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درباره برتیناتماس با ماهوش مصنوعی رایگانایمیل رایگانمترجم رایگانDNS رایگانهواشناسیکاوش برتیناپشتیبانیتبلیغ در برتینا
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www.nature.com/articles/jhg2013114PDF

The promise of whole-exome sequencing in medical genetics

B Rabbani, M Tekin, N Mahdieh - Journal of human genetics, 2014 - nature.com
۸۳۱ ارجاع2014

Massively parallel DNA-sequencing systems provide sequence of huge numbers of different DNA strands at once. These technologies are revolutionizing our understanding in medical …

pubs.acs.org/aamick/article-abstract/8/33/21107/1474599PDF

Temperature-responsive smart nanocarriers for delivery of therapeutic agents: applications and recent advances

…, H Ghahramanzadeh Asl, Z Mahdieh… - … applied materials & …, 2016 - ACS Publications
۵۲۴ ارجاع2016

Smart drug delivery systems (DDSs) have attracted the attention of many scientists, as carriers that can be stimulated by changes in environmental parameters such as temperature, pH, …

www.nature.com/articles/jhg201291PDF

Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders

B Rabbani, N Mahdieh, K Hosomichi… - Journal of human …, 2012 - nature.com
۳۰۹ ارجاع2012

Traditional approaches for gene mapping from candidate gene studies to positional cloning strategies have been applied for Mendelian disorders. Since 2005, next-generation …

arxiv.org/abs/2312.11805PDF

Gemini: a family of highly capable multimodal models

…, YG Li, Y Cheng, A Ittycheriah, M Mahdieh… - arXiv preprint arXiv …, 2023 - arxiv.org
۱۰۶۳۵ ارجاع2023

This report introduces a new family of multimodal models, Gemini, that exhibit remarkable capabilities across image, audio, video, and text understanding. The Gemini family consists of …

arxiv.org/abs/2403.05530PDF

Gemini 1.5: Unlocking multimodal understanding across millions of tokens of context

…, K Hui, K Haridasan, V Campos, M Mahdieh… - arXiv preprint arXiv …, 2024 - arxiv.org
۴۶۵۶ ارجاع2024

In this report, we introduce the Gemini 1.5 family of models, representing the next generation of highly compute-efficient multimodal models capable of recalling and reasoning over fine-…

www.sciencedirect.com/science/article/pii/S1026309812000697

Green biosynthesis of silver nanoparticles by Spirulina platensis

M Mahdieh, A Zolanvari, AS Azimee - Scientia Iranica, 2012 - Elsevier
۲۹۱ ارجاع2012

Crystallized silver nanoparticles (SNPs) have been biosynthesized by Spirulina platensis in an aqueous system. An aqueous solution of silver ions was treated with a live biomass of …

www.nature.com/articles/jhg201096PDF

Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations

N Mahdieh, B Rabbani, S Wiley, MT Akbari… - Journal of human …, 2010 - nature.com
۱۳۱ ارجاع2010

Hearing loss (HL) is the most prevalent sensory defect affecting 1 in 500 neonates. Genetic factors are involved in half of the cases. The extreme heterogeneity of HL makes it difficult to …

academic.oup.com/pcp/article-abstract/49/5/801/1911042PDF

Drought Stress Alters Water Relations and Expression of PIP-Type Aquaporin Genes in Nicotiana tabacum Plants

M Mahdieh, A Mostajeran, T Horie… - Plant and Cell …, 2008 - academic.oup.com
۲۹۴ ارجاع2008

Plasma membrane intrinsic proteins (PIPs), a type of aquaporins, mediate water transport in many plant species. In this study, we investigated the relationship between the functions of …

journals.sagepub.com/doi/abs/10.1016/j.otohns.2007.03.033

Hearing loss in Behçet syndrome

…, GM Mehdi, HM Reza, T Mahdieh… - … —Head and Neck …, 2007 - journals.sagepub.com
۳۷ ارجاع2007

OBJECTIVE: To determine the prevalence and characteristics of hearing loss in Behçet syndrome. STUDY DESIGN AND SETTING: This study included 27 patients with Behçet …

pmc.ncbi.nlm.nih.gov/articles/PMC3883366/PDF

An overview of mutation detection methods in genetic disorders

N Mahdieh, B Rabbani - Iranian journal of pediatrics, 2013 - pmc.ncbi.nlm.nih.gov
۲۰۳ ارجاع2013

Genetic disorders are traditionally categorized into three main groups: single-gene, chromosomal, and multifactorial disorders. Single gene or Mendelian disorders result from errors in …

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