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You searched for subject:(Li Fraumeni syndrome). Showing records 1 – 29 of 29 total matches.

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University of Toronto

1. Villani, Anita. Investigation of PIN1 as a Genetic Modifier in Li-Fraumeni Syndrome.

Degree: 2015, University of Toronto

Li-Fraumeni syndrome (LFS) is a heterogeneous cancer predisposition syndrome caused by germline mutations in TP53. Some of this phenotypic variability can be explained by presence… (more)

Subjects/Keywords: Li-Fraumeni Syndrome; modifier; p53; PIN1; 0992

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APA (6th Edition):

Villani, A. (2015). Investigation of PIN1 as a Genetic Modifier in Li-Fraumeni Syndrome. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/75192

Chicago Manual of Style (16th Edition):

Villani, Anita. “Investigation of PIN1 as a Genetic Modifier in Li-Fraumeni Syndrome.” 2015. Masters Thesis, University of Toronto. Accessed December 01, 2020. http://hdl.handle.net/1807/75192.

MLA Handbook (7th Edition):

Villani, Anita. “Investigation of PIN1 as a Genetic Modifier in Li-Fraumeni Syndrome.” 2015. Web. 01 Dec 2020.

Vancouver:

Villani A. Investigation of PIN1 as a Genetic Modifier in Li-Fraumeni Syndrome. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1807/75192.

Council of Science Editors:

Villani A. Investigation of PIN1 as a Genetic Modifier in Li-Fraumeni Syndrome. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/75192


Universidade do Rio Grande do Sul

2. Hütten, Michele Oliveira. Atuação da mutação R337H em TP53 em pacientes de Li-Fraumeni em autofagia, senescência e função mitocondrial.

Degree: 2016, Universidade do Rio Grande do Sul

Introdução: As síndromes de Li-Fraumeni (LFS) e Li-Fraumeni Like (LFL) são síndromes hereditárias de predisposição a câncer frequentemente associadas à mutações germinativas no gene TP53.… (more)

Subjects/Keywords: Li-Fraumeni syndrome; Síndrome de Li-Fraumeni; Síndrome de Li-Fraumeni Like; Autophagy; Senescence; p53; TP53

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APA (6th Edition):

Hütten, M. O. (2016). Atuação da mutação R337H em TP53 em pacientes de Li-Fraumeni em autofagia, senescência e função mitocondrial. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/173139

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):

Hütten, Michele Oliveira. “Atuação da mutação R337H em TP53 em pacientes de Li-Fraumeni em autofagia, senescência e função mitocondrial.” 2016. Thesis, Universidade do Rio Grande do Sul. Accessed December 01, 2020. http://hdl.handle.net/10183/173139.

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

MLA Handbook (7th Edition):

Hütten, Michele Oliveira. “Atuação da mutação R337H em TP53 em pacientes de Li-Fraumeni em autofagia, senescência e função mitocondrial.” 2016. Web. 01 Dec 2020.

Vancouver:

Hütten MO. Atuação da mutação R337H em TP53 em pacientes de Li-Fraumeni em autofagia, senescência e função mitocondrial. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2016. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10183/173139.

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

Council of Science Editors:

Hütten MO. Atuação da mutação R337H em TP53 em pacientes de Li-Fraumeni em autofagia, senescência e função mitocondrial. [Thesis]. Universidade do Rio Grande do Sul; 2016. Available from: http://hdl.handle.net/10183/173139

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


Texas Medical Center

3. Ross, Jessica L. The Psychosocial Effects of the Li-Fraumeni Education and Early Detection (LEAD) Program on Indivdiuals with Li-Fraumeni Syndrome.

Degree: MS, 2016, Texas Medical Center

Li-Fraumeni syndrome (LFS) is a hereditary cancer syndrome that leads to an increased risk of multiple cancers. In the past five years new screening… (more)

Subjects/Keywords: Li-Fraumeni Syndrome; psychosocial effects; LEAD Program; comprehensive Li-Fraumeni Syndrome screening; cancer screening; psychosocial; Oncology; Psychological Phenomena and Processes

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APA (6th Edition):

Ross, J. L. (2016). The Psychosocial Effects of the Li-Fraumeni Education and Early Detection (LEAD) Program on Indivdiuals with Li-Fraumeni Syndrome. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/662

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):

Ross, Jessica L. “The Psychosocial Effects of the Li-Fraumeni Education and Early Detection (LEAD) Program on Indivdiuals with Li-Fraumeni Syndrome.” 2016. Thesis, Texas Medical Center. Accessed December 01, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/662.

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

MLA Handbook (7th Edition):

Ross, Jessica L. “The Psychosocial Effects of the Li-Fraumeni Education and Early Detection (LEAD) Program on Indivdiuals with Li-Fraumeni Syndrome.” 2016. Web. 01 Dec 2020.

Vancouver:

Ross JL. The Psychosocial Effects of the Li-Fraumeni Education and Early Detection (LEAD) Program on Indivdiuals with Li-Fraumeni Syndrome. [Internet] [Thesis]. Texas Medical Center; 2016. [cited 2020 Dec 01]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/662.

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

Council of Science Editors:

Ross JL. The Psychosocial Effects of the Li-Fraumeni Education and Early Detection (LEAD) Program on Indivdiuals with Li-Fraumeni Syndrome. [Thesis]. Texas Medical Center; 2016. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/662

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


University of Toronto

4. Pan, Anna Jing Wei. Patched Domain-containing 4 (PTCH53) Identified in Li-Fraumeni Syndrome Patient-derived Cells.

Degree: 2018, University of Toronto

Germline TP53 mutations are the primary underlying etiologic cause of Li-Fraumeni syndrome. Lack of predictability in age-of-onset, cancer phenotypes, and likelihood of subsequent malignancies, highlights… (more)

Subjects/Keywords: Alternative splicing; Hedgehog signalling; Li-Fraumeni syndrome; p53; Patched; PTCH53; 0369

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APA (6th Edition):

Pan, A. J. W. (2018). Patched Domain-containing 4 (PTCH53) Identified in Li-Fraumeni Syndrome Patient-derived Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91562

Chicago Manual of Style (16th Edition):

Pan, Anna Jing Wei. “Patched Domain-containing 4 (PTCH53) Identified in Li-Fraumeni Syndrome Patient-derived Cells.” 2018. Masters Thesis, University of Toronto. Accessed December 01, 2020. http://hdl.handle.net/1807/91562.

MLA Handbook (7th Edition):

Pan, Anna Jing Wei. “Patched Domain-containing 4 (PTCH53) Identified in Li-Fraumeni Syndrome Patient-derived Cells.” 2018. Web. 01 Dec 2020.

Vancouver:

Pan AJW. Patched Domain-containing 4 (PTCH53) Identified in Li-Fraumeni Syndrome Patient-derived Cells. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1807/91562.

Council of Science Editors:

Pan AJW. Patched Domain-containing 4 (PTCH53) Identified in Li-Fraumeni Syndrome Patient-derived Cells. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91562


University of Toronto

5. Paramathas, Sangeetha. Investigating the use of circulating tumor DNA for cancer surveillance and early detection in (pediatric) sarcomas and Li-Fraumeni Syndrome.

