΠ½Ρ‹ΠΉ Π°Π½Π°Π»ΠΈΠ· частоты ΠΈ распрСдСлСния Π°Π»Π»Π΅Π»ΡŒΠ½Ρ‹Ρ… Π²Π°Ρ€ΠΈΠ°Π½Ρ‚ΠΎΠ² Π³Π΅Π½ΠΎΠ² HLA-DRB1 ΠΈ HLA-DQA1ΠΏΠΎΠΊΠ°Π·Π°Π», Ρ‡Ρ‚ΠΎ DRB1*0301, DRB1*1101-1104 ΠΈ DQA1*0501 ΡΠ²Π»ΡΡŽΡ‚ΡΡ аллСлями-агрСссорами Ρƒ ΠΆΠ΅Π½Ρ‰ΠΈΠ½ с Ρ€Π°Π½Π½ΠΈΠΌΠΈ Ρ€Π΅ΠΏΡ€ΠΎΠ΄ΡƒΠΊΡ‚ΠΈΠ²Π½Ρ‹ΠΌΠΈ потСрями (РРП). Бовокупная гомология аллСльного ΠΏΠΎΠ»ΠΈΠΌΠΎΡ€Ρ„ΠΈΠ·ΠΌΠ° локусов HLA-DRB1 ΠΈ HLA-DQA1 Π±ΠΎΠ»Π΅Π΅ 50 % ΠΌΠ΅ΠΆΠ΄Ρƒ ΠΏΠ°Ρ€Ρ‚Π½Π΅Ρ€Π°ΠΌΠΈ ΡƒΠ²Π΅Π»ΠΈΡ‡ΠΈΠ²Π°Π΅Ρ‚ риск РРП ΠΏΠΎΡ‡Ρ‚ΠΈ Π² Ρ‡Π΅Ρ‚Ρ‹Ρ€Π΅ Ρ€Π°Π·Π°. Π’Ρ‹Π²ΠΎΠ΄Ρ‹. ВыявлСнныС хромосомныС Π°Π½Π΅ΡƒΠΏΠ»ΠΎΠΈΠ΄ΠΈΠΈ Π² ΠΌΠ°Ρ‚Π΅Ρ€ΠΈΠ°Π»Π΅ ΡΠ°ΠΌΠΎΠΏΡ€ΠΎΠΈΠ·Π²ΠΎΠ»ΡŒΠ½Ρ‹Ρ… Π²Ρ‹ΠΊΠΈΠ΄Ρ‹ΡˆΠ΅ΠΉ ΠΈ измСнСния Π² Π³Π΅Π½Π°Ρ… Π³Π»Π°Π²Π½ΠΎΠ³ΠΎ комплСкса гистосовмСстимости Ρƒ супруТСских ΠΏΠ°Ρ€ ΠΌΠΎΠ³ΡƒΡ‚ Π²Ρ‹Π·Ρ‹Π²Π°Ρ‚ΡŒ Π½Π°Ρ€ΡƒΡˆΠ΅Π½ΠΈΡ Ρ€Π΅ΠΏΡ€ΠΎΠ΄ΡƒΠΊΡ‚ΠΈΠ²Π½ΠΎΠΉ Ρ„ΡƒΠ½ΠΊΡ†ΠΈΠΈ ΠΈ ΡΠ»ΠΈΠΌΠΈΠ½Π°Ρ†ΠΈΡŽ ΠΏΠ»ΠΎΠ΄Π° Π² Ρ€Π°Π½Π½Π΅ΠΌ ΠΏΠ΅Ρ€ΠΈΠΎΠ΄Π΅ бСрСмСнности

    Electron and hole states in quantum-dot quantum wells within a spherical 8-band model

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    In order to study heterostructures composed both of materials with strongly different parameters and of materials with narrow band gaps, we have developed an approach, which combines the spherical 8-band effective-mass Hamiltonian and the Burt's envelope function representation. Using this method, electron and hole states are calculated in CdS/HgS/CdS/H_2O and CdTe/HgTe/CdTe/H_2O quantum-dot quantum-well heterostructures. Radial components of the wave functions of the lowest S and P electron and hole states in typical quantum-dot quantum wells (QDQWs) are presented as a function of radius. The 6-band-hole components of the radial wave functions of an electron in the 8-band model have amplitudes comparable with the amplitude of the corresponding 2-band-electron component. This is a consequence of the coupling between the conduction and valence bands, which gives a strong nonparabolicity of the conduction band. At the same time, the 2-band-electron component of the radial wave functions of a hole in the 8-band model is small compared with the amplitudes of the corresponding 6-band-hole components. It is shown that in the CdS/HgS/CdS/H_2O QDQW holes in the lowest states are strongly localized in the well region (HgS). On the contrary, electrons in this QDQW and both electron and holes in the CdTe/HgTe/CdTe/H_2O QDQW are distributed through the entire dot. The importance of the developed theory for QDQWs is proven by the fact that in contrast to our rigorous 8-band model, there appear spurious states within the commonly used symmetrized 8-band model.Comment: 15 pages, 5 figures, E-mail addresses: [email protected], [email protected]
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