куртка кожаная chromosome chromosome ch036emqnu41



Шорты Chromosome Chromosome CH036EMFPRJ8 Шорты Chromosome Chromosome CH036EMFPRJ8 Новинка

Шорты Chromosome Chromosome CH036EMFPRJ8

1970 руб.
Шорты Chromosome. Цвет: черный. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRI6 Шорты Chromosome Chromosome CH036EMFPRI6 Новинка

Шорты Chromosome Chromosome CH036EMFPRI6

1880 руб.
Шорты Chromosome. Цвет: синий. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRK1 Шорты Chromosome Chromosome CH036EMFPRK1 Новинка

Шорты Chromosome Chromosome CH036EMFPRK1

1740 руб.
Шорты Chromosome. Цвет: хаки. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRK3 Шорты Chromosome Chromosome CH036EMFPRK3 Новинка

Шорты Chromosome Chromosome CH036EMFPRK3

1640 руб.
Шорты Chromosome. Цвет: желтый. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRK4 Шорты Chromosome Chromosome CH036EMFPRK4 Новинка

Шорты Chromosome Chromosome CH036EMFPRK4

2140 руб.
Шорты Chromosome. Цвет: синий. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRJ7 Шорты Chromosome Chromosome CH036EMFPRJ7 Новинка

Шорты Chromosome Chromosome CH036EMFPRJ7

1740 руб.
Шорты Chromosome. Цвет: хаки. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRI9 Шорты Chromosome Chromosome CH036EMFPRI9 Новинка

Шорты Chromosome Chromosome CH036EMFPRI9

1740 руб.
Шорты Chromosome. Цвет: синий. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRK5 Шорты Chromosome Chromosome CH036EMFPRK5 Новинка

Шорты Chromosome Chromosome CH036EMFPRK5

1970 руб.
Шорты Chromosome. Цвет: бежевый. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRJ1 Шорты Chromosome Chromosome CH036EMFPRJ1 Новинка

Шорты Chromosome Chromosome CH036EMFPRJ1

1740 руб.
Шорты Chromosome. Цвет: бежевый. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRJ6 Шорты Chromosome Chromosome CH036EMFPRJ6 Новинка

Шорты Chromosome Chromosome CH036EMFPRJ6

1740 руб.
Шорты Chromosome. Цвет: серый. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRJ2 Шорты Chromosome Chromosome CH036EMFPRJ2 Новинка

Шорты Chromosome Chromosome CH036EMFPRJ2

1740 руб.
Шорты Chromosome. Цвет: синий. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRJ4 Шорты Chromosome Chromosome CH036EMFPRJ4 Новинка

Шорты Chromosome Chromosome CH036EMFPRJ4

1740 руб.
Шорты Chromosome. Цвет: серый. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRI7 Шорты Chromosome Chromosome CH036EMFPRI7 Новинка

Шорты Chromosome Chromosome CH036EMFPRI7

1730 руб.
Шорты Chromosome. Цвет: серый. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRJ3 Шорты Chromosome Chromosome CH036EMFPRJ3 Новинка

Шорты Chromosome Chromosome CH036EMFPRJ3

2090 руб.
Шорты Chromosome. Цвет: хаки. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRJ0 Шорты Chromosome Chromosome CH036EMFPRJ0 Новинка

Шорты Chromosome Chromosome CH036EMFPRJ0

1740 руб.
Шорты Chromosome. Цвет: хаки. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRK2 Шорты Chromosome Chromosome CH036EMFPRK2 Новинка

Шорты Chromosome Chromosome CH036EMFPRK2

2070 руб.
Шорты Chromosome. Цвет: бежевый. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRK0 Шорты Chromosome Chromosome CH036EMFPRK0 Новинка

Шорты Chromosome Chromosome CH036EMFPRK0

1740 руб.
Шорты Chromosome. Цвет: серый. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRJ5 Шорты Chromosome Chromosome CH036EMFPRJ5 Новинка

Шорты Chromosome Chromosome CH036EMFPRJ5

1740 руб.
Шорты Chromosome. Цвет: синий. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRI8 Шорты Chromosome Chromosome CH036EMFPRI8 Новинка

