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You searched for +publisher:"Universidade Estadual de Campinas" +contributor:("Soma, Mithitaka"). Showing records 1 – 4 of 4 total matches.

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Universidade Estadual de Campinas

1. Gonçalves, Claudia Estela, 1970-. Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia.

Degree: 2014, Universidade Estadual de Campinas

 Abstract: The Fanconi Anemia (FA) is a genetic disorder characterized by multiple congenital and hematological abnormalities and predisposition to a variety of tumors. The worldwide… (more)

Subjects/Keywords: Anemia de Fanconi; Neoplasias; Genótipo; Síndromes mielodisplásicas; Mutação; Instabilidade cromossomica; Fanconi anemia; Neoplasms; Genotype; Myelodysplastic syndromes; Mutation; Chromosomal instability

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

APA (6th Edition):

Gonçalves, Claudia Estela, 1. (2014). Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/308602

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):

Gonçalves, Claudia Estela, 1970-. “Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia.” 2014. Thesis, Universidade Estadual de Campinas. Accessed October 29, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/308602.

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

MLA Handbook (7th Edition):

Gonçalves, Claudia Estela, 1970-. “Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia.” 2014. Web. 29 Oct 2020.

Vancouver:

Gonçalves, Claudia Estela 1. Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia. [Internet] [Thesis]. Universidade Estadual de Campinas; 2014. [cited 2020 Oct 29]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308602.

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

Council of Science Editors:

Gonçalves, Claudia Estela 1. Estudo molecular do gene FANCA em pacientes com quadro clínico de Anemia de Fanconi: Molecular study of the gene FANCA in patients with compatible clinical of Fanconi Anemia. [Thesis]. Universidade Estadual de Campinas; 2014. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308602

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


Universidade Estadual de Campinas

2. Amstalden, Lucila Gobby. Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer.

Degree: 2011, Universidade Estadual de Campinas

 Abstract: Breast Cancer (BC) is the cancer type more commonly occurs among women with estimative of 49.240 new cases in 2010. The BC presents risk… (more)

Subjects/Keywords: Mamas - Câncer; Fanconi, Anemia de; Metástase; Câncer; Sequência de nucleotídeos; Breast - Cancer; Fanconi anemia; Metastasis; Cancer; Nucleotides sequence

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

APA (6th Edition):

Amstalden, L. G. (2011). Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/308580

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):

Amstalden, Lucila Gobby. “Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer.” 2011. Thesis, Universidade Estadual de Campinas. Accessed October 29, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/308580.

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

MLA Handbook (7th Edition):

Amstalden, Lucila Gobby. “Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer.” 2011. Web. 29 Oct 2020.

Vancouver:

Amstalden LG. Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer. [Internet] [Thesis]. Universidade Estadual de Campinas; 2011. [cited 2020 Oct 29]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308580.

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

Council of Science Editors:

Amstalden LG. Análise do complexo gênico FANCD2/FANCI em mulheres brasileiras com câncer de mama herediitário: Analysis of the gene complex FANCD2/FANCI in Brazilian womem with hereditary breast cancer. [Thesis]. Universidade Estadual de Campinas; 2011. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308580

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


Universidade Estadual de Campinas

3. Rueda, Lidiane Camila, 1982-. Investigação de mutações nos genes MLH1 e MSH2 em portadores de câncer colorretal hereditário sem polipose (HNPCC): Investigation of mutations in MLH1 and MSH2 genes in carriers with Hereditary Nonpolyposis Colorectal Cancer (HNPCC).

Degree: 2013, Universidade Estadual de Campinas

 Abstract: Colorectal cancer has high importance because of its incidence and morbidity. Among the hereditary cases, the hereditary nonpolyposis colorectal cancer (HNPCC) or Lynch syndrome,… (more)

Subjects/Keywords: Gene MLH1; Gene MSH2; Neoplasias colorretais hereditárias sem polipose; Gene, MLH1; Gene, MSH2; Colorectal neoplasms, Hereditary nonpolyposis; Lynch Syndrome

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

APA (6th Edition):

