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You searched for subject:(GJB2). Showing records 1 – 8 of 8 total matches.

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1. Melo, Uirá Souto. Estudo epidemiológico e genético da surdez em dois municípios do estado da Paraíba, Brasil.

Degree: Mestrado, Biologia (Genética), 2013, University of São Paulo

Os estados do Nordeste brasileiro concentram elevadas taxas de pessoas com deficiências, mas pouco se estudou a respeito de suas causas. O objetivo desse estudo… (more)

Subjects/Keywords: Epidemiologia; Epidemiology; GJB2; GJB2; Hearing loss; Surdez

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APA (6th Edition):

Melo, U. S. (2013). Estudo epidemiológico e genético da surdez em dois municípios do estado da Paraíba, Brasil. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-19032014-132211/ ;

Chicago Manual of Style (16th Edition):

Melo, Uirá Souto. “Estudo epidemiológico e genético da surdez em dois municípios do estado da Paraíba, Brasil.” 2013. Masters Thesis, University of São Paulo. Accessed August 25, 2019. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-19032014-132211/ ;.

MLA Handbook (7th Edition):

Melo, Uirá Souto. “Estudo epidemiológico e genético da surdez em dois municípios do estado da Paraíba, Brasil.” 2013. Web. 25 Aug 2019.

Vancouver:

Melo US. Estudo epidemiológico e genético da surdez em dois municípios do estado da Paraíba, Brasil. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2019 Aug 25]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-19032014-132211/ ;.

Council of Science Editors:

Melo US. Estudo epidemiológico e genético da surdez em dois municípios do estado da Paraíba, Brasil. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-19032014-132211/ ;

2. Carvalho, Simone da Costa e Silva. Estudo do Papel do Gene SLC26A4 na Surdez Neurossensorial Não-Sindrômica Pré-Lingual em uma Série de Casos no Sudeste Brasileiro.

Degree: Mestrado, Genética, 2015, University of São Paulo

 A audição representa a principal fonte para o aprendizado da fala e linguagem durante a infância e a surdez e a privação de estímulos auditivos… (more)

Subjects/Keywords: Diagnóstico molecular; GJB2; GJB2; Hereditary hearing loss; Molecular diagnosis; SLC26A4; SLC26A4; Surdez hereditária

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APA (6th Edition):

Carvalho, S. d. C. e. S. (2015). Estudo do Papel do Gene SLC26A4 na Surdez Neurossensorial Não-Sindrômica Pré-Lingual em uma Série de Casos no Sudeste Brasileiro. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17135/tde-28072015-121136/ ;

Chicago Manual of Style (16th Edition):

Carvalho, Simone da Costa e Silva. “Estudo do Papel do Gene SLC26A4 na Surdez Neurossensorial Não-Sindrômica Pré-Lingual em uma Série de Casos no Sudeste Brasileiro.” 2015. Masters Thesis, University of São Paulo. Accessed August 25, 2019. http://www.teses.usp.br/teses/disponiveis/17/17135/tde-28072015-121136/ ;.

MLA Handbook (7th Edition):

Carvalho, Simone da Costa e Silva. “Estudo do Papel do Gene SLC26A4 na Surdez Neurossensorial Não-Sindrômica Pré-Lingual em uma Série de Casos no Sudeste Brasileiro.” 2015. Web. 25 Aug 2019.

Vancouver:

Carvalho SdCeS. Estudo do Papel do Gene SLC26A4 na Surdez Neurossensorial Não-Sindrômica Pré-Lingual em uma Série de Casos no Sudeste Brasileiro. [Internet] [Masters thesis]. University of São Paulo; 2015. [cited 2019 Aug 25]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17135/tde-28072015-121136/ ;.