Шорты Chromosome Chromosome CH036EMFPRI8

1440 руб.
Шорты Chromosome. Цвет: зеленый. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Шорты Chromosome Chromosome CH036EMFPRJ9 Шорты Chromosome Chromosome CH036EMFPRJ9 Новинка

Шорты Chromosome Chromosome CH036EMFPRJ9

2440 руб.
Шорты Chromosome. Цвет: синий. Сезон: Осень-зима 2019/2020. С бесплатной доставкой и примеркой на Lamoda.
Kurt Benirschke, Tao C. Hsu Chromosome Atlas. Fish, Amphibians, Reptiles and Birds: Volume 1 Kurt Benirschke, Tao C. Hsu Chromosome Atlas. Fish, Amphibians, Reptiles and Birds: Volume 1 Новинка

Kurt Benirschke, Tao C. Hsu Chromosome Atlas. Fish, Amphibians, Reptiles and Birds: Volume 1

9052 руб.
Книга "Chromosome Atlas. Fish, Amphibians, Reptiles and Birds: Volume 1".
Samuel Rajendran Raphael Chromosome Segregation Defects of Adult Teleost Fish Brain Samuel Rajendran Raphael Chromosome Segregation Defects of Adult Teleost Fish Brain Новинка

Samuel Rajendran Raphael Chromosome Segregation Defects of Adult Teleost Fish Brain

3944 руб.
In contrast to most other vertebrates,teleost fish exhibit an unparalleled capacity to generate stem cells in both the intact and the injured adult brain.My research is focused on the occurrence, the extent and the fate of aneuploid cells (genome-modified individual cells characterized by the loss or gain of whole chromosomes) generated in the teleostean brain. Aneuploidy arises through various chromosome segregation defects during the mitotic divisions of newly-generated cells in the adult brain. Aneuploidy is observed in ~80% of the newly-generated stem cells of the adult brain,but occurs at a very low rate in liver tissue, as shown by metaphase chromosome spreads and flow-cytometric DNA content analysis. The mitotic machinery of adult brain cells was examined for chromosome segregation defects which showed lagging chromosomes at metaphase and anaphase, as well as micronuclei and anaphase bridges,in the intact adult brain. In conclusion,my research demonstrates the evidence of the generation and maintenance of aneuploid cells in the adult fish brain that arise through chromosome missegregation which is a widespread phenomenon in the teleostean central nervous system.
Sarah Jacobs Deciphering Human Chromosome 16. Index to the Report Sarah Jacobs Deciphering Human Chromosome 16. Index to the Report Новинка

Sarah Jacobs Deciphering Human Chromosome 16. Index to the Report

4014 руб.
Deciphering Human Chromosome 16: We Report Here, and Deciphering Human Chromosome 16: Index to the Report, by Sarah Jacobs, use text in a visual way to document the ethical, economic, political and philosophical polemics associated with mapping the human genome. The Report is an ebook which contains links to over 240 websites collected in the months following publication in the journal Nature of ¿The sequence and analysis of duplication-rich human chromosome 16¿ ( Vol. 432. December 2004). Its contents change over time as the websites change, migrate or disappear. It is available as a FREE DOWNLOAD from the publisher at www.informationasmaterial.com .The Index sets fragments collected from the websites against the background of the earlier draft sequence originally published by Project Gutenberg. The solid physicality of the Index contrasts with the ever changing Report although vagaries of the printing process ensure that each copy of the Index is unique.
Subhoshmita Mondal Histone acetylation and Histone methylation Subhoshmita Mondal Histone acetylation and Histone methylation Новинка

Subhoshmita Mondal Histone acetylation and Histone methylation

3212 руб.
Acetylation of explicit residues of histones is associated with gene activity and may play elementary role in transcriptional regulation. Bromodomains, motifs found in several eukaryotic transcription factors, exclusively interact with acetyl-lysines in histones. p300 is functionally conserved transcriptional coactivators for various transcription factors and have intrinsic acetyltransferase activity. The covalent alteration of histone tails has regulatory roles in various nuclear processes, such as organization of transcription and mitotic chromosome condensation. Among the different groups of enzymes identified to catalyze the covalent modification, the most topical additions are the histone methyltransferases (HMTases), whose functions are now being characterized. G9A is a novel mammalian HMTase that prefer lysine. Specific chromosome translocations commonly found in human leukemia engross rearrangements of genes which are implicated in the regulation of hematopoiesis. Further, the detail shows that the chromosome translocations often results in the expression of gene products.
Margaret Barch J. The AGT Cytogenetics Laboratory Manual Margaret Barch J. The AGT Cytogenetics Laboratory Manual Новинка

