«LYSOSOMAL» தொடர்புடைய ஆங்கிலம் புத்தகங்கள்
பின்வரும் புத்தக விவரத்தொகுப்புத் தேர்ந்தெடுப்பில்
lysosomal இன் பயன்பாட்டைக் கண்டறியுங்கள்.
lysosomal தொடர்பான புத்தகங்கள் மற்றும் ஆங்கிலம் இலக்கியத்தில் அதன் பயன்பாட்டுச் சூழலை வழங்குவதற்கு அதிலிருந்து பெறப்பட்ட சுருக்கமான சாரங்களைத் தொடர்புபடுத்துகின்றன.
1
Lysosomal Storage Disorders: Principles and Practice
This book presents an overview of lysosomal storage disorders, and provides the reader with an understanding of clinical features, associated complications, and diagnosis and management approaches.
Gregory M. Pastores,
2010
2
Lysosomal Storage Disorders
Disease specific chapters provide thorough reviews of the clinical features of lysosomal storage disorders, their molecular basis and the commercial or experimental therapeutic approaches sought in this area.
John A. Barranger, Mario Cabrera-Salazar,
2007
3
Lysosomal Storage Disorders: A Practical Guide
Awareness of lysomal storage disorders needs to be raised and there is very substantial pharmaceutical interest to do so. The disorders are often viewed as obscurities but in fact they are treatable.
Atul Mehta, Bryan Winchester,
2012
4
Lysosomal Disorders of the Brain: Recent Advances in ...
Details recent advances in the molecular and cellular pathologies of a variety of lysosomal storage diseases. Also discusses the development of effective therapies.
Frances M. Platt, Steven U. Walkley,
2004
5
Nervous System
Lysosomal Storage Diseases—Advances in ...
Nervous System Lysosomal Storage Diseases—Advances in Research and Treatment: 2012 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Nervous System Lysosomal Storage Diseas in a ...
6
Molecular Basis of
Lysosomal Storage Disorders
Molecular Basis of Lysosomal Storage Disorders
7
P38 MAPKs Coordinately Regulate Distinct Phases of Autophagy ...
p38 mitogen-activated protein kinases (MAPKs) control the endocytic trafficking of various growth-related cell surface receptors and transporters.
Shankar Varadarajan,
2008
8
Selective Enhancement of
Lysosomal Responses Clears ...
Protein deposition is a characteristic of Alzheimer's disease (AD) in which pathogenic accumulations of paired helical filaments (PHFs) and amyloid-beta peptides (e.g.
9
Pathophysiology of
Lysosomal Transport
The book also examines the transfer of macromolecules into the lysosomes, describes the analogy between mammalian lysosomes and vacuoles of plants and fungi, and reviews non-mediated transport.
10
Unrestrained Molecular Dynamics Simulations of Human ...
Molecular dynamics (MD) simulations have been performed at the atomic level to study autoproteolysis in human glycosylasparaginase (GA) precursor and the Finnish mutation AGUFIN.
William Michael York,
2007
«LYSOSOMAL» வார்த்தையைக் கொண்டுள்ள புதிய உருப்படிகள்
பின்வரும் செய்தி உருப்படிகளின் சூழலில்
lysosomal என்ற வார்த்தையைப் பயன்படுத்துவது பற்றியும் எப்படிப் பயன்படுத்துவது என்பதைப் பற்றியும் தேசிய மற்றும் பன்னாட்டு அச்சகங்கள் என்ன பேசியிருக்கின்றன என்பதைக் கண்டறியுங்கள்.
Visualizing lipid-formulated siRNA release from endosomes and …
By contrast, the late endosomal (Rab9) and lysosomal (LAMP1) markers were just being recruited or completely absent, respectively, at the time of release (Fig. «Nature.com, ஜூலை 15»
First - BioMed Central
... cholesteanol, lysosomal enzymes, quantitative assessment of amino acids) [14], and genetic testing for SCA1,2,3,6,7 was performed. All results were normal. «BMC Blogs Network, ஜூலை 15»
Listening to Yellen Cost You 80%
Alexion Pharmaceuticals, for instance, has an upcoming FDA decision on September 8 for Kanuma, its treatment of lysosomal acid lipase ... «Motley Fool, ஜூலை 15»
Shares of Amicus Therapeutics, Inc. (NASDAQ:FOLD) Sees Large …
... as pharmacological chaperones for treating a range of diseases, including lysosomal storage diseases and diseases of neurodegeneration. «Insider Trading Report, ஜூலை 15»
"Saving Eliza" campaign helps another child
Sanfilippo is a lysosomal storage disease, described in my first post about Eliza. Mutations in any of four genes cause it. Will, with type B, is 1 in ... «Medical Xpress, ஜூலை 15»
Amicus Therapeutics Given Consensus Recommendation of "Buy …
... of next-generation medicines for a range of rare and orphan diseases, with a focus on improved therapies for lysosomal storage disorders. «Dakota Financial News, ஜூலை 15»
“Saving Eliza” Campaign Helps Another Child
Sanfilippo is a lysosomal storage disease, described in my first post about Eliza. Mutations in any of four genes cause it. Will, with type B, is 1 in ... «PLoS Blogs, ஜூலை 15»
Dr. Charles W. Richard Joins uniQure as Senior Vice President to …
... a biotechnology company focused on developing second-generation enzyme replacement therapies for rare lysosomal storage diseases, ... «Nasdaq, ஜூலை 15»
Pre-Market News Report on: BioMarin Pharmaceutical (NASDAQ …
Its commercial products comprise Vimizim, an enzyme replacement therapy for the treatment of MPS IV A, a lysosomal storage disorder; Naglazyme, ... «wsnewspublishers, ஜூலை 15»
Parkinson's Disease: The Devil Is in the Protein
This past February, Lysosomal Therapeutics announced it had raised $20 million in Series A financing from Atlas Venture, Roche Ventures, ... «Genetic Engineering & Biotechnology News, ஜூலை 15»