Council of Science Editors:

Carvalho SdCeS. Estudo do Papel do Gene SLC26A4 na Surdez Neurossensorial Não-Sindrômica Pré-Lingual em uma Série de Casos no Sudeste Brasileiro. [Masters Thesis]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/17/17135/tde-28072015-121136/ ;

3. Παμπάνος, Ανδρέας. Μελέτη της επίδρασης της μεταλλαγής 35delG του γονιδίου της συνδετίνης (κονεξίνης 26) σε ασθενείς ελληνικής καταγωγής με προομιλητική βαρηκοϊα.

Degree: 2003, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

Subjects/Keywords: Νευροαισθητήρια βαρηκοΐα; Deafness; GJB2 gene

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APA (6th Edition):

Παμπάνος, . . (2003). Μελέτη της επίδρασης της μεταλλαγής 35delG του γονιδίου της συνδετίνης (κονεξίνης 26) σε ασθενείς ελληνικής καταγωγής με προομιλητική βαρηκοϊα. (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/13751

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):

Παμπάνος, Ανδρέας. “Μελέτη της επίδρασης της μεταλλαγής 35delG του γονιδίου της συνδετίνης (κονεξίνης 26) σε ασθενείς ελληνικής καταγωγής με προομιλητική βαρηκοϊα.” 2003. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed August 25, 2019. http://hdl.handle.net/10442/hedi/13751.

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

MLA Handbook (7th Edition):

Παμπάνος, Ανδρέας. “Μελέτη της επίδρασης της μεταλλαγής 35delG του γονιδίου της συνδετίνης (κονεξίνης 26) σε ασθενείς ελληνικής καταγωγής με προομιλητική βαρηκοϊα.” 2003. Web. 25 Aug 2019.

Vancouver:

Παμπάνος . Μελέτη της επίδρασης της μεταλλαγής 35delG του γονιδίου της συνδετίνης (κονεξίνης 26) σε ασθενείς ελληνικής καταγωγής με προομιλητική βαρηκοϊα. [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2003. [cited 2019 Aug 25]. Available from: http://hdl.handle.net/10442/hedi/13751.

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

Council of Science Editors:

Παμπάνος . Μελέτη της επίδρασης της μεταλλαγής 35delG του γονιδίου της συνδετίνης (κονεξίνης 26) σε ασθενείς ελληνικής καταγωγής με προομιλητική βαρηκοϊα. [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2003. Available from: http://hdl.handle.net/10442/hedi/13751

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

4. 정, 연훈. Gunctional study of gap junction in GJB2 mutations associated with hereditary hearing loss.

Degree: 2001, Ajou University

Doctor Advisors/Committee Members: 정, 연훈.

Subjects/Keywords: 유전성 난청; GJB2 유전자 변이; 세포간극; Hereditary hearing loss

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APA (6th Edition):

정, . (2001). Gunctional study of gap junction in GJB2 mutations associated with hereditary hearing loss. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/2224 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000008623

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):

정, 연훈. “Gunctional study of gap junction in GJB2 mutations associated with hereditary hearing loss.” 2001. Thesis, Ajou University. Accessed August 25, 2019. http://repository.ajou.ac.kr/handle/201003/2224 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000008623.

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

MLA Handbook (7th Edition):

정, 연훈. “Gunctional study of gap junction in GJB2 mutations associated with hereditary hearing loss.” 2001. Web. 25 Aug 2019.

Vancouver:

정 . Gunctional study of gap junction in GJB2 mutations associated with hereditary hearing loss. [Internet] [Thesis]. Ajou University; 2001. [cited 2019 Aug 25]. Available from: http://repository.ajou.ac.kr/handle/201003/2224 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000008623.