Degree: PhD, 2020, University of Toronto

 Circulating tumor DNA (ctDNA) is a biomarker that has been shown to be valuable in a variety of contexts in clinical oncology such as determining… (more)

Subjects/Keywords: ctDNA; Early Detection; Li-Fraumeni Syndrome; Liquid Biopsies; Sarcomas; Surveillance; 0992

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APA (6th Edition):

Paramathas, S. (2020). Investigating the use of circulating tumor DNA for cancer surveillance and early detection in (pediatric) sarcomas and Li-Fraumeni Syndrome. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/101212

Chicago Manual of Style (16th Edition):

Paramathas, Sangeetha. “Investigating the use of circulating tumor DNA for cancer surveillance and early detection in (pediatric) sarcomas and Li-Fraumeni Syndrome.” 2020. Doctoral Dissertation, University of Toronto. Accessed December 01, 2020. http://hdl.handle.net/1807/101212.

MLA Handbook (7th Edition):

Paramathas, Sangeetha. “Investigating the use of circulating tumor DNA for cancer surveillance and early detection in (pediatric) sarcomas and Li-Fraumeni Syndrome.” 2020. Web. 01 Dec 2020.

Vancouver:

Paramathas S. Investigating the use of circulating tumor DNA for cancer surveillance and early detection in (pediatric) sarcomas and Li-Fraumeni Syndrome. [Internet] [Doctoral dissertation]. University of Toronto; 2020. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1807/101212.

Council of Science Editors:

Paramathas S. Investigating the use of circulating tumor DNA for cancer surveillance and early detection in (pediatric) sarcomas and Li-Fraumeni Syndrome. [Doctoral Dissertation]. University of Toronto; 2020. Available from: http://hdl.handle.net/1807/101212


University of Toronto

6. Sauberli-Stewart, Katherine. Transcriptomic Signature of Radiation Response in Li-Fraumeni Syndrome.

Degree: 2019, University of Toronto

Li-Fraumeni Syndrome (LFS) is an inherited cancer predisposition disorder associated with a germline mutation in the TP53 tumour suppressor gene. Impaired p53, important in the… (more)

Subjects/Keywords: Cancer; LFS; Li-Fraumeni Syndrome; Radiation; RNA; second malignancy; 0992

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APA (6th Edition):

Sauberli-Stewart, K. (2019). Transcriptomic Signature of Radiation Response in Li-Fraumeni Syndrome. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/98347

Chicago Manual of Style (16th Edition):

Sauberli-Stewart, Katherine. “Transcriptomic Signature of Radiation Response in Li-Fraumeni Syndrome.” 2019. Masters Thesis, University of Toronto. Accessed December 01, 2020. http://hdl.handle.net/1807/98347.

MLA Handbook (7th Edition):

Sauberli-Stewart, Katherine. “Transcriptomic Signature of Radiation Response in Li-Fraumeni Syndrome.” 2019. Web. 01 Dec 2020.

Vancouver:

Sauberli-Stewart K. Transcriptomic Signature of Radiation Response in Li-Fraumeni Syndrome. [Internet] [Masters thesis]. University of Toronto; 2019. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1807/98347.

Council of Science Editors:

Sauberli-Stewart K. Transcriptomic Signature of Radiation Response in Li-Fraumeni Syndrome. [Masters Thesis]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/98347


University of South Carolina

7. Berenson, Emily Anne. The Psychosocial Burden of LI-Fraumeni Syndrome Tumor Surveillance on Mutation and Non-Mutation Carriers Within Families.

Degree: MSin Genetic Counseling, Genetic Counseling, 2020, University of South Carolina

  Individuals undergoing Li-Fraumeni syndrome (LFS) tumor surveillance are known to experience a significant psychosocial burden due to financial, emotional and logistical stresses. This study… (more)

Subjects/Keywords: LI-Fraumeni Syndrome Tumor; Mutation; Non-Mutation Carriers; family

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APA (6th Edition):

Berenson, E. A. (2020). The Psychosocial Burden of LI-Fraumeni Syndrome Tumor Surveillance on Mutation and Non-Mutation Carriers Within Families. (Masters Thesis). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/5861

Chicago Manual of Style (16th Edition):

Berenson, Emily Anne. “The Psychosocial Burden of LI-Fraumeni Syndrome Tumor Surveillance on Mutation and Non-Mutation Carriers Within Families.” 2020. Masters Thesis, University of South Carolina. Accessed December 01, 2020. https://scholarcommons.sc.edu/etd/5861.

MLA Handbook (7th Edition):

Berenson, Emily Anne. “The Psychosocial Burden of LI-Fraumeni Syndrome Tumor Surveillance on Mutation and Non-Mutation Carriers Within Families.” 2020. Web. 01 Dec 2020.

Vancouver:

Berenson EA. The Psychosocial Burden of LI-Fraumeni Syndrome Tumor Surveillance on Mutation and Non-Mutation Carriers Within Families. [Internet] [Masters thesis]. University of South Carolina; 2020. [cited 2020 Dec 01]. Available from: https://scholarcommons.sc.edu/etd/5861.

Council of Science Editors:

Berenson EA. The Psychosocial Burden of LI-Fraumeni Syndrome Tumor Surveillance on Mutation and Non-Mutation Carriers Within Families. [Masters Thesis]. University of South Carolina; 2020. Available from: https://scholarcommons.sc.edu/etd/5861


Universidade do Rio Grande do Sul

8. Santos, João Paulo Franco dos. Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria.

Degree: 2016, Universidade do Rio Grande do Sul

Objetivo: Até 10% dos casos de câncer de mama estão associados com uma síndrome genética de predisposição ao câncer. A identificação de possíveis portadores dessas… (more)

Subjects/Keywords: Breast cancer; Síndrome de Li-Fraumeni; Neoplasias da mama; Genetic counselling; Hereditary cancer syndromes; Hereditary breast and ovarian cancer syndrome; Li-Fraumeni syndrome

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APA (6th Edition):

Santos, J. P. F. d. (2016). Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/143202

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):

Santos, João Paulo Franco dos. “Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria.” 2016. Thesis, Universidade do Rio Grande do Sul. Accessed December 01, 2020. http://hdl.handle.net/10183/143202.

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

MLA Handbook (7th Edition):

Santos, João Paulo Franco dos. “Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria.” 2016. Web. 01 Dec 2020.

Vancouver:

Santos JPFd. Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2016. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10183/143202.

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

Council of Science Editors:

Santos JPFd. Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria. [Thesis]. Universidade do Rio Grande do Sul; 2016. Available from: http://hdl.handle.net/10183/143202

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


Texas Medical Center

9. Copeland, Allison. ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME.

Degree: MS, 2013, Texas Medical Center

Li- Fraumeni Syndrome (LFS) is a rare autosomal dominant hereditary cancer syndrome caused by mutations in the TP53 gene that predisposes individuals to a… (more)

Subjects/Keywords: Li-Fraumeni syndrome; predictive testing; genetic testing; minors; genetic counseling; Medicine and Health Sciences

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APA (6th Edition):

Copeland, A. (2013). ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/363

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):

Copeland, Allison. “ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME.” 2013. Thesis, Texas Medical Center. Accessed December 01, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/363.

