نتایج جستجو برای: chromosome type

تعداد نتایج: 1443937  

Journal: :The American Journal of Human Genetics 1998

Journal: :Microbiology resource announcements 2021

We report a de novo -assembled draft genome sequence of the Indian Staphylococcus aureus type 88 (ST88) strain LVP-7, isolated from an ocular infection. The harbors Panton-Valentine leukocidin phage, V staphylococcal cassette chromosome mec element, delta-hemolysin-converting Newman phage ΦNM3, and pathogenicity island SaPI3, encoding superantigen enterotoxin B.

Alfredo Orrico, Ambra Cortesi Andrea Giansanti Chiara Pescucci Francesca Gerundino Giuseppina Marseglia Paola Piomboni Roberto Ponchietti

Chromosomal defects are relatively frequent in infertile men however, translocations between the Y chromosome and autosomes are rare and less than 40 cases of Y-autosome translocation have been reported. In particular, only three individuals has been described with a Y;21 translocation, up to now. We report on an additional case of an infertile man in whom a Y;21 translocation was associated wi...

Journal: :Diabetes 2002
Daniela Contu Laura Morelli Patrizia Zavattari Rosanna Lampis Efisio Angius Paola Frongia Daniela Murru Mario Maioli Paolo Francalacci John A Todd Francesco Cucca

A male excess in Sardinian type 1 diabetic cases has previously been reported and was largely restricted to those patients carrying the HLA-DR3/nonDR4 genotype. In the present study, we have measured the male- to-female (M:F) ratio in a sample set of 542 newly collected, early-onset type 1 diabetic Sardinian patients. This data not only confirm the excess of male type 1 diabetic patients overal...

Journal: :Proceedings of the National Academy of Sciences 2016

Journal: :Diabetes 2001
A Parker J Meyer S Lewitzky J S Rennich G Chan J D Thomas M Orho-Melander M Lehtovirta C Forsblom A Hyrkkö M Carlsson C Lindgren L C Groop

Genome-wide nonparametric linkage analysis of 480 sib-pairs affected with type 2 diabetes revealed linkage to a previously unreported susceptibility locus on chromosome 18p11. This result improved with stringent subphenotyping using age- and sex-adjusted BMI, ultimately reaching a logarithm of odds of 3.82 (allele sharing 0.6654) at a point between markers D18S976 and D18S391 when the most obes...

2000

The mammalian in vivo chromosome aberration test is used for the detection of structural chromosome aberrations induced by the test substance to the bone marrow cells of animals, usually rodents (1)(2)(3)(4). Structural chromosome aberrations may be of two types, chromosome or chromatid. An increase in polyploidy may indicate that a chemical has the potential to induce numerical aberrations. Wi...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 1996
X F Wu M R Spitz G L Delclos T H Connor Y Zhao M J Siciliano T C Hsu

In a previous study of lung cancer, we showed that bleomycin, a radiomimetic agent, induced breaks preferentially on chromosomes 4 and 5. The molecular cytogenetic study reported here, using chromosome painting and G banding, was designed to assess whether the chromatid breaks induced by bleomycin could survive as chromosome-type aberrations after treated lymphocyte populations were allowed to ...

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