نتایج جستجو برای: آنتی پورتر sos1

تعداد نتایج: 18300  

Journal: :Conjeturas 2022

Noonan syndrome (NS) is a heterogeneous autosomal dominant disorder caused by germline mutations in genes belonging RAS-MAPK pathway. Herein, we described two patients with developmental delay and syndromic features from Central Brazil diagnosed NS using an exome sequencing target gene panel. Germline mutation that participates the signaling pathway are associated disorders share particular cli...

هدف از این پژوهش، امکان­سنجی تولید دارویی با ترکیب طبیعی برای درمان بیماری اسهال در دام است. بعد از ارزیابی فنی و کار آزمایشگاهی، توجیه مالی تولید داروی ضد اسهال با ساختار طبیعی در یک بازه زمانی پنج ساله انجام شد. نتایج حاصل از آنالیز داده­ها نشان داد تولید این دارو با نرخ تنزیل 18 درصد دارای ارزش فعلی خالص 621/1 میلیون ریال و نرخ بازده داخلی 45 درصدی امکان­پذیر است. دوره بازگشت سرمایه سه سال و...

2015
Payal Sanadhya Parinita Agarwal Pradeep K. Agarwal

Salinity adversely affects plant growth and development, and disturbs intracellular ion homeostasis, resulting in cellular toxicity. Plants that tolerate salinity, halophytes, do so by manifesting numerous physiological and biochemical processes in coordination to alleviate cellular ionic imbalance. The present study was undertaken to analyse the salt tolerance mechanism in Aeluropus lagopoides...

Journal: :Biochemistry 2009
Caleb B McDonald Kenneth L Seldeen Brian J Deegan Amjad Farooq

Ubiquitously encountered in a wide variety of cellular processes, the Grb2-Sos1 interaction is mediated through the combinatorial binding of nSH3 and cSH3 domains of Grb2 to various sites containing PXpsiPXR motifs within Sos1. Here, using isothermal titration calorimetry, we demonstrate that while the nSH3 domain binds with affinities in the physiological range to all four sites containing PXp...

2013
Jayakumar Bose Yanjie Xie Wenbiao Shen Sergey Shabala

Reactive oxygen species (ROS) production is a common denominator in a variety of biotic and abiotic stresses, including salinity. In recent years, haem oxygenase (HO; EC 1.14.99.3) has been described as an important component of the antioxidant defence system in both mammalian and plant systems. Moreover, a recent report on Arabidopsis demonstrated that HO overexpression resulted in an enhanced...

Journal: :Current Biology 2001
Tracy M Saxton Alec M Cheng Siew Hwa Ong Yong Lu Ryuichi Sakai James C Cross Tony Pawson

BACKGROUND The mammalian Grb2 adaptor protein binds pTyr-X-Asn motifs through its SH2 domain, and engages downstream targets such as Sos1 and Gab1 through its SH3 domains. Grb2 thereby couples receptor tyrosine kinases to the Ras-MAP kinase pathway, and potentially to phosphatidylinositol (PI) 3'-kinase. By creating a null (Delta) allele of mouse Grb2, we have shown that Grb2 is required for en...

Journal: :Revista espanola de cardiologia 2012
Begoña Ezquieta José L Santomé Atilano Carcavilla Encarna Guillén-Navarro Antonio Pérez-Aytés Jaime Sánchez del Pozo Sixto García-Miñaur Emilia Castillo Milagros Alonso Teresa Vendrell Alfredo Santana Enrique Maroto Liliana Galbis

INTRODUCTION AND OBJECTIVES Molecular characterization of congenital heart diseases now includes the not infrequent dysmorphic Noonan syndrome. A study of 6 genes of the RAS-MAPK pathway in Spanish patients is presented: the impact of heart disease, clinical expressivity, and diagnostic yield are investigated. METHODS The study included 643 patients (and 182 family members) diagnosed by dysmo...

2017
Xinrui Liu Bin Song Shanji Li Nan Wang Hongfa Yang

Low-grade gliomas (LGGs) are associated with neurological disability. The present study used microRNA (miRNA) expression profiles to identify risk miRNAs for potential prognosis of cerebral LGGs. miRNA expression profiles and clinical data from 408 patients with cerebral LGGs were obtained from the Cancer Genome Atlas database. Risk miRNAs were identified by plotting Kaplan‑Meier curves and Cox...

Journal: :Journal of medical genetics 2015
Guilherme Lopes Yamamoto Meire Aguena Monika Gos Christina Hung Jacek Pilch Somayyeh Fahiminiya Anna Abramowicz Ingrid Cristian Michelle Buscarilli Michel Satya Naslavsky Alexsandra C Malaquias Mayana Zatz Olaf Bodamer Jacek Majewski Alexander A L Jorge Alexandre C Pereira Chong Ae Kim Maria Rita Passos-Bueno Débora Romeo Bertola

BACKGROUND Noonan syndrome is an autosomal dominant, multisystemic disorder caused by dysregulation of the RAS/mitogen activated protein kinase (MAPK) pathway. Heterozygous, pathogenic variants in 11 known genes account for approximately 80% of cases. The identification of novel genes associated with Noonan syndrome has become increasingly challenging, since they might be responsible for very s...

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