Relevant bibliographies by topics / Molecular genetics

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Molecular genetics'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Molecular genetics"

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G. Ushakiran, S. Ganga Sai Pradeepa, S. Lavanya, T. Sahithi Priya, and P Krishna Kumari. "Molecular genetics." World Journal of Advanced Research and Reviews 20, no. 3 (2023): 1035–39. http://dx.doi.org/10.30574/wjarr.2023.20.3.2057.

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Molecular genetics, is the study of the biochemical mechanisms of It is the study of the biochemical nature of the genetic material and it’s control of phenotype. It is the study of the connection between genotype and phenotype the connection was a chemical one. Molecular genetics often applies an "investigative approach" to determine the structure and function of genes in an organism's genome using genetic screens. Molecular genetics is a powerful methodology for linking mutations to genetic conditions that may aid the search for treatments for various genetics diseases. This field has provid
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G., Ushakiran, Ganga Sai Pradeepa S., Lavanya S., Sahithi Priya T., and Krishna Kumari P. "Molecular genetics." World Journal of Advanced Research and Reviews 20, no. 3 (2023): 1035–39. https://doi.org/10.5281/zenodo.12749963.

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Molecular genetics, is the study of the biochemical mechanisms of It is the study of the biochemical nature of the genetic material and it’s control of phenotype. It is the study of the connection between genotype and phenotype the connection was a chemical one. Molecular genetics often applies an "investigative approach" to determine the structure and function of genes in an organism's genome using genetic screens. Molecular genetics is a powerful methodology for linking mutations to genetic conditions that may aid the search for treatments for various genetics  diseases. This fiel
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Athanasiou, Y., M. Zavros, M. Arsali, et al. "GENETIC DISEASES AND MOLECULAR GENETICS." Nephrology Dialysis Transplantation 29, suppl 3 (2014): iii339—iii350. http://dx.doi.org/10.1093/ndt/gfu162.

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Stekrova, J., J. Reiterova, V. Elisakova, et al. "Genetic diseases and molecular genetics." Clinical Kidney Journal 4, suppl 2 (2011): 4.s2.28. http://dx.doi.org/10.1093/ndtplus/4.s2.28.

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Legendre, C., D. Cohen, Y. Delmas, et al. "Genetic diseases and molecular genetics." Nephrology Dialysis Transplantation 28, suppl 1 (2013): i309—i321. http://dx.doi.org/10.1093/ndt/gft126.

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D, Bhuvana. "Innovations in Molecular Biology-Cutting-Edge Breakthroughs in Molecular Genetics." Annals of Experimental and Molecular Biology 6, no. 1 (2024): 1–4. http://dx.doi.org/10.23880/aemb-16000121.

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The field of molecular biology has experienced significant breakthroughs in recent years, driven by cutting-edge technologies and innovative research strategies. This abstract provides a concise overview of some key advancement that has shaped the landscape of molecular biology. One prominent area of progress involves the CRISPR-Cas9 gene editing system, which has revolutionized genetic manipulation. Researchers have refined and expanded its applications, enabling precise modifications to the genome for therapeutic purposes, functional genomics, and the development of genetically modified orga
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Wierzbicki, Anthony S. "Genetics and molecular biology: Genetic epidemiology." Current Opinion in Lipidology 15, no. 6 (2004): 699–701. http://dx.doi.org/10.1097/00041433-200412000-00011.

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Bakhshilloyevna, Sultonova Dildor. "Biochemistry and molecular genetics of human glycogenoses." American Journal of Applied Sciences 7, no. 7 (2025): 78–82. https://doi.org/10.37547/tajas/volume07issue07-08.

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Most of the glycogen metabolism disorders that affect skeletal muscle involve enzymes of glycogenolysis (myophosphorylase ( PYGM ), glycogen debranching enzyme ( AGL ), phosphorylase b -kinase ( PHKB )) and glycolysis (phosphofructokinase ( PFK ), phosphoglyceromutase ( PGAM 2), aldolase A ( ALDOA ), β -enolase ( ENO 3)); however, 3 of them involve glycogen synthesis (glycogenin-1 ( GYG 1), glycogen synthase ( GSE ), and debranching enzyme ( GBE 1)). Many present with exercise-induced cramps and rhabdomyolysis with more intense exercise (ie, PYGM , PFK , PGAM 2), while others present with musc
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Vázquez, José. "Molecular Genetics." American Biology Teacher 65, no. 8 (2003): 634. http://dx.doi.org/10.2307/4451575.

