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Aedes
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B01.050.500.131.617.720.500.500.750.712.500.875.100 |
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Leptospiraceae
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B03.851.475 |
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Pea Proteins
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J02.500.428.920.500 |
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WAGR Syndrome
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C13.351.937.820.535.585.950 |
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ATP Binding Cassette Transporter, Subfamily G, Member 8
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D12.776.395.550.020.457.875 |
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Neuromuscular Junction
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D009469 |
[The synapse between a neuron and a muscle.
] |
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Mandibular Neoplasms
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C05.500.607.442 |
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Neuromuscular Depolarizing Agents
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D009467 |
[Drugs that interrupt transmission at the skeletal neuromuscular junction by causing sustained depolarization of the motor end plate. These agents are primarily used as adjuvants in surgical anesthesia to cause skeletal muscle relaxation.
] |
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Neuromuscular Diseases
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D009468 |
[A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA.
] |
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Peptide Termination Factors
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D010454 |
[Proteins that are involved in the peptide chain termination reaction (PEPTIDE CHAIN TERMINATION, TRANSLATIONAL) on RIBOSOMES. They include codon-specific class-I release factors, which recognize stop signals (TERMINATOR CODON) in the MESSENGER RNA; and codon-nonspecific class-II release factors.
] |
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Neurons, Efferent
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D009476 |
[Neurons which send impulses peripherally to activate muscles or secretory cells.
] |
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Peptides
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D010455 |
[Members of the class of compounds composed of AMINO ACIDS joined together by peptide bonds between adjacent amino acids into linear, branched or cyclical structures. OLIGOPEPTIDES are composed of approximately 2-12 amino acids. Polypeptides are composed of approximately 13 or more amino acids. PROTEINS are linear polypeptides that are normally synthesized on RIBOSOMES.
] |
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Hereditary Sensory and Autonomic Neuropathies
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D009477 |
[A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4)
] |
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Peptides, Cyclic
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D010456 |
[Peptides whose amino acid residues are linked together forming a circular chain. Some of them are ANTI-INFECTIVE AGENTS; some are biosynthesized non-ribosomally (PEPTIDE BIOSYNTHESIS, NON-RIBOSOMAL).
, Ribosomally synthesized homodetic plant cyclic peptides that have N-to-C amide bonds rather than disulfide bonds.
] |
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Neurons
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D009474 |
[The basic cellular units of nervous tissue. Each neuron consists of a body, an axon, and dendrites. Their purpose is to receive, conduct, and transmit impulses in the NERVOUS SYSTEM.
] |
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Peptidoglycan
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D010457 |
[A structural polymer of the bacterial cell envelope consisting of sugars and amino acids which is responsible for both shape determination and cellular integrity under osmotic stress in virtually all bacteria.
] |
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Neurons, Afferent
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D009475 |
[Neurons which conduct NERVE IMPULSES to the CENTRAL NERVOUS SYSTEM.
] |
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Peptidyl Transferases
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D010458 |
[Acyltransferases that use AMINO ACYL TRNA as the amino acid donor in formation of a peptide bond. There are ribosomal and non-ribosomal peptidyltransferases.
] |
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Neuronal Ceroid-Lipofuscinoses
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D009472 |
[This type is caused by mutation in the gene (CLN1or PPT1) encoding palmitoyl-protein thioesterase (THIOLESTER HYDROLASES), an enzyme involved in catabolism of lipid-modified proteins.
, This type is caused by mutation in the CLN3 gene encoding a lysosomal integral membrane protein (Battenin).
, This type is caused by mutation in the CLN2 gene encoding tripeptidyl-peptidase I, a lysosomal serine protease.
, A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure.
] |
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Peptococcaceae
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D010459 |
[A family of bacteria found in the mouth and intestinal and respiratory tracts of man and other animals as well as in the human female urogenital tract. Its organisms are also found in soil and on cereal grains.
] |
