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You searched for subject:( SCID). Showing records 1 – 30 of 61 total matches.

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University of Debrecen

1. Kupcha, Anna. Early identification and neonatal screening of severe combined immunodeficiencies .

Degree: DE – Általános Orvostudományi Kar, 2014, University of Debrecen

 The thesis discusses the importance of the early identification and neonatal screening of severe combined immunodeficiency. It emphasizes the importance of implementation of worldwide-national newborn… (more)

Subjects/Keywords: Newborn screening; SCID

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APA (6th Edition):

Kupcha, A. (2014). Early identification and neonatal screening of severe combined immunodeficiencies . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/194848

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):

Kupcha, Anna. “Early identification and neonatal screening of severe combined immunodeficiencies .” 2014. Thesis, University of Debrecen. Accessed January 19, 2020. http://hdl.handle.net/2437/194848.

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

MLA Handbook (7th Edition):

Kupcha, Anna. “Early identification and neonatal screening of severe combined immunodeficiencies .” 2014. Web. 19 Jan 2020.

Vancouver:

Kupcha A. Early identification and neonatal screening of severe combined immunodeficiencies . [Internet] [Thesis]. University of Debrecen; 2014. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2437/194848.

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

Council of Science Editors:

Kupcha A. Early identification and neonatal screening of severe combined immunodeficiencies . [Thesis]. University of Debrecen; 2014. Available from: http://hdl.handle.net/2437/194848

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


Washington State University

2. [No author]. Neutralizing antibody-mediated control of lentivirus infection .

Degree: 2010, Washington State University

 NEUTRALIZING ANTIBODY-MEDIATED CONTROL OF LENTIVIRUS INFECTIONAbstractby Sandra D. Taylor, Ph.D.Washington State UniversityDecember 2010Chair: Robert H. MealeyVaccines preventing HIV-1 infection will likely elicit antibodies that neutralize… (more)

Subjects/Keywords: antibody; EIAV; neutralization; resistance; SCID

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APA (6th Edition):

author], [. (2010). Neutralizing antibody-mediated control of lentivirus infection . (Thesis). Washington State University. Retrieved from http://hdl.handle.net/2376/2791

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):

author], [No. “Neutralizing antibody-mediated control of lentivirus infection .” 2010. Thesis, Washington State University. Accessed January 19, 2020. http://hdl.handle.net/2376/2791.

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

MLA Handbook (7th Edition):

author], [No. “Neutralizing antibody-mediated control of lentivirus infection .” 2010. Web. 19 Jan 2020.

Vancouver:

author] [. Neutralizing antibody-mediated control of lentivirus infection . [Internet] [Thesis]. Washington State University; 2010. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2376/2791.

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

Council of Science Editors:

author] [. Neutralizing antibody-mediated control of lentivirus infection . [Thesis]. Washington State University; 2010. Available from: http://hdl.handle.net/2376/2791

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


University of Ottawa

3. Cavar, Marko. Mutational Analysis of CD127 and Its Role in Immunological Diseases .

Degree: 2016, University of Ottawa

 Interleukin (IL) -7 is an essential non-redundant cytokine that influences T-cell differentiation, proliferation, homeostasis and T-cell functions. In T-cells, IL-7 signals are transduced via IL-7's… (more)

Subjects/Keywords: CD127; Autoimmune; SCID; Interleukin-7; Multiple Sclerosis

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APA (6th Edition):

Cavar, M. (2016). Mutational Analysis of CD127 and Its Role in Immunological Diseases . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/34404

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):

Cavar, Marko. “Mutational Analysis of CD127 and Its Role in Immunological Diseases .” 2016. Thesis, University of Ottawa. Accessed January 19, 2020. http://hdl.handle.net/10393/34404.

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

MLA Handbook (7th Edition):

Cavar, Marko. “Mutational Analysis of CD127 and Its Role in Immunological Diseases .” 2016. Web. 19 Jan 2020.

Vancouver:

Cavar M. Mutational Analysis of CD127 and Its Role in Immunological Diseases . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/10393/34404.

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

Council of Science Editors:

Cavar M. Mutational Analysis of CD127 and Its Role in Immunological Diseases . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/34404

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


University of Toronto

4. Dhanju, Rupreet. Lung Complications in Adenosine Deaminase (ADA) Deficiency: A Mouse Model for the Human Disease.

Degree: 2012, University of Toronto

Recently, we discovered patients with inherited adenosine deaminase (ADA) deficiency are predisposed to pulmonary alveolar proteinosis (PAP). PAP is characterized by the accumulation of surfactant… (more)

Subjects/Keywords: Adenosine Deaminase; SCID; Pulmonary Alveolar Proteinosis; 0306

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APA (6th Edition):

Dhanju, R. (2012). Lung Complications in Adenosine Deaminase (ADA) Deficiency: A Mouse Model for the Human Disease. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33397

Chicago Manual of Style (16th Edition):

Dhanju, Rupreet. “Lung Complications in Adenosine Deaminase (ADA) Deficiency: A Mouse Model for the Human Disease.” 2012. Masters Thesis, University of Toronto. Accessed January 19, 2020. http://hdl.handle.net/1807/33397.

MLA Handbook (7th Edition):

Dhanju, Rupreet. “Lung Complications in Adenosine Deaminase (ADA) Deficiency: A Mouse Model for the Human Disease.” 2012. Web. 19 Jan 2020.

Vancouver:

Dhanju R. Lung Complications in Adenosine Deaminase (ADA) Deficiency: A Mouse Model for the Human Disease. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1807/33397.

Council of Science Editors:

Dhanju R. Lung Complications in Adenosine Deaminase (ADA) Deficiency: A Mouse Model for the Human Disease. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33397

5. Hauck, Fabian. Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK.

Degree: Docteur es, Immunologie, 2013, Université Paris Descartes – Paris V

Les lymphocytes T sont caractérisés par l’expression d’un récepteur à l’antigène des cellules T (TCR), soit le preTCR, soit le γδ TCR et le αβ… (more)

Subjects/Keywords: PID; SCID; CID; TCR; T cell; Lck; Zap-70; Itk; PID; SCID; CID; TCR; T cell; Lck; Zap-70; Itk; 616.079

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APA (6th Edition):

Hauck, F. (2013). Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2013PA05T031

Chicago Manual of Style (16th Edition):

Hauck, Fabian. “Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK.” 2013. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed January 19, 2020. http://www.theses.fr/2013PA05T031.

MLA Handbook (7th Edition):

Hauck, Fabian. “Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK.” 2013. Web. 19 Jan 2020.

Vancouver:

Hauck F. Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2013. [cited 2020 Jan 19]. Available from: http://www.theses.fr/2013PA05T031.

Council of Science Editors:

Hauck F. Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2013. Available from: http://www.theses.fr/2013PA05T031

6. Bouis, Delphine. Etude des conséquences d’un gain de fonction de Sting chez la souris : modèle STING V154M/WT : Studying consequences of Sting Gain-of-function in mice : STING V154M/WT mouse model.

