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Titlebook: Genetics and Genomics for the Cardiologist; Gian Antonio Danieli Book 2002 Springer Science+Business Media New York 2002 Chromosom.DNA.car

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發(fā)表于 2025-3-21 19:59:49 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Genetics and Genomics for the Cardiologist
編輯Gian Antonio Danieli
視頻videohttp://file.papertrans.cn/383/382694/382694.mp4
叢書名稱Basic Science for the Cardiologist
圖書封面Titlebook: Genetics and Genomics for the Cardiologist;  Gian Antonio Danieli Book 2002 Springer Science+Business Media New York 2002 Chromosom.DNA.car
描述.Genetics and Genomics for the Cardiologist. is a concise, but comprehensive volume for the clinical cardiologist or medical student interested in learning how molecular genetics is now being applied to prevention and treatment of heart diseases, from DNA tests to pharmacogenomics and gene-based therapeutics. The volume, written in a plain language, contains detailed figures. A rich glossary, three appendices, many references and several URLs provide additional sources of information.
出版日期Book 2002
關(guān)鍵詞Chromosom; DNA; cardiovascular; genes; genetics; hypertension; transgenic animals
版次1
doihttps://doi.org/10.1007/978-1-4615-1025-3
isbn_softcover978-1-4613-5357-7
isbn_ebook978-1-4615-1025-3Series ISSN 1566-0753
issn_series 1566-0753
copyrightSpringer Science+Business Media New York 2002
The information of publication is updating

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From Genome to Clinical Phenotype,every single day), possibly with the exception of those (the so-called “housekeeping genes”) coding for products involved in general functions of all cell types. Many genes produce tissue-specific or stage-specific isoforms, by tissue-specific promoters or by tissue-specific alternative splicing.
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發(fā)表于 2025-3-22 03:52:38 | 只看該作者
Identifying Disease Genes in Humans,ossible that a genetically inherited disease is first detected in a family as an isolated case. Often isolated cases are simply due to chance, in regular segregation of a pathogenic mutation in a given family. Let’s consider for instance a family in which a dominant mutation with reduced penetrance
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https://doi.org/10.1007/978-3-531-92749-7 inheritance”. In principle, mutations in mitochondrial DNA will be transmitted to all the children of the same mother, but only daughters will pass a mtDNA mutation to next generation. On the contrary, mutations in DNA carried by chromosomes will follow the rules dictated by chromosomal duplication, recombination and segregation.
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發(fā)表于 2025-3-22 20:42:57 | 只看該作者
The Human Genome, inheritance”. In principle, mutations in mitochondrial DNA will be transmitted to all the children of the same mother, but only daughters will pass a mtDNA mutation to next generation. On the contrary, mutations in DNA carried by chromosomes will follow the rules dictated by chromosomal duplication, recombination and segregation.
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https://doi.org/10.1007/978-3-531-92749-7es of chromosomes (22 autosomes, X chromosome, Y chromosome, mitochondrial DNA) which are present within our cells. All these DNA molecules are transmitted from cell to cell and from generation to generation: chromosomes by mitosis and meiosis, mitochondrial DNA by replication followed by mitochondr
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https://doi.org/10.1007/978-3-476-04170-8every single day), possibly with the exception of those (the so-called “housekeeping genes”) coding for products involved in general functions of all cell types. Many genes produce tissue-specific or stage-specific isoforms, by tissue-specific promoters or by tissue-specific alternative splicing.
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