1.35 g

Sifat Campuran Herbisida Ammonium glufosinat 135 g/l + Imazetapir 40 g/l + Karfentrazon etil 7 g/l) terhadap beberapa gulma

Journal: :Kultivasi 2021

Factor V Leiden and Prothrombin 20210A Mutations among Turkish Pediatric Leukemia Patients

2012

Dilara Fatma Akın Kadir Sipahi Tuğba Kayaalp Yonca Eğin Serpil Taşdelen Emin Kürekçi Üstün Ezer Nejat Akar

This study was undertaken to determine the prevalence of the Factor V 1691 G-A and PT 20210 G-A mutations in Turkish children with leukemia. We genotyped 135 pediatric leukemia patients with for these mutations. Eleven (8%) of the 135 patients were heterozygous for the FV 1691 G-A mutation. Seven (5,1%) of the patients carried the PT 20210 G-A heterozygous mutation. Of the 135 patients, only th...

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Complete Genome Assemblies for Two Single-Chromosome Vibrio cholerae Isolates, Strains 1154-74 (Serogroup O49) and 10432-62 (Serogroup O27)

2015

S L Johnson A Khiani K A Bishop-Lilly C Chapman M Patel K Verratti H Teshima A C Munk D C Bruce C S Han G Xie K W Davenport P Chain S Sozhamannan

Here, we report the completed genome sequences for two non-O1/non-O139 Vibrio cholerae isolates. Each isolate has only a single chromosome, as opposed to the normal paradigm of two chromosomes found in all other V. cholerae isolates.

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A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers.

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2001

W W Wang A B Spurdle P Kolachana B Bove B Modan S M Ebbers G Suthers M A Tucker D J Kaufman M M Doody R E Tarone M Daly H Levavi H Pierce A Chetrit G H Yechezkel G Chenevix-Trench K Offit A K Godwin J P Struewing

RAD51 colocalizes with both BRCA1 and BRCA2, and genetic variants in RAD51 would be candidate BRCA1/2 modifiers. We searched for RAD51 polymorphisms by sequencing 20 individuals. We compared the polymorphism allele frequencies between female BRCA1/2 mutation carriers with and without breast or ovarian cancer and between population-based ovarian cancer cases with BRCA1/2 mutations to cases and c...

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a functional polymorphism in promoter of the cxcl10 gene (-135 g/a) associated with pulmonary tuberculosis

Journal: :archives of clinical infectious diseases 0

mohsen taheri genetics of non-communicable diseases research center, zahedan university of medical sciences, zahedan, ir iran; department of genetics, school of medicine, zahedan university of medical sciences, zahedan, ir iran; department of genetics, school of medicine, zahedan university of medical sciences, zahedan, ir iran. tel: +98-5413425793, fax: +98-5413425796 hamid reza kouhpayeh research center for infectious diseases and tropical medicine, zahedan university of medical sciences, zahedan, ir iran toraj hosseinalizadeh research center for infectious diseases and tropical medicine, zahedan university of medical sciences, zahedan, ir iran mohammad naderi research center for infectious diseases and tropical medicine, zahedan university of medical sciences, zahedan, ir iran gholamreza bahari department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran mohammad hashemi department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran

background: genetic variation influences susceptibility/resistance to tuberculosis. cxcl10 is involved in t-cell migration and stimulation of natural killer cells in mycobacterium tuberculosis infection. objectives: we aimed to investigate the genetic polymorphisms in promoter of the cxcl10 gene in patients with pulmonary tuberculosis (ptb) and healthy controls, to clarify whether polymorphisms...

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RAD51 homologous recombination repair gene haplotypes and risk of acute myeloid leukaemia.

Journal: :Leukemia research 2007

Sara Rollinson Alexandra G Smith James M Allan Peter J Adamson Kathryn Scott Christine F Skibola Martyn T Smith Gareth J Morgan

Homologous recombination (HR) is one of the main pathways for the repair of DNA double strand breaks (DSBs). To investigate whether inherited variants in genes encoding proteins that repair DSBs by HR modulate acute myeloid leukaemia (AML) risk, we have examined the frequency of two variants in the 5' untranslated region (UTR) of RAD51 (RAD51 135 G>C and the RAD51 172 G>T) in a large case-contr...

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Association between RAD51 135 G/C polymorphism and risk of 3 common gynecological cancers

Journal: :Medicine 2018

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Abstract 135

Journal: :Plastic and Reconstructive Surgery - Global Open 2020

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135. Einleitung

Journal: :Langenbecks Archiv f�r Chirurgie 1983

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Carborane-Based Metal−Organic Framework with High Methane and Hydrogen Storage Capacities

2013

Robert D. Kennedy Vaiva Krungleviciute Daniel J. Clingerman Joseph E. Mondloch Yang Peng Christopher E. Wilmer Amy A. Sarjeant Randall Q. Snurr Joseph T. Hupp Taner Yildirim Omar K. Farha Chad A. Mirkin

A Cu−carborane-based metal−organic framework (MOF), NU-135, which contains a quasi-spherical para-carborane moiety, has been synthesized and characterized. NU-135 exhibits a pore volume of 1.02 cm/g and a gravimetric BET surface area of ca. 2600 m/g, and thus represents the first highly porous carborane-based MOF. As a consequence of the unique geometry of the carborane unit, NU-135 has a very ...

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