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

Council of Science Editors:

정 . Gunctional study of gap junction in GJB2 mutations associated with hereditary hearing loss. [Thesis]. Ajou University; 2001. Available from: http://repository.ajou.ac.kr/handle/201003/2224 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000008623

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


Universidade de Lisboa

5. Correia, Bárbara Isabel de Carvalho. Analysis of DFNB1 locus in presbycusis.

Degree: 2017, Universidade de Lisboa

Tese de mestrado, Biologia Molecular e Genética, Universidade de Lisboa, Faculdade de Ciências, 2017

Introdução: O ouvido é um órgão sensorial que tem como função… (more)

Subjects/Keywords: Presbiacusia; Estudos funcionais; locus DFNB1; Mutações em GJB2 e GJB6; Teses de mestrado - 2017; Departamento de Biologia Vegetal

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APA (6th Edition):

Correia, B. I. d. C. (2017). Analysis of DFNB1 locus in presbycusis. (Thesis). Universidade de Lisboa. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/30529

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):

Correia, Bárbara Isabel de Carvalho. “Analysis of DFNB1 locus in presbycusis.” 2017. Thesis, Universidade de Lisboa. Accessed August 25, 2019. https://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/30529.

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

MLA Handbook (7th Edition):

Correia, Bárbara Isabel de Carvalho. “Analysis of DFNB1 locus in presbycusis.” 2017. Web. 25 Aug 2019.

Vancouver:

Correia BIdC. Analysis of DFNB1 locus in presbycusis. [Internet] [Thesis]. Universidade de Lisboa; 2017. [cited 2019 Aug 25]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/30529.

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

Council of Science Editors:

Correia BIdC. Analysis of DFNB1 locus in presbycusis. [Thesis]. Universidade de Lisboa; 2017. Available from: https://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/30529

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

6. Silva, Ronaldo Serafim Abreu. Susceptibilidade genética à perda auditiva induzida por ruído (PAIR).

Degree: PhD, Biologia (Genética), 2008, University of São Paulo

 A exposição contínua ao ruído de alta intensidade é o fator ambiental mais importante como causa de problemas auditivos em adultos. Esses tipos de perdas… (more)

Subjects/Keywords: Gjb2 GSTM1 e GSTT1 genes polimorphisms; MT-RNR1 e MT-TS1 mutations; Deafness mutations; Genetic susceptibility; Mutações associadas à surdez; Mutações nos genes mitocondriais MT-RNR1 e MT-TS1; NIHL; PAIR; Polimorfismos dos genes Gjb2 GSTM1 e GSTT1; Susceptibilidade genética

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APA (6th Edition):

Silva, R. S. A. (2008). Susceptibilidade genética à perda auditiva induzida por ruído (PAIR). (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-16062008-160637/ ;

Chicago Manual of Style (16th Edition):

Silva, Ronaldo Serafim Abreu. “Susceptibilidade genética à perda auditiva induzida por ruído (PAIR).” 2008. Doctoral Dissertation, University of São Paulo. Accessed August 25, 2019. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-16062008-160637/ ;.

MLA Handbook (7th Edition):

Silva, Ronaldo Serafim Abreu. “Susceptibilidade genética à perda auditiva induzida por ruído (PAIR).” 2008. Web. 25 Aug 2019.

Vancouver:

Silva RSA. Susceptibilidade genética à perda auditiva induzida por ruído (PAIR). [Internet] [Doctoral dissertation]. University of São Paulo; 2008. [cited 2019 Aug 25]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-16062008-160637/ ;.

Council of Science Editors:

Silva RSA. Susceptibilidade genética à perda auditiva induzida por ruído (PAIR). [Doctoral Dissertation]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-16062008-160637/ ;

7. Supinger, Rachel Christine. Process Review of <I>GJB6</i> Reflex Testing in Individuals with 0 or 1 <i>GJB2</i> Pathogenic Variants and Non-Syndromic Hearing Loss.

