File | Title | Manuscript Id |
Chapter Introduction | lodish8e_ch11_1.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_1_dlap.xml | 572b8b0d757a2efc31000000 |
11.1 Overview of Transmembrane Transport
| lodish8e_ch11_2.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_2_dlap.xml | 572b8b0d757a2efc31000000 |
Only Gases and Small Uncharged Molecules Cross Membranes by Simple Diffusion
| lodish8e_ch11_3.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_3_dlap.xml | 572b8b0d757a2efc31000000 |
Three Main Classes of Membrane Proteins Transport Molecules and Ions Across Cellular Membranes
| lodish8e_ch11_4.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_4_dlap.xml | 572b8b0d757a2efc31000000 |
Key Concepts of Section 11.1 | lodish8e_ch11_5.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_5_dlap.xml | 572b8b0d757a2efc31000000 |
11.2 Facilitated Transport of Glucose and Water
| lodish8e_ch11_6.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_6_dlap.xml | 572b8b0d757a2efc31000000 |
Uniport Transport Is Faster and More Specific than Simple Diffusion
| lodish8e_ch11_7.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_7_dlap.xml | 572b8b0d757a2efc31000000 |
The Low Km of the GLUT1 Uniporter Enables It to Transport Glucose into Most Mammalian Cells
| lodish8e_ch11_8.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_8_dlap.xml | 572b8b0d757a2efc31000000 |
The Human Genome Encodes a Family of Sugar-Transporting GLUT Proteins
| lodish8e_ch11_9.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_9_dlap.xml | 572b8b0d757a2efc31000000 |
Transport Proteins Can Be Studied Using Artificial Membranes and Recombinant Cells
| lodish8e_ch11_10.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_10_dlap.xml | 572b8b0d757a2efc31000000 |
Osmotic Pressure Causes Water to Move Across Membranes
| lodish8e_ch11_11.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_11_dlap.xml | 572b8b0d757a2efc31000000 |
Aquaporins Increase the Water Permeability of Cellular Membranes
| lodish8e_ch11_12.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_12_dlap.xml | 572b8b0d757a2efc31000000 |
Key Concepts of Section 11.2 | lodish8e_ch11_13.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_13_dlap.xml | 572b8b0d757a2efc31000000 |
11.3 ATP-Powered Pumps and the Intracellular Ionic Environment
| lodish8e_ch11_14.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_14_dlap.xml | 572b8b0d757a2efc31000000 |
There Are Four Main Classes of ATP-Powered Pumps
| lodish8e_ch11_15.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_15_dlap.xml | 572b8b0d757a2efc31000000 |
ATP-Powered Ion Pumps Generate and Maintain Ionic Gradients Across Cellular Membranes
| lodish8e_ch11_16.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_16_dlap.xml | 572b8b0d757a2efc31000000 |
Muscle Relaxation Depends on Ca2+ ATPases That Pump Ca2+ from the Cytosol into the Sarcoplasmic Reticulum
| lodish8e_ch11_17.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_17_dlap.xml | 572b8b0d757a2efc31000000 |
The Mechanism of Action of the Ca2+ Pump Is Known in Detail
| lodish8e_ch11_18.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_18_dlap.xml | 572b8b0d757a2efc31000000 |
Calmodulin Regulates the Plasma-Membrane Pumps That Control Cytosolic Ca2+ Concentrations
| lodish8e_ch11_19.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_19_dlap.xml | 572b8b0d757a2efc31000000 |
The Na+/K+ ATPase Maintains the Intracellular Na+ and K+ Concentrations in Animal Cells
| lodish8e_ch11_20.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_20_dlap.xml | 572b8b0d757a2efc31000000 |
V-Class H+ ATPases Maintain the Acidity of Lysosomes and Vacuoles
| lodish8e_ch11_21.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_21_dlap.xml | 572b8b0d757a2efc31000000 |
ABC Proteins Export a Wide Variety of Drugs and Toxins from the Cell
| lodish8e_ch11_22.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_22_dlap.xml | 572b8b0d757a2efc31000000 |
Certain ABC Proteins “Flip†Phospholipids and Other Lipid-Soluble Substrates from One Membrane Leaflet to the Other
| lodish8e_ch11_23.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_23_dlap.xml | 572b8b0d757a2efc31000000 |
The ABC Cystic Fibrosis Transmembrane Regulator Is a Chloride Channel, Not a Pump
| lodish8e_ch11_24.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_24_dlap.xml | 572b8b0d757a2efc31000000 |
Key Concepts of Section 11.3 | lodish8e_ch11_25.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_25_dlap.xml | 572b8b0d757a2efc31000000 |
11.4 Nongated Ion Channels and the Resting Membrane Potential
| lodish8e_ch11_26.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_26_dlap.xml | 572b8b0d757a2efc31000000 |