Degree: Docteur es, Immunologie, 2018, Université de Strasbourg

Des mutations gains de fonction du gène STING chez l’Homme (telles que V155M) déclenchent une pathologie autoinflammatoire sévère de type interféronopathie, le SAVI (Sting associated… (more)

Subjects/Keywords: STING; V154M; SCID; IFN I; Développement lymphoïde; STING; V154M; SCID; IFN I; Lymphoid development; 572.8; 616.9

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APA (6th Edition):

Bouis, D. (2018). Etude des conséquences d’un gain de fonction de Sting chez la souris : modèle STING V154M/WT : Studying consequences of Sting Gain-of-function in mice : STING V154M/WT mouse model. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2018STRAJ063

Chicago Manual of Style (16th Edition):

Bouis, Delphine. “Etude des conséquences d’un gain de fonction de Sting chez la souris : modèle STING V154M/WT : Studying consequences of Sting Gain-of-function in mice : STING V154M/WT mouse model.” 2018. Doctoral Dissertation, Université de Strasbourg. Accessed January 19, 2020. http://www.theses.fr/2018STRAJ063.

MLA Handbook (7th Edition):

Bouis, Delphine. “Etude des conséquences d’un gain de fonction de Sting chez la souris : modèle STING V154M/WT : Studying consequences of Sting Gain-of-function in mice : STING V154M/WT mouse model.” 2018. Web. 19 Jan 2020.

Vancouver:

Bouis D. Etude des conséquences d’un gain de fonction de Sting chez la souris : modèle STING V154M/WT : Studying consequences of Sting Gain-of-function in mice : STING V154M/WT mouse model. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2018. [cited 2020 Jan 19]. Available from: http://www.theses.fr/2018STRAJ063.

Council of Science Editors:

Bouis D. Etude des conséquences d’un gain de fonction de Sting chez la souris : modèle STING V154M/WT : Studying consequences of Sting Gain-of-function in mice : STING V154M/WT mouse model. [Doctoral Dissertation]. Université de Strasbourg; 2018. Available from: http://www.theses.fr/2018STRAJ063


University of Alberta

7. Hsi Dickie, Belinda. Advancing the Alb-uPA/SCID/Bg Chimeric Mouse.

Degree: PhD, Department of Surgery, 2009, University of Alberta

 The feasibility of the Alb-uPA/SCID/Bg chimeric mouse as a model for Hepatitis C Virus (HCV) infection was assessed experimentally by (1) the infection and treatment… (more)

Subjects/Keywords: Hepatitis C; Mouse Model; Transgenic mice; Alb-uPA/SCID/Beige mouse

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APA (6th Edition):

Hsi Dickie, B. (2009). Advancing the Alb-uPA/SCID/Bg Chimeric Mouse. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/rr171x54d

Chicago Manual of Style (16th Edition):

Hsi Dickie, Belinda. “Advancing the Alb-uPA/SCID/Bg Chimeric Mouse.” 2009. Doctoral Dissertation, University of Alberta. Accessed January 19, 2020. https://era.library.ualberta.ca/files/rr171x54d.

MLA Handbook (7th Edition):

Hsi Dickie, Belinda. “Advancing the Alb-uPA/SCID/Bg Chimeric Mouse.” 2009. Web. 19 Jan 2020.

Vancouver:

Hsi Dickie B. Advancing the Alb-uPA/SCID/Bg Chimeric Mouse. [Internet] [Doctoral dissertation]. University of Alberta; 2009. [cited 2020 Jan 19]. Available from: https://era.library.ualberta.ca/files/rr171x54d.

Council of Science Editors:

Hsi Dickie B. Advancing the Alb-uPA/SCID/Bg Chimeric Mouse. [Doctoral Dissertation]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/rr171x54d


Royal Holloway, University of London

8. Prakash, Versha. Gene editing in PRKDC severe combined immunodeficiency and ataxia telangiectasia.

Degree: PhD, 2017, Royal Holloway, University of London

 Primary immunodeficiencies (PIDs) are inherited diseases of the immune system. A variety of molecular defects can cause PIDs, including mutations in genes PRKDC and ATM… (more)

Subjects/Keywords: Gene editing; CRISPR-Cas; Radiosensitive SCID; Ataxia Telangiectasia; PRKDC

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APA (6th Edition):

Prakash, V. (2017). Gene editing in PRKDC severe combined immunodeficiency and ataxia telangiectasia. (Doctoral Dissertation). Royal Holloway, University of London. Retrieved from https://pure.royalholloway.ac.uk/portal/en/publications/gene-editing-in-prkdc-severe-combined-immunodeficiency-and-ataxia-telangiectasia(480a3d06-4c85-4783-99f3-0a375831d283).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792683

Chicago Manual of Style (16th Edition):

Prakash, Versha. “Gene editing in PRKDC severe combined immunodeficiency and ataxia telangiectasia.” 2017. Doctoral Dissertation, Royal Holloway, University of London. Accessed January 19, 2020. https://pure.royalholloway.ac.uk/portal/en/publications/gene-editing-in-prkdc-severe-combined-immunodeficiency-and-ataxia-telangiectasia(480a3d06-4c85-4783-99f3-0a375831d283).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792683.

MLA Handbook (7th Edition):

Prakash, Versha. “Gene editing in PRKDC severe combined immunodeficiency and ataxia telangiectasia.” 2017. Web. 19 Jan 2020.

Vancouver:

Prakash V. Gene editing in PRKDC severe combined immunodeficiency and ataxia telangiectasia. [Internet] [Doctoral dissertation]. Royal Holloway, University of London; 2017. [cited 2020 Jan 19]. Available from: https://pure.royalholloway.ac.uk/portal/en/publications/gene-editing-in-prkdc-severe-combined-immunodeficiency-and-ataxia-telangiectasia(480a3d06-4c85-4783-99f3-0a375831d283).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792683.

Council of Science Editors:

Prakash V. Gene editing in PRKDC severe combined immunodeficiency and ataxia telangiectasia. [Doctoral Dissertation]. Royal Holloway, University of London; 2017. Available from: https://pure.royalholloway.ac.uk/portal/en/publications/gene-editing-in-prkdc-severe-combined-immunodeficiency-and-ataxia-telangiectasia(480a3d06-4c85-4783-99f3-0a375831d283).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792683

9. Christou, Niki. De la caractérisation des Cellules Initiant le Cancer Colorectal vers un biomarqueur pronostique et de surveillance des sujets traités pour cancer colorectal : From characterization of colorectal cancer initiating cells to a prognostic biomarker and monotoring of patients treated for colorectal cancer.