Degree: MS, Genetic Counseling, 2017, The Ohio State University

 The gene most commonly implicated in autosomal recessive non-syndromic hearing loss (NSHL) is <i>GJB2</i>. Homozygous deletions within the gene <i>GJB6</i>, as well as a heterozygous… (more)

Subjects/Keywords: Genetics; hearing loss; GJB2; GJB6; non-syndromic hearing loss; reflex testing; process review

…2 GJB2 Gene… …4 GJB2-Related Syndromic Hearing Loss… …4 GJB2-Related NSHL… …26 Aim 1: Identify current laboratory practices in genetic testing of GJB2 and GJB6… …26 Aim 2: Examine the frequency and distribution of GJB2 variants and the 309 kb deletion… 

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APA (6th Edition):

Supinger, R. C. (2017). Process Review of <I>GJB6</i> Reflex Testing in Individuals with 0 or 1 <i>GJB2</i> Pathogenic Variants and Non-Syndromic Hearing Loss. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1492470064058105

Chicago Manual of Style (16th Edition):

Supinger, Rachel Christine. “Process Review of <I>GJB6</i> Reflex Testing in Individuals with 0 or 1 <i>GJB2</i> Pathogenic Variants and Non-Syndromic Hearing Loss.” 2017. Masters Thesis, The Ohio State University. Accessed August 25, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1492470064058105.

MLA Handbook (7th Edition):

Supinger, Rachel Christine. “Process Review of <I>GJB6</i> Reflex Testing in Individuals with 0 or 1 <i>GJB2</i> Pathogenic Variants and Non-Syndromic Hearing Loss.” 2017. Web. 25 Aug 2019.

Vancouver:

Supinger RC. Process Review of <I>GJB6</i> Reflex Testing in Individuals with 0 or 1 <i>GJB2</i> Pathogenic Variants and Non-Syndromic Hearing Loss. [Internet] [Masters thesis]. The Ohio State University; 2017. [cited 2019 Aug 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1492470064058105.

Council of Science Editors:

Supinger RC. Process Review of <I>GJB6</i> Reflex Testing in Individuals with 0 or 1 <i>GJB2</i> Pathogenic Variants and Non-Syndromic Hearing Loss. [Masters Thesis]. The Ohio State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1492470064058105

8. Sheffield, Abraham Matthias. Gene therapy for hereditary hearing loss: lessons from a mouse model.

Degree: PhD, Genetics, 2012, University of Iowa

  Hearing impairment is the most common sensory deficit worldwide, affecting at least one child in every one thousand born. Gene therapy targeting the inner… (more)

Subjects/Keywords: Gene therapy; GJB2; Hearing loss; Mouse Model; RNA interference; Viral vectors; Genetics

…mutation in GJB2 which encodes connexin 26, a gap junction protein expressed in the supporting… …RNAitherapy to the GJB2-R75W transgenic mouse, a model of severe-to-profound dominantnegative… …described two previously unreported phenotypes in the GJB2-R75W transgenic mouse model: skin… …8 GJB2 (CX26) and Other Connexins… …13 GJB2 Mutations… 

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

APA (6th Edition):

Sheffield, A. M. (2012). Gene therapy for hereditary hearing loss: lessons from a mouse model. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/2984

Chicago Manual of Style (16th Edition):

Sheffield, Abraham Matthias. “Gene therapy for hereditary hearing loss: lessons from a mouse model.” 2012. Doctoral Dissertation, University of Iowa. Accessed August 25, 2019. https://ir.uiowa.edu/etd/2984.

MLA Handbook (7th Edition):

Sheffield, Abraham Matthias. “Gene therapy for hereditary hearing loss: lessons from a mouse model.” 2012. Web. 25 Aug 2019.

Vancouver:

Sheffield AM. Gene therapy for hereditary hearing loss: lessons from a mouse model. [Internet] [Doctoral dissertation]. University of Iowa; 2012. [cited 2019 Aug 25]. Available from: https://ir.uiowa.edu/etd/2984.

Council of Science Editors:

Sheffield AM. Gene therapy for hereditary hearing loss: lessons from a mouse model. [Doctoral Dissertation]. University of Iowa; 2012. Available from: https://ir.uiowa.edu/etd/2984

.