Overview

The FactsBooks Series has established itself as the best source of easily-accessible and accurate facts about protein groups. Described as a growing series of excellent manuals by Molecular Medicine Today, and essential works of reference by Trends in Biochemical Sciences, the FactsBooks have become the most popular comprehensive data resources available. Using an easy-to-follow format and drawing from meticulous research, the Factsbooks will keep you up-to-date with the latest advances in structure, amino acid sequences, physicochemical properties, and biological activity. The Gene Knockout FactsBook contains entries, grouped into subject disciplines, covering immunology, neurobiology, development, cancer, and other knockouts. It describes more than 600 gene knockouts described and listed in alphabetical order for easy reference.

Full Product Details

Author:   Tak W. Mak (The Campbell Family Institute for Breast Cancer Research, Ontario, Canada)
Publisher:   Elsevier Science Publishing Co Inc
Imprint:   Academic Press Inc
Volume:   v. 1-2
Dimensions:   Width: 15.20cm , Height: 4.80cm , Length: 23.50cm
Weight:   1.800kg
ISBN:  

9780124660441

ISBN 10:   0124660444
Pages:   1140
Publication Date:   26 October 1998
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Unknown
Availability:   Out of stock  

Table of Contents

5-HT1B. 5-HT2c. ACE. ACP5. AROSIN. ACTIVIN REC TYPE II. ACTIVIN/INHIBIN BETA B. ACTIVIN/INHIBIN BETA A. Ada. Ae1. AGA. AGT. AGTR1A. AGTR2. AHR. Alox12p. Alpha Galactosidase. Alpha Lactalbumin. Alpha-Globin. Alpha-Inhibin. Alx-4. AML-1. ANP. Ant1. AP-2. Apo A-1. ApoA-II. ApoB. Apobec-1. ApoC-I. ApoC-III. ApoE. APP. APRT. ARNT. ASGPR2. Asmase. ASS. ATF-2. B7.1. B7.2. Bax. Bcl-x. Bcl2. Bcl6. Bcr. BDNF. Beta C Chain. Beta IL-3. Beta-2 Microglobulin. BETA-CATENIN. BF-1. BF-2. BK2R. BMP1. BMP2. BMP4. BMP7. Bmp8a. Bmp8b. BMPR. Brca1. Brca2. C-erb Aalpha. C-kit. C-mpl. C-rel. C-ROS. C/EBP a. C/EBP beta (NF-IL6). C/EBP delta. C3. C5aR. Calbindin. Calretinin. CART HOMEOPROT1. Casein-Beta. CBFA1. Cbfb. CBS. CCHB1. CCR2. CCR5. CD11a. CD11Bcd14. Cd19. CD1d1. CD22. CD23. CD24. CD28. CD3 Epsilon. CD3 Eta. CD3 Zeta. CD3 Zeta/Eta. CD30. CD31. CD34. CD4. CD40. CD40L. CD43. CD44. CD45. CD5. CD79a. CD8 Alpha. CD8 Beta. CD81. Cdk5. CDX1. Cdx2. CEL. CFTR. CGT. CHK/HYL. Ciap1. CIS. CNTF. CNTFR-Alpha. Collagen III. Collagen V. Complement Factor B. Connexin 26. Connexin 32. Connexin 37. Connexin 40. Cox-2. CPP32. CRABPI. CRABPII. CREB. CREM. CRH. CTLA-4. Cyclin A2. Cyclin D2. CYP1A2. CYP1B1. CYP2E1. CYP7A1. Cytokeratin 10. D1. D3. Dad1. DAG1. DESMIN. DLL1. DNA Ligase I. DNA METHYLTRANSFERASE. DSG3. E-CADHERIN. E-Selectin. E2-2. E2A. E2F-1. EAAC-1. EAP. EBF. ECE-1. ECE-2. EDNRA. EDNRB. EGFR. EKLF. Emr1. EMX1. EMX2. ENDOTHELIN-1. ENDOTHRLIN-3. ENGRAILED-1. ENOS. EphA8. EphB2. Epo. EpoR. ER. ErbB2. ErbB4. ERCC-1. ET-2. ETS2. EVX2. Fac. Factor IX. FADD. FAH. FAK. Fas. Fc Epsilon R Alpha. Fc Gamma R IIB. Fc Gamma R III. FcR Gamma. FGF3. FGF4. FGF5. FGF7. FGFR1. Fgr. Fibrinogen Alpha. Fibrinogen Gamma. FIBRONECTIN. FKH6. FLAP. Fli-1. FLK. FLT1. FOLLISTATIN. Fosb. FucTVII. FUR. FYN. G Alpha 13. G Alpha I2. G Alpha I3. G Alpha o. G Alpha q. G-CSF. GABA(A)-R-Alpha6. GABA(A)-R-Beta3. Galectin-1. GalTase. GAP. GAP43. GATA-1. GATA-2. GATA-4. GDF9. GDNF. GFAP. GK. GLI2. GLP-1R. Glucocerebrosidase. GluR2. GLUT4. Glycoprotein Alpha Subunit. GOOSECOID. Gp130. Gp91 Phox. GR. Granzyme A. Granzyme B. GRF1. GSHPx-1. Gz Alpha. H-2A Alpha. H-2A Beta. H19. H1R. H2-M