Margaret Barch J. The AGT Cytogenetics Laboratory Manual

18052.97 руб.
Cytogenetics is the study of chromosome morphology, structure, pathology, function, and behavior. The field has evolved to embrace molecular cytogenetic changes, now termed cytogenomics. Cytogeneticists utilize an assortment of procedures to investigate the full complement of chromosomes and/or a targeted region within a specific chromosome in metaphase or interphase. Tools include routine analysis of G-banded chromosomes, specialized stains that address specific chromosomal structures, and molecular probes, such as fluorescence in situ hybridization (FISH) and chromosome microarray analysis, which employ a variety of methods to highlight a region as small as a single, specific genetic sequence under investigation. The AGT Cytogenetics Laboratory Manual, Fourth Edition offers a comprehensive description of the diagnostic tests offered by the clinical laboratory and explains the science behind them. One of the most valuable assets is its rich compilation of laboratory-tested protocols currently being used in leading laboratories, along with practical advice for nearly every area of interest to cytogeneticists. In addition to covering essential topics that have been the backbone of cytogenetics for over 60 years, such as the basic components of a cell, use of a microscope, human tissue processing for cytogenetic analysis (prenatal, constitutional, and neoplastic), laboratory safety, and the mechanisms behind chromosome rearrangement and aneuploidy, this edition introduces new and expanded chapters by experts in the field. Some of these new topics include a unique collection of chromosome heteromorphisms; clinical examples of genomic imprinting; an example-driven overview of chromosomal microarray; mathematics specifically geared for the cytogeneticist; usage of ISCN’s cytogenetic language to describe chromosome changes; tips for laboratory management; examples of laboratory information systems; a collection of internet and library resources; and a special chapter on animal chromosomes for the research and zoo cytogeneticist. The range of topics is thus broad yet comprehensive, offering the student a resource that teaches the procedures performed in the cytogenetics laboratory environment, and the laboratory professional with a peer-reviewed reference that explores the basis of each of these procedures. This makes it a useful resource for researchers, clinicians, and lab professionals, as well as students in a university or medical school setting.
Todd Eckdahl Hemophilia. The Royal Disease Todd Eckdahl Hemophilia. The Royal Disease Новинка

Todd Eckdahl Hemophilia. The Royal Disease

6602 руб.
Hemophilia is a genetic disease that impairs the normal process of blood clotting and results in uncontrolled external and internal bleeding. The reader of this book will learn how a diagnosis of hemophilia is made by blood clot­ting tests and measurements of clotting factor levels in blood. The book describes how hemophilia A and B are caused by mutations in genes that encode clotting factor VIII and clotting factor IX, respectively, both of which are carried on the X chromosome. As a result, almost all children born with hemophilia A and B are boys. Hemophilia C is caused by mutations in the clotting factor XI gene on chromosome 4, and occurs in males and females with equal frequency. The author details the use of factor replacement therapy to treat hemophilia, and evaluates the prospects for curing hemophilia through gene therapy and genome editing.
B.C. Blackman The third-chromosome group of mutant characters of Drosophila melanogaster B.C. Blackman The third-chromosome group of mutant characters of Drosophila melanogaster Новинка

B.C. Blackman The third-chromosome group of mutant characters of Drosophila melanogaster

1275 руб.
Эта книга — репринт оригинального издания 1923 года, созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Khamsa Parveen, Israr Ahmad Mapping of RAPD primers on chromosome 2A of common wheat Khamsa Parveen, Israr Ahmad Mapping of RAPD primers on chromosome 2A of common wheat Новинка

Khamsa Parveen, Israr Ahmad Mapping of RAPD primers on chromosome 2A of common wheat

