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You searched for subject:(maltase). Showing records 1 – 5 of 5 total matches.

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University of Waterloo

1. Jones, Kyra Jill Jacques. Molecular Mechanism of Starch Digestion by Family 31 Glycoside Hydrolases: Structural Characterization and Inhibition Studies of C-terminal Maltase Glycoamylase and Sucrase Isomaltase.

Degree: 2014, University of Waterloo

 Although carbohydrates are a principal component of the human diet, the mechanism of the final stages of starch digestion is not fully understood. One approach… (more)

Subjects/Keywords: Starch; Family 31 Glycoside Hydrolase; Sucrase Isomaltase; Maltase Glucoamylase; Digestion

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

APA (6th Edition):

Jones, K. J. J. (2014). Molecular Mechanism of Starch Digestion by Family 31 Glycoside Hydrolases: Structural Characterization and Inhibition Studies of C-terminal Maltase Glycoamylase and Sucrase Isomaltase. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/8333

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):

Jones, Kyra Jill Jacques. “Molecular Mechanism of Starch Digestion by Family 31 Glycoside Hydrolases: Structural Characterization and Inhibition Studies of C-terminal Maltase Glycoamylase and Sucrase Isomaltase.” 2014. Thesis, University of Waterloo. Accessed July 24, 2019. http://hdl.handle.net/10012/8333.

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

MLA Handbook (7th Edition):

Jones, Kyra Jill Jacques. “Molecular Mechanism of Starch Digestion by Family 31 Glycoside Hydrolases: Structural Characterization and Inhibition Studies of C-terminal Maltase Glycoamylase and Sucrase Isomaltase.” 2014. Web. 24 Jul 2019.

Vancouver:

Jones KJJ. Molecular Mechanism of Starch Digestion by Family 31 Glycoside Hydrolases: Structural Characterization and Inhibition Studies of C-terminal Maltase Glycoamylase and Sucrase Isomaltase. [Internet] [Thesis]. University of Waterloo; 2014. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/10012/8333.

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

Council of Science Editors:

Jones KJJ. Molecular Mechanism of Starch Digestion by Family 31 Glycoside Hydrolases: Structural Characterization and Inhibition Studies of C-terminal Maltase Glycoamylase and Sucrase Isomaltase. [Thesis]. University of Waterloo; 2014. Available from: http://hdl.handle.net/10012/8333

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


University of Cincinnati

2. Cecchi, Alana. Analysis of Parental Perception of Swallowing and Voice in Infants and Children with Pompe Disease.

Degree: MS, Medicine: Genetic Counseling, 2011, University of Cincinnati

 Pompe disease is an autosomal recessive lysosomal storage disease caused by a deficiency of the enzyme acid a-glucosidase (GAA). It is a heterogeneous neuromuscular condition… (more)

Subjects/Keywords: Surgery; Pompe disease; Glycogen storage disease type II; Acid maltase deficiency; Oropharyngeal dysfunction; Voice disorders

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APA (6th Edition):

Cecchi, A. (2011). Analysis of Parental Perception of Swallowing and Voice in Infants and Children with Pompe Disease. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1307125630

Chicago Manual of Style (16th Edition):

Cecchi, Alana. “Analysis of Parental Perception of Swallowing and Voice in Infants and Children with Pompe Disease.” 2011. Masters Thesis, University of Cincinnati. Accessed July 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1307125630.

MLA Handbook (7th Edition):

Cecchi, Alana. “Analysis of Parental Perception of Swallowing and Voice in Infants and Children with Pompe Disease.” 2011. Web. 24 Jul 2019.

Vancouver:

Cecchi A. Analysis of Parental Perception of Swallowing and Voice in Infants and Children with Pompe Disease. [Internet] [Masters thesis]. University of Cincinnati; 2011. [cited 2019 Jul 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1307125630.

Council of Science Editors:

Cecchi A. Analysis of Parental Perception of Swallowing and Voice in Infants and Children with Pompe Disease. [Masters Thesis]. University of Cincinnati; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1307125630


Universidade Federal de Santa Maria

3. Vera Maria Machado da Silva. SOBREVIVÊNCIA, CRESCIMENTO, PARÂMETROS METABÓLICOS E ENZIMÁTICOS EM JUNDIÁS (Rhamdia quelen) EXPOSTOS AO COBRE.

Degree: 2006, Universidade Federal de Santa Maria

O objetivo deste estudo foi verificar a concentração letal média em 96 h (CL50) para o cobre, bem como o efeito da exposição ao cobre… (more)

Subjects/Keywords: psicultura; jundiá; enzimas; cobre; ZOOTECNIA; lethal concentration; growth; metabolic parameters; acetylcholinesterase; amylase; maltase; silver catfish (Rhamdia quelen.)

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

APA (6th Edition):

Silva, V. M. M. d. (2006). SOBREVIVÊNCIA, CRESCIMENTO, PARÂMETROS METABÓLICOS E ENZIMÁTICOS EM JUNDIÁS (Rhamdia quelen) EXPOSTOS AO COBRE. (Thesis). Universidade Federal de Santa Maria. Retrieved from http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=687

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):

Silva, Vera Maria Machado da. “SOBREVIVÊNCIA, CRESCIMENTO, PARÂMETROS METABÓLICOS E ENZIMÁTICOS EM JUNDIÁS (Rhamdia quelen) EXPOSTOS AO COBRE.” 2006. Thesis, Universidade Federal de Santa Maria. Accessed July 24, 2019. http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=687.

