File | Title | Manuscript Id |
Chapter Introduction | lodish8e_ch22_1.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_1_dlap.xml | 57335f41757a2ede7e000005 |
22.1 Neurons and Glia: Building Blocks of the Nervous System
| lodish8e_ch22_2.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_2_dlap.xml | 57335f41757a2ede7e000005 |
Information Flows Through Neurons from Dendrites to Axons
| lodish8e_ch22_3.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_3_dlap.xml | 57335f41757a2ede7e000005 |
Information Moves Along Axons as Pulses of Ion Flow Called Action Potentials
| lodish8e_ch22_4.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_4_dlap.xml | 57335f41757a2ede7e000005 |
Information Flows Between Neurons via Synapses
| lodish8e_ch22_5.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_5_dlap.xml | 57335f41757a2ede7e000005 |
The Nervous System Uses Signaling Circuits Composed of Multiple Neurons
| lodish8e_ch22_6.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_6_dlap.xml | 57335f41757a2ede7e000005 |
Glial Cells Form Myelin Sheaths and Support Neurons
| lodish8e_ch22_7.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_7_dlap.xml | 57335f41757a2ede7e000005 |
Neural Stem Cells Form Nerve and Glial Cells in the Central Nervous System
| lodish8e_ch22_8.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_8_dlap.xml | 57335f41757a2ede7e000005 |
Key Concepts of Section 22.1 | lodish8e_ch22_9.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_9_dlap.xml | 57335f41757a2ede7e000005 |
22.2 Voltage-Gated Ion Channels and the Propagation of Action Potentials
| lodish8e_ch22_10.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_10_dlap.xml | 57335f41757a2ede7e000005 |
The Magnitude of the Action Potential Is Close to ENa and Is Caused by Na+ Influx Through Open Na+ Channels
| lodish8e_ch22_11.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_11_dlap.xml | 57335f41757a2ede7e000005 |
Sequential Opening and Closing of Voltage-Gated Na+ and K+ Channels Generate Action Potentials
| lodish8e_ch22_12.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_12_dlap.xml | 57335f41757a2ede7e000005 |
Action Potentials Are Propagated Unidirectionally Without Diminution
| lodish8e_ch22_13.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_13_dlap.xml | 57335f41757a2ede7e000005 |
Nerve Cells Can Conduct Many Action Potentials in the Absence of ATP
| lodish8e_ch22_14.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_14_dlap.xml | 57335f41757a2ede7e000005 |
All Voltage-Gated Ion Channels Have Similar Structures
| lodish8e_ch22_15.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_15_dlap.xml | 57335f41757a2ede7e000005 |
Voltage-Sensing S4 α Helices Move in Response to Membrane Depolarization
| lodish8e_ch22_16.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_16_dlap.xml | 57335f41757a2ede7e000005 |
Movement of the Channel-Inactivating Segment into the Open Pore Blocks Ion Flow
| lodish8e_ch22_17.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_17_dlap.xml | 57335f41757a2ede7e000005 |
Myelination Increases the Velocity of Impulse Conduction
| lodish8e_ch22_18.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_18_dlap.xml | 57335f41757a2ede7e000005 |
Action Potentials “Jump†from Node to Node in Myelinated Axons
| lodish8e_ch22_19.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_19_dlap.xml | 57335f41757a2ede7e000005 |
Two Types of Glia Produce Myelin Sheaths
| lodish8e_ch22_20.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_20_dlap.xml | 57335f41757a2ede7e000005 |
Light-Activated Ion Channels and Optogenetics
| lodish8e_ch22_21.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_21_dlap.xml | 57335f41757a2ede7e000005 |
Key Concepts of Section 22.2 | lodish8e_ch22_22.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_22_dlap.xml | 57335f41757a2ede7e000005 |
22.3 Communication at Synapses
| lodish8e_ch22_23.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_23_dlap.xml | 57335f41757a2ede7e000005 |
Formation of Synapses Requires Assembly of Presynaptic and Postsynaptic Structures
| lodish8e_ch22_24.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_24_dlap.xml | 57335f41757a2ede7e000005 |
Neurotransmitters Are Transported into Synaptic Vesicles by H+-Linked Antiport Proteins
| lodish8e_ch22_25.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_25_dlap.xml | 57335f41757a2ede7e000005 |
Three Pools of Synaptic Vesicles Loaded with Neurotransmitter Are Present in the Presynaptic Terminal
