File | Title | Manuscript Id |
Chapter Introduction | lodish8e_ch21_1.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_1_dlap.xml | 57335f01757a2ed17f000002 |
21.1 Early Mammalian Development
| lodish8e_ch21_2.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_2_dlap.xml | 57335f01757a2ed17f000002 |
Fertilization Unifies the Genome
| lodish8e_ch21_3.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_3_dlap.xml | 57335f01757a2ed17f000002 |
Cleavage of the Mammalian Embryo Leads to the First Differentiation Events
| lodish8e_ch21_4.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_4_dlap.xml | 57335f01757a2ed17f000002 |
Key Concepts of Section 21.1 | lodish8e_ch21_5.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_5_dlap.xml | 57335f01757a2ed17f000002 |
21.2 Embryonic Stem Cells and Induced Pluripotent Stem Cells
| lodish8e_ch21_6.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_6_dlap.xml | 57335f01757a2ed17f000002 |
The Inner Cell Mass Is the Source of ES Cells
| lodish8e_ch21_7.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_7_dlap.xml | 57335f01757a2ed17f000002 |
Multiple Factors Control the Pluripotency of ES Cells
| lodish8e_ch21_8.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_8_dlap.xml | 57335f01757a2ed17f000002 |
Animal Cloning Shows That Differentiation Can Be Reversed
| lodish8e_ch21_9.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_9_dlap.xml | 57335f01757a2ed17f000002 |
Somatic Cells Can Generate iPS Cells
| lodish8e_ch21_10.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_10_dlap.xml | 57335f01757a2ed17f000002 |
ES and iPS Cells Can Generate Functional Differentiated Human Cells
| lodish8e_ch21_11.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_11_dlap.xml | 57335f01757a2ed17f000002 |
Key Concepts of Section 21.2 | lodish8e_ch21_12.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_12_dlap.xml | 57335f01757a2ed17f000002 |
21.3 Stem Cells and Niches in Multicellular Organisms
| lodish8e_ch21_13.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_13_dlap.xml | 57335f01757a2ed17f000002 |
Adult Planaria Contain Pluripotent Stem Cells
| lodish8e_ch21_14.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_14_dlap.xml | 57335f01757a2ed17f000002 |
Multipotent Somatic Stem Cells Give Rise to Both Stem Cells and Differentiating Cells
| lodish8e_ch21_15.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_15_dlap.xml | 57335f01757a2ed17f000002 |
Stem Cells for Different Tissues Occupy Sustaining Niches
| lodish8e_ch21_16.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_16_dlap.xml | 57335f01757a2ed17f000002 |
Germ-Line Stem Cells Produce Sperm or Oocytes
| lodish8e_ch21_17.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_17_dlap.xml | 57335f01757a2ed17f000002 |
Intestinal Stem Cells Continuously Generate All the Cells of the Intestinal Epithelium
| lodish8e_ch21_18.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_18_dlap.xml | 57335f01757a2ed17f000002 |
Hematopoietic Stem Cells Form All Blood Cells
| lodish8e_ch21_19.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_19_dlap.xml | 57335f01757a2ed17f000002 |
Rare Types of Cells Constitute the Niche for Hematopoietic Stem Cells
| lodish8e_ch21_20.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_20_dlap.xml | 57335f01757a2ed17f000002 |
Meristems Are Niches for Stem Cells in Plants
| lodish8e_ch21_21.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_21_dlap.xml | 57335f01757a2ed17f000002 |
A Negative Feedback Loop Maintains the Size of the Shoot Apical Stem-Cell Population
| lodish8e_ch21_22.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_22_dlap.xml | 57335f01757a2ed17f000002 |
The Root Meristem Resembles the Shoot Meristem in Structure and Function
| lodish8e_ch21_23.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_23_dlap.xml | 57335f01757a2ed17f000002 |
Key Concepts of Section 21.3 | lodish8e_ch21_24.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_24_dlap.xml | 57335f01757a2ed17f000002 |
21.4 Mechanisms of Cell Polarity and Asymmetric Cell Division
| lodish8e_ch21_25.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_25_dlap.xml | 57335f01757a2ed17f000002 |
