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Allgemeinbegriff

Molekulargenetik

Genetik, Molekularbiologie

Subject heading	Molekulargenetik
Definition	Teilgebiet der Genetik, das mit biochemischen Methoden die chemische Struktur und den Stoffwechsel des genetischen Materials (Nukleinsäuren) sowie die Codierung und differenzielle Ausprägung der genetischen Information aufklärt.
Synonym	Molekulare Genetik Biochemische Genetik
Broader term	Genetik Molekularbiologie
Topic	Biochemie, Biophysik, Zytologie
Source	B Wissen
Record type	Allgemeinbegriff
GND-Identifier	4039987-4
Record ID	040399877
Topic of show all Fluorescence In Situ Hybridization (FISH) : Application Guide Genetic and functional analysis of the calcium-sensing receptor in chronic pancreatitis Molecular syndromology Vol.17.2026,No.1 „Die Evolution der DNA-Analyse: Vom Labor zur digitalen Revolution“ : „Ein Blick auf die Fortschritte, die unsere genetischen Daten neu definieren“ Characterization of segmental chromosomal aberration of chromosome 17q gain in Neuroblastoma Classification of biopsy findings in individuals with hereditary glomerulopathies using molecular genetic testing and proteomics Development of molecular genetic tools for coccolithophores and proteomic analysis of Chrysotila carterae’s calcitic scales Dissecting gene metabolite relationships in the Medicago truncatula terpenome after Aphanomyces euteiches infection Establishing a new method for automatized UPD detection in exome sequencing data applied on a large cohort Genetic engineering in the oilseed crop camelina: establishment and application Identification of Novel Germline Genetic Variants Associated with Pancreatic Cancer Risk by Using Genome-Wide Studies Modeling the Tissue-Specific Somatic Mutation Rate Along the Genome Based on Genomic Features Molecular characterization of rare genetic diseases with progeroid features Molecular syndromology Vol.16.2025,No.1 Molecular syndromology Vol.16.2025,No.2 Molecular syndromology Vol.16.2025,No.3 Molecular syndromology Vol.16.2025,No.4 Molecular syndromology Vol.16.2025,No.5 Molecular syndromology Vol.16.2025,No.6 Molekulargenetische Charakterisierung syndromaler, genetischer Erkrankungen mittels Next-Generation-Sequencing Nematode genetics beyond Caenorhabditis elegans: Adapting modern genetic tools to phylogenetically distant nematodes Aberrant gene expression prediction from sequence and implications in health and disease Biotech Frontiers: Journeying Through Genetic Exploration Das Buch der Gene und Genome Development of the BonnMu transposon resource in maize (Zea mays L.) and its application in characterizing the magenta root dwarf 1 (mrd1) mutant Effective strategies incorporating genomic selection to improve short- and long-term genetic gain in plant breeding programs Entwicklung eines molekulargenetischen Panels zur Detektion von Mutationen im TP53 Gen mittels ClearSEEK™ Biochemie Enzyklopädie der Cannabiszucht : Fachbuch der Hanfgenetik Generation and analysis of a novel, cre-inducible knock-in mouse strain to assess the leukemogenic potential of the mutation H3.3-K27M in the context of Mll5-deficiency Genetic factors of horn-related traits in small ruminants with special reference to the polled intersex syndrome (PIS) in the goat Integrating deep learning and genetic approaches to uncover molecular mechanisms of cellular organization Laboratory Guide to the Methods in Biochemical Genetics Molecular mechanisms of colorectal cancer: MACC1 and the novel IER2 gene Molecular syndromology Vol.15.2024,No.1 Molecular syndromology Vol.15.2024,No.2 Molecular syndromology Vol.15.2024,No.3 Molecular syndromology Vol.15.2024,No.4 Molecular syndromology Vol.15.2024,No.5 Molecular syndromology Vol.15.2024,No.6 Prioritizing coronary artery disease candidate genes using gene panel sequencing data from 54k+ Europeans Psychologische und molekulargenetische Aspekte interindividueller Differenzen in Angstbewältigungsstrategien Techniken der individualisierten molekulargenetischen Diagnostik Understanding multimorbidity with big data in genomics Untersuchung und Identifizierung molekulargenetischer Ursachen bei Kindern und Jugendlichen mit Verdacht auf eine erbliche Nierenerkrankung Alignment-free Phylogenetic Placement and its Applications Analysis of whole-genome sequencing data from ICGC-PanCancer project Anwendung molekulargenetischer Methoden zur Gewinnung neuer Erkenntnisse für die Diagnostik und Behandlung ausgewählter Infektions- und Tumorerkrankungen Assessment of phenotypic, genomic and novel approaches for soybean breeding in Central Europe Das Gen : Eine sehr persönliche Geschichte \| Der New York Times-Bestseller Design and application of methods for genome inference Die Wissenschaft der Genetik - Wie uns unser Erbgut beeinflusst Die Wissenschaft der Genetik - Wie uns unser Erbgut beeinflusst Discovery and evolution of novel Cre-type tyrosine site-specific recombinases for advanced genome engineering Diverse molekulare Ursachen unklarer autosomal dominanter tubulointerstitieller Nierenerkrankungen Functional dissection of the meiotic drive of female-inherited accessory chromosomes in Zymoseptoria tritici Gen oder Nicht-Gen : Wer weiß das schon so genau Genomic profiling in rare kidney disease Identification of genetic risk factors for Parkinson’s disease Identification of structural variations from whole genome sequencing of cancer patients Identifikation eines neuen Pathomechanismus zur Entstehung einer 46,XY-Gonadendysgenesie

