|
|
|
|
LEADER |
00000cam a2200000Mi 4500 |
001 |
SCIDIR_on1005613269 |
003 |
OCoLC |
005 |
20231120010222.0 |
006 |
m o d |
007 |
cr |n|---||||| |
008 |
171007s2017 mou ob 001 0 eng d |
040 |
|
|
|a EBLCP
|b eng
|e pn
|c EBLCP
|d OCLCQ
|d YDX
|d N$T
|d OPELS
|d IDEBK
|d MERUC
|d MERER
|d OCLCF
|d UPM
|d TXM
|d NLE
|d GZM
|d D6H
|d GZM
|d U3W
|d LQU
|d OCLCQ
|d S2H
|d OCLCO
|d OCLCQ
|d OCLCO
|d COM
|d OCLCQ
|d CASUM
|d SFB
|
019 |
|
|
|a 1005138897
|a 1005190661
|a 1012827255
|a 1012893254
|a 1013783942
|a 1013905581
|a 1014351871
|a 1017715763
|a 1019997170
|a 1022756743
|a 1027161767
|a 1029446211
|a 1105193947
|a 1105573109
|
020 |
|
|
|a 9780128092606
|
020 |
|
|
|a 0128092602
|
020 |
|
|
|z 9780128092521
|
020 |
|
|
|z 0128092521
|
035 |
|
|
|a (OCoLC)1005613269
|z (OCoLC)1005138897
|z (OCoLC)1005190661
|z (OCoLC)1012827255
|z (OCoLC)1012893254
|z (OCoLC)1013783942
|z (OCoLC)1013905581
|z (OCoLC)1014351871
|z (OCoLC)1017715763
|z (OCoLC)1019997170
|z (OCoLC)1022756743
|z (OCoLC)1027161767
|z (OCoLC)1029446211
|z (OCoLC)1105193947
|z (OCoLC)1105573109
|
050 |
|
4 |
|a RA1224.4.M86
|b M89 2018
|
072 |
|
7 |
|a SCI
|x 027000
|2 bisacsh
|
082 |
0 |
4 |
|a 616/.042
|2 23
|
100 |
1 |
|
|a Kumar, Ashutosh.
|
245 |
1 |
0 |
|a Mutagenicity.
|
264 |
|
1 |
|a Saint Louis :
|b Elsevier Science,
|c 2017.
|
300 |
|
|
|a 1 online resource (352 pages)
|
336 |
|
|
|a text
|b txt
|2 rdacontent
|
337 |
|
|
|a computer
|b c
|2 rdamedia
|
338 |
|
|
|a online resource
|b cr
|2 rdacarrier
|
588 |
0 |
|
|a Print version record.
|
500 |
|
|
|a ACKNOWLEDGMENT.
|
504 |
|
|
|a Includes bibliographical references and index.
|
505 |
0 |
|
|a Front Cover; MUTAGENICITY: ASSAYS AND APPLICATIONS ; MUTAGENICITY: ASSAYS AND APPLICATIONS ; Copyright; CONTENTS; LIST OF CONTRIBUTORS; FOREWORD; PREFACE; ACKNOWLEDGMENTS; 1 -- Mutagenesis, Genetic Disorders and Diseases; 1. INTRODUCTION; 2. MUTAGENS; 2.1 Physical Mutagens; 2.2 Chemical Mutagens; 2.3 Biological Mutagens; 3. MUTATIONS; 3.1 Break in Homologous Chromosome; 3.2 Breaks in Nonhomologous Chromosomes; 4. DNA DAMAGE RESPONSE AND REPAIR; 5. DNA REPAIR PATHWAYS; 5.1 Direct Repair; 5.2 Single-Strand Break Repair; 5.2.1 Base Excision Repair; 5.2.2 Nucleotide Excision Repair.
|
505 |
8 |
|
|a 5.2.3 Mismatch Repair5.2.4 Interstrand Cross-Linking Repair; 5.3 Double-Strand DNA Breaks Repair; 6. GENETIC DISORDERS AND DISEASES; 6.1 Noonan Syndrome (OMIM 163950); 6.2 Costello Syndrome (OMIM 218040); 6.3 Cardio-Facio-Cutaneous Syndrome (OMIM 115150); 6.4 Hirschsprung Disease (OMIM 142623); 6.5 Hutchinsons-Gilford Progeria Syndrome (OMIM 176670); 6.6 Cancer; 6.7 Parkinson Disease (OMIM 168600); 6.8 Alzheimer Disease (OMIM 104300); 6.9 Ataxia-Telangiectasia (OMIM 208900); 6.10 Seckel Syndrome (OMIM 210600); 6.11 Cockayne Syndrome (OMIM 216400); 6.12 Fanconi Anemia (OMIM 227650).