The Intrinsic Polarity Program Depends on a Positive Feedback Loop Involving Cdc42
| lodish8e_ch21_26.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_26_dlap.xml | 57335f01757a2ed17f000002 |
Cell Polarization Before Cell Division Follows a Common Hierarchy of Steps
| lodish8e_ch21_27.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_27_dlap.xml | 57335f01757a2ed17f000002 |
Polarized Membrane Traffic Allows Yeast to Grow Asymmetrically During Mating
| lodish8e_ch21_28.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_28_dlap.xml | 57335f01757a2ed17f000002 |
The Par Proteins Direct Cell Asymmetry in the Nematode Embryo
| lodish8e_ch21_29.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_29_dlap.xml | 57335f01757a2ed17f000002 |
The Par Proteins and Other Polarity Complexes Are Involved in Epithelial-Cell Polarity
| lodish8e_ch21_30.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_30_dlap.xml | 57335f01757a2ed17f000002 |
The Planar Cell Polarity Pathway Orients Cells Within an Epithelium
| lodish8e_ch21_31.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_31_dlap.xml | 57335f01757a2ed17f000002 |
The Par Proteins Are Involved in Asymmetric Division of Stem Cells
| lodish8e_ch21_32.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_32_dlap.xml | 57335f01757a2ed17f000002 |
Key Concepts of Section 21.4 | lodish8e_ch21_33.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_33_dlap.xml | 57335f01757a2ed17f000002 |
21.5 Cell Death and Its Regulation
| lodish8e_ch21_34.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_34_dlap.xml | 57335f01757a2ed17f000002 |
Most Programmed Cell Death Occurs Through Apoptosis
| lodish8e_ch21_35.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_35_dlap.xml | 57335f01757a2ed17f000002 |
Evolutionarily Conserved Proteins Participate in the Apoptotic Pathway
| lodish8e_ch21_36.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_36_dlap.xml | 57335f01757a2ed17f000002 |
Caspases Amplify the Initial Apoptotic Signal and Destroy Key Cellular Proteins
| lodish8e_ch21_37.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_37_dlap.xml | 57335f01757a2ed17f000002 |
Neurotrophins Promote Survival of Neurons
| lodish8e_ch21_38.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_38_dlap.xml | 57335f01757a2ed17f000002 |
Mitochondria Play a Central Role in Regulation of Apoptosis in Vertebrate Cells
| lodish8e_ch21_39.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_39_dlap.xml | 57335f01757a2ed17f000002 |
The Pro-apoptotic Proteins Bax and Bak Form Pores and Holes in the Outer Mitochondrial Membrane
| lodish8e_ch21_40.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_40_dlap.xml | 57335f01757a2ed17f000002 |
Release of Cytochrome c and SMAC/DIABLO Proteins from Mitochondria Leads to Formation of the Apoptosome and Caspase Activation
| lodish8e_ch21_41.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_41_dlap.xml | 57335f01757a2ed17f000002 |
Trophic Factors Induce Inactivation of Bad, a Pro-apoptotic BH3-Only Protein
| lodish8e_ch21_42.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_42_dlap.xml | 57335f01757a2ed17f000002 |
Vertebrate Apoptosis Is Regulated by BH3-Only Pro-apoptotic Proteins That Are Activated by Environmental Stresses
| lodish8e_ch21_43.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_43_dlap.xml | 57335f01757a2ed17f000002 |
Two Types of Cell Murder Are Triggered by Tumor Necrosis Factor, Fas Ligand, and Related Death Signals
| lodish8e_ch21_44.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_44_dlap.xml | 57335f01757a2ed17f000002 |
Key Concepts of Section 21.5 | lodish8e_ch21_45.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_45_dlap.xml | 57335f01757a2ed17f000002 |
Key Terms
| lodish8e_ch21_46.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_46_dlap.xml | 57335f01757a2ed17f000002 |
Review the Concepts
| lodish8e_ch21_47.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_47_dlap.xml | 57335f01757a2ed17f000002 |
References
| lodish8e_ch21_48.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_48_dlap.xml | 57335f01757a2ed17f000002 |
Perspectives for the Future
| lodish8e_ch21_49.html | 57335f01757a2ed17f000002 |
DLAP questions | lodish8e_ch21_49_dlap.xml | 57335f01757a2ed17f000002 |