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Katalog der Deutschen Nationalbibliothek

Molekulargenetik

Fluorescence In Situ Hybridization (FISH) : Application Guide

Genetic and functional analysis of the calcium-sensing receptor in chronic pancreatitis

Molecular syndromology

„Die Evolution der DNA-Analyse: Vom Labor zur digitalen Revolution“ : „Ein Blick auf die Fortschritte, die unsere genetischen Daten neu definieren“

Characterization of segmental chromosomal aberration of chromosome 17q gain in Neuroblastoma

Classification of biopsy findings in individuals with hereditary glomerulopathies using molecular genetic testing and proteomics

Development of molecular genetic tools for coccolithophores and proteomic analysis of Chrysotila carterae’s calcitic scales

Dissecting gene metabolite relationships in the Medicago truncatula terpenome after Aphanomyces euteiches infection

Establishing a new method for automatized UPD detection in exome sequencing data applied on a large cohort

Genetic engineering in the oilseed crop camelina: establishment and application

Identification of Novel Germline Genetic Variants Associated with Pancreatic Cancer Risk by Using Genome-Wide Studies

Modeling the Tissue-Specific Somatic Mutation Rate Along the Genome Based on Genomic Features

Molecular characterization of rare genetic diseases with progeroid features

Molecular syndromology

Molecular syndromology

Molecular syndromology

Molecular syndromology

Molecular syndromology

Molecular syndromology

Molekulargenetische Charakterisierung syndromaler, genetischer Erkrankungen mittels Next-Generation-Sequencing

Nematode genetics beyond Caenorhabditis elegans: Adapting modern genetic tools to phylogenetically distant nematodes

Aberrant gene expression prediction from sequence and implications in health and disease

Biotech Frontiers: Journeying Through Genetic Exploration

Das Buch der Gene und Genome

Development of the BonnMu transposon resource in maize (Zea mays L.) and its application in characterizing the magenta root dwarf 1 (mrd1) mutant

Effective strategies incorporating genomic selection to improve short- and long-term genetic gain in plant breeding programs

Entwicklung eines molekulargenetischen Panels zur Detektion von Mutationen im TP53 Gen mittels ClearSEEK™ Biochemie

Enzyklopädie der Cannabiszucht : Fachbuch der Hanfgenetik

Generation and analysis of a novel, cre-inducible knock-in mouse strain to assess the leukemogenic potential of the mutation H3.3-K27M in the context of Mll5-deficiency

Genetic factors of horn-related traits in small ruminants with special reference to the polled intersex syndrome (PIS) in the goat

Integrating deep learning and genetic approaches to uncover molecular mechanisms of cellular organization

Laboratory Guide to the Methods in Biochemical Genetics

Molecular mechanisms of colorectal cancer: MACC1 and the novel IER2 gene

Molecular syndromology

Molecular syndromology

Molecular syndromology

Molecular syndromology

Molecular syndromology

Molecular syndromology

Prioritizing coronary artery disease candidate genes using gene panel sequencing data from 54k+ Europeans

Psychologische und molekulargenetische Aspekte interindividueller Differenzen in Angstbewältigungsstrategien

Techniken der individualisierten molekulargenetischen Diagnostik

Understanding multimorbidity with big data in genomics

Untersuchung und Identifizierung molekulargenetischer Ursachen bei Kindern und Jugendlichen mit Verdacht auf eine erbliche Nierenerkrankung

Alignment-free Phylogenetic Placement and its Applications

Analysis of whole-genome sequencing data from ICGC-PanCancer project

Anwendung molekulargenetischer Methoden zur Gewinnung neuer Erkenntnisse für die Diagnostik und Behandlung ausgewählter Infektions- und Tumorerkrankungen

Assessment of phenotypic, genomic and novel approaches for soybean breeding in Central Europe

Das Gen : Eine sehr persönliche Geschichte | Der New York Times-Bestseller

Design and application of methods for genome inference

Die Wissenschaft der Genetik - Wie uns unser Erbgut beeinflusst

Die Wissenschaft der Genetik - Wie uns unser Erbgut beeinflusst

Discovery and evolution of novel Cre-type tyrosine site-specific recombinases for advanced genome engineering

Diverse molekulare Ursachen unklarer autosomal dominanter tubulointerstitieller Nierenerkrankungen

Functional dissection of the meiotic drive of female-inherited accessory chromosomes in Zymoseptoria tritici

Gen oder Nicht-Gen : Wer weiß das schon so genau

Genomic profiling in rare kidney disease

Identification of genetic risk factors for Parkinson’s disease

Identification of structural variations from whole genome sequencing of cancer patients

Identifikation eines neuen Pathomechanismus zur Entstehung einer 46,XY-Gonadendysgenesie