Degree: Docteur es, Biologie-Santé, 2017, Limoges

Le Cancer Colo Rectal (CCR) est la deuxième cause de mortalité par cancer dans le monde. Le risque de récidive après traitement curatif atteint 45%… (more)

Subjects/Keywords: Cancer colorectal; Cellules initiant le cancer; Membrane chorio allantoidienne; Souris SCID; E cadherine; Colorectal cancer; Cancer initiating cells; Chorio allantoid membrane; SCID mice; E cadherin; 616.994

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APA (6th Edition):

Christou, N. (2017). De la caractérisation des Cellules Initiant le Cancer Colorectal vers un biomarqueur pronostique et de surveillance des sujets traités pour cancer colorectal : From characterization of colorectal cancer initiating cells to a prognostic biomarker and monotoring of patients treated for colorectal cancer. (Doctoral Dissertation). Limoges. Retrieved from http://www.theses.fr/2017LIMO0007

Chicago Manual of Style (16th Edition):

Christou, Niki. “De la caractérisation des Cellules Initiant le Cancer Colorectal vers un biomarqueur pronostique et de surveillance des sujets traités pour cancer colorectal : From characterization of colorectal cancer initiating cells to a prognostic biomarker and monotoring of patients treated for colorectal cancer.” 2017. Doctoral Dissertation, Limoges. Accessed January 19, 2020. http://www.theses.fr/2017LIMO0007.

MLA Handbook (7th Edition):

Christou, Niki. “De la caractérisation des Cellules Initiant le Cancer Colorectal vers un biomarqueur pronostique et de surveillance des sujets traités pour cancer colorectal : From characterization of colorectal cancer initiating cells to a prognostic biomarker and monotoring of patients treated for colorectal cancer.” 2017. Web. 19 Jan 2020.

Vancouver:

Christou N. De la caractérisation des Cellules Initiant le Cancer Colorectal vers un biomarqueur pronostique et de surveillance des sujets traités pour cancer colorectal : From characterization of colorectal cancer initiating cells to a prognostic biomarker and monotoring of patients treated for colorectal cancer. [Internet] [Doctoral dissertation]. Limoges; 2017. [cited 2020 Jan 19]. Available from: http://www.theses.fr/2017LIMO0007.

Council of Science Editors:

Christou N. De la caractérisation des Cellules Initiant le Cancer Colorectal vers un biomarqueur pronostique et de surveillance des sujets traités pour cancer colorectal : From characterization of colorectal cancer initiating cells to a prognostic biomarker and monotoring of patients treated for colorectal cancer. [Doctoral Dissertation]. Limoges; 2017. Available from: http://www.theses.fr/2017LIMO0007


Dalhousie University

10. Fernando, T R G Wasundara. EFFICACY AND SAFETY OF DOCOSAHEXAENOIC ACID ACYLATED PHLORIDZIN FOR TREATING TRIPLE NEGATIVE BREAST CANCER.

Degree: MS, Faculty of Agriculture, 2014, Dalhousie University

 Phloridzin (PZ), a polyphenol compound found in apple, exerts glucose transporter inhibitory and estrogen-like effects. Therapeutic applications of PZ are limited due to its poor… (more)

Subjects/Keywords: Triple negative breast cancer; tumor suppression; NOD-SCID; phloridzin; docosahexaenoic acid; PZ-DHA

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APA (6th Edition):

Fernando, T. R. G. W. (2014). EFFICACY AND SAFETY OF DOCOSAHEXAENOIC ACID ACYLATED PHLORIDZIN FOR TREATING TRIPLE NEGATIVE BREAST CANCER. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/54032

Chicago Manual of Style (16th Edition):

Fernando, T R G Wasundara. “EFFICACY AND SAFETY OF DOCOSAHEXAENOIC ACID ACYLATED PHLORIDZIN FOR TREATING TRIPLE NEGATIVE BREAST CANCER.” 2014. Masters Thesis, Dalhousie University. Accessed January 19, 2020. http://hdl.handle.net/10222/54032.

MLA Handbook (7th Edition):

Fernando, T R G Wasundara. “EFFICACY AND SAFETY OF DOCOSAHEXAENOIC ACID ACYLATED PHLORIDZIN FOR TREATING TRIPLE NEGATIVE BREAST CANCER.” 2014. Web. 19 Jan 2020.

Vancouver:

Fernando TRGW. EFFICACY AND SAFETY OF DOCOSAHEXAENOIC ACID ACYLATED PHLORIDZIN FOR TREATING TRIPLE NEGATIVE BREAST CANCER. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/10222/54032.

Council of Science Editors:

Fernando TRGW. EFFICACY AND SAFETY OF DOCOSAHEXAENOIC ACID ACYLATED PHLORIDZIN FOR TREATING TRIPLE NEGATIVE BREAST CANCER. [Masters Thesis]. Dalhousie University; 2014. Available from: http://hdl.handle.net/10222/54032


University of Minnesota

11. Multhaup, Megan Marie. Gene therapy for Athabascan SCID.

Degree: PhD, 2010, University of Minnesota

 Artemis is an endonuclease characterized as a key factor involved in both nonhomologous end joining (NHEJ) and variable (diversity) joining (V(D)J) recombination. Mutations in the… (more)

Subjects/Keywords: Artemis; Gene Therapy; Immunodeficiency; Lentivirus; SCID; Molecular, Cellular, Developmental Biology and Genetics

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APA (6th Edition):

Multhaup, M. M. (2010). Gene therapy for Athabascan SCID. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/97761

Chicago Manual of Style (16th Edition):

Multhaup, Megan Marie. “Gene therapy for Athabascan SCID.” 2010. Doctoral Dissertation, University of Minnesota. Accessed January 19, 2020. http://purl.umn.edu/97761.

MLA Handbook (7th Edition):

Multhaup, Megan Marie. “Gene therapy for Athabascan SCID.” 2010. Web. 19 Jan 2020.

Vancouver:

Multhaup MM. Gene therapy for Athabascan SCID. [Internet] [Doctoral dissertation]. University of Minnesota; 2010. [cited 2020 Jan 19]. Available from: http://purl.umn.edu/97761.

Council of Science Editors:

Multhaup MM. Gene therapy for Athabascan SCID. [Doctoral Dissertation]. University of Minnesota; 2010. Available from: http://purl.umn.edu/97761


University of Alberta

12. Chen, Ran. STUDIES OF HEPATITIS B VIRUS AND HEPATITIS C VIRUS IN SCID/BEIGE-ALB/UPA CHIMERIC MICE.

Degree: PhD, Department of Medical Microbiology and Immunology, 2014, University of Alberta

 Both hepatitis C virus (HCV) and hepatitis B virus (HBV) infections represent major global public health problems. Interferon (IFN) has been an important factor in… (more)

Subjects/Keywords: SCID/BEIGE-ALB/UPA CHIMERIC MOUSE MODEL; INTERFERON; HEPATITIS B VIRUS; HEPATITIS C VIRUS

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APA (6th Edition):

Chen, R. (2014). STUDIES OF HEPATITIS B VIRUS AND HEPATITIS C VIRUS IN SCID/BEIGE-ALB/UPA CHIMERIC MICE. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/h702q7680

Chicago Manual of Style (16th Edition):

Chen, Ran. “STUDIES OF HEPATITIS B VIRUS AND HEPATITIS C VIRUS IN SCID/BEIGE-ALB/UPA CHIMERIC MICE.” 2014. Doctoral Dissertation, University of Alberta. Accessed January 19, 2020. https://era.library.ualberta.ca/files/h702q7680.

