Descriptor English: | Calcium Channels, L-Type | ||||||
Descriptor Spanish: |
Canales de Calcio Tipo L
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Descriptor Portuguese: | Canais de Cálcio Tipo L | ||||||
Descriptor French: | Canaux calciques de type L | ||||||
Entry term(s): |
Calcium Channel, L-Type Calcium Channel, Long-Lasting Calcium Channels, L Type Calcium Channels, Long-Lasting Channel, Long-Lasting Calcium Dihydropyridine Receptor Dihydropyridine Receptors L Type Calcium Channel L Type Calcium Channels L Type VDCC L Type VDCC alpha 1 Subunit L Type VDCC alpha 2 Subunit L Type VDCC beta Subunit L Type VDCC delta Subunit L Type VDCC gamma Subunit L Type Voltage Dependent Calcium Channel L Type Voltage Dependent Calcium Channels L-Type Calcium Channel L-Type Calcium Channels L-Type VDCC L-Type VDCC alpha-1 Subunit L-Type VDCC alpha-2 Subunit L-Type VDCC beta Subunit L-Type VDCC delta Subunit L-Type VDCC gamma Subunit L-Type Voltage-Dependent Calcium Channel L-Type Voltage-Dependent Calcium Channels Long Lasting Calcium Channel Long Lasting Calcium Channels Long-Lasting Calcium Channel Long-Lasting Calcium Channels Receptor, Dihydropyridine Receptors, Dihydropyridine VDCC, L-Type |
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Tree number(s): |
D12.776.157.530.400.150.400 D12.776.543.550.450.150.400 D12.776.543.585.400.150.400 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D020746 | ||||||
Scope note: | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
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Allowable Qualifiers: |
AD administration & dosage AE adverse effects AN analysis BI biosynthesis BL blood CF cerebrospinal fluid CH chemistry CL classification CS chemical synthesis DE drug effects DF deficiency EC economics GE genetics HI history IM immunology IP isolation & purification ME metabolism PD pharmacology PH physiology PK pharmacokinetics PO poisoning RE radiation effects SD supply & distribution ST standards TO toxicity TU therapeutic use UL ultrastructure UR urine |
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Previous Indexing: |
Calcium Channels (1993-1999) Muscle Proteins (1993-1999) |
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Public MeSH Note: | 2000; DIHYDROPYRIDINE RECEPTOR (now L-TYPE CALCIUM CHANNELS) was indexed under CALCIUM CHANNELS & MUSCLE PROTEINS 1993-1999 |
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History Note: | 2000; use L-TYPE CALCIUM CHANNELS (NM) 1993-1999 |
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Entry Version: | VDCC L |
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DeCS ID: | 34475 | ||||||
Unique ID: | D020746 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 2000/01/01 | ||||||
Date of Entry: | 1999/11/04 | ||||||
Revision Date: | 2020/05/27 |
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CHEMICALS AND DRUGS
Amino Acids, Peptides, and Proteins [D12]Amino Acids, Peptides, and Proteins -
CHEMICALS AND DRUGS
Amino Acids, Peptides, and Proteins [D12]Amino Acids, Peptides, and Proteins -
CHEMICALS AND DRUGS
Amino Acids, Peptides, and Proteins [D12]Amino Acids, Peptides, and Proteins
|
Calcium Channels, L-Type
- Preferred
Receptors, Dihydropyridine
- Narrower
L-Type VDCC delta Subunit
- Narrower
L-Type VDCC alpha-2 Subunit
- Narrower
L-Type VDCC beta Subunit
- Narrower
L-Type VDCC gamma Subunit
- Narrower
Concept UI |
M0328046 |
Scope note | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
Preferred term | Calcium Channels, L-Type |
Entry term(s) |
Calcium Channel, L-Type Calcium Channel, Long-Lasting Calcium Channels, L Type Calcium Channels, Long-Lasting Channel, Long-Lasting Calcium L Type Calcium Channel L Type Calcium Channels L Type VDCC L Type Voltage Dependent Calcium Channel L Type Voltage Dependent Calcium Channels L-Type Calcium Channel L-Type Calcium Channels L-Type VDCC L-Type Voltage-Dependent Calcium Channel L-Type Voltage-Dependent Calcium Channels Long Lasting Calcium Channel Long Lasting Calcium Channels Long-Lasting Calcium Channel Long-Lasting Calcium Channels VDCC, L-Type |
Concept UI |
M0333104 |
Scope note | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
Scope note | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
Preferred term | Receptors, Dihydropyridine |
Entry term(s) |
Dihydropyridine Receptor Dihydropyridine Receptors L Type VDCC alpha 1 Subunit L-Type VDCC alpha-1 Subunit Receptor, Dihydropyridine |
Concept UI |
M0333270 |
Scope note | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
Scope note | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
Preferred term | L-Type VDCC delta Subunit |
Entry term(s) |
L Type VDCC delta Subunit |
Concept UI |
M0337686 |
Scope note | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
Scope note | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
Preferred term | L-Type VDCC alpha-2 Subunit |
Entry term(s) |
L Type VDCC alpha 2 Subunit |
Concept UI |
M0333269 |
Scope note | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
Scope note | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
Preferred term | L-Type VDCC beta Subunit |
Entry term(s) |
L Type VDCC beta Subunit |
Concept UI |
M0333271 |
Scope note | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
Scope note | Long-lasting voltage-gated CALCIUM CHANNELS found in both excitable and non-excitable tissue. They are responsible for normal myocardial and vascular smooth muscle contractility. Five subunits (alpha-1, alpha-2, beta, gamma, and delta) make up the L-type channel. The alpha-1 subunit is the binding site for calcium-based antagonists. Dihydropyridine-based calcium antagonists are used as markers for these binding sites. |
Preferred term | L-Type VDCC gamma Subunit |
Entry term(s) |
L Type VDCC gamma Subunit |
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