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statatm ic 10 1 software  (STATA Corporation)


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    Structured Review

    STATA Corporation statatm ic 10 1 software
    Statatm Ic 10 1 Software, supplied by STATA Corporation, used in various techniques. Bioz Stars score: 99/100, based on 36606 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/statatm+10+1+software/STATA+1%2E0/pm27836039-112-23-26
    Average 99 stars, based on 36606 article reviews
    statatm ic 10 1 software - by Bioz Stars, 2026-09
    99/100 stars

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    Software:

    Article Title: Infectious causes of posterior uveitis and panuveitis in Thailand.
    Article Snippet: Purpose To determine the infectious causes of posterior uveitis (PU) and panuveitis (panU) in Thailand.. Methods We investigated the infectious causes of uveitis involving the posterior segment of the eye by using real-time polymerase chain reaction (PCR) for cytomegalovirus (CMV), herpes simplex virus (HSV-1, HSV-2), varicella zoster virus and Toxoplasma gondii (T. gondii) DNA in intraocular samples of 80 human immunodeficiency virus (HIV)-negative patients.. Additionally, in 61 patients, we performed Goldmann–Witmer coefficient (GWC) analysis for T. gondii.

    Article Title: Mitochondrial cytochrome c oxidase subunit II variations predict adverse prognosis in cytogenetically normal acute myeloid leukaemia.
    Article Snippet: Alterations in the two catalytic genes Cytochrome c oxidase subunit I and II (COI, COII) have recently been suggested to have an adverse impact on prognosis in AML patients.. In order to explore this in further detail, we sequenced these two mitochondrial genes in diagnostic bone marrow or blood samples in 235 AML patients.. In 37 (16%) patients, a nonsynonymous variation in either COI or COII could be demonstrated.

    Article Title: Characterization and prognostic significance of mitochondrial DNA variations in acute myeloid leukemia.
    Article Snippet: A cc ep te d A rt ic le © 2013 John Wiley & Sons A/S Recent studies have suggested that mutations in the mitochondrial genome (mtDNA) may play a role in the development and response to treatment in human cancer.. The aim of the present study was to investigate whether mtDNA variations have any prognostic relevance, to clarify the spectra of mtDNA variation, and to determine if there was any correlation to known prognostic factors in acute myeloid leukemia (AML).. To elucidate this, we sequenced the entire mtDNA in 56 AML patients and 14 control subjects.



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