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Vázquez, José. "Molecular Genetics." American Biology Teacher 68, no. 4 (2006): 253–54. http://dx.doi.org/10.2307/4451977.

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Dissertations / Theses on the topic "Molecular genetics"

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Bruiners, Natalie. "Molecular genetic analysis of preterm labour." Thesis, Stellenbosch : Stellenbosch University, 2007. http://hdl.handle.net/10019.1/17741.

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Thesis (MSc)--University of Stellenbosch, 2007.<br>ENGLISH ABSTRACT: The World Health Organisation (WHO) has defined preterm labour as the onset of labour before 37 completed weeks of gestation with an incidence ranging between 5-10%. Although patient care has improved, the rate of preterm birth has slowly been increasing and currently impacts significantly on maternal and fetal mortality and morbidity. The complex condition of preterm labour involves multiple etiologies and risk factors, which complicates the search for candidate markers and / or biomarkers. The aim of this prospective
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Fourie, Mariesa. "Molecular characterization and further shortening of recombinant forms of the Lr19 translocation." Thesis, Link to the online version, 2005. http://hdl.handle.net/10019/189.

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Hedmark, Eva. "Conservation Genetics of Scandinavian Wolverines." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Universitetsbiblioteket [distributör], 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-6636.

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Howell, Viive Maarika. "Molecular Genetics of Hyperparathyroidism." University of Sydney, 2005. http://hdl.handle.net/2123/6022.

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Doctor of Philosophy(PhD)<br>Hyperparathyroidism, a disease of the parathyroid glands, is one of the most common endocrinopathies, having a prevalence of 1 – 3 per 1000 individuals. It is characterised by calcium insensitive hypersecretion of parathyroid hormone, and increased cell proliferation. While the treatment for familial as well as many sporadic tumours associated with hyperparathyroidism includes parathyroidectomy, the extent of surgery and the follow-up monitoring regime, are dependent on accurate clinical and histopathological classification of the lesion. However, overlaps in histo
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Wallace, Robyn. "Molecular genetics of epilepsy /." Title page, contents and summary only, 1997. http://web4.library.adelaide.edu.au/theses/09PH/09phw193.pdf.

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Thesis (Ph. D.)--University of Adelaide, Dept. of Paediatrics, 1997.<br>Errata pasted onto back end-paper. Copies of author's previously published articles inserted. Includes bibliographical references (leaves 157-176).
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Busfield, Frances. "Molecular genetics of dementia." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.336329.

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Hill, Margaret J. "Molecular genetics of tabtoxin." Thesis, University of East Anglia, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.292600.

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Asumalahti, Kati. "Molecular genetics of psoriasis." Helsinki : University of Helsinki, 2003. http://ethesis.helsinki.fi/julkaisut/laa/kliin/vk/asumalahti/.

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Law, Bic-fai Fian, and 羅璧輝. "Molecular genetics of esophageal squamous cell carcinoma." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2006. http://hub.hku.hk/bib/B3660446X.

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Sjödin, Per. "Effects of Selection and Demography on DNA Polymorphism in Black Mustard (Brassica nigra)." Doctoral thesis, Uppsala universitet, Evolutionär funktionsgenomik, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-6633.

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The evolution of three genes from the CONSTANS-LIKE gene family is studied in Brassica nigra. We use a combination of population genetic and phylogenetic techniques in order to assess the relative importance of selection and demography on the pattern of DNA variation. The analysis is complicated by the fact that they are recent duplicates of each other and hence there is a potential redundancy factor that has to be considered. The relationship between two of the genes, COa and COb, is however much closer than between any relationship to the third gene, COL1. The three genes are all suspected t
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Books on the topic "Molecular genetics"

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Hancock, J. T. Molecular genetics. Butterworth-Heinemann, 1999.

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Smith-Keary, Peter. Molecular Genetics. Macmillan Education UK, 1991. http://dx.doi.org/10.1007/978-1-349-11732-1.

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D, Dickson. Molecular genetics. Brunel University, 1994.

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J, Benz Edward, ed. Molecular genetics. Churchill Livingstone, 1989.

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J, Benz Edward, ed. Molecular genetics. Churchill Livingstone, 1989.

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Ian, Sudbery, ed. Human molecular genetics. 3rd ed. Pearson Prentice Hall, 2009.

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Sudbery, Peter. Human molecular genetics. Longman, 1998.

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Strachan, Tom. Human molecular genetics. BIOS Scientific, 1996.

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Dale, Jeremy. Molecular genetics of bacteria. 2nd ed. J. Wiley, 1994.

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Dale, Jeremy. Molecular genetics of bacteria. 4th ed. John Wiley & Sons, 2004.

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Book chapters on the topic "Molecular genetics"

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le Maire, Marc, Raymond Chabaud, and Guy Hervé. "Molecular Genetics." In Laboratory Guide to Biochemistry, Enzymology, and Protein Physical Chemistry. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3820-2_2.

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Reuter, Martin, Andrea Felten, and Christian Montag. "Molecular Genetics." In Neuroeconomics. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-35923-1_23.

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Hangay, George, Susan V. Gruner, F. W. Howard, et al. "Molecular Genetics." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_4660.

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Jeffery, Austin. "Molecular Genetics." In Encyclopedia of Personality and Individual Differences. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-24612-3_777.

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Jeffery, Austin. "Molecular Genetics." In Encyclopedia of Personality and Individual Differences. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-28099-8_777-1.

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Gorczyca, Wojciech. "Molecular Genetics." In Atlas of Differential Diagnosis in Neoplastic Hematopathology, 4th ed. CRC Press, 2021. http://dx.doi.org/10.1201/9781003120445-08.

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Graf, Ulrich, Nancy van Schaik, and Friedrich E. Würgler. "Molecular Biology." In Drosophila Genetics. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-76805-7_8.

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Foroud, Tatiana, and Daniel L. Koller. "Genetic Inheritance and Population Genetics." In Molecular Genetic Pathology. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-405-6_14.

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Foroud, Tatiana, and Daniel L. Koller. "Genetic Inheritance and Population Genetics." In Molecular Genetic Pathology. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-4800-6_5.

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Twfieg, Mohammed-Elfatih, and M. Dawn Teare. "Molecular Genetics and Genetic Variation." In Methods in Molecular Biology. Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60327-416-6_1.

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Conference papers on the topic "Molecular genetics"

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Giannelli, B. F. "MOLECULAR GENETICS OF HAEMOPHILIA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643981.

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Haemophilia B, an X-linked recessive disease with an incidence of 1/30,000 newborn males, is due to defects in the gene for coagulation factor IX, which is on the long am of the X chromosome at band Xq27.1. This gene consists of approximately 34 Kb and contains 8 exons which specify a mRtfc of 2803 residues coding for a protein of 415 aa preceded by a prepro signal peptide of 46 aa. Coripanson of the functional domains of the factor IX protein with the exon structure of the gene supports the exon/protein domain hypothesis of gene evolution. The factor IX gene seems to be formed by a number of
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MENDLEWICZ, J. "MOLECULAR GENETICS IN PSYCHIATRY RESEARCH." In IX World Congress of Psychiatry. WORLD SCIENTIFIC, 1994. http://dx.doi.org/10.1142/9789814440912_0004.

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Sari, Lili Nur Indah, and Elza Ibrahim Auerkari. "Molecular Genetics and Epigenetics of Ankyloglossia." In 11th International Dentistry Scientific Meeting (IDSM 2017). Atlantis Press, 2018. http://dx.doi.org/10.2991/idsm-17.2018.14.

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Monica, Monica, and Elza Ibrahim Auerkari. "Molecular Genetics of Peutz-Jegher Syndrome." In 11th International Dentistry Scientific Meeting (IDSM 2017). Atlantis Press, 2018. http://dx.doi.org/10.2991/idsm-17.2018.19.

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Utami, Wulan Sri, Ferry Pergamus Gultom, Harismanto, and Elza Ibrahim Auerkari. "Molecular genetics and epigenetics of ameloblastoma." In ADVANCES IN INTELLIGENT APPLICATIONS AND INNOVATIVE APPROACH. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0140214.

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"Molecular phylogeny of plant 14-3-3 proteins family." In Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Novosibirsk ICG SB RAS 2021, 2021. http://dx.doi.org/10.18699/plantgen2021-133.

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"Molecular, сytogenetic, and morphological features of primary octoploid triticale". У Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 2019. http://dx.doi.org/10.18699/plantgen2019-055.

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Antonarakis, E. "The Molecular Genetics of Hemophilia A Stylianos." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643980.

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Hemophilia A is a common X linked hereditary disorder of blood coagulation due to deficiency of factor 8. The gene for factor 8 has been cloned and characterized (Nature 312:326-342, 1984). It is divided into 26 exons and 25 introns and spans 186 kb of DNA. The CGNA is 9 kb and codes for 2351 amino acids. The first 19 amino acids comprise the secretory leader peptide and the mature excreted polypeptide consists of 2332 amino acids. The nucleotide sequence of the exons and the exon-intron junctions is known and the complete amino acid sequence has been deducedSeveral laboratories have used clon
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Weitz, C., Y. Miyake, K. Shinzato, E. Montag, and J. Nathans. "Studies on the molecular genetics of tritanopia." In OSA Annual Meeting. Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.fm3.

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Tritanopia differs fundamentally from other inherited anomalies of color vision. Its autosomal dominant tranmission1 implies a mechanism unlike that of protanopia or deuteranopia. Because people with tritanopis lack a measurable blue-cone electroretinographic response,2 the defect is likely localized within blue-cone photoreceptors. These findings suggest that a mutant gene product actively interferes with blue-cone function or viability. Could a mutation in the gene encoding the blue-sensitive visual pigment3 be responsible for tritanopia? To test this hypothesis we have used the polymerase c
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Neitz, Maureen. "Molecular genetics of red-green color vision." In OSA Annual Meeting. Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.fm2.

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Genes encoding cone pigments sensitive to middle-to-long wavelengths lie in a head-to-tail tandem array on the X-chromosome. Although two X-encoded genes, one for long-wavelength-sensitive pigments and one for middle-wavelength-sensitive pigments, are sufficient to serve trichromatic color vision, most people have more than two such genes. The arrangement, location, and degree of homology of the pigment genes promote recombination within the tandem arrays. Such recombination events produce pigment-gene complements that differ in the number and sequences of individual genes and in the interrela
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Reports on the topic "Molecular genetics"

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Beitz, Donald, Micha Ron, Albert E. Freeman, Moshe Shani, Alan Myers, and B. T. McDaniel. Mitochondrial Molecular Genetics and Milk Production. United States Department of Agriculture, 1993. http://dx.doi.org/10.32747/1993.7603822.bard.

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Cullen, D. Molecular genetics of ligninase expression. Progress report. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/81012.

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Chamovitz, Daniel A., and Zhenbiao Yang. Chemical Genetics of the COP9 Signalosome: Identification of Novel Regulators of Plant Development. United States Department of Agriculture, 2011. http://dx.doi.org/10.32747/2011.7699844.bard.

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This was an exploratory one-year study to identify chemical regulators of the COP9 signalosome. Chemical Genetics uses small molecules to modify or disrupt the function of specific genes/proteins. This is in contrast to classical genetics, in which mutations disrupt the function of genes. The underlying concept is that the functions of most proteins can be altered by the binding of a chemical, which can be found by screening large libraries for compounds that specifically affect a biological, molecular or biochemical process. In addition to screens for chemicals which inhibit specific biologic
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Ow, David W. ow@pgec ams usda gov. Molecular Genetics of Metal Detoxification: Prospects for Phytoremediation. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/781718.

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Ow, David W. Molecular Genetics of Metal Detoxification: Prospects for Phytoremediation. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/828166.

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Konisky, J. Genetics and molecular biology of methanogen genes. Final report. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/555346.

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Cahaner, Avigdor, Susan J. Lamont, E. Dan Heller, and Jossi Hillel. Molecular Genetic Dissection of Complex Immunocompetence Traits in Broilers. United States Department of Agriculture, 2003. http://dx.doi.org/10.32747/2003.7586461.bard.

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Objectives: (1) Evaluate Immunocompetence-OTL-containing Chromosomal Regions (ICRs), marked by microsatellites or candidate genes, for magnitude of direct effect and for contribution to relationships among multiple immunocompetence, disease-resistance, and growth traits, in order to estimate epistatic and pleiotropic effects and to predict the potential breeding applications of such markers. (2) Evaluate the interaction of the ICRs with genetic backgrounds from multiple sources and of multiple levels of genetic variation, in order to predict the general applicability of molecular genetic marke
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Fox, Jacob, and Hassan Fathallan-Shaykh. Molecular Genetics Techniques to Develop New Treatments for Brain Cancers. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/900310.

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Gunsalus, R. P. Molecular biology and genetics of the acetate-utilizing methanogenic bacteria. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6967641.

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Robert P. Gunsalus. Molecular Biology and Genetics of the Acetate-Utilizing Methanogenic Bacteria. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/859404.

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