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

MLA Handbook (7th Edition):

Copeland, Allison. “ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME.” 2013. Web. 01 Dec 2020.

Vancouver:

Copeland A. ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME. [Internet] [Thesis]. Texas Medical Center; 2013. [cited 2020 Dec 01]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/363.

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

Council of Science Editors:

Copeland A. ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME. [Thesis]. Texas Medical Center; 2013. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/363

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


Texas Medical Center

10. Parham, Emily A. EVALUATION OF CURRENT CLINICAL CRITERIA FOR LI-FRAUMENI SYNDROME IN A DIVERSE SAMPLE OF TP53 MUTATION CARRIERS.

Degree: MS, 2014, Texas Medical Center

Li-Fraumeni syndrome (LFS) is a hereditary cancer predisposition syndrome caused by heterozyogous germline mutations in the TP53 gene and characterized by an excess of… (more)

Subjects/Keywords: Li fraumeni syndrome; sarcoma; tp53; genetic testing; Medical Genetics; Medicine and Health Sciences; Neoplasms; Oncology

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APA (6th Edition):

Parham, E. A. (2014). EVALUATION OF CURRENT CLINICAL CRITERIA FOR LI-FRAUMENI SYNDROME IN A DIVERSE SAMPLE OF TP53 MUTATION CARRIERS. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/459

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):

Parham, Emily A. “EVALUATION OF CURRENT CLINICAL CRITERIA FOR LI-FRAUMENI SYNDROME IN A DIVERSE SAMPLE OF TP53 MUTATION CARRIERS.” 2014. Thesis, Texas Medical Center. Accessed December 01, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/459.

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

MLA Handbook (7th Edition):

Parham, Emily A. “EVALUATION OF CURRENT CLINICAL CRITERIA FOR LI-FRAUMENI SYNDROME IN A DIVERSE SAMPLE OF TP53 MUTATION CARRIERS.” 2014. Web. 01 Dec 2020.

Vancouver:

Parham EA. EVALUATION OF CURRENT CLINICAL CRITERIA FOR LI-FRAUMENI SYNDROME IN A DIVERSE SAMPLE OF TP53 MUTATION CARRIERS. [Internet] [Thesis]. Texas Medical Center; 2014. [cited 2020 Dec 01]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/459.

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

Council of Science Editors:

Parham EA. EVALUATION OF CURRENT CLINICAL CRITERIA FOR LI-FRAUMENI SYNDROME IN A DIVERSE SAMPLE OF TP53 MUTATION CARRIERS. [Thesis]. Texas Medical Center; 2014. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/459

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


University of Toronto

11. Guha, Tanya. DNA methylation alterations associated with tumorigenicity in germline TP53-mediated cancer susceptibility.

Degree: PhD, 2018, University of Toronto

Aberrations in the epigenome, including DNA methylation alterations, are known to play an important role in tumor initiation and progression. However, the extent of interplay… (more)

Subjects/Keywords: cancer pre-disposition; circulating DNA; early cancer detection; epigenetics; Li-Fraumeni syndrome; methylation; 0992

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APA (6th Edition):

Guha, T. (2018). DNA methylation alterations associated with tumorigenicity in germline TP53-mediated cancer susceptibility. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/95656

Chicago Manual of Style (16th Edition):

Guha, Tanya. “DNA methylation alterations associated with tumorigenicity in germline TP53-mediated cancer susceptibility.” 2018. Doctoral Dissertation, University of Toronto. Accessed December 01, 2020. http://hdl.handle.net/1807/95656.

MLA Handbook (7th Edition):

Guha, Tanya. “DNA methylation alterations associated with tumorigenicity in germline TP53-mediated cancer susceptibility.” 2018. Web. 01 Dec 2020.

Vancouver:

Guha T. DNA methylation alterations associated with tumorigenicity in germline TP53-mediated cancer susceptibility. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1807/95656.

Council of Science Editors:

Guha T. DNA methylation alterations associated with tumorigenicity in germline TP53-mediated cancer susceptibility. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/95656


University of Toronto

12. Samuel, Nardin. Genetic and Epigenetic Crosstalk Define TP53-mediated Human Cancer Susceptibility.

Degree: PhD, 2016, University of Toronto

 Deregulation of epigenetic programming is crucial to tumorigenesis, yet the extent to which epigenetics plays a role in cancer susceptibility remains unclear. This work details… (more)

Subjects/Keywords: Cancer susceptibility; DNA methylation; epigenetics; Li-Fraumeni Syndrome; miR-34A; TP53; 0369

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APA (6th Edition):

Samuel, N. (2016). Genetic and Epigenetic Crosstalk Define TP53-mediated Human Cancer Susceptibility. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/76809

Chicago Manual of Style (16th Edition):

Samuel, Nardin. “Genetic and Epigenetic Crosstalk Define TP53-mediated Human Cancer Susceptibility.” 2016. Doctoral Dissertation, University of Toronto. Accessed December 01, 2020. http://hdl.handle.net/1807/76809.

MLA Handbook (7th Edition):

Samuel, Nardin. “Genetic and Epigenetic Crosstalk Define TP53-mediated Human Cancer Susceptibility.” 2016. Web. 01 Dec 2020.

Vancouver:

Samuel N. Genetic and Epigenetic Crosstalk Define TP53-mediated Human Cancer Susceptibility. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1807/76809.

Council of Science Editors:

Samuel N. Genetic and Epigenetic Crosstalk Define TP53-mediated Human Cancer Susceptibility. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76809


Universidade do Rio Grande do Sul

13. Giacomazzi, Juliana. Prevalência da mutação germinativa TP53 p.R337H em indivíduos com tumores do espectro da Síndrome de Li-Fraumeni.

Degree: 2012, Universidade do Rio Grande do Sul

 Introdução: Estudos prévios têm indicado que uma mutação germinativa específica no gene TP53, p.R337H está associada a efeito fundador no Brasil e é muito frequente… (more)

Subjects/Keywords: TP53 gene; Síndrome de Li-Fraumeni; Neoplasias da mama; TP53 p.R337H mutation; Li-Fraumeni syndrome; Proteína supressora de tumor p53; Breast neoplasm; Childhood cancer; Phyllodes tumor

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APA (6th Edition):

Giacomazzi, J. (2012). Prevalência da mutação germinativa TP53 p.R337H em indivíduos com tumores do espectro da Síndrome de Li-Fraumeni. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/115624

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):

Giacomazzi, Juliana. “Prevalência da mutação germinativa TP53 p.R337H em indivíduos com tumores do espectro da Síndrome de Li-Fraumeni.” 2012. Thesis, Universidade do Rio Grande do Sul. Accessed December 01, 2020. http://hdl.handle.net/10183/115624.

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

MLA Handbook (7th Edition):

Giacomazzi, Juliana. “Prevalência da mutação germinativa TP53 p.R337H em indivíduos com tumores do espectro da Síndrome de Li-Fraumeni.” 2012. Web. 01 Dec 2020.

Vancouver:

Giacomazzi J. Prevalência da mutação germinativa TP53 p.R337H em indivíduos com tumores do espectro da Síndrome de Li-Fraumeni. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2012. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10183/115624.

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

Council of Science Editors:

Giacomazzi J. Prevalência da mutação germinativa TP53 p.R337H em indivíduos com tumores do espectro da Síndrome de Li-Fraumeni. [Thesis]. Universidade do Rio Grande do Sul; 2012. Available from: http://hdl.handle.net/10183/115624

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


Universidade Estadual de Campinas

14. Mastellaro, Maria José, 1955-. Tumores adrenocorticais na infância = impacto da exposição hormonal e do tratamento no crescimento e desenvolvimento, estado atual de saúde de sobreviventes à longo prazo e susceptibilidade familiar ao câncer relacionada à mutação germinativa do gene "TP53" R337H = Childhood adrenocortical tumors: impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation: Childhood adrenocortical tumors : impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation.

Degree: 2016, Universidade Estadual de Campinas

 Abstract: INTRODUCTION: the incidence of the adrenocortical tumor (ACT) in children is 18 fold higher in southeastern and southern regions of Brazil than in other… (more)

Subjects/Keywords: Carcinoma adrenocortical; Genes P53; Síndrome de Li-Fraumeni; Mutação em linhagem germinativa; Crescimento e desenvolvimento; Adrenocortical carcinoma; Genes, p53; Li-Fraumeni syndrome; Germ-line mutation; Growth and development

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APA (6th Edition):

Mastellaro, Maria José, 1. (2016). Tumores adrenocorticais na infância = impacto da exposição hormonal e do tratamento no crescimento e desenvolvimento, estado atual de saúde de sobreviventes à longo prazo e susceptibilidade familiar ao câncer relacionada à mutação germinativa do gene "TP53" R337H = Childhood adrenocortical tumors: impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation: Childhood adrenocortical tumors : impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/321838

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):

Mastellaro, Maria José, 1955-. “Tumores adrenocorticais na infância = impacto da exposição hormonal e do tratamento no crescimento e desenvolvimento, estado atual de saúde de sobreviventes à longo prazo e susceptibilidade familiar ao câncer relacionada à mutação germinativa do gene "TP53" R337H = Childhood adrenocortical tumors: impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation: Childhood adrenocortical tumors : impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation.” 2016. Thesis, Universidade Estadual de Campinas. Accessed December 01, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/321838.

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

MLA Handbook (7th Edition):

Mastellaro, Maria José, 1955-. “Tumores adrenocorticais na infância = impacto da exposição hormonal e do tratamento no crescimento e desenvolvimento, estado atual de saúde de sobreviventes à longo prazo e susceptibilidade familiar ao câncer relacionada à mutação germinativa do gene "TP53" R337H = Childhood adrenocortical tumors: impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation: Childhood adrenocortical tumors : impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation.” 2016. Web. 01 Dec 2020.

Vancouver:

Mastellaro, Maria José 1. Tumores adrenocorticais na infância = impacto da exposição hormonal e do tratamento no crescimento e desenvolvimento, estado atual de saúde de sobreviventes à longo prazo e susceptibilidade familiar ao câncer relacionada à mutação germinativa do gene "TP53" R337H = Childhood adrenocortical tumors: impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation: Childhood adrenocortical tumors : impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation. [Internet] [Thesis]. Universidade Estadual de Campinas; 2016. [cited 2020 Dec 01]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/321838.

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

Council of Science Editors:

Mastellaro, Maria José 1. Tumores adrenocorticais na infância = impacto da exposição hormonal e do tratamento no crescimento e desenvolvimento, estado atual de saúde de sobreviventes à longo prazo e susceptibilidade familiar ao câncer relacionada à mutação germinativa do gene "TP53" R337H = Childhood adrenocortical tumors: impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation: Childhood adrenocortical tumors : impact on growth and development of adrenal cortex hormones exposure, the current health status of long-term survivors and familial cancer susceptibility in carriers of the "TP53" R337H mutation. [Thesis]. Universidade Estadual de Campinas; 2016. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/321838

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


Vrije Universiteit Amsterdam

15. Ruijs, M.W.G. Li-Fraumeni syndrome, clinical and molecular genetics .

Degree: 2010, Vrije Universiteit Amsterdam

Subjects/Keywords: Li-Fraumeni syndrome; hereditary cancer syndrome; clinical genetics

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APA (6th Edition):

Ruijs, M. W. G. (2010). Li-Fraumeni syndrome, clinical and molecular genetics . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/21516

Chicago Manual of Style (16th Edition):

Ruijs, M W G. “Li-Fraumeni syndrome, clinical and molecular genetics .” 2010. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed December 01, 2020. http://hdl.handle.net/1871/21516.

MLA Handbook (7th Edition):

Ruijs, M W G. “Li-Fraumeni syndrome, clinical and molecular genetics .” 2010. Web. 01 Dec 2020.

Vancouver:

Ruijs MWG. Li-Fraumeni syndrome, clinical and molecular genetics . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2010. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1871/21516.

Council of Science Editors:

Ruijs MWG. Li-Fraumeni syndrome, clinical and molecular genetics . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2010. Available from: http://hdl.handle.net/1871/21516


University of Oulu

16. Huusko, P. (Pia). Predisposing genes in hereditary breast and ovarian cancer.

Degree: 1999, University of Oulu

 Abstract In the present study, mutations in BRCA1 and BRCA2, the two major genes predisposing individuals to hereditary breast and ovarian cancer, were screened in… (more)

Subjects/Keywords: BRCA1; BRCA2; Li-Fraumeni syndrome; founder mutations

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APA (6th Edition):

Huusko, P. (. (1999). Predisposing genes in hereditary breast and ovarian cancer. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9514254422

Chicago Manual of Style (16th Edition):

Huusko, P (Pia). “Predisposing genes in hereditary breast and ovarian cancer.” 1999. Doctoral Dissertation, University of Oulu. Accessed December 01, 2020. http://urn.fi/urn:isbn:9514254422.

MLA Handbook (7th Edition):

Huusko, P (Pia). “Predisposing genes in hereditary breast and ovarian cancer.” 1999. Web. 01 Dec 2020.

Vancouver:

Huusko P(. Predisposing genes in hereditary breast and ovarian cancer. [Internet] [Doctoral dissertation]. University of Oulu; 1999. [cited 2020 Dec 01]. Available from: http://urn.fi/urn:isbn:9514254422.

Council of Science Editors:

Huusko P(. Predisposing genes in hereditary breast and ovarian cancer. [Doctoral Dissertation]. University of Oulu; 1999. Available from: http://urn.fi/urn:isbn:9514254422


Texas Medical Center

17. Peng, Gang. Germline Mutation Detection in Next Generation Sequencing Data and TP53 Mutation Carrier Probability Estimation for Li-Fraumeni Syndrome.

Degree: PhD, 2015, Texas Medical Center

  Next generation sequencing technology has been widely used in genomic analysis, but its application has been compromised by the missing true variants, especially when… (more)

Subjects/Keywords: Next Generation Sequencing; Variant Calling; Mendelian; Risk Prediction; Li-Fraumeni Syndrome; Germline Mutation; TP53; Multi-platform; Bayesian; Bioinformatics; Biostatistics; Genetics

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APA (6th Edition):

Peng, G. (2015). Germline Mutation Detection in Next Generation Sequencing Data and TP53 Mutation Carrier Probability Estimation for Li-Fraumeni Syndrome. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/619

Chicago Manual of Style (16th Edition):

Peng, Gang. “Germline Mutation Detection in Next Generation Sequencing Data and TP53 Mutation Carrier Probability Estimation for Li-Fraumeni Syndrome.” 2015. Doctoral Dissertation, Texas Medical Center. Accessed December 01, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/619.

MLA Handbook (7th Edition):

Peng, Gang. “Germline Mutation Detection in Next Generation Sequencing Data and TP53 Mutation Carrier Probability Estimation for Li-Fraumeni Syndrome.” 2015. Web. 01 Dec 2020.

Vancouver:

Peng G. Germline Mutation Detection in Next Generation Sequencing Data and TP53 Mutation Carrier Probability Estimation for Li-Fraumeni Syndrome. [Internet] [Doctoral dissertation]. Texas Medical Center; 2015. [cited 2020 Dec 01]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/619.

Council of Science Editors:

Peng G. Germline Mutation Detection in Next Generation Sequencing Data and TP53 Mutation Carrier Probability Estimation for Li-Fraumeni Syndrome. [Doctoral Dissertation]. Texas Medical Center; 2015. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/619


Texas Medical Center

18. Wong, Justin. Omics Approaches to Uncover Germline and Somatic Variation Underlying Inherited Sarcomagenesis.

Degree: PhD, 2018, Texas Medical Center

  Sarcomas are rare mesenchymal tumors, making up 15% of all childhood and 1% of all adult tumors. They account for a disproportionate share of… (more)

Subjects/Keywords: Li-Fraumeni Syndrome; Sarcomas; Inherited Cancer Syndromes; Sarcomagenesis; Comparative genomics; Bioinformatics; Genetics; Genomics; Medicine and Health Sciences; Oncology

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APA (6th Edition):

Wong, J. (2018). Omics Approaches to Uncover Germline and Somatic Variation Underlying Inherited Sarcomagenesis. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/869

Chicago Manual of Style (16th Edition):

Wong, Justin. “Omics Approaches to Uncover Germline and Somatic Variation Underlying Inherited Sarcomagenesis.” 2018. Doctoral Dissertation, Texas Medical Center. Accessed December 01, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/869.

MLA Handbook (7th Edition):

Wong, Justin. “Omics Approaches to Uncover Germline and Somatic Variation Underlying Inherited Sarcomagenesis.” 2018. Web. 01 Dec 2020.

Vancouver:

Wong J. Omics Approaches to Uncover Germline and Somatic Variation Underlying Inherited Sarcomagenesis. [Internet] [Doctoral dissertation]. Texas Medical Center; 2018. [cited 2020 Dec 01]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/869.

Council of Science Editors:

Wong J. Omics Approaches to Uncover Germline and Somatic Variation Underlying Inherited Sarcomagenesis. [Doctoral Dissertation]. Texas Medical Center; 2018. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/869


The Ohio State University

19. Spees, Colleen K. Dysregulation of p53 Gene Expression in Human Prostate Carcinogenesis and Its Relationship to Angiogenesis.

Degree: PhD, Allied Medical Professions, 2011, The Ohio State University

 Prostate cancer is a common malignancy in affluent nations. Indeed, it is the most common visceral malignancy in American men impacting over 200,000 annually. The… (more)

Subjects/Keywords: Cellular Biology; Epidemiology; Genetics; Health Sciences; Oncology; p53; TP53; prostate cancer; angiogenesis; Li Fraumeni Syndrome; LFS

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APA (6th Edition):

Spees, C. K. (2011). Dysregulation of p53 Gene Expression in Human Prostate Carcinogenesis and Its Relationship to Angiogenesis. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1313523656

Chicago Manual of Style (16th Edition):

Spees, Colleen K. “Dysregulation of p53 Gene Expression in Human Prostate Carcinogenesis and Its Relationship to Angiogenesis.” 2011. Doctoral Dissertation, The Ohio State University. Accessed December 01, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1313523656.

MLA Handbook (7th Edition):

Spees, Colleen K. “Dysregulation of p53 Gene Expression in Human Prostate Carcinogenesis and Its Relationship to Angiogenesis.” 2011. Web. 01 Dec 2020.

Vancouver:

Spees CK. Dysregulation of p53 Gene Expression in Human Prostate Carcinogenesis and Its Relationship to Angiogenesis. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2020 Dec 01]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1313523656.

Council of Science Editors:

Spees CK. Dysregulation of p53 Gene Expression in Human Prostate Carcinogenesis and Its Relationship to Angiogenesis. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1313523656


Université Paris-Sud – Paris XI

20. Sagne, Charlotte. Polymorphisms in G-quadruplex regions of the TP53 tumour suppressor gene : Impact on cancer susceptibility and expression of p53 N-terminal isoforms : Polymorphismes situés dans les régions de type G-quadruplexe du gène suppresseur de tumeur TP53 : Impact sur la susceptibilité au cancer et l’expression des isoformes en N-terminal de p53.

Degree: Docteur es, Biologie, 2013, Université Paris-Sud – Paris XI

Le gène TP53 est extrêmement polymorphique avec 85 polymorphismes décrits. Certains de ces polymorphismes sont associés à une augmentation du risque de cancer, par exemple… (more)

Subjects/Keywords: Protéine suppresseur de tumeur; P53; Isoformes; Polymorphismes; Rs17878362; Épissage alternatif; Structure de type G-quadruplexe; Syndrome de Li-Fraumeni; Méta-analyse; Tumour suppressor protein; P53; Isoforms; Polymorphisms; Rs17878362; Alternative splicing; G-quadruplex structure; Li-Fraumeni syndrome; Meta-analysis

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APA (6th Edition):

Sagne, C. (2013). Polymorphisms in G-quadruplex regions of the TP53 tumour suppressor gene : Impact on cancer susceptibility and expression of p53 N-terminal isoforms : Polymorphismes situés dans les régions de type G-quadruplexe du gène suppresseur de tumeur TP53 : Impact sur la susceptibilité au cancer et l’expression des isoformes en N-terminal de p53. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2013PA11T072

Chicago Manual of Style (16th Edition):

Sagne, Charlotte. “Polymorphisms in G-quadruplex regions of the TP53 tumour suppressor gene : Impact on cancer susceptibility and expression of p53 N-terminal isoforms : Polymorphismes situés dans les régions de type G-quadruplexe du gène suppresseur de tumeur TP53 : Impact sur la susceptibilité au cancer et l’expression des isoformes en N-terminal de p53.” 2013. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed December 01, 2020. http://www.theses.fr/2013PA11T072.

MLA Handbook (7th Edition):

Sagne, Charlotte. “Polymorphisms in G-quadruplex regions of the TP53 tumour suppressor gene : Impact on cancer susceptibility and expression of p53 N-terminal isoforms : Polymorphismes situés dans les régions de type G-quadruplexe du gène suppresseur de tumeur TP53 : Impact sur la susceptibilité au cancer et l’expression des isoformes en N-terminal de p53.” 2013. Web. 01 Dec 2020.

Vancouver:

Sagne C. Polymorphisms in G-quadruplex regions of the TP53 tumour suppressor gene : Impact on cancer susceptibility and expression of p53 N-terminal isoforms : Polymorphismes situés dans les régions de type G-quadruplexe du gène suppresseur de tumeur TP53 : Impact sur la susceptibilité au cancer et l’expression des isoformes en N-terminal de p53. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2013. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2013PA11T072.

Council of Science Editors:

Sagne C. Polymorphisms in G-quadruplex regions of the TP53 tumour suppressor gene : Impact on cancer susceptibility and expression of p53 N-terminal isoforms : Polymorphismes situés dans les régions de type G-quadruplexe du gène suppresseur de tumeur TP53 : Impact sur la susceptibilité au cancer et l’expression des isoformes en N-terminal de p53. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2013. Available from: http://www.theses.fr/2013PA11T072

21. Marcel, Virginie. Régulation transcriptionnelle des isoformes de la protéine suppresseur de tumeur p53 tronquée dans leur région amino-terminale : impact des polymorphismes du gène TP53 : Transcriptional regulation of N-truncated isoforms of the p53 tumor suppressor : impact of the TP53 polymorphisms.

Degree: Docteur es, Biologie moléculaire, 2009, Université Claude Bernard – Lyon I

Le gène suppresseur de tumeurs TP53 exprime plusieurs isoformes, dont Δ40p53 (perte du domaine de transactivation) et Δ133p53 (perte du domaine de transactivation et d’une… (more)

Subjects/Keywords: Protéine suppresseur de tumeur p53; Isoformes; Régulation transcriptionnelle; Structures de type G-quadruplexe; Effet modificateur; Épissage alternatif; Syndrome Li-Fraumeni; Promoteur interne; Tumor suppressor protein p53; Isoforms; Transcriptional regulation; Structures such as G-quadruplex; Modifying effect; Alternative splicing; Li-Fraumeni Syndrome; Internal promoter; 572.8

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APA (6th Edition):

Marcel, V. (2009). Régulation transcriptionnelle des isoformes de la protéine suppresseur de tumeur p53 tronquée dans leur région amino-terminale : impact des polymorphismes du gène TP53 : Transcriptional regulation of N-truncated isoforms of the p53 tumor suppressor : impact of the TP53 polymorphisms. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2009LYO10088

Chicago Manual of Style (16th Edition):

Marcel, Virginie. “Régulation transcriptionnelle des isoformes de la protéine suppresseur de tumeur p53 tronquée dans leur région amino-terminale : impact des polymorphismes du gène TP53 : Transcriptional regulation of N-truncated isoforms of the p53 tumor suppressor : impact of the TP53 polymorphisms.” 2009. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed December 01, 2020. http://www.theses.fr/2009LYO10088.

MLA Handbook (7th Edition):

Marcel, Virginie. “Régulation transcriptionnelle des isoformes de la protéine suppresseur de tumeur p53 tronquée dans leur région amino-terminale : impact des polymorphismes du gène TP53 : Transcriptional regulation of N-truncated isoforms of the p53 tumor suppressor : impact of the TP53 polymorphisms.” 2009. Web. 01 Dec 2020.

Vancouver:

Marcel V. Régulation transcriptionnelle des isoformes de la protéine suppresseur de tumeur p53 tronquée dans leur région amino-terminale : impact des polymorphismes du gène TP53 : Transcriptional regulation of N-truncated isoforms of the p53 tumor suppressor : impact of the TP53 polymorphisms. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2009. [cited 2020 Dec 01]. Available from: http://www.theses.fr/2009LYO10088.

Council of Science Editors:

Marcel V. Régulation transcriptionnelle des isoformes de la protéine suppresseur de tumeur p53 tronquée dans leur région amino-terminale : impact des polymorphismes du gène TP53 : Transcriptional regulation of N-truncated isoforms of the p53 tumor suppressor : impact of the TP53 polymorphisms. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2009. Available from: http://www.theses.fr/2009LYO10088


Texas Medical Center

22. Newman, Leslie A. Attitudes of Parents at risk of inheriting Li-Fraumeni Syndrome towards predictive genetic testing in their minor-aged children.

Degree: MS, 2010, Texas Medical Center

Li-Fraumeni Syndrome (LFS) is a hereditary cancer syndrome which predisposes individuals to cancer beginning in childhood. These risks are spread across a lifetime, from early… (more)

Subjects/Keywords: Li-Fraumeni Syndrome; genetic testing; children; Bioethics and Medical Ethics; Genetics

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APA (6th Edition):

Newman, L. A. (2010). Attitudes of Parents at risk of inheriting Li-Fraumeni Syndrome towards predictive genetic testing in their minor-aged children. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/38

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):

Newman, Leslie A. “Attitudes of Parents at risk of inheriting Li-Fraumeni Syndrome towards predictive genetic testing in their minor-aged children.” 2010. Thesis, Texas Medical Center. Accessed December 01, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/38.

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

MLA Handbook (7th Edition):

Newman, Leslie A. “Attitudes of Parents at risk of inheriting Li-Fraumeni Syndrome towards predictive genetic testing in their minor-aged children.” 2010. Web. 01 Dec 2020.

Vancouver:

Newman LA. Attitudes of Parents at risk of inheriting Li-Fraumeni Syndrome towards predictive genetic testing in their minor-aged children. [Internet] [Thesis]. Texas Medical Center; 2010. [cited 2020 Dec 01]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/38.