MLA Handbook (7th Edition):

Chen, Ran. “STUDIES OF HEPATITIS B VIRUS AND HEPATITIS C VIRUS IN SCID/BEIGE-ALB/UPA CHIMERIC MICE.” 2014. Web. 19 Jan 2020.

Vancouver:

Chen R. STUDIES OF HEPATITIS B VIRUS AND HEPATITIS C VIRUS IN SCID/BEIGE-ALB/UPA CHIMERIC MICE. [Internet] [Doctoral dissertation]. University of Alberta; 2014. [cited 2020 Jan 19]. Available from: https://era.library.ualberta.ca/files/h702q7680.

Council of Science Editors:

Chen R. STUDIES OF HEPATITIS B VIRUS AND HEPATITIS C VIRUS IN SCID/BEIGE-ALB/UPA CHIMERIC MICE. [Doctoral Dissertation]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/h702q7680


Universiteit Utrecht

13. Wempe, F. High mortality among young wetterhoun dogs due to an immunodeficiency.

Degree: 2009, Universiteit Utrecht

 The Wetterhoun is an old Dutch hunting dogbreed which consists of a very small population. Inbreeding is a big risk within the population and the… (more)

Subjects/Keywords: Diergeneeskunde; SCID, Severe Combined Immuno Deficiency, Primary immunodefciency, pup mortality, Wetterhoun dog

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APA (6th Edition):

Wempe, F. (2009). High mortality among young wetterhoun dogs due to an immunodeficiency. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/35031

Chicago Manual of Style (16th Edition):

Wempe, F. “High mortality among young wetterhoun dogs due to an immunodeficiency.” 2009. Doctoral Dissertation, Universiteit Utrecht. Accessed January 19, 2020. http://dspace.library.uu.nl:8080/handle/1874/35031.

MLA Handbook (7th Edition):

Wempe, F. “High mortality among young wetterhoun dogs due to an immunodeficiency.” 2009. Web. 19 Jan 2020.

Vancouver:

Wempe F. High mortality among young wetterhoun dogs due to an immunodeficiency. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2009. [cited 2020 Jan 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/35031.

Council of Science Editors:

Wempe F. High mortality among young wetterhoun dogs due to an immunodeficiency. [Doctoral Dissertation]. Universiteit Utrecht; 2009. Available from: http://dspace.library.uu.nl:8080/handle/1874/35031


Penn State University

14. Xu, Tongtong. Anti-Cancer Effects of Phenolic-rich Extracts of Button Mushrooms (Agaricus bisporus).

Degree: PhD, Food Science, 2012, Penn State University

 Standard therapies for the treatments of cancer have limitations, including lack of effectiveness against hormone-refractory tumors and toxic side-effects. Dietary anti-cancer compounds have attracted increasing… (more)

Subjects/Keywords: Agaricus bisporus; mushrooms; cancer; phenolic compounds; apoptosis; microarray; SCID mice; xenograft tumor

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APA (6th Edition):

Xu, T. (2012). Anti-Cancer Effects of Phenolic-rich Extracts of Button Mushrooms (Agaricus bisporus). (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/17505

Chicago Manual of Style (16th Edition):

Xu, Tongtong. “Anti-Cancer Effects of Phenolic-rich Extracts of Button Mushrooms (Agaricus bisporus).” 2012. Doctoral Dissertation, Penn State University. Accessed January 19, 2020. https://etda.libraries.psu.edu/catalog/17505.

MLA Handbook (7th Edition):

Xu, Tongtong. “Anti-Cancer Effects of Phenolic-rich Extracts of Button Mushrooms (Agaricus bisporus).” 2012. Web. 19 Jan 2020.

Vancouver:

Xu T. Anti-Cancer Effects of Phenolic-rich Extracts of Button Mushrooms (Agaricus bisporus). [Internet] [Doctoral dissertation]. Penn State University; 2012. [cited 2020 Jan 19]. Available from: https://etda.libraries.psu.edu/catalog/17505.

Council of Science Editors:

Xu T. Anti-Cancer Effects of Phenolic-rich Extracts of Button Mushrooms (Agaricus bisporus). [Doctoral Dissertation]. Penn State University; 2012. Available from: https://etda.libraries.psu.edu/catalog/17505


Université de Sherbrooke

15. Provençal, Philippe. Étude de biomarqueurs pour la maladie de Fabry dans les tissus de souris NOD/SCID/Fabry .

Degree: 2017, Université de Sherbrooke

 La maladie de Fabry est une maladie lysosomale présentant une grande hétérogénéité phénotypique et génotypique. Elle est causée par des mutations au niveau du gène… (more)

Subjects/Keywords: Maladie de Fabry; Spectrométrie de masse; Globotriaosylcéramide (Gb3); Souris NOD/SCID/Fabry; Biomarqueur; Thérapie génique

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APA (6th Edition):

Provençal, P. (2017). Étude de biomarqueurs pour la maladie de Fabry dans les tissus de souris NOD/SCID/Fabry . (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/10972

Chicago Manual of Style (16th Edition):

Provençal, Philippe. “Étude de biomarqueurs pour la maladie de Fabry dans les tissus de souris NOD/SCID/Fabry .” 2017. Masters Thesis, Université de Sherbrooke. Accessed January 19, 2020. http://hdl.handle.net/11143/10972.

MLA Handbook (7th Edition):

Provençal, Philippe. “Étude de biomarqueurs pour la maladie de Fabry dans les tissus de souris NOD/SCID/Fabry .” 2017. Web. 19 Jan 2020.

Vancouver:

Provençal P. Étude de biomarqueurs pour la maladie de Fabry dans les tissus de souris NOD/SCID/Fabry . [Internet] [Masters thesis]. Université de Sherbrooke; 2017. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/11143/10972.

Council of Science Editors:

Provençal P. Étude de biomarqueurs pour la maladie de Fabry dans les tissus de souris NOD/SCID/Fabry . [Masters Thesis]. Université de Sherbrooke; 2017. Available from: http://hdl.handle.net/11143/10972


University of Saskatchewan

16. Karkare, Sharayu A 1993-. Targeted therapy of osteosarcoma with radiolabeled monoclonal antibody to an insulin-like growth factor-2 receptor.

Degree: 2017, University of Saskatchewan

 Osteosarcoma (OS) represents 3.4% of all childhood cancers with overall survival of 70% not improving in 30 years. The consistent surface overexpression of insulin-like growth… (more)

Subjects/Keywords: RIT; OS; IGF2R; SPECT-CT; TRT; mAb; Lutetium-177; Actinium-225; PDX; SCID

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APA (6th Edition):

Karkare, S. A. 1. (2017). Targeted therapy of osteosarcoma with radiolabeled monoclonal antibody to an insulin-like growth factor-2 receptor. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12331

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):

Karkare, Sharayu A 1993-. “Targeted therapy of osteosarcoma with radiolabeled monoclonal antibody to an insulin-like growth factor-2 receptor.” 2017. Thesis, University of Saskatchewan. Accessed January 19, 2020. http://hdl.handle.net/10388/12331.

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

MLA Handbook (7th Edition):

Karkare, Sharayu A 1993-. “Targeted therapy of osteosarcoma with radiolabeled monoclonal antibody to an insulin-like growth factor-2 receptor.” 2017. Web. 19 Jan 2020.

Vancouver:

Karkare SA1. Targeted therapy of osteosarcoma with radiolabeled monoclonal antibody to an insulin-like growth factor-2 receptor. [Internet] [Thesis]. University of Saskatchewan; 2017. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/10388/12331.

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

Council of Science Editors:

Karkare SA1. Targeted therapy of osteosarcoma with radiolabeled monoclonal antibody to an insulin-like growth factor-2 receptor. [Thesis]. University of Saskatchewan; 2017. Available from: http://hdl.handle.net/10388/12331

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


Iowa State University

17. Waide, Emily Hannah. Molecular and quantitative genetic basis and control of severe combined immunodeficiency and porcine reproductive and respiratory syndrome in pigs.

Degree: 2015, Iowa State University

 Disease causes large economic losses in the swine industry, not only through the cost of medical treatment, but also due to reduced production performance of… (more)

Subjects/Keywords: Genetics; genomics; molecular genetics; pigs; PRRS; quantitative genetics; SCID; Agriculture; Animal Diseases; Animal Sciences; Genetics

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APA (6th Edition):

Waide, E. H. (2015). Molecular and quantitative genetic basis and control of severe combined immunodeficiency and porcine reproductive and respiratory syndrome in pigs. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/14878

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):

Waide, Emily Hannah. “Molecular and quantitative genetic basis and control of severe combined immunodeficiency and porcine reproductive and respiratory syndrome in pigs.” 2015. Thesis, Iowa State University. Accessed January 19, 2020. https://lib.dr.iastate.edu/etd/14878.

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

MLA Handbook (7th Edition):

Waide, Emily Hannah. “Molecular and quantitative genetic basis and control of severe combined immunodeficiency and porcine reproductive and respiratory syndrome in pigs.” 2015. Web. 19 Jan 2020.

Vancouver:

Waide EH. Molecular and quantitative genetic basis and control of severe combined immunodeficiency and porcine reproductive and respiratory syndrome in pigs. [Internet] [Thesis]. Iowa State University; 2015. [cited 2020 Jan 19]. Available from: https://lib.dr.iastate.edu/etd/14878.

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

Council of Science Editors:

Waide EH. Molecular and quantitative genetic basis and control of severe combined immunodeficiency and porcine reproductive and respiratory syndrome in pigs. [Thesis]. Iowa State University; 2015. Available from: https://lib.dr.iastate.edu/etd/14878

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


University of Alberta

18. Mohajerani, Seyed Amir. Immortalized human hepatocyte, an alternate model for the study of the propagation of HCV in vivo and in vitro.

Degree: MS, Department of Surgery, 2010, University of Alberta

 The chimeric Alb-uPA SCID mouse that has been transplanted with human hepatocytes is a model to facilitate in vivo study of HCV. We explored further… (more)

Subjects/Keywords: Immortalized human hepatocyte, HCV, SCID-uPA mice, de-immortalization, tamoxifen, Cre recombinase, JFH1, viral entry, HCV life cycle

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APA (6th Edition):

Mohajerani, S. A. (2010). Immortalized human hepatocyte, an alternate model for the study of the propagation of HCV in vivo and in vitro. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/mp48sc78n

Chicago Manual of Style (16th Edition):

Mohajerani, Seyed Amir. “Immortalized human hepatocyte, an alternate model for the study of the propagation of HCV in vivo and in vitro.” 2010. Masters Thesis, University of Alberta. Accessed January 19, 2020. https://era.library.ualberta.ca/files/mp48sc78n.

MLA Handbook (7th Edition):

Mohajerani, Seyed Amir. “Immortalized human hepatocyte, an alternate model for the study of the propagation of HCV in vivo and in vitro.” 2010. Web. 19 Jan 2020.

Vancouver:

Mohajerani SA. Immortalized human hepatocyte, an alternate model for the study of the propagation of HCV in vivo and in vitro. [Internet] [Masters thesis]. University of Alberta; 2010. [cited 2020 Jan 19]. Available from: https://era.library.ualberta.ca/files/mp48sc78n.

Council of Science Editors:

Mohajerani SA. Immortalized human hepatocyte, an alternate model for the study of the propagation of HCV in vivo and in vitro. [Masters Thesis]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/mp48sc78n


University of Alberta

19. Pang, Daniel. To HAV or not to HAV: Novel hepatitis A virus (HAV) infection in a chimeric mouse model.

Degree: MS, Department of Medical Microbiology and Immunology, 2013, University of Alberta

 Chimpanzees have been previously used to study HAV infection in vivo but they are expensive and difficult to maintain and thus, there is a need… (more)

Subjects/Keywords: small animal model; hcv; hepatitis a virus; chimeric mouse model; hav; SCID-beige/Alb-uPA; hepatitis c virus

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APA (6th Edition):

Pang, D. (2013). To HAV or not to HAV: Novel hepatitis A virus (HAV) infection in a chimeric mouse model. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/9p290b669

Chicago Manual of Style (16th Edition):

Pang, Daniel. “To HAV or not to HAV: Novel hepatitis A virus (HAV) infection in a chimeric mouse model.” 2013. Masters Thesis, University of Alberta. Accessed January 19, 2020. https://era.library.ualberta.ca/files/9p290b669.

MLA Handbook (7th Edition):

Pang, Daniel. “To HAV or not to HAV: Novel hepatitis A virus (HAV) infection in a chimeric mouse model.” 2013. Web. 19 Jan 2020.

Vancouver:

Pang D. To HAV or not to HAV: Novel hepatitis A virus (HAV) infection in a chimeric mouse model. [Internet] [Masters thesis]. University of Alberta; 2013. [cited 2020 Jan 19]. Available from: https://era.library.ualberta.ca/files/9p290b669.