Rueda, Lidiane Camila, 1. (2013). Investigação de mutações nos genes MLH1 e MSH2 em portadores de câncer colorretal hereditário sem polipose (HNPCC): Investigation of mutations in MLH1 and MSH2 genes in carriers with Hereditary Nonpolyposis Colorectal Cancer (HNPCC). (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/308604

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):

Rueda, Lidiane Camila, 1982-. “Investigação de mutações nos genes MLH1 e MSH2 em portadores de câncer colorretal hereditário sem polipose (HNPCC): Investigation of mutations in MLH1 and MSH2 genes in carriers with Hereditary Nonpolyposis Colorectal Cancer (HNPCC).” 2013. Thesis, Universidade Estadual de Campinas. Accessed October 29, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/308604.

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

MLA Handbook (7th Edition):

Rueda, Lidiane Camila, 1982-. “Investigação de mutações nos genes MLH1 e MSH2 em portadores de câncer colorretal hereditário sem polipose (HNPCC): Investigation of mutations in MLH1 and MSH2 genes in carriers with Hereditary Nonpolyposis Colorectal Cancer (HNPCC).” 2013. Web. 29 Oct 2020.

Vancouver:

Rueda, Lidiane Camila 1. Investigação de mutações nos genes MLH1 e MSH2 em portadores de câncer colorretal hereditário sem polipose (HNPCC): Investigation of mutations in MLH1 and MSH2 genes in carriers with Hereditary Nonpolyposis Colorectal Cancer (HNPCC). [Internet] [Thesis]. Universidade Estadual de Campinas; 2013. [cited 2020 Oct 29]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308604.

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

Council of Science Editors:

Rueda, Lidiane Camila 1. Investigação de mutações nos genes MLH1 e MSH2 em portadores de câncer colorretal hereditário sem polipose (HNPCC): Investigation of mutations in MLH1 and MSH2 genes in carriers with Hereditary Nonpolyposis Colorectal Cancer (HNPCC). [Thesis]. Universidade Estadual de Campinas; 2013. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308604

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


Universidade Estadual de Campinas

4. Furgeri, Daniela Tenório, 1983-. Estudo de polimorfismos nos genes TCF7L2 e ADRA2A associados à gravidade clínica da fibrose cística = Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis: Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis.

Degree: 2013, Universidade Estadual de Campinas

 Abstract: Cystic fibrosis (CF) is an autosomal recessive disease with characteristics of complex disease. Clinical complications appear to be a decisive factor in the prognosis… (more)

Subjects/Keywords: Genótipo; Fenótipo; Genes modificadores; Diabetes Mellitus; Regulador de condutância transmembrana em fibrose cística; Genotype; Phenotype; Genes, Modifier; Diabetes Mellitus; Cystic fibrosis transmembrane conductance regulator

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

APA (6th Edition):

Furgeri, Daniela Tenório, 1. (2013). Estudo de polimorfismos nos genes TCF7L2 e ADRA2A associados à gravidade clínica da fibrose cística = Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis: Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/308578

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):

Furgeri, Daniela Tenório, 1983-. “Estudo de polimorfismos nos genes TCF7L2 e ADRA2A associados à gravidade clínica da fibrose cística = Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis: Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis.” 2013. Thesis, Universidade Estadual de Campinas. Accessed October 29, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/308578.

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

MLA Handbook (7th Edition):

Furgeri, Daniela Tenório, 1983-. “Estudo de polimorfismos nos genes TCF7L2 e ADRA2A associados à gravidade clínica da fibrose cística = Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis: Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis.” 2013. Web. 29 Oct 2020.

Vancouver:

Furgeri, Daniela Tenório 1. Estudo de polimorfismos nos genes TCF7L2 e ADRA2A associados à gravidade clínica da fibrose cística = Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis: Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis. [Internet] [Thesis]. Universidade Estadual de Campinas; 2013. [cited 2020 Oct 29]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308578.

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

Council of Science Editors:

Furgeri, Daniela Tenório 1. Estudo de polimorfismos nos genes TCF7L2 e ADRA2A associados à gravidade clínica da fibrose cística = Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis: Study of polymorphisms in ADRA2A and TCF7L2 genes associated with clinical gravity of cystic fibrosis. [Thesis]. Universidade Estadual de Campinas; 2013. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/308578

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

.