نتایج جستجو برای: q27

تعداد نتایج: 214  

Journal: :تحقیقات اقتصادی 0
غلامعلی شرزه ای دانشیار دانشکده ی اقتصاد دانشگاه تهران وحید ماجد استادیار دانشکده ی اقتصاد دانشگاه علوم اقتصادی

development projects in natural water resources like rivers and lakes, specially transferring water to use in agriculture, domestic and industrial sector without considering environmental values, causes irrecoverable and irreversible damage to ecosystem and future options. if we consider the future generation and species rights, those damages and costs can be very much than we take in. the abov...

2018
Yan-Wei Sha Li-Bin Mei Liang-Kai Zheng Rui-Hua Tian Lu Ding Zhi-Yong Ji Qing Zhang Ping Li

cases found that 11 patients (61.1%) had a homozygous deletion of a 200‐kb fragment of the DPY19L gene, two (11.1%) had a homozygous nonsynonymous mutation in exon 8 (p.R298C), one (5.6%) had a homozygous new splice site mutation at the junction of exon‐intron 16 (c.1579_1580 + 4delAGGTAAinsTCAT), and four (22.2%) had no mutations in DPY19L2, SPATA16, or PICK1.4 In humans, the DPY19L2 gene is l...

Journal: :Journal of bacteriology 1969
A M Reiner

Three polynucleotide phosphorylase mutations, isolated in heavily mutagenized Escherichia coli strains Q7, Q13, and Q27, were characterized after their transfer by P1 transduction to nearly isogenic strains which lack ribonuclease I. Each strain has a different altered form of polynucleotide phosphorylase. One enzyme exhibited sharply reduced activity under all conditions tested. A second had r...

2017
Marianna De Cinque Orazio Palumbo Ermelinda Mazzucco Antonella Simone Pietro Palumbo Renata Ciavatta Giuliana Maria Rosangela Ferese Stefano Gambardella Antonella Angiolillo Massimo Carella Silvio Garofalo

Terminal deletion of chromosome 6q is a rare chromosomal abnormality associated with variable phenotype spectrum. Although intellectual disability, facial dysmorphism, seizures and brain abnormalities are typical features of this syndrome, genotype-phenotype correlation needs to be better understood. We report the case of a 6-year-old Caucasian boy with a clinical diagnosis of intellectual disa...

2014
Lucinda Sanders Sandrine Jayne Ben Kennedy Fiona Miall Sietse M Aukema Reiner Siebert Simon D Wagner Martin J S Dyer

The WHO classification of lymphomas allows for a group of diseases that have features intermediate between those of Burkitt lymphoma and diffuse large B-cell lymphoma. These are a diverse group of diseases whose genetics and clinical course are yet to be fully described. We report an unusual case of high grade B-cell lymphoma, intermediate between DLBCL and BL, lacking CD10 expression in which ...

2006
Nathan Fiala

This paper adds to the existing literature on the estimation of future consumption patterns. I first forecast the demand of beef, chicken and pig products for the years 2020 and 2040 using a simultaneous equations model for the world and specific regions. Then, using existing research on “best existing case” scenarios of the ecological impact of different foods, I estimate the land usage and gr...

Journal: :Blood 2004
Geraldine Guasch Bénédicte Delaval Christine Arnoulet Min-Jue Xie Luc Xerri Danielle Sainty Daniel Birnbaum Marie-Joséphe Pébusque

Constitutive activation of aberrant fibroblast growth factor receptor 1 (FGFR1) kinase as a consequence of gene fusion such as FOP-FGFR1 associated with t(6; 8)(q27;p11-12) translocation, is the hallmark of an atypical aggressive stem cell myeloproliferative disorder (MPD) in humans. In this study, we show that expression of FOP-FGFR1 in primary bone marrow cells induced by retroviral transduct...

Journal: :In vivo 2016
Julia Landin Walter Weber

BACKGROUND/AIM Pancreatic neuroendocrine tumors (PNETs) are uncommon malignancies of largely unknown pathogenesis. Observations on patients and their families can provide clues on etiology. PATIENTS AND METHODS In a medical oncology practice cohort of 2,087 patients 5 females and 2 males with PNETs have been identified. RESULTS Observations of etiologic interest have been made in 2 patients...

Journal: :Cancer genetics and cytogenetics 1997
M R Teixeira H Qvist K E Giercksky P J Bøhler S Heim

Epithelial proliferative lesions of the appendix are rare and have never been studied cytogenetically. We present the chromosomal banding analysis of four successfully short-term cultured samples from pseudomyxoma peritonei lesions originating from a cystadenoma of the appendix. All four sample contained clonal chromosome abnormalities. In three of them, the clone 46,XX,der(6)?del(6)(q16q21)?de...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید