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You searched for subject:(recessive genes). Showing records 1 – 6 of 6 total matches.

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Indian Institute of Science

1. Singhmar, Pooja. Functional Analysis Of Primary Microcephaly Gene Product ASPM.

Degree: PhD, Faculty of Science, 2013, Indian Institute of Science

 Autosomal recessive primary microcephaly (MCPH) is defined by congenital microcephaly and associated mental retardation with head circumference of the affected individual at least 3 standard… (more)

Subjects/Keywords: Microcephaly Gene; Autosomal Recessive Primary Microcephaly (MCPH); Abnormal Spindle-like, Micrcephaly Associated Protein (ASPM); MCPH Genes; Microcephaly Protein; Neurology

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APA (6th Edition):

Singhmar, P. (2013). Functional Analysis Of Primary Microcephaly Gene Product ASPM. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/2060

Chicago Manual of Style (16th Edition):

Singhmar, Pooja. “Functional Analysis Of Primary Microcephaly Gene Product ASPM.” 2013. Doctoral Dissertation, Indian Institute of Science. Accessed May 05, 2021. http://etd.iisc.ac.in/handle/2005/2060.

MLA Handbook (7th Edition):

Singhmar, Pooja. “Functional Analysis Of Primary Microcephaly Gene Product ASPM.” 2013. Web. 05 May 2021.

Vancouver:

Singhmar P. Functional Analysis Of Primary Microcephaly Gene Product ASPM. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2013. [cited 2021 May 05]. Available from: http://etd.iisc.ac.in/handle/2005/2060.

Council of Science Editors:

Singhmar P. Functional Analysis Of Primary Microcephaly Gene Product ASPM. [Doctoral Dissertation]. Indian Institute of Science; 2013. Available from: http://etd.iisc.ac.in/handle/2005/2060


Freie Universität Berlin

2. Neubert, Gerda. Hereditary microcephalies: characterization of the pathomechanism of autosomal recessive primary microcephaly type 3 and clinical-genetic aspect of Angelman syndrome.

Degree: 2016, Freie Universität Berlin

 Microcephaly describes the clinical finding of a reduced occipital-frontal circumference by at least two standard deviations. Hereditary microcephaly appears congenital (primary) or postnatal (secondary), isolated… (more)

Subjects/Keywords: Angelman syndrome; autosomal recessive primary microcephaly; MCPH3; Cdk5rap2; housekeeping genes; mESC; neural differentiation; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Neubert, G. (2016). Hereditary microcephalies: characterization of the pathomechanism of autosomal recessive primary microcephaly type 3 and clinical-genetic aspect of Angelman syndrome. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-14222

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Neubert, Gerda. “Hereditary microcephalies: characterization of the pathomechanism of autosomal recessive primary microcephaly type 3 and clinical-genetic aspect of Angelman syndrome.” 2016. Thesis, Freie Universität Berlin. Accessed May 05, 2021. http://dx.doi.org/10.17169/refubium-14222.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Neubert, Gerda. “Hereditary microcephalies: characterization of the pathomechanism of autosomal recessive primary microcephaly type 3 and clinical-genetic aspect of Angelman syndrome.” 2016. Web. 05 May 2021.

Vancouver:

Neubert G. Hereditary microcephalies: characterization of the pathomechanism of autosomal recessive primary microcephaly type 3 and clinical-genetic aspect of Angelman syndrome. [Internet] [Thesis]. Freie Universität Berlin; 2016. [cited 2021 May 05]. Available from: http://dx.doi.org/10.17169/refubium-14222.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Neubert G. Hereditary microcephalies: characterization of the pathomechanism of autosomal recessive primary microcephaly type 3 and clinical-genetic aspect of Angelman syndrome. [Thesis]. Freie Universität Berlin; 2016. Available from: http://dx.doi.org/10.17169/refubium-14222

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

3. Simone Consuelo de Amorim. Estudo da condução nervosa em pacientes com a síndrome SPOAN.

Degree: 2013, University of São Paulo

 Introdução: A síndrome SPOAN é uma doença neurodegenerativa, de transmissão genética autossômica recessiva, até o momento reconhecida apenas no Brasil, que caracteriza-se por: paraplegia espástica,… (more)

Subjects/Keywords: Atrofia óptica; Doença de Charcot-Marie-Tooth; Genes recessivos; Nervo fibular; Nervo mediano; Nervo tibial; Nervo ulnar; Neuropatia hereditária motora e sensorial; Paraplegia espástica; Polineuropatias; Charcot-Marie-Tooth disease; Median nerve; Optic atrophy; Peroneal nerve; Polyneuropathy; Recessive genes; Sensitive-motor hereditary neuropathy; Spastic paraplegia; Tibial nerve; Ulnar nerve

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APA (6th Edition):

Amorim, S. C. d. (2013). Estudo da condução nervosa em pacientes com a síndrome SPOAN. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5138/tde-05112013-154543/

Chicago Manual of Style (16th Edition):

Amorim, Simone Consuelo de. “Estudo da condução nervosa em pacientes com a síndrome SPOAN.” 2013. Doctoral Dissertation, University of São Paulo. Accessed May 05, 2021. http://www.teses.usp.br/teses/disponiveis/5/5138/tde-05112013-154543/.

MLA Handbook (7th Edition):

Amorim, Simone Consuelo de. “Estudo da condução nervosa em pacientes com a síndrome SPOAN.” 2013. Web. 05 May 2021.

Vancouver:

Amorim SCd. Estudo da condução nervosa em pacientes com a síndrome SPOAN. [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2021 May 05]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5138/tde-05112013-154543/.

Council of Science Editors:

Amorim SCd. Estudo da condução nervosa em pacientes com a síndrome SPOAN. [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/5/5138/tde-05112013-154543/

4. Stam, P. The effect of initial linkage disequilibrium and natural selection in pooled populations : experiments with Tribolium and simulation.

Degree: 1972, Landbouwhogeschool Wageningen

 <p/>In chapter 2 a number of the mechanisms are discussed through which genetic polymorphisms can be maintained in natural populations: overdominance, frequency dependent selection and… (more)

Subjects/Keywords: biometrie; dominantie; genen; genetica; heritability; overerving; koppeling; recessieve genen; recessiviteit; geslachtskoppeling; tenebrionidae; statistische analyse; kernerfelijkheid; Genetica (algemeen); biometry; dominance; genes; genetics; heritability; inheritance; linkage; recessive genes; recessiveness; sex linkage; tenebrionidae; statistical analysis; nuclear inheritance; Genetics (General)

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APA (6th Edition):

Stam, P. (1972). The effect of initial linkage disequilibrium and natural selection in pooled populations : experiments with Tribolium and simulation. (Doctoral Dissertation). Landbouwhogeschool Wageningen. Retrieved from http://library.wur.nl/WebQuery/wurpubs/421747 ; urn:nbn:nl:ui:32-421747 ; urn:nbn:nl:ui:32-421747 ; http://library.wur.nl/WebQuery/wurpubs/421747

Chicago Manual of Style (16th Edition):

Stam, P. “The effect of initial linkage disequilibrium and natural selection in pooled populations : experiments with Tribolium and simulation.” 1972. Doctoral Dissertation, Landbouwhogeschool Wageningen. Accessed May 05, 2021. http://library.wur.nl/WebQuery/wurpubs/421747 ; urn:nbn:nl:ui:32-421747 ; urn:nbn:nl:ui:32-421747 ; http://library.wur.nl/WebQuery/wurpubs/421747.

MLA Handbook (7th Edition):

Stam, P. “The effect of initial linkage disequilibrium and natural selection in pooled populations : experiments with Tribolium and simulation.” 1972. Web. 05 May 2021.

Vancouver:

Stam P. The effect of initial linkage disequilibrium and natural selection in pooled populations : experiments with Tribolium and simulation. [Internet] [Doctoral dissertation]. Landbouwhogeschool Wageningen; 1972. [cited 2021 May 05]. Available from: http://library.wur.nl/WebQuery/wurpubs/421747 ; urn:nbn:nl:ui:32-421747 ; urn:nbn:nl:ui:32-421747 ; http://library.wur.nl/WebQuery/wurpubs/421747.

Council of Science Editors:

Stam P. The effect of initial linkage disequilibrium and natural selection in pooled populations : experiments with Tribolium and simulation. [Doctoral Dissertation]. Landbouwhogeschool Wageningen; 1972. Available from: http://library.wur.nl/WebQuery/wurpubs/421747 ; urn:nbn:nl:ui:32-421747 ; urn:nbn:nl:ui:32-421747 ; http://library.wur.nl/WebQuery/wurpubs/421747


York University

5. Gulri, Manpreet Kaur. Investigating the Role of Selected Epigenetic Silencing Marks in Determining Mouse Skeletal Muscle Oxidative Phenotype.

Degree: MSc -MS, Kinesiology & Health Science, 2020, York University

 Epigenetic regulation of gene expression supports skeletal muscle phenotypic plasticity. The role of epigenetic silencing marks in maintaining muscle phenotype and in supporting muscle plasticity… (more)

Subjects/Keywords: Kinesiology; Epigenetic; Silencing marks; Histone modification; Genes; Gene silencing; Gene repression; Gene activation; Transcriptional repression; Transcriptional activation; h3k27me3; ezh2; mdm2; Exercise; Endurance; Endurance exercise; Endurance training; Exercise training; Skeletal muscle; Mouse; Mice; c57bl6; c2c12; c2c12 differentiation; c2c12 myoblasts; Long term training; Short term training; Muscle phenotype; Skeletal muscle phenotype; Oxidative muscle; Glycolytic muscle; Slow-twitch; Fast-twitch; Kinesiology; Physiology; Genetics; Post-translational modifications; Ptms; Histone methyltransferase; e3 ubiquitin ligase; prc2; Polycomb recessive complex 2

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APA (6th Edition):

Gulri, M. K. (2020). Investigating the Role of Selected Epigenetic Silencing Marks in Determining Mouse Skeletal Muscle Oxidative Phenotype. (Masters Thesis). York University. Retrieved from http://hdl.handle.net/10315/37891

Chicago Manual of Style (16th Edition):

Gulri, Manpreet Kaur. “Investigating the Role of Selected Epigenetic Silencing Marks in Determining Mouse Skeletal Muscle Oxidative Phenotype.” 2020. Masters Thesis, York University. Accessed May 05, 2021. http://hdl.handle.net/10315/37891.

MLA Handbook (7th Edition):

Gulri, Manpreet Kaur. “Investigating the Role of Selected Epigenetic Silencing Marks in Determining Mouse Skeletal Muscle Oxidative Phenotype.” 2020. Web. 05 May 2021.

Vancouver:

Gulri MK. Investigating the Role of Selected Epigenetic Silencing Marks in Determining Mouse Skeletal Muscle Oxidative Phenotype. [Internet] [Masters thesis]. York University; 2020. [cited 2021 May 05]. Available from: http://hdl.handle.net/10315/37891.

Council of Science Editors:

Gulri MK. Investigating the Role of Selected Epigenetic Silencing Marks in Determining Mouse Skeletal Muscle Oxidative Phenotype. [Masters Thesis]. York University; 2020. Available from: http://hdl.handle.net/10315/37891

6. Pavan, S.N.C. Exploring recessive resistance to the powdery mildew disease.

Degree: 2011, NARCIS

  The powdery mildew disease, caused by obligate biotrophic fungi belonging to the Ascomycete order of Erysiphales, is common among higher plants and represents one… (more)

Subjects/Keywords: planten; ziekteresistentie; plantenziekteverwekkende schimmels; erysiphaceae; recessieve genen; solanum lycopersicum; wilde verwanten; oidium neolycopersici; erysiphe pisi; genetische analyse; verdedigingsmechanismen; plantenveredeling; marker assisted breeding; Resistentieveredeling; Plantenverdediging en -resistentie; plants; disease resistance; plant pathogenic fungi; erysiphaceae; recessive genes; solanum lycopersicum; wild relatives; oidium neolycopersici; erysiphe pisi; genetic analysis; defence mechanisms; plant breeding; marker assisted breeding; Resistance Breeding; Plant Defence, Plant Resistance

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APA (6th Edition):

Pavan, S. N. C. (2011). Exploring recessive resistance to the powdery mildew disease. (Doctoral Dissertation). NARCIS. Retrieved from http://library.wur.nl/WebQuery/wurpubs/414418 ; urn:nbn:nl:ui:32-414418 ; urn:nbn:nl:ui:32-414418 ; http://library.wur.nl/WebQuery/wurpubs/414418

Chicago Manual of Style (16th Edition):

Pavan, S N C. “Exploring recessive resistance to the powdery mildew disease.” 2011. Doctoral Dissertation, NARCIS. Accessed May 05, 2021. http://library.wur.nl/WebQuery/wurpubs/414418 ; urn:nbn:nl:ui:32-414418 ; urn:nbn:nl:ui:32-414418 ; http://library.wur.nl/WebQuery/wurpubs/414418.

MLA Handbook (7th Edition):

Pavan, S N C. “Exploring recessive resistance to the powdery mildew disease.” 2011. Web. 05 May 2021.

Vancouver:

Pavan SNC. Exploring recessive resistance to the powdery mildew disease. [Internet] [Doctoral dissertation]. NARCIS; 2011. [cited 2021 May 05]. Available from: http://library.wur.nl/WebQuery/wurpubs/414418 ; urn:nbn:nl:ui:32-414418 ; urn:nbn:nl:ui:32-414418 ; http://library.wur.nl/WebQuery/wurpubs/414418.

Council of Science Editors:

Pavan SNC. Exploring recessive resistance to the powdery mildew disease. [Doctoral Dissertation]. NARCIS; 2011. Available from: http://library.wur.nl/WebQuery/wurpubs/414418 ; urn:nbn:nl:ui:32-414418 ; urn:nbn:nl:ui:32-414418 ; http://library.wur.nl/WebQuery/wurpubs/414418

.