Color Atlas of GeneticsThieme, 2001 - 457 páginas |
Contenido
16 | |
26 | |
34 | |
40 | |
Recombinant | 52 |
Advances in Genetics | 84 |
Changes in | 128 |
Independent Distribution of | 136 |
Oxygen and Electron Transport | 336 |
13 | 348 |
Homeostasis | 358 |
Developmental Program for Individual | 362 |
Fundamentals | 367 |
Immune System | 368 |
Genetic Diversity Generated by Somatic | 374 |
Evolution of the Immunoglobulin | 380 |
Linkage and Recombination | 144 |
Linkage Analysis | 150 |
Distribution of Genes in a Population | 156 |
Twins | 162 |
Geographical Distribution of Genes | 168 |
Polytene Chromosomes | 174 |
Special Structure at the Ends of | 180 |
The G and RBanding Patterns of | 186 |
In Situ Hybridization | 192 |
Translocation | 198 |
Regulation and Expression | 204 |
Chromosomal Location | 249 |
The Cell Nucleus and Ribosomal | 276 |
Control of Gene Expression in Bacteria | 282 |
Odorant Receptor Gene Family | 286 |
Homeobox Genes | 292 |
Repression | 385 |
Mammalian Sex Determination | 386 |
Cellular Oncogenes | 392 |
Eukaryotic Cells | 394 |
Retinoblastoma | 398 |
Mitochondrial Genetics | 400 |
Formal Genetics | 406 |
Monogenic Diseases | 410 |
Hemoglobin | 412 |
General References | 421 |
Genomics | 430 |
Index | 442 |
CelltoCellInteractions | 443 |
Hemoglobin Genes | 447 |
Peroxisomal Diseases | 453 |
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Términos y frases comunes
Aa aa activity allele amino acids analysis antigen bacteria base pairs binding Biology cancer CBFA1 cDNA cell division cellular centromere chain chro chromatids chromo chromosome cloning codon coli complex contains crossing-over cycle defective deficiency ch deletion disease disorders DNA fragments DNA sequences domains Drosophila dystrophin embryonic enzyme eukaryotic exons Figure adapted frequency function gene loci gene product genetic genotypes growth factor helix hemoglobin hereditary heterozygotes heterozygous homologous homozygous human genome hybridization inactivation individual intracellular introns locus marker meiosis membrane ment Metabolic metaphase methylation mitochondrial mitosis Molecular molecules mosome mouse mRNA mutation normal nucleotide nucleotide base occur peptide phage phenotype plasmid polymerase polymorphism protein receptor recombination References region replication result ribosomal signal somatic Southern blot specific splicing strand structure subunits syndrome synthesis telomere Thalassemia tion transcription translocation transmembrane trisomy tumor viral virus X chromosome yeast York
Pasajes populares
Página 6 - It has not escaped our notice that the specific pairing we have postulated immediately suggests a possible copying mechanism for the genetic material.
Página 324 - Mutation in the DNA mismatch repair gene homologue hMLHl is associated with hereditary non-polyposis colon cancer.
Página 110 - Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors.
Página 274 - Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens. N. Engl. J. Med.
Página 330 - Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia. Nature 306:277, 1983 7.
Referencias a este libro
Grundlagen der Strahlungsphysik und des Strahlenschutzes Hanno Krieger Sin vista previa disponible - 2007 |
Molekularmedizinische Grundlagen von hereditären Tumorerkrankungen: mit 90 ... Detlev Ganten,Klaus Ruckpaul Sin vista previa disponible - 2001 |