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

MLA Handbook (7th Edition):

Silva, Vera Maria Machado da. “SOBREVIVÊNCIA, CRESCIMENTO, PARÂMETROS METABÓLICOS E ENZIMÁTICOS EM JUNDIÁS (Rhamdia quelen) EXPOSTOS AO COBRE.” 2006. Web. 24 Jul 2019.

Vancouver:

Silva VMMd. SOBREVIVÊNCIA, CRESCIMENTO, PARÂMETROS METABÓLICOS E ENZIMÁTICOS EM JUNDIÁS (Rhamdia quelen) EXPOSTOS AO COBRE. [Internet] [Thesis]. Universidade Federal de Santa Maria; 2006. [cited 2019 Jul 24]. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=687.

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

Council of Science Editors:

Silva VMMd. SOBREVIVÊNCIA, CRESCIMENTO, PARÂMETROS METABÓLICOS E ENZIMÁTICOS EM JUNDIÁS (Rhamdia quelen) EXPOSTOS AO COBRE. [Thesis]. Universidade Federal de Santa Maria; 2006. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=687

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

4. Hagemans, Marloes. Pompe disease in children and adults: natural course, disease severity and impact on daily life; results from an international patient survey.

Degree: Department of Pediatrics, 2006, Erasmus University Medical Center

 textabstractPompe disease is a lysosomal storage disorder caused by deficiency of the enzyme acid alpha-glucosidase and mainly characterized by progressive skeletal muscle weakness. Research on… (more)

Subjects/Keywords: Pomp Disease; acid maltase deficiency; alpha-glucosidase deficiency; patient reported outcome measures

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

APA (6th Edition):

Hagemans, M. (2006). Pompe disease in children and adults: natural course, disease severity and impact on daily life; results from an international patient survey. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/9453

Chicago Manual of Style (16th Edition):

Hagemans, Marloes. “Pompe disease in children and adults: natural course, disease severity and impact on daily life; results from an international patient survey.” 2006. Doctoral Dissertation, Erasmus University Medical Center. Accessed July 24, 2019. http://hdl.handle.net/1765/9453.

MLA Handbook (7th Edition):

Hagemans, Marloes. “Pompe disease in children and adults: natural course, disease severity and impact on daily life; results from an international patient survey.” 2006. Web. 24 Jul 2019.

Vancouver:

Hagemans M. Pompe disease in children and adults: natural course, disease severity and impact on daily life; results from an international patient survey. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2006. [cited 2019 Jul 24]. Available from: http://hdl.handle.net/1765/9453.

Council of Science Editors:

Hagemans M. Pompe disease in children and adults: natural course, disease severity and impact on daily life; results from an international patient survey. [Doctoral Dissertation]. Erasmus University Medical Center; 2006. Available from: http://hdl.handle.net/1765/9453


Universidad del Rosario

5. Niño Martínez, Monica Yasmin. Identificación y caracterización de las mutaciones en el gen GAA en pacientes colombianos afectados por la enfermedad de Pompe.

Degree: 2013, Universidad del Rosario

La Enfermedad de Pompe (EP) es un desorden metabólico caracterizado por la deficiencia de alfa-glucosidasa acida (GAA), una enzima que cataliza la hidrolisis de las… (more)

Subjects/Keywords: Enfermedad de Pompe, Enfermedad de almacenamiento de glucógeno tipo II; alfa glucosidasa acida humana; Trastornos del metabolismo::Investigaciones; GAA gene; acid maltase deficiency; ENFERMEDAD DEL ALMACENAMIENTO DE GLUCÓGENO TIPO II - INVESTIGACIONES

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

APA (6th Edition):

Niño Martínez, M. Y. (2013). Identificación y caracterización de las mutaciones en el gen GAA en pacientes colombianos afectados por la enfermedad de Pompe. (Thesis). Universidad del Rosario. Retrieved from http://repository.urosario.edu.co/handle/10336/4485

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):

Niño Martínez, Monica Yasmin. “Identificación y caracterización de las mutaciones en el gen GAA en pacientes colombianos afectados por la enfermedad de Pompe.” 2013. Thesis, Universidad del Rosario. Accessed July 24, 2019. http://repository.urosario.edu.co/handle/10336/4485.

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

MLA Handbook (7th Edition):

Niño Martínez, Monica Yasmin. “Identificación y caracterización de las mutaciones en el gen GAA en pacientes colombianos afectados por la enfermedad de Pompe.” 2013. Web. 24 Jul 2019.

Vancouver:

Niño Martínez MY. Identificación y caracterización de las mutaciones en el gen GAA en pacientes colombianos afectados por la enfermedad de Pompe. [Internet] [Thesis]. Universidad del Rosario; 2013. [cited 2019 Jul 24]. Available from: http://repository.urosario.edu.co/handle/10336/4485.

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

Council of Science Editors:

Niño Martínez MY. Identificación y caracterización de las mutaciones en el gen GAA en pacientes colombianos afectados por la enfermedad de Pompe. [Thesis]. Universidad del Rosario; 2013. Available from: http://repository.urosario.edu.co/handle/10336/4485

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

.