Council of Science Editors:

Pang D. To HAV or not to HAV: Novel hepatitis A virus (HAV) infection in a chimeric mouse model. [Masters Thesis]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/9p290b669


University of Oulu

20. Kantojärvi, L. (Liisa). Personality disorders in the Northern Finland 1966 Birth Cohort Study.

Degree: 2008, University of Oulu

Abstract Personality disorders (PDs) are relatively common mental disorders associating with other psychiatric disorders and disability. The aim of the study was to determine the… (more)

Subjects/Keywords: DSM-III-R; Finland; SCID; TCI; comorbidity; family structure; hospital treatment; personality disorder; population study; temperament; perherakenne; persoonallisuushäiriö; sairaalahoito; väestötutkimus; yhteissairastavuus

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APA (6th Edition):

Kantojärvi, L. (. (2008). Personality disorders in the Northern Finland 1966 Birth Cohort Study. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514288487

Chicago Manual of Style (16th Edition):

Kantojärvi, L (Liisa). “Personality disorders in the Northern Finland 1966 Birth Cohort Study.” 2008. Doctoral Dissertation, University of Oulu. Accessed January 19, 2020. http://urn.fi/urn:isbn:9789514288487.

MLA Handbook (7th Edition):

Kantojärvi, L (Liisa). “Personality disorders in the Northern Finland 1966 Birth Cohort Study.” 2008. Web. 19 Jan 2020.

Vancouver:

Kantojärvi L(. Personality disorders in the Northern Finland 1966 Birth Cohort Study. [Internet] [Doctoral dissertation]. University of Oulu; 2008. [cited 2020 Jan 19]. Available from: http://urn.fi/urn:isbn:9789514288487.

Council of Science Editors:

Kantojärvi L(. Personality disorders in the Northern Finland 1966 Birth Cohort Study. [Doctoral Dissertation]. University of Oulu; 2008. Available from: http://urn.fi/urn:isbn:9789514288487


Universiteit Utrecht

21. Verfuurden, B. The genetic background of immune deficiency related mortality among Wetterhoun pups.

Degree: 2008, Universiteit Utrecht

 For about 17 years the Friese Staby and Wetterhoun association has been dealing with unexplained mortality among Wetterhoun pups. The clinical signs and the results… (more)

Subjects/Keywords: Diergeneeskunde; Severe combined immunodeficiency (SCID), Wetterhoun, DNA PKcs, KU70, KU80, Artemis, DNA Ligase IV, XRCC4, RAG1, RAG2

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APA (6th Edition):

Verfuurden, B. (2008). The genetic background of immune deficiency related mortality among Wetterhoun pups. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/33496

Chicago Manual of Style (16th Edition):

Verfuurden, B. “The genetic background of immune deficiency related mortality among Wetterhoun pups.” 2008. Masters Thesis, Universiteit Utrecht. Accessed January 19, 2020. http://dspace.library.uu.nl:8080/handle/1874/33496.

MLA Handbook (7th Edition):

Verfuurden, B. “The genetic background of immune deficiency related mortality among Wetterhoun pups.” 2008. Web. 19 Jan 2020.

Vancouver:

Verfuurden B. The genetic background of immune deficiency related mortality among Wetterhoun pups. [Internet] [Masters thesis]. Universiteit Utrecht; 2008. [cited 2020 Jan 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/33496.

Council of Science Editors:

Verfuurden B. The genetic background of immune deficiency related mortality among Wetterhoun pups. [Masters Thesis]. Universiteit Utrecht; 2008. Available from: http://dspace.library.uu.nl:8080/handle/1874/33496


Universiteit Utrecht

22. Latour, B.L. Regenerating an Immune System: Gene Therapy and Stem Cell Transplantation for Severe Combined Immune Deficiency.

Degree: 2013, Universiteit Utrecht

 Primary immunodeficiencies (PIDs) are a subset of immunologically based, inherited diseases that predispose affected individuals to a variety of infections, allergies, and autoimmune disorders, and… (more)

Subjects/Keywords: Severe Combined Immune Deficiency (SCID); hematopoietic stem cell transplantation (HSCT); gene therapy; insertional mutagenesis; LMO2; viral integration; primary immunodeficiency (PID)

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APA (6th Edition):

Latour, B. L. (2013). Regenerating an Immune System: Gene Therapy and Stem Cell Transplantation for Severe Combined Immune Deficiency. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/285783

Chicago Manual of Style (16th Edition):

Latour, B L. “Regenerating an Immune System: Gene Therapy and Stem Cell Transplantation for Severe Combined Immune Deficiency.” 2013. Masters Thesis, Universiteit Utrecht. Accessed January 19, 2020. http://dspace.library.uu.nl:8080/handle/1874/285783.

MLA Handbook (7th Edition):

Latour, B L. “Regenerating an Immune System: Gene Therapy and Stem Cell Transplantation for Severe Combined Immune Deficiency.” 2013. Web. 19 Jan 2020.

Vancouver:

Latour BL. Regenerating an Immune System: Gene Therapy and Stem Cell Transplantation for Severe Combined Immune Deficiency. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2020 Jan 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/285783.

Council of Science Editors:

Latour BL. Regenerating an Immune System: Gene Therapy and Stem Cell Transplantation for Severe Combined Immune Deficiency. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/285783

23. 小酒, 慶一. A novel TK-NOG based humanized mouse model for the study of HBV and HCV infections. : HBV及びHCV感染症研究のための新たなTK-NOGベースヒト化マウスモデルの検討.

Degree: 博士(医学), 2014, Hiroshima University / 広島大学

 The immunodeficient mice transplanted with human hepatocytes are available for the study of the human hepatitis viruses. Recently, human hepatocytes were also successfully transplanted in… (more)

Subjects/Keywords: Human hepatocyte chimeric mouse; TK-NOG mouse; uPA-SCID mouse; Hepatitis B virus; Hepatitis C virus; Human serum albumin

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APA (6th Edition):

小酒, . (2014). A novel TK-NOG based humanized mouse model for the study of HBV and HCV infections. : HBV及びHCV感染症研究のための新たなTK-NOGベースヒト化マウスモデルの検討. (Thesis). Hiroshima University / 広島大学. Retrieved from http://ir.lib.hiroshima-u.ac.jp/00040621

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):

小酒, 慶一. “A novel TK-NOG based humanized mouse model for the study of HBV and HCV infections. : HBV及びHCV感染症研究のための新たなTK-NOGベースヒト化マウスモデルの検討.” 2014. Thesis, Hiroshima University / 広島大学. Accessed January 19, 2020. http://ir.lib.hiroshima-u.ac.jp/00040621.

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

MLA Handbook (7th Edition):

小酒, 慶一. “A novel TK-NOG based humanized mouse model for the study of HBV and HCV infections. : HBV及びHCV感染症研究のための新たなTK-NOGベースヒト化マウスモデルの検討.” 2014. Web. 19 Jan 2020.

Vancouver:

小酒 . A novel TK-NOG based humanized mouse model for the study of HBV and HCV infections. : HBV及びHCV感染症研究のための新たなTK-NOGベースヒト化マウスモデルの検討. [Internet] [Thesis]. Hiroshima University / 広島大学; 2014. [cited 2020 Jan 19]. Available from: http://ir.lib.hiroshima-u.ac.jp/00040621.