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

Council of Science Editors:

Newman LA. Attitudes of Parents at risk of inheriting Li-Fraumeni Syndrome towards predictive genetic testing in their minor-aged children. [Thesis]. Texas Medical Center; 2010. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/38

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

23. Badr, Idsaid. The Role of miR-605 and its Variant in Li-Fraumeni Syndrome.

Degree: 2014, University of Toronto

Li-Fraumeni Syndrome (LFS) is a rare cancer predisposition syndrome, typically involving germline mutations in the TP53 gene. Despite the high penetrance of TP53 mutations, LFS… (more)

Subjects/Keywords: MicroRNA; Li-Fraumeni Syndrome; p53; Single Nucleotide Polymorphism; 0369; 0307

…and tumors, and later by the finding that patients with Li-Fraumeni Syndrome had inherited… …ultimately apoptosis. 8 1.2 Li-Fraumeni Syndrome In addition to being the most mutated gene in… …peculiar familiar cancer syndrome, called Li-Fraumeni Syndrome (LFS)4,62. LFS was first… …1.2.5 Secondary Modifiers in Li-Fraumeni Syndrome The TP53 PEX4 polymorphism, which results in… …impact p53 activity are plausible modifier events in patients with Li-Fraumeni syndrome. More… 

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APA (6th Edition):

Badr, I. (2014). The Role of miR-605 and its Variant in Li-Fraumeni Syndrome. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/44027

Chicago Manual of Style (16th Edition):

Badr, Idsaid. “The Role of miR-605 and its Variant in Li-Fraumeni Syndrome.” 2014. Masters Thesis, University of Toronto. Accessed December 01, 2020. http://hdl.handle.net/1807/44027.

MLA Handbook (7th Edition):

Badr, Idsaid. “The Role of miR-605 and its Variant in Li-Fraumeni Syndrome.” 2014. Web. 01 Dec 2020.

Vancouver:

Badr I. The Role of miR-605 and its Variant in Li-Fraumeni Syndrome. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1807/44027.

Council of Science Editors:

Badr I. The Role of miR-605 and its Variant in Li-Fraumeni Syndrome. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/44027


Ohio University

24. Ayanga, Bernard Aguya. IDENTIFICATION OF GENES THAT COOPERATE WITH P53 IN TUMORIGENESIS.

Degree: PhD, Chemistry (Arts and Sciences), 2006, Ohio University

Li-Fraumeni syndrome is a rare inherited disorder that greatly increases the risk of developing several types of cancer, particularly in children and young adults.… (more)

Subjects/Keywords: p53; Li-Fraumeni syndrome; Loss of Heterozygosity; Metastasis; Cancer; Stat5a

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APA (6th Edition):

Ayanga, B. A. (2006). IDENTIFICATION OF GENES THAT COOPERATE WITH P53 IN TUMORIGENESIS. (Doctoral Dissertation). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1161966086

Chicago Manual of Style (16th Edition):

Ayanga, Bernard Aguya. “IDENTIFICATION OF GENES THAT COOPERATE WITH P53 IN TUMORIGENESIS.” 2006. Doctoral Dissertation, Ohio University. Accessed December 01, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1161966086.

MLA Handbook (7th Edition):

Ayanga, Bernard Aguya. “IDENTIFICATION OF GENES THAT COOPERATE WITH P53 IN TUMORIGENESIS.” 2006. Web. 01 Dec 2020.

Vancouver:

Ayanga BA. IDENTIFICATION OF GENES THAT COOPERATE WITH P53 IN TUMORIGENESIS. [Internet] [Doctoral dissertation]. Ohio University; 2006. [cited 2020 Dec 01]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1161966086.

Council of Science Editors:

Ayanga BA. IDENTIFICATION OF GENES THAT COOPERATE WITH P53 IN TUMORIGENESIS. [Doctoral Dissertation]. Ohio University; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1161966086

25. Achatz, Maria Isabel Alves de Souza Waddington. Modificadores de penetrância de mutações germinativas no gene TP53 em famílias brasileiras com diagnóstico clínico da síndrome de Li-Fraumeni e Li-Fraumeni like: impacto dos polimorfismos intragênicos do TP53 e de genes.

Degree: PhD, Oncologia, 2008, University of São Paulo

A síndrome de Li-Fraumeni (LFS) e sua variante like (LFL) são associadas a mutações germinativas no gene TP53 e predispõe ao alto risco para múltiplos… (more)

Subjects/Keywords: Adrenocortical carcinoma; Carcinoma adrenocortical; Deleção de genes; Gene deletion; Genetic polymorphism; Genetic predisposition to disease; Germline mutation; Li-Fraumeni syndrome; Mutação em linhagem germinativa; Polimorfismo genético; Predisposição genética para doença; Proteína supressora de tumor p53; Proteínas proto-oncogênicas c-mdm2; Proto-oncogene proteins c-mdm2; Síndrome de Li-Fraumeni; Tumor suppressor protein p53

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APA (6th Edition):

Achatz, M. I. A. d. S. W. (2008). Modificadores de penetrância de mutações germinativas no gene TP53 em famílias brasileiras com diagnóstico clínico da síndrome de Li-Fraumeni e Li-Fraumeni like: impacto dos polimorfismos intragênicos do TP53 e de genes. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5155/tde-29012009-172419/ ;

Chicago Manual of Style (16th Edition):

Achatz, Maria Isabel Alves de Souza Waddington. “Modificadores de penetrância de mutações germinativas no gene TP53 em famílias brasileiras com diagnóstico clínico da síndrome de Li-Fraumeni e Li-Fraumeni like: impacto dos polimorfismos intragênicos do TP53 e de genes.” 2008. Doctoral Dissertation, University of São Paulo. Accessed December 01, 2020. http://www.teses.usp.br/teses/disponiveis/5/5155/tde-29012009-172419/ ;.

MLA Handbook (7th Edition):

Achatz, Maria Isabel Alves de Souza Waddington. “Modificadores de penetrância de mutações germinativas no gene TP53 em famílias brasileiras com diagnóstico clínico da síndrome de Li-Fraumeni e Li-Fraumeni like: impacto dos polimorfismos intragênicos do TP53 e de genes.” 2008. Web. 01 Dec 2020.

Vancouver:

Achatz MIAdSW. Modificadores de penetrância de mutações germinativas no gene TP53 em famílias brasileiras com diagnóstico clínico da síndrome de Li-Fraumeni e Li-Fraumeni like: impacto dos polimorfismos intragênicos do TP53 e de genes. [Internet] [Doctoral dissertation]. University of São Paulo; 2008. [cited 2020 Dec 01]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5155/tde-29012009-172419/ ;.

Council of Science Editors:

Achatz MIAdSW. Modificadores de penetrância de mutações germinativas no gene TP53 em famílias brasileiras com diagnóstico clínico da síndrome de Li-Fraumeni e Li-Fraumeni like: impacto dos polimorfismos intragênicos do TP53 e de genes. [Doctoral Dissertation]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/5/5155/tde-29012009-172419/ ;


Texas Medical Center

26. Li, Jialu. Statistical Methods for Two Problems in Cancer Research: Analysis of RNA-seq Data from Archival Samples and Characterization of Onset of Multiple Primary Cancers.

Degree: PhD, 2017, Texas Medical Center

  My dissertation is focused on quantitative methodology development and application for two important topics in translational and clinical cancer research. The first topic was… (more)

Subjects/Keywords: Formalin-fixation and paraffin-embedding tissue; Gene expression; Library preparation; Breast cancer tissue; Coding region enrichment; RNA sequencing; age-at-onset penetrance; familywise likelihood; multiple primary cancers; Li-Fraumeni syndrome; recurrent event model; Bioinformatics; Biostatistics; Computational Biology; Genomics; Medicine and Health Sciences; Statistical Models; Survival Analysis

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APA (6th Edition):

Li, J. (2017). Statistical Methods for Two Problems in Cancer Research: Analysis of RNA-seq Data from Archival Samples and Characterization of Onset of Multiple Primary Cancers. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/740

Chicago Manual of Style (16th Edition):

Li, Jialu. “Statistical Methods for Two Problems in Cancer Research: Analysis of RNA-seq Data from Archival Samples and Characterization of Onset of Multiple Primary Cancers.” 2017. Doctoral Dissertation, Texas Medical Center. Accessed December 01, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/740.

