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Amyloid Deposit -- See Plaque, Amyloid


Accumulations of extracellularly deposited AMYLOID FIBRILS within tissues
  1
 

Amyloid Deposits -- See Plaque, Amyloid


Accumulations of extracellularly deposited AMYLOID FIBRILS within tissues
  1
  Amyloid fibril protein (Alzheimer's) -- 2 Related Subjects   2
 

Amyloid Fibrils -- See Amyloid


A fibrous protein complex that consists of proteins folded into a specific cross beta-pleated sheet structure. This fibrillar structure has been found as an alternative folding pattern for a variety of functional proteins. Deposits of amyloid in the form of AMYLOID PLAQUES are associated with a variety of degenerative diseases. The amyloid structure has also been found in a number of functional proteins that are unrelated to disease
  1
Amyloid -- metabolism. : Adapting proteostasis to ameliorate aggregation-associated amyloid diseases / Jeffery W. Kelly  2018 1
Amyloid -- Periodicals : Amyloid (Online)  1994- 1
 

Amyloid Plaque -- See Plaque, Amyloid


Accumulations of extracellularly deposited AMYLOID FIBRILS within tissues
  1
 

Amyloid Plaques -- See Plaque, Amyloid


Accumulations of extracellularly deposited AMYLOID FIBRILS within tissues
  1
Amyloid Precursor Protein Secretases -- pharmacology. : BACE : Lead Target for Orchestrated Therapy of Alzheimer's Disease / edited by Varghese John  2010 1
Amyloid Precursor Protein Secretases -- therapeutic use. : BACE : Lead Target for Orchestrated Therapy of Alzheimer's Disease / edited by Varghese John  2010 1
  Amyloid Protein A4 -- 2 Related Subjects   2
  Amyloid protein precursor -- 2 Related Subjects   2
 

Amyloid Proteins -- See Amyloidogenic Proteins


Proteins that form the core of amyloid fibrils. For example, the core of amyloid A is formed from amyloid A protein, also known as serum amyloid A protein or SAA protein
  1
 

Amyloid Substance -- See Amyloid


A fibrous protein complex that consists of proteins folded into a specific cross beta-pleated sheet structure. This fibrillar structure has been found as an alternative folding pattern for a variety of functional proteins. Deposits of amyloid in the form of AMYLOID PLAQUES are associated with a variety of degenerative diseases. The amyloid structure has also been found in a number of functional proteins that are unrelated to disease
  1
Amyloidogenic Proteins. : Amyloid fibrils as functional nanomaterials / Juliet Gerrard  2017 1
Amyloidogenic Proteins -- toxicity. : Non-fibrillar amyloidogenic protein assemblies : common cytotoxins underlying degenerative diseases / Farid Rahimi, Gal Bitan, editors  2012 1
 

Amyloidoses -- See Amyloidosis


A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits
  1
  Amyloidosis -- 3 Related Subjects   3
Amyloidosis.   8
Amyloidosis -- Complications. : The kidney in plasma cell dyscrasias / volume editor, Guillermo A. Herrera  2007 1
Amyloidosis -- diagnosis.   4
Amyloidosis -- drug therapy. : Adapting proteostasis to ameliorate aggregation-associated amyloid diseases / Jeffery W. Kelly  2018 1
Amyloidosis -- etiology. : Protein misfolding diseases : current and emerging principles and therapies / edited by Marina Ramirez-Alvarado, Jeffery W. Kelly, Christopher M. Dobson  2010 1
Amyloidosis -- genetics. : Water and biomolecules : physical chemistry of life phenomena / Kunihiro Kuwajima [and others] (editors)  2009 1
Amyloidosis -- pathology. : Amyloid and related disorders : surgical pathology and clinical correlations / Maria M. Picken, Ahmet Dogan, Guillermo A. Herrera, editors  2012 1
Amyloidosis -- Periodicals : Amyloid (Online)  1994- 1
Amyloidosis -- physiopathology.   2
Amyloidosis -- therapy.   3
Amyloidosis -- Treatment.   3
 

Amylomaize Starch -- See Starch


Any of a group of polysaccharides of the general formula (C6-H10-O5)n, composed of a long-chain polymer of glucose in the form of amylose and amylopectin. It is the chief storage form of energy reserve (carbohydrates) in plants
  1
 

Amyloplast -- See Plastids


Self-replicating cytoplasmic organelles of plant and algal cells that contain pigments and may synthesize and accumulate various substances. PLASTID GENOMES are used in phylogenetic studies
  1
 

Amyloplasts -- See Plastids


Self-replicating cytoplasmic organelles of plant and algal cells that contain pigments and may synthesize and accumulate various substances. PLASTID GENOMES are used in phylogenetic studies
  1
  Amylum -- 2 Related Subjects   2
  Amyotonia congenita -- 2 Related Subjects   2
Amyotrophic lateral sclerosis.   40
Amyotrophic lateral sclerosis -- Australia. : Morbidity of Vietnam veterans : multiple sclerosis and motor neurone disease in Vietnam veterans : supplementary report no. 3  2001 1
Amyotrophic lateral sclerosis -- Biography.   3
Amyotrophic Lateral Sclerosis -- complications.   2
Amyotrophic Lateral Sclerosis -- diagnosis.   3
Amyotrophic Lateral Sclerosis -- epidemiology. : The clinical features of amyotrophic lateral sclerosis : diagnosis, natural history and epidemiology / Kevin Talbot  2016 1
Amyotrophic Lateral Sclerosis -- etiology.   2
Amyotrophic lateral sclerosis -- Fiction. : Every breath / Nicholas Sparks  2018 1
Amyotrophic Lateral Sclerosis -- genetics.   3
Amyotrophic lateral sclerosis -- Guam. : The island of the colorblind : and, Cycad island / by Oliver Sacks  1997 1
 

Amyotrophic Lateral Sclerosis, Guam Form -- See Amyotrophic Lateral Sclerosis


A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
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Amyotrophic lateral sclerosis -- Handbooks, manuals, etc. : The motor neurone disease handbook / edited by Matthew Kiernan  2007 1
Amyotrophic Lateral Sclerosis -- immunology. : Neuroinflammation in ALS : cause or consequence? / Philip Van Damme  2016 1
Amyotrophic Lateral Sclerosis -- metabolism. : Oligodendroglia/MCT1 are an unexpected contributor to CNS toxicity/neurodegeneration / Jeffrey D. Rothstein  2013 1
Amyotrophic lateral sclerosis -- Nursing. : Aspects of care for staff of residential care facilities : Motor neurone disease  2006 1
Amyotrophic lateral sclerosis -- Palliative treatment.   2
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