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

Council of Science Editors:

小酒 . A novel TK-NOG based humanized mouse model for the study of HBV and HCV infections. : HBV及びHCV感染症研究のための新たなTK-NOGベースヒト化マウスモデルの検討. [Thesis]. Hiroshima University / 広島大学; 2014. Available from: http://ir.lib.hiroshima-u.ac.jp/00040621

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

24. M. CHIRIVA INTERNATI. PRECLINICAL TESTING OF GALECTIN-3C FOR MULTIPLE MYELOMA.

Degree: 2012, Università degli Studi di Milano

 The American Cancer Society expects that there will be more than 20,000 new cases of multiple myeloma (MM) in the US in 2011 and despite… (more)

Subjects/Keywords: multiple myeloma; cancer; B cells; galectin-3C; bortezomib; animal model; nod/scid; Settore BIO/16 - Anatomia Umana

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APA (6th Edition):

INTERNATI, M. C. (2012). PRECLINICAL TESTING OF GALECTIN-3C FOR MULTIPLE MYELOMA. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/168390

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):

INTERNATI, M. CHIRIVA. “PRECLINICAL TESTING OF GALECTIN-3C FOR MULTIPLE MYELOMA.” 2012. Thesis, Università degli Studi di Milano. Accessed January 19, 2020. http://hdl.handle.net/2434/168390.

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

MLA Handbook (7th Edition):

INTERNATI, M. CHIRIVA. “PRECLINICAL TESTING OF GALECTIN-3C FOR MULTIPLE MYELOMA.” 2012. Web. 19 Jan 2020.

Vancouver:

INTERNATI MC. PRECLINICAL TESTING OF GALECTIN-3C FOR MULTIPLE MYELOMA. [Internet] [Thesis]. Università degli Studi di Milano; 2012. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2434/168390.

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

Council of Science Editors:

INTERNATI MC. PRECLINICAL TESTING OF GALECTIN-3C FOR MULTIPLE MYELOMA. [Thesis]. Università degli Studi di Milano; 2012. Available from: http://hdl.handle.net/2434/168390

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


University of Debrecen

25. Akhigbe, Benny. Severe Combined Immunodeficiency .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 Severe Combined Immunodeficiency(SCID)is a primary immunodeficiency.It gained public attention in the 1970's,a boy had to live in a sterile environment,a bubble, to have any chance… (more)

Subjects/Keywords: Severe Combined Immunodeficiency; X-SCID; Gene Therapy

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APA (6th Edition):

Akhigbe, B. (n.d.). Severe Combined Immunodeficiency . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/233533

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Akhigbe, Benny. “Severe Combined Immunodeficiency .” Thesis, University of Debrecen. Accessed January 19, 2020. http://hdl.handle.net/2437/233533.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Akhigbe, Benny. “Severe Combined Immunodeficiency .” Web. 19 Jan 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Akhigbe B. Severe Combined Immunodeficiency . [Internet] [Thesis]. University of Debrecen; [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2437/233533.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Akhigbe B. Severe Combined Immunodeficiency . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/233533

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Iowa State University

26. Boettcher, Adeline Nicole. Development and characterization of an immunologically humanized and cancer xenograft model in pigs with severe combined immunodeficiency (SCID).

Degree: 2019, Iowa State University

 Swine with severe combined immunodeficiency (SCID) are an emerging large animal model for biomedical research. There have been several SCID pig models described since our… (more)

Subjects/Keywords: Biomedical Animal Models; Cancer; SCID; Severe Combined Immunodeficiency; Swine; xenotransplantation; Cell Biology; Developmental Biology; Molecular Biology

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APA (6th Edition):

Boettcher, A. N. (2019). Development and characterization of an immunologically humanized and cancer xenograft model in pigs with severe combined immunodeficiency (SCID). (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/16975

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):

Boettcher, Adeline Nicole. “Development and characterization of an immunologically humanized and cancer xenograft model in pigs with severe combined immunodeficiency (SCID).” 2019. Thesis, Iowa State University. Accessed January 19, 2020. https://lib.dr.iastate.edu/etd/16975.

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

MLA Handbook (7th Edition):

Boettcher, Adeline Nicole. “Development and characterization of an immunologically humanized and cancer xenograft model in pigs with severe combined immunodeficiency (SCID).” 2019. Web. 19 Jan 2020.

Vancouver:

Boettcher AN. Development and characterization of an immunologically humanized and cancer xenograft model in pigs with severe combined immunodeficiency (SCID). [Internet] [Thesis]. Iowa State University; 2019. [cited 2020 Jan 19]. Available from: https://lib.dr.iastate.edu/etd/16975.

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

Council of Science Editors:

Boettcher AN. Development and characterization of an immunologically humanized and cancer xenograft model in pigs with severe combined immunodeficiency (SCID). [Thesis]. Iowa State University; 2019. Available from: https://lib.dr.iastate.edu/etd/16975

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


Leiden University

27. Wiekmeijer, A.S. In vivo modelling of normal and pathological human T-cell development.

Degree: 2016, Leiden University

 This thesis describes novel insights in human T-cell development by transplanting human HSPCs in severe immunodeficient NSG mice. First, an in vivo model was optimized… (more)

Subjects/Keywords: T-cell development; Human; NSG mouse; SCID; T-ALL; T-cell development; Human; NSG mouse; SCID; T-ALL

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wiekmeijer, A. S. (2016). In vivo modelling of normal and pathological human T-cell development. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/42846

Chicago Manual of Style (16th Edition):

Wiekmeijer, A S. “In vivo modelling of normal and pathological human T-cell development.” 2016. Doctoral Dissertation, Leiden University. Accessed January 19, 2020. http://hdl.handle.net/1887/42846.

MLA Handbook (7th Edition):

Wiekmeijer, A S. “In vivo modelling of normal and pathological human T-cell development.” 2016. Web. 19 Jan 2020.

Vancouver:

Wiekmeijer AS. In vivo modelling of normal and pathological human T-cell development. [Internet] [Doctoral dissertation]. Leiden University; 2016. [cited 2020 Jan 19]. Available from: http://hdl.handle.net/1887/42846.

Council of Science Editors:

Wiekmeijer AS. In vivo modelling of normal and pathological human T-cell development. [Doctoral Dissertation]. Leiden University; 2016. Available from: http://hdl.handle.net/1887/42846


University of Alberta

28. Abbasi Dezfouli, Meysam. Lipid Modified Polymers for Transfection of Human CRL Fibroblasts, and for siRNA Mediated MDR Reversal in Melanoma Cancer Therapy.