MLA Handbook (7th Edition):

Li, Jialu. “Statistical Methods for Two Problems in Cancer Research: Analysis of RNA-seq Data from Archival Samples and Characterization of Onset of Multiple Primary Cancers.” 2017. Web. 01 Dec 2020.

Vancouver:

Li J. Statistical Methods for Two Problems in Cancer Research: Analysis of RNA-seq Data from Archival Samples and Characterization of Onset of Multiple Primary Cancers. [Internet] [Doctoral dissertation]. Texas Medical Center; 2017. [cited 2020 Dec 01]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/740.

Council of Science Editors:

Li J. Statistical Methods for Two Problems in Cancer Research: Analysis of RNA-seq Data from Archival Samples and Characterization of Onset of Multiple Primary Cancers. [Doctoral Dissertation]. Texas Medical Center; 2017. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/740


University of Lund

27. Magnusson, Susanne. Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations.

Degree: 2012, University of Lund

 The etiology of childhood cancer is largely unknown. Approximately 1-10% of all childhood tumors are associated with known cancer predisposition syndromes. However, the contribution may… (more)

Subjects/Keywords: Cancer and Oncology; Childhood cancer; hereditary factors; breast cancer; survival; hereditary breast and ovarian cancer; hereditary non-polyposis colorectal cancer; familial malignant melanoma; BRCA1; BRCA2; mismatch repair; CDKN2A; familial risk; multiple childhood tumors; Li-Fraumeni syndrome; TP53; adrenocortical carcinoma; choroid plexus tumors; rhabdomyosarcoma

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APA (6th Edition):

Magnusson, S. (2012). Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/2364386 ; https://portal.research.lu.se/ws/files/3867820/2364415.pdf

Chicago Manual of Style (16th Edition):

Magnusson, Susanne. “Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations.” 2012. Doctoral Dissertation, University of Lund. Accessed December 01, 2020. https://lup.lub.lu.se/record/2364386 ; https://portal.research.lu.se/ws/files/3867820/2364415.pdf.

MLA Handbook (7th Edition):

Magnusson, Susanne. “Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations.” 2012. Web. 01 Dec 2020.

Vancouver:

Magnusson S. Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations. [Internet] [Doctoral dissertation]. University of Lund; 2012. [cited 2020 Dec 01]. Available from: https://lup.lub.lu.se/record/2364386 ; https://portal.research.lu.se/ws/files/3867820/2364415.pdf.

Council of Science Editors:

Magnusson S. Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations. [Doctoral Dissertation]. University of Lund; 2012. Available from: https://lup.lub.lu.se/record/2364386 ; https://portal.research.lu.se/ws/files/3867820/2364415.pdf

28. Shlien, Adam. Genomic DNA Copy Number Variations and Cancer: Studies of Li-Fraumeni Syndrome and its Variants.

Degree: 2010, University of Toronto

Copy number variations (CNVs) are a major source of inter-individual genetic difference, accounting for a greater proportion of the human genome than other forms of… (more)

Subjects/Keywords: Cancer; Genomics; Copy number variations; Copy number variants; Li-Fraumeni syndrome; p53; TP53; 0369

…13 1.2 Li-Fraumeni Syndrome… …15 1.2.1 Genetic Etiology of Li-Fraumeni Syndrome… …are the six most frequent sites of TP53 mutation 19 Figure 4 - Li-Fraumeni syndrome… …Li-Fraumeni syndrome Figure 2 - Inherited deletions and duplications in 4 LFS families. 63… …the Li-Fraumeni cancer predisposition syndrome 78-79 Supplementary Figure 1 - CNV… 

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

APA (6th Edition):

Shlien, A. (2010). Genomic DNA Copy Number Variations and Cancer: Studies of Li-Fraumeni Syndrome and its Variants. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32050

Chicago Manual of Style (16th Edition):

Shlien, Adam. “Genomic DNA Copy Number Variations and Cancer: Studies of Li-Fraumeni Syndrome and its Variants.” 2010. Doctoral Dissertation, University of Toronto. Accessed December 01, 2020. http://hdl.handle.net/1807/32050.

MLA Handbook (7th Edition):

Shlien, Adam. “Genomic DNA Copy Number Variations and Cancer: Studies of Li-Fraumeni Syndrome and its Variants.” 2010. Web. 01 Dec 2020.

Vancouver:

Shlien A. Genomic DNA Copy Number Variations and Cancer: Studies of Li-Fraumeni Syndrome and its Variants. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1807/32050.

Council of Science Editors:

Shlien A. Genomic DNA Copy Number Variations and Cancer: Studies of Li-Fraumeni Syndrome and its Variants. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/32050

29. Bhutani, Kunal. Limiting Biases in Biological Data Analysis by Pooling Information.

Degree: Bioinformatics & Systems Bio, 2017, University of California – San Diego

 Innovations in the design and implementation of high-throughput technologies has shifted biological research from hypothesis-driven inquiries to large data-driven studies. Scientists can now jointly interrogate… (more)

Subjects/Keywords: Bioinformatics; Genetics; Statistics; Bayesian Statistics; Complex Diseases; Li-Fraumeni Syndrome; N-of-1 Studies; Population Genetics; Stem Cells

…TWAS. 8 1.3 Metabolomics and Li-Fraumeni Syndrome Single subject or N-of-1 studies and… …syndrome[LFJ69]. Li-Fraumeni patients have a high incidence of cancer during their… …molecular surveillance study of an individual a germline p53 mutation, which causes Li-Fraumeni… …sites (TFBS), MutSig genes, and Familial Syndrome Cancer Genes (Methods)… 

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APA (6th Edition):

Bhutani, K. (2017). Limiting Biases in Biological Data Analysis by Pooling Information. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/1mv9d8n8

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):

Bhutani, Kunal. “Limiting Biases in Biological Data Analysis by Pooling Information.” 2017. Thesis, University of California – San Diego. Accessed December 01, 2020. http://www.escholarship.org/uc/item/1mv9d8n8.

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

MLA Handbook (7th Edition):

Bhutani, Kunal. “Limiting Biases in Biological Data Analysis by Pooling Information.” 2017. Web. 01 Dec 2020.

Vancouver:

Bhutani K. Limiting Biases in Biological Data Analysis by Pooling Information. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2020 Dec 01]. Available from: http://www.escholarship.org/uc/item/1mv9d8n8.

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

Council of Science Editors:

Bhutani K. Limiting Biases in Biological Data Analysis by Pooling Information. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/1mv9d8n8

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

.