نتایج جستجو برای: nt3

تعداد نتایج: 263  

2017
Jaya Padmanabhan

During development of the nervous system an excess number of neural progenitor cells are generated and approximately half of these cells are eliminated by programmed cell death (PCD) or apoptosis (Farinelli and Greene, 1996; Jacobson et al., 1997; Oppenheim, 1991; Raff, 1992; Raff et al., 1993). The apoptosis and elimination of the excess number of precursor cells enable the proper synaptic int...

Journal: :Molecular phylogenetics and evolution 2006
Brice P Noonan Paul T Chippindale

Since the early 1970s, boine snakes (Boidae: Boinae) have served as a prime example of a group whose current distribution was shaped by vicariant events associated with the fragmentation of the supercontinent Gondwana. Early phylogenetic treatments of this group, and what were thought to be closely related groups (Erycinae and Pythoninae) based on morphological features, produced a relatively s...

2015
Ramu Venkatesan Eunhee Ji Sun Yeou Kim

Alzheimer’s disease (AD), characterized by progressive dementia and deterioration of cognitive function, is an unsolved social and medical problem. Age, nutrition, and toxins are the most common causes of AD. However, currently no credible treatment is available for AD. Traditional herbs and phytochemicals may delay its onset and slow its progression and also allow recovery by targeting multipl...

2017
Bechan Sharma

The progressive dementia and deterioration of cognitive functions have been characterised as Alzheimer’s disease (AD). The most common causes of Alzheimer’s disease include aging, nutrition, and toxins. It has been reported to be an unsolved sociomedical problem because of their lack of proper treatment in present scenario. The plant based principles and phytochemicals from traditional herbs mi...

Journal: :Mechanisms of Development 2009
Claire E. Kelly Konstantinos Ampatzis Shinya Tanaka James E. Dixon Vasso Episkopou Wai Tam

Vertebrate neurotrophins (NTs: NGF, BDNF, NT3, NT4) form a family of signalling molecules with key functions in nervous system development and function. They regulate cell survival, axon guidance and targeting, synaptic formation and function, learning and memory. Deficient NGF function occurs in Alzheimer’s disease and alterations in BDNF function underlie psychiatric and cognitive disorders s...

Journal: :Neurobiology of disease 2006
Mara Dierssen Mònica Gratacòs Ignasi Sahún Miguel Martín Xavier Gallego Alejandro Amador-Arjona María Martínez de Lagrán Patricia Murtra Eulalia Martí Miguel A Pujana Isidre Ferrer Esther Dalfó Carmen Martínez-Cué Jesús Flórez Jesús F Torres-Peraza Jordi Alberch Rafael Maldonado Cristina Fillat Xavier Estivill

Accumulating evidence has suggested that neurotrophins participate in the pathophysiology of mood disorders. We have developed transgenic mice overexpressing the full-length neurotrophin-3 receptor TrkC (TgNTRK3) in the central nervous system. TgNTRK3 mice show increased anxiety-like behavior and enhancement of panic reaction in the mouse defense test battery, along with an increase in the numb...

ژورنال: :فیض 0
محمدتقی قربانیان mohammad taghi ghorbanian faculty of biology, damghan university, damghan, i. r. iran.ایران، دامغان، دانشگاه دامغان، کدپستی 1565- 14155 مریم حاجی قاسم کاشانی maryam haji-ghasem-kashani لیلی حسین پور leili hossein-pour لیلا میرزائیان leila mirzaiyan

سابقه و هدف: بافت چربی منبع قابل دسترسی برای سلول های بنیادی (adipose tissue-derived mesenchymal stem cells adscs) است. فاکتورهای نوروتروفیک، مولکول هایی هستند که در بقا، تکثیر و تمایز سلول های بنیادی نقش حیاتی دارند. هدف از این مطالعه بررسی ظرفیت تکثیری و قابلیت بیان فاکتورهای نوروتروفیک (ngf، cntf، nt3، nt4، gdnf و bdnf) و همچنین بیان فیلامان بینابینی سلول های پیش ساز عصبی (نستین) در adscها م...

2010
Youe Li Jose M. Manaligod Daniel L. Weeks

BACKGROUND INFORMATION The BOR (branchio-oto-renal) syndrome is a dominant disorder most commonly caused by mutations in the EYA1 (Eyes Absent 1) gene. Symptoms commonly include deafness and renal anomalies. RESULTS We have used the embryos of the frog Xenopus laevis as an animal model for early ear development to examine the effects of different EYA1 mutations. Four eya1 mRNAs encoding prote...

Journal: :NeuroImage 2013
Meredith N. Braskie Omid Kohannim Neda Jahanshad Ming-Chang Chiang Marina Barysheva Arthur W. Toga John M. Ringman Grant W. Montgomery Katie L. McMahon Greig I. de Zubicaray Nicholas G. Martin Margaret J. Wright Paul M. Thompson

The NTRK3 gene (also known as TRKC) encodes a high affinity receptor for the neurotrophin 3'-nucleotidase (NT3), which is implicated in oligodendrocyte and myelin development. We previously found that white matter integrity in young adults is related to common variants in genes encoding neurotrophins and their receptors. This underscores the importance of neurotrophins for white matter developm...

Journal: :Development 2005
Elia Benito-Gutiérrez Christian Nake Marta Llovera Joan X Comella Jordi Garcia-Fernàndez

Neurotrophins (Nt) and their tyrosine kinase Trk receptors play an essential role in the development and maintenance of the complex vertebrate nervous system. Invertebrate genome sequencing projects have suggested that the Nt/Trk system is a vertebrate innovation. We describe the isolation and characterisation of the amphioxus Trk receptor, AmphiTrk. Its ancestral link to vertebrate Trk recepto...

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