Degree: PhD, Department of Biomedical Engineering, 2010, University of Alberta

 Gene delivery for therapeutic purposes is quickly emerging as the best potential treatment option for inherited genetic diseases and cancer. Viral gene carriers have been… (more)

Subjects/Keywords: Chemotherapy; Fibroblast; Plasmid DNA; Transfection; SCID Mice; Multidrug Resistance; Polymer; siRNA; Non Viral Gene Delivery; Doxorubicin; Tumor; Paclitaxel; In Vivo Gene Delivery; P-glycoprotein; Melanoma Cancer

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APA (6th Edition):

Abbasi Dezfouli, M. (2010). Lipid Modified Polymers for Transfection of Human CRL Fibroblasts, and for siRNA Mediated MDR Reversal in Melanoma Cancer Therapy. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/jq085k82z

Chicago Manual of Style (16th Edition):

Abbasi Dezfouli, Meysam. “Lipid Modified Polymers for Transfection of Human CRL Fibroblasts, and for siRNA Mediated MDR Reversal in Melanoma Cancer Therapy.” 2010. Doctoral Dissertation, University of Alberta. Accessed January 19, 2020. https://era.library.ualberta.ca/files/jq085k82z.

MLA Handbook (7th Edition):

Abbasi Dezfouli, Meysam. “Lipid Modified Polymers for Transfection of Human CRL Fibroblasts, and for siRNA Mediated MDR Reversal in Melanoma Cancer Therapy.” 2010. Web. 19 Jan 2020.

Vancouver:

Abbasi Dezfouli M. Lipid Modified Polymers for Transfection of Human CRL Fibroblasts, and for siRNA Mediated MDR Reversal in Melanoma Cancer Therapy. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2020 Jan 19]. Available from: https://era.library.ualberta.ca/files/jq085k82z.

Council of Science Editors:

Abbasi Dezfouli M. Lipid Modified Polymers for Transfection of Human CRL Fibroblasts, and for siRNA Mediated MDR Reversal in Melanoma Cancer Therapy. [Doctoral Dissertation]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/jq085k82z


Universiteit Utrecht

29. Vercauteren, Suzanne Maria. Normal and Leukemic Hematopoiesis.

Degree: 2003, Universiteit Utrecht

 Acute Myeloid Leukemia (AML) is a clonal myeloproliferative disease characterized by an uncontrolled proliferation and block in differentiation of myeloid committed blood cells in the… (more)

Subjects/Keywords: Geneeskunde; AML; stem cells; NOD/SCID; CD133; CD33; telomerase; Notch4; Jagged1

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Vercauteren, S. M. (2003). Normal and Leukemic Hematopoiesis. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/508

Chicago Manual of Style (16th Edition):

Vercauteren, Suzanne Maria. “Normal and Leukemic Hematopoiesis.” 2003. Doctoral Dissertation, Universiteit Utrecht. Accessed January 19, 2020. http://dspace.library.uu.nl:8080/handle/1874/508.

MLA Handbook (7th Edition):

Vercauteren, Suzanne Maria. “Normal and Leukemic Hematopoiesis.” 2003. Web. 19 Jan 2020.

Vancouver:

Vercauteren SM. Normal and Leukemic Hematopoiesis. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2003. [cited 2020 Jan 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/508.

Council of Science Editors:

Vercauteren SM. Normal and Leukemic Hematopoiesis. [Doctoral Dissertation]. Universiteit Utrecht; 2003. Available from: http://dspace.library.uu.nl:8080/handle/1874/508

30. 井上, 光弘; イノウエ, ミツヒロ. 新規癌抗原SPARCを標的とした癌免疫療法の開発 : シンキ ガン コウゲン SPARC オ ヒョウテキ トシタ ガン メンエキ リョウホウ ノ カイハツ; Identification of a novel tumor-associated antigen, SPARC, as a possible target for immunotherapy of gastric, colorectal, and pancreatic cancers.

Degree: Kumamoto University / 熊本大学

cDNAマイクロアレイ解析により、スキルス胃癌に高発現する新規癌関連抗原遺伝子として、SPARC (Secreted Protein Acidic and Rich in Cysteine) が同定されている。また、すでにSPARCは、マウスにおいて抗腫瘍免疫を誘導できることが知られている。本研究は、SPARCによるヒト細胞傷害性T細胞(CTL) の誘導を検討し、SPARCを標的とした癌免疫療法の可能性を探ることを目的とする。

It is important to identify tumor-associated antigens (TAAs) to direct the immune system to attack… (more)

Subjects/Keywords: CTL; CDNAマイクロアレイ; SPARC遺伝子; NOD/Shi-scid IL2rgammanull(NOG)

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APA (6th Edition):

井上, 光弘; イノウエ, . (n.d.). 新規癌抗原SPARCを標的とした癌免疫療法の開発 : シンキ ガン コウゲン SPARC オ ヒョウテキ トシタ ガン メンエキ リョウホウ ノ カイハツ; Identification of a novel tumor-associated antigen, SPARC, as a possible target for immunotherapy of gastric, colorectal, and pancreatic cancers. (Thesis). Kumamoto University / 熊本大学. Retrieved from http://hdl.handle.net/2298/16776

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

井上, 光弘; イノウエ, ミツヒロ. “新規癌抗原SPARCを標的とした癌免疫療法の開発 : シンキ ガン コウゲン SPARC オ ヒョウテキ トシタ ガン メンエキ リョウホウ ノ カイハツ; Identification of a novel tumor-associated antigen, SPARC, as a possible target for immunotherapy of gastric, colorectal, and pancreatic cancers.” Thesis, Kumamoto University / 熊本大学. Accessed January 19, 2020. http://hdl.handle.net/2298/16776.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

井上, 光弘; イノウエ, ミツヒロ. “新規癌抗原SPARCを標的とした癌免疫療法の開発 : シンキ ガン コウゲン SPARC オ ヒョウテキ トシタ ガン メンエキ リョウホウ ノ カイハツ; Identification of a novel tumor-associated antigen, SPARC, as a possible target for immunotherapy of gastric, colorectal, and pancreatic cancers.” Web. 19 Jan 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

井上, 光弘; イノウエ . 新規癌抗原SPARCを標的とした癌免疫療法の開発 : シンキ ガン コウゲン SPARC オ ヒョウテキ トシタ ガン メンエキ リョウホウ ノ カイハツ; Identification of a novel tumor-associated antigen, SPARC, as a possible target for immunotherapy of gastric, colorectal, and pancreatic cancers. [Internet] [Thesis]. Kumamoto University / 熊本大学; [cited 2020 Jan 19]. Available from: http://hdl.handle.net/2298/16776.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

井上, 光弘; イノウエ . 新規癌抗原SPARCを標的とした癌免疫療法の開発 : シンキ ガン コウゲン SPARC オ ヒョウテキ トシタ ガン メンエキ リョウホウ ノ カイハツ; Identification of a novel tumor-associated antigen, SPARC, as a possible target for immunotherapy of gastric, colorectal, and pancreatic cancers. [Thesis]. Kumamoto University / 熊本大学; Available from: http://hdl.handle.net/2298/16776

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

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