| lodish8e_ch22_26.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_26_dlap.xml | 57335f41757a2ede7e000005 |
Influx of Ca2+ Triggers Release of Neurotransmitters
| lodish8e_ch22_27.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_27_dlap.xml | 57335f41757a2ede7e000005 |
A Calcium-Binding Protein Regulates Fusion of Synaptic Vesicles with the Plasma Membrane
| lodish8e_ch22_28.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_28_dlap.xml | 57335f41757a2ede7e000005 |
Fly Mutants Lacking Dynamin Cannot Recycle Synaptic Vesicles
| lodish8e_ch22_29.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_29_dlap.xml | 57335f41757a2ede7e000005 |
Signaling at Synapses Is Terminated by Degradation or Reuptake of Neurotransmitters
| lodish8e_ch22_30.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_30_dlap.xml | 57335f41757a2ede7e000005 |
Opening of Acetylcholine-Gated Cation Channels Leads to Muscle Contraction
| lodish8e_ch22_31.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_31_dlap.xml | 57335f41757a2ede7e000005 |
All Five Subunits in the Nicotinic Acetylcholine Receptor Contribute to the Ion Channel
| lodish8e_ch22_32.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_32_dlap.xml | 57335f41757a2ede7e000005 |
Nerve Cells Integrate Many Inputs to Make an All-or-None Decision to Generate an Action Potential
| lodish8e_ch22_33.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_33_dlap.xml | 57335f41757a2ede7e000005 |
Gap Junctions Allow Direct Communication Between Neurons and Between Glia
| lodish8e_ch22_34.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_34_dlap.xml | 57335f41757a2ede7e000005 |
Key Concepts of Section 22.3 | lodish8e_ch22_35.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_35_dlap.xml | 57335f41757a2ede7e000005 |
22.4 Sensing the Environment: Touch, Pain, Taste, and Smell
| lodish8e_ch22_36.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_36_dlap.xml | 57335f41757a2ede7e000005 |
Mechanoreceptors Are Gated Cation Channels
| lodish8e_ch22_37.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_37_dlap.xml | 57335f41757a2ede7e000005 |
Pain Receptors Are Also Gated Cation Channels
| lodish8e_ch22_38.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_38_dlap.xml | 57335f41757a2ede7e000005 |
Five Primary Tastes Are Sensed by Subsets of Cells in Each Taste Bud
| lodish8e_ch22_39.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_39_dlap.xml | 57335f41757a2ede7e000005 |
A Plethora of Receptors Detect Odors
| lodish8e_ch22_40.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_40_dlap.xml | 57335f41757a2ede7e000005 |
Each Olfactory Receptor Neuron Expresses a Single Type of Odorant Receptor
| lodish8e_ch22_41.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_41_dlap.xml | 57335f41757a2ede7e000005 |
Key Concepts of Section 22.4 | lodish8e_ch22_42.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_42_dlap.xml | 57335f41757a2ede7e000005 |
22.5 Forming and Storing Memories
| lodish8e_ch22_43.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_43_dlap.xml | 57335f41757a2ede7e000005 |
Memories Are Formed by Changing the Number or Strength of Synapses Between Neurons
| lodish8e_ch22_44.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_44_dlap.xml | 57335f41757a2ede7e000005 |
The Hippocampus Is Required for Memory Formation
| lodish8e_ch22_45.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_45_dlap.xml | 57335f41757a2ede7e000005 |
Multiple Molecular Mechanisms Contribute to Synaptic Plasticity
| lodish8e_ch22_46.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_46_dlap.xml | 57335f41757a2ede7e000005 |
Formation of Long-Term Memories Requires Gene Expression
| lodish8e_ch22_47.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_47_dlap.xml | 57335f41757a2ede7e000005 |
Key Concepts of Section 22.5 | lodish8e_ch22_48.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_48_dlap.xml | 57335f41757a2ede7e000005 |
Key Terms
| lodish8e_ch22_49.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_49_dlap.xml | 57335f41757a2ede7e000005 |
Review the Concepts
| lodish8e_ch22_50.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_50_dlap.xml | 57335f41757a2ede7e000005 |
Extended References
| lodish8e_ch22_51.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_51_dlap.xml | 57335f41757a2ede7e000005 |
Perspectives for the Future
| lodish8e_ch22_52.html | 57335f41757a2ede7e000005 |
DLAP questions | lodish8e_ch22_52_dlap.xml | 57335f41757a2ede7e000005 |