8364 руб.
Common (bread) wheat is an allohexaploid species (Triticum aestivum L.) with 3 compensating genomes AABBDD (2n=6x=42 chromosomes). Traditionally genetic and physical mapping in this most important cereal crop has been based on molecular markers (RFLPs, PCR, Insitu hubridisation etc). The recent development in producing deletion lines of common wheat (using Aegilops cylindricum genome) has revolutionized the physical mapping of wheat chromosomes. During present study, deletion lines of chromosomes 2A of common wheat were used to identify RAPD (Randomly Amplified Polymorphic DNA) based molecular markers specific for short and/or long arm of chromosome 2A. Out of the 7 RAPD primers used, OPA-07 showed useful polymorphism. By comparing the C-banding karyotype of the deletion lines, it is inferred that the primer (OPA-07) anneals to the distal half of the long arm of chromosome 2A.
Ali Al-Marzoqi,Mohammed Sabri Abdul-Razzaq and Mohammed Aboud Muhsin Male Infertility: Molecular Approaches to Diagnosis Ali Al-Marzoqi,Mohammed Sabri Abdul-Razzaq and Mohammed Aboud Muhsin Male Infertility: Molecular Approaches to Diagnosis Новинка

Ali Al-Marzoqi,Mohammed Sabri Abdul-Razzaq and Mohammed Aboud Muhsin Male Infertility: Molecular Approaches to Diagnosis

4755 руб.
Male infertility is a multifactorial syndrome encompassing a wide variety of ‎disorders. In more than half of infertile men, the cause of their infertility is ‎mysterious (idiopathic) and could be congenital or acquired.‎ The causes are known in less than half of these cases, out of which genetic or ‎inherited disease and specific abnormalities in the Y chromosome are major ‎factors. About 10-20 percent of males presenting without sperm in the ‎ejaculate carry a deletion of the Y chromosome Male genetic factor of infertility accounts for about half the cases of couple ‎infertility and in around 50% of cases its etiology remains unknown. Molecular ‎genetic techniques have unveiled a number of etiopathogenetic factors, ‎including microdeletions of the Yq. Y chromosome microdeletions removing ‎the AZoospermia Factor (AZF) regions are the most frequent molecular genetic ‎causes of oligo/azoospermia).‎
Sajiro Makino An atlas of the chromosome numbers in animals Sajiro Makino An atlas of the chromosome numbers in animals Новинка

Sajiro Makino An atlas of the chromosome numbers in animals

903 руб.
Эта книга — репринт оригинального издания (издательство "Ames, Iowa State College Press", 1951 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Кожаная куртка Gilman One Кожаная куртка Кожаная куртка Gilman One Кожаная куртка Новинка

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Cytogenetics is the study of chromosome morphology, structure, pathology, function, and behavior. The field has evolved to embrace molecular cytogenetic changes, now termed cytogenomics. Cytogeneticists utilize an assortment of procedures to investigate the full complement of chromosomes and/or a targeted region within a specific chromosome in metaphase or interphase. Tools include routine analysis of G-banded chromosomes, specialized stains that address specific chromosomal structures, and molecular probes, such as fluorescence in situ hybridization (FISH) and chromosome microarray analysis, which employ a variety of methods to highlight a region as small as a single, specific genetic sequence under investigation. The AGT Cytogenetics Laboratory Manual, Fourth Edition offers a comprehensive description of the diagnostic tests offered by the clinical laboratory and explains the science behind them. One of the most valuable assets is its rich compilation of laboratory-tested protocols currently being used in leading laboratories, along with practical advice for nearly every area of interest to cytogeneticists. In addition to covering essential topics that have been the backbone of cytogenetics for over 60 years, such as the basic components of a cell, use of a microscope, human tissue processing for cytogenetic analysis (prenatal, constitutional, and neoplastic), laboratory safety, and the mechanisms behind chromosome rearrangement and aneuploidy, this edition introduces new and expanded chapters by experts in the field. Some of these new topics include a unique collection of chromosome heteromorphisms; clinical examples of genomic imprinting; an example-driven overview of chromosomal microarray; mathematics specifically geared for the cytogeneticist; usage of ISCN’s cytogenetic language to describe chromosome changes; tips for laboratory management; examples of laboratory information systems; a collection of internet and library resources; and a special chapter on animal chromosomes for the research and zoo cytogeneticist. The range of topics is thus broad yet comprehensive, offering the student a resource that teaches the procedures performed in the cytogenetics laboratory environment, and the laboratory professional with a peer-reviewed reference that explores the basis of each of these procedures. This makes it a useful resource for researchers, clinicians, and lab professionals, as well as students in a university or medical school setting.
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