Selective Movement of Ions Creates a Transmembrane Electric Gradient
| lodish8e_ch11_27.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_27_dlap.xml | 572b8b0d757a2efc31000000 |
The Resting Membrane Potential in Animal Cells Depends Largely on the Outward Flow of K+ Ions Through Open K+ Channels
| lodish8e_ch11_28.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_28_dlap.xml | 572b8b0d757a2efc31000000 |
Ion Channels Are Selective for Certain Ions by Virtue of a Molecular “Selectivity Filterâ€Â
| lodish8e_ch11_29.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_29_dlap.xml | 572b8b0d757a2efc31000000 |
Patch Clamps Permit Measurement of Ion Movements Through Single Channels
| lodish8e_ch11_30.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_30_dlap.xml | 572b8b0d757a2efc31000000 |
Novel Ion Channels Can Be Characterized by a Combination of Oocyte Expression and Patch Clamping
| lodish8e_ch11_31.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_31_dlap.xml | 572b8b0d757a2efc31000000 |
Key Concepts of Section 11.4 | lodish8e_ch11_32.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_32_dlap.xml | 572b8b0d757a2efc31000000 |
11.5 Cotransport by Symporters and Antiporters
| lodish8e_ch11_33.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_33_dlap.xml | 572b8b0d757a2efc31000000 |
Na+ Entry into Mammalian Cells Is Thermodynamically Favored
| lodish8e_ch11_34.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_34_dlap.xml | 572b8b0d757a2efc31000000 |
Na+-Linked Symporters Enable Animal Cells to Import Glucose and Amino Acids Against High Concentration Gradients
| lodish8e_ch11_35.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_35_dlap.xml | 572b8b0d757a2efc31000000 |
A Bacterial Na+/Amino Acid Symporter Reveals How Symport Works
| lodish8e_ch11_36.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_36_dlap.xml | 572b8b0d757a2efc31000000 |
A Na+-Linked Ca2+ Antiporter Regulates the Strength of Cardiac Muscle Contraction
| lodish8e_ch11_37.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_37_dlap.xml | 572b8b0d757a2efc31000000 |
Several Cotransporters Regulate Cytosolic pH
| lodish8e_ch11_38.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_38_dlap.xml | 572b8b0d757a2efc31000000 |
An Anion Antiporter Is Essential for Transport of CO2 by Erythrocytes
| lodish8e_ch11_39.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_39_dlap.xml | 572b8b0d757a2efc31000000 |
Numerous Transport Proteins Enable Plant Vacuoles to Accumulate Metabolites and Ions
| lodish8e_ch11_40.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_40_dlap.xml | 572b8b0d757a2efc31000000 |
Key Concepts of Section 11.5 | lodish8e_ch11_41.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_41_dlap.xml | 572b8b0d757a2efc31000000 |
11.6 Transcellular Transport
| lodish8e_ch11_42.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_42_dlap.xml | 572b8b0d757a2efc31000000 |
Multiple Transport Proteins Are Needed to Move Glucose and Amino Acids Across Epithelia
| lodish8e_ch11_43.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_43_dlap.xml | 572b8b0d757a2efc31000000 |
Simple Rehydration Therapy Depends on the Osmotic Gradient Created by Absorption of Glucose and Na+ | lodish8e_ch11_44.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_44_dlap.xml | 572b8b0d757a2efc31000000 |
Parietal Cells Acidify the Stomach Contents While Maintaining a Neutral Cytosolic pH
| lodish8e_ch11_45.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_45_dlap.xml | 572b8b0d757a2efc31000000 |
Bone Resorption Requires the Coordinated Function of a V-Class Proton Pump and a Specific Chloride Channel
| lodish8e_ch11_46.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_46_dlap.xml | 572b8b0d757a2efc31000000 |
Key Concepts of Section 11.6 | lodish8e_ch11_47.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_47_dlap.xml | 572b8b0d757a2efc31000000 |
Key Terms
| lodish8e_ch11_48.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_48_dlap.xml | 572b8b0d757a2efc31000000 |
Review the Concepts
| lodish8e_ch11_49.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_49_dlap.xml | 572b8b0d757a2efc31000000 |
Extended References
| lodish8e_ch11_50.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_50_dlap.xml | 572b8b0d757a2efc31000000 |
Perspectives for the Future
| lodish8e_ch11_51.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_51_dlap.xml | 572b8b0d757a2efc31000000 |
Classic Experiment 11-1: Stumbling upon Active Transport | lodish8e_ch11_52.html | 572b8b0d757a2efc31000000 |
DLAP questions | lodish8e_ch11_52_dlap.xml | 572b8b0d757a2efc31000000 |