Alpha. Hck. HDH. HEB. HePTP. HES1. Hexa. Hexb. HGF. HL. HLX. HNF 3 Gamma. HNF-3BETA. HNF-4. HO-1. HO-2. HNF-3BETA. HNF-4. HO-1. HO-2. HOXA1. HOXA1 3RARE. HOXA10. HOXA11. HOXA13. HOXA2. HOXA3. HOXA4. HOXA5. HOXA6. HOXA7. HOXA9. HOXB1. HOXB2. HOXB3. HOXB4. HOXB5. HOXB6. HOXB7. HOXB8. HOXB9. HOXC10. HOXC12. HOXC13. HOXC4. HOXC5. HOXC8. HOXC9. HOXD10. HOXD11. HOXD12. HOXD13. HOXD3. HOXD4. HOXD8. HOXD9. HPRT. HS1. HS2. HS3. IAP. ICAM-1. ICAM-2. ICE. ICSBP. IFN Gamma. IFN Gamma R. IFN Type 1R. IgD. IgE. IGF1. IGF1R. IGF2. IGF2R. IGFBP2. Igh iE. Igh-J. Igh-J + iE. Igk iE. Igk-C. IgM Transmembrane. Ikapa B Alpha. Ikaros. IL-1 Beta. IL-11 Ra 1. IL-12 Alpha. IL-12 Beta. IL-1R1. IL-1ra. IL-2. IL-2R Alpha. IL-2R Beta. IL-2R Gamma. IL-4. IL-5. IL-6. IL-7. IL-7R. IL-8R. INOS. INTEGRIN ALPHA1. INTEGRIN ALPHA3. INTEGRIN ALPHA4. INTEGRIN ALPHA5. INTEGRIN ALPHA6. INTEGRIN ALPHA9. INTEGRIN ALPHAV. Integrin Beta 3. Integrin Beta 6. INTEGRIN BETA 1. Invariant Chain. IP3R1. IR. IRF-1. IRF-2. IRF-4. IRS-1. Isl-1. ITF. JAK3. Keratin 14. Krox-20. Ku80. Kv3.1. Kvbeta 1. L-12LO. L-selectin. LAG3. Lambda 5. LCAT. Lck. LDLR. LEF-1. Leukotriene. LIF. LIFR-beta. LIM1. LMO2. LMP-2. LMP-7. LPL. LRP. LTA4 Hydrolase. Ly-6A. Lyl-1. Lymphotoxin Beta. Lyn. M-CK. Mad1. MAM. MAOA. MAP1b. MASH1. MASH2. Matrilysin. MDR1A. MDR1B. MDR2. Megalin. MEL-18. MET. Mgat1. Mgat3. MGluR1. MGluR2. MGluR4. MGluR5. MGluR6. MHOX. MIP-1 Alpha. MIS. MLH1. MLL. MPR46. MPV17. MR. MRP. MSH2. MSR-A. MT I and MT II. MTF-1. Mu Opiate Receptor. MUG1. Musk. MYB. MYF5. MYF6. MYOD. MYOGENIN. N-CADHERIN. N-myc. NCAM. NEP. Neuregulin. NF-Atp. NF-kappa B (p50). NFATC1. NFKB2. NGF. NKX2-5. NMDAR-1. NMDAR-2A. NMDAR-2B. NMDAR-2C. NNOS. NOTCH1. NRF-2. NT3. NT4. NURR1. OAT. OBF-1. Oct-2. OMP. Otx1. OTX2. P-Cadherin. P-Selectin. P18NF-E2. P38 Kinase. P45NF-E2. P47 Phox. P48. P53. P75NGFR. PAX2. PAX4. PAX7. PDGF Beta-R. PDGF-A. PDGF-B. PDX1. Perforin. Phox2a. PKR. PLAKOGLOBIN. PLB. PLC Gamma 1. PLG. PLP. PMS2. PPAR Alpha. PPCA. PR. PRESENILIN 1. PRLR. PrP. PS2. PTH-PTHrP. PTHrP. PU.1. RAG-1. RAG-2. RAP. RAR ALPHA. RAR BETA. RAR GAMMA. Rb. RBP-J KAPPA. Rel A. Rel B. RXR ALPHA. RXR BETA. RXR GAMMA. RyR1. RyR3. Sc1. ScCKmit. SDF-1/PBSF. SEK1. Sez-6. SF-1. SHH. SHP-2. SLN1. Smad4. SOD1. SOD2. SOD3. SP-A. SP-B. SPALT. SRD5A1. Srm. STAR. Stat3. Stat1. STAT4. STAT5a. STAT6. STK. Switch Gamma 1. Syk. Synaptotamin 1. T-PA. TAL-1. TAP-1. Tau. Tcf-1. TCP 10 bt. TCR Alpha.

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Author Information

Tak W. Mak received his Ph.D. in biochemistry in 1972 from the University of Alberta after completing undergraduate and graduate studies at the University of Wisconsin. In 1997, he was appointed Professor at the University of Toronto. He is also Vice President of Research/Director of the The Campbell Family Institute for Breast Cancer Research. He has co-authored over 350 scientific papers and is a member on numerous advisory boards of scientific journals and medical centers.Mak is best recognized for the discovery of the T-cell receptor in 1984, and is a leader in the development of knockout mice for the analysis of gene function. He has also made significant contributions in the areas of virology, immunology, genetics, molecular signaling, and cancer biology. His laboratory has ongoing efforts to understand the changes in gene function that occur when cells become cancerous, cell signaling pathways, and the role of apoptosis in development and disease.

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