Primary Immunodeficiency Diseases
A Molecular & Cellular Approach
Second Edition
ISBN13: 9780195147742ISBN10: 019514774X
Hardback,
776 pages
Aug 2006,
In Stock
Price:
$125.00 (05)Table of Contents
1.
Genetically Determined Immunodeficiency Diseases: A Perspective
,
2.
Genetic Principles and Technologies in the Study of Immune Disorders
,
3.
Mammalian Hematopoietic Development and Function
,
4.
T-Cell Development
,
5.
Molecular Mechanisms Guiding B-Cell Development
,
6.
Signal Transduction by T and B Lymphocyte Antigen Receptors
,
7.
Regulation of Lymphocyte Responses, Cell Trafficking and Lymphoid Organ Development
,
8.
The Phagocytic System
,
Part II Syndromes.
9.
X-linked Severe Combined Immunodeficiency
,
10.
Autosomal Recessive SCID Due to Defects of Cytokine Signaling Pathways
,
11.
Recombination Defects
,
12.
Immunodeficiency Due to Defects of Purine Metabolism
,
13.
CD45 Deficiency
,
14.
SCID Due to Defects in T-Cell-Receptor-Associated Protein Kinases
,
15.
Human Interleukin-2 Receptor Alpha Deficiency
,
16.
CD3 and CD8 Deficiencies
,
17.
Molecular Basis of Major Histocompatibility Complex Class II Deficiency
,
18.
Peptide Transporter Defects in HLA Class I Deficiency
,
19.
CD40, CD40 Ligand, and theHyper-IgM Syndrome
,
20.
Autosomal Hyper-IgM Syndromes Caused by an Intrinsic B-cell Defect
,
21.
X-linked Agammaglobulinemia: A Defect of Btk Tyrosine Kinase
,
22.
Autosomal Recessive Agammaglobulinemia
,
23.
Genetic Approach to Common Variable Immunodeficiency and IgA Deficiency
,
24.
Defects in Apoptosis with Autoimmune Manifestations
,
25.
Autoimmune Polyendocrinopathy, Candidiasis and Ectodermal Dystrophy (APECED)
,
26.
Immune Dysregulation, Polyendocrinopathy, Enteropathy; X-linked (IPEX)
,
27.
Periodic Fever Syndromes
,
28.
Inherited Disorders of the Interleukin-12/23-Interferon Gamma Axis
,
29.
Ataxia-Telangiectasia
,
30.
DNA Breakage and Repair Associated Syndromes Other Than Ataxia-Telangiectasia
,
31.
The Wiskott-Aldrich Syndrome
,
32.
X-linked Lymphoproliferative Disease (XLP) due to Defects of SH2D1A
,
33.
DiGeorge Syndrome: A Chromosome 22q11.2 Deletion Syndrome
,
34.
Hyper IgE Recurrent Infection Syndromes
,
35.
Immunodeficiency with Centromere Instability and Facial Anomalies
,
36.
Immunodeficiencies with Associated Manifestations of Skin, Hair, Teeth, and Skeleton
,
37.
Chronic Granulomatous Disease
,
38.
Cell Adhesion and Leukocyte Adhesion Defects
,
39.
Cyclic and Congenital Neutropenia Due to Defects in Neutrophil Elastase
,
40.
Chediak-Higashi Syndrome
,
41.
Inherited Hemophagocytic Syndromes
,
42.
Genetically Determined Deficiencies of the Complement System
,
Part III Assessment and Treatment.
43.
Assessment of the Immune System
,
44.
Genetic Aspects of Primary Immunodeficiencies
,
45.
Immunodeficiency Information Systems
,
46.
Conventional Therapy of Primary Immunodeficiency Diseases
,
47.
Bone Marrow Transplantation for Primary Immunodeficiency Diseases
,
48.
Gene Therapy
,