|
505 |
8 |
|
|a 6.13 Bloom Syndrome (OMIM 210900)6.14 Werner Syndrome (OMIM 277700); 6.15 Xeroderma Pigmentosum (OMIM 278700); 7. SUMMARY; ACKNOWLEDGMENT; REFERENCES; 2 -- Detection of Mutation in Prokaryotic Cells; 1. INTRODUCTION; 2. MATERIALS AND METHODOLOGIES; 2.1 Preparation of Mammalian Liver S9 Fraction; 2.1.1 Induction of Rat Liver Enzymes; 2.1.2 Removal of Liver From Rats; 2.1.3 Preparation of Liver S9 Fraction; 2.2 Preparation of Reagents; 2.2.1 Vogel-Bonner (VB Salt) Solution (50�); 2.2.2 Glucose Solution (10% W/V); 2.2.3 Minimal Glucose Agar Plates; 2.2.4 Histidine-Biotin Solution (0.5mM).
|
505 |
8 |
|
|a 2.2.5 Top Agar Supplemented With Histidine-Biotin Solution2.2.6 Buffers for Metabolic Activation; 2.2.6.1 Sodium Phosphate Buffer (0.1mM, pH 7.4); 2.2.6.2 To Activate the NADP Regenerating System in Presence of Liver S9 Fraction; 2.3 Methodology; 2.3.1 Culture Preparation; 2.3.2 Genetic Analysis of the Tester Strains; 2.3.3 Histidine and Biotin (his, bio) or Tryptophan (trp) Dependence; 2.3.4 rfa (Deep Rough) Mutation; 2.3.5 Treatment of Culture; 2.3.6 Plating of Treated Culture; 3. RESULT EVALUATION; 4. RESULT INTERPRETATION; 5. EXPERIMENTAL DESIGN; 6. PRECAUTION; REFERENCES; FURTHER READING.
|
505 |
8 |
|
|a 3 -- Detection of Gene Mutation in Cultured Mammalian Cells1. INTRODUCTION; 2. PCR-BASED MUTATION DETECTION; 3. DETECTION OF MUTATIONS BY DENATURING GRADIENT GEL ELECTROPHORESIS; 4. SINGLE-STRAND CONFORMATION POLYMORPHISM; 5. HETERODUPLEX ANALYSIS; 6. MICROARRAY; 7. ARRAYED PRIMER EXTENSION TECHNOLOGY; 8. SINGLE-BASE EXTENSION-TAGS TECHNOLOGY; 9. ATOMIC FORCE MICROSCOPY; 10. FLUORESCENCE IN SITU HYBRIDIZATION; 11. DNA SEQUENCING; 12. KARYOTYPING; 13. HYPOXANTHINE PHOSPHORIBOSYL TRANSFERASE, THYMIDINE KINASE, AND XANTHINE-GUANINE PHOSPHORIBOSYL TRANSFERASE GENE MUTATION DET ... ; 14. CONCLUSION.
|
650 |
|
0 |
|a Mutagenicity testing.
|
650 |
|
2 |
|a Mutagenicity Tests
|0 (DNLM)D009152
|
650 |
|
6 |
|a Mutag�enicit�e.
|0 (CaQQLa)201-0244933
|
650 |
|
7 |
|a SCIENCE
|x Life Sciences
|x Evolution.
|2 bisacsh
|
650 |
|
7 |
|a Mutagenicity testing.
|2 fast
|0 (OCoLC)fst01031140
|
655 |
|
0 |
|a Electronic books.
|
655 |
|
4 |
|a Internet Resources.
|
700 |
1 |
|
|a Dobrovolsky, Vasily N.
|
700 |
1 |
|
|a Dhawan, Alok.
|
700 |
1 |
|
|a Shanker, Rishi.
|
776 |
0 |
8 |
|i Print version:
|a Kumar, Ashutosh.
|t Mutagenicity: Assays and Applications.
|d Saint Louis : Elsevier Science, �2017
|z 9780128092521
|
856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/book/9780128092521
|z Texto completo
|