Results 111 to 120 of about 1,967 (171)

グローバルコミュニケーションと域学連携に関する予備的研究 [PDF]

open access: yes, 2019
本研究の目的は、近年の外国人訪問客や在留外国人の増加にともなうグローバルコミュニケーションの重要性から、特に災害に関する防災・減災・復興に資するコミュニケーションモデルの構築に取り組むことにある。また、岡山県立大学を中心とする地方創生推進事業(COC+)の学問的成果を活用し、ポスト岡山創生学の位置付けにもなりうる域学連携としての教育研究カリキュラムにつなげることでもある。具体的には、メディア・フレームの視座から海外メディアに表出される災害という実態に近似的な<世界>を検証する。また ...
関根 紳太郎
core   +1 more source

Gene expression analysis of the biocontrol fungus Trichoderma harzianum in the presence of tomato plants, chitin, or glucose using a high-density oligonucleotide microarray

open access: yesBMC Microbiology, 2009
Background It has recently been shown that the Trichoderma fungal species used for biocontrol of plant diseases are capable of interacting with plant roots directly, behaving as symbiotic microorganisms.
Suárez M Belén   +4 more
doaj   +1 more source

Evaluación continua con Goodle-GMS a más de 800 alumnos en Ingeniería Química [PDF]

open access: yes, 2014
El objetivo de esta experiencia ha sido la de establecer un sistema de evaluación continua en asignaturas con gran cantidad de alumnos de forma que no supongan un excesivo trabajo para el docente, que permita generar una retroalimentación a los alumnos ...
Cornejo Fernández-Gao, Ana   +4 more
core  

ALP1 and ELP1 – novel genetic modifiers of LIKE HETEROCHROMATIN PROTEIN 1 participate in Polycomb mediated gene repression in Arabidopsis [PDF]

open access: yes, 2012
Polycomb Group (PcG) proteins are involved in the inheritance of phenotypic traits by repressing the expression of target genes through binding of chromatin. In Arabidopsis thaliana several Polycomb Repressive Complexes (PRCs) are active during different
Hartwig, Benjamin
core  

Role of Elp1 in neural crest cell migration, differentiation and target tissue innervation in Familial Dysautonomia

open access: yesThe FASEB Journal, 2013
A highly conserved germline point mutation located in the donor splice site of intron 20 of the human Elp1 gene leads to loss of its encoded protein and causes familial dysautonomia (FD; Riley‐Day Syndrome; hereditary sensory and autonomic neuropathy, type 3; HSAN3), an autosomal recessive disease characterized by severe and progressive sympathetic and
Marisa Z. Jackson   +2 more
openaire   +1 more source

A second case report of medulloblastoma in a patient carrying biallelic pathogenic MUTYH germline variants

open access: yes
Neuropathology and Applied Neurobiology, Volume 50, Issue 2, April 2024.
Selene Cipri   +9 more
wiley   +1 more source

The evolutionary impact of childhood cancer on the human gene pool

open access: yesNature Communications
Germline pathogenic variants associated with increased childhood mortality must be subject to natural selection. Here, we analyze publicly available germline genetic metadata from 4,574 children with cancer [11 studies; 1,083 whole exome sequences (WES),
Ulrik Kristoffer Stoltze   +6 more
doaj   +1 more source

Assessment of Electrode Configurations of Electrical Impedance Myography for the Evaluation of Neuromuscular Diseases [PDF]

open access: yes, 2015
Electrical impedance myography (EIM) is a painless, noninvasive approach to measure the neuromuscular disease status. EIM parameters- resistance (R), reactance (X) and phase (θ) depend significantly on subcutaneous fat thickness, muscle size and inter ...
Fazle Rabbi, Khondokar Mohammad
core   +1 more source

Loss of the Familial Dysautonomia gene Elp1 in cerebellar granule cell progenitors leads to ataxia in mice [PDF]

open access: gold
F. Manz   +18 more
openalex   +1 more source

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