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You searched for subject:(neuronal ceroid lipofuscinosis). Showing records 1 – 28 of 28 total matches.

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University of Rochester

1. Getty, Amanda L. Studies of the Cell Biology of CLN3 and Cell Motility Defects in the Cln3-/- Mouse.

Degree: PhD, 2011, University of Rochester

 Juvenile neuronal ceroid lipofuscinosis (JNCL) is a pediatric lysosomal storage disorder that results from autosomal recessively inherited mutations in CLN3. Neurodegeneration and accumulation of autofluorescent… (more)

Subjects/Keywords: Batten Disease; Juvenile Neuronal Ceroid Lipofuscinosis; Myosin-IIB

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

APA (6th Edition):

Getty, A. L. (2011). Studies of the Cell Biology of CLN3 and Cell Motility Defects in the Cln3-/- Mouse. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/14610

Chicago Manual of Style (16th Edition):

Getty, Amanda L. “Studies of the Cell Biology of CLN3 and Cell Motility Defects in the Cln3-/- Mouse.” 2011. Doctoral Dissertation, University of Rochester. Accessed January 17, 2021. http://hdl.handle.net/1802/14610.

MLA Handbook (7th Edition):

Getty, Amanda L. “Studies of the Cell Biology of CLN3 and Cell Motility Defects in the Cln3-/- Mouse.” 2011. Web. 17 Jan 2021.

Vancouver:

Getty AL. Studies of the Cell Biology of CLN3 and Cell Motility Defects in the Cln3-/- Mouse. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1802/14610.

Council of Science Editors:

Getty AL. Studies of the Cell Biology of CLN3 and Cell Motility Defects in the Cln3-/- Mouse. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/14610


University of Adelaide

2. Lensink, Ingrid L. Characterisation of the Batten disease gene, CLN3 / Ingrid Lensink.

Degree: 2000, University of Adelaide

The gene for CLN3 had been cloned and sequenced. The project involved determining the major mutation in this gene, which is a 1.02 kb deletion in approxiamately 85 % of all disease chromosomes. Advisors/Committee Members: Dept. of Cytogenetics and Molecular Genetics (school).

Subjects/Keywords: Neuronal ceroid-lipofuscinosis Genetic aspects

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APA (6th Edition):

Lensink, I. L. (2000). Characterisation of the Batten disease gene, CLN3 / Ingrid Lensink. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/19738

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):

Lensink, Ingrid L. “Characterisation of the Batten disease gene, CLN3 / Ingrid Lensink.” 2000. Thesis, University of Adelaide. Accessed January 17, 2021. http://hdl.handle.net/2440/19738.

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

MLA Handbook (7th Edition):

Lensink, Ingrid L. “Characterisation of the Batten disease gene, CLN3 / Ingrid Lensink.” 2000. Web. 17 Jan 2021.

Vancouver:

Lensink IL. Characterisation of the Batten disease gene, CLN3 / Ingrid Lensink. [Internet] [Thesis]. University of Adelaide; 2000. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/2440/19738.

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

Council of Science Editors:

Lensink IL. Characterisation of the Batten disease gene, CLN3 / Ingrid Lensink. [Thesis]. University of Adelaide; 2000. Available from: http://hdl.handle.net/2440/19738

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


University of Melbourne

3. von Eisenhart-Rothe, Philipp Johannes. Impact of lipofuscin accumulation on retinal degeneration in the mouse model of the Neuronal Ceroid Lipofuscinosis variant CLN6.

Degree: 2018, University of Melbourne

 Failure of the autophagy-lysosomal pathway and accumulation of lipofuscin in the retinal pigment epithelium (RPE) has been suggested to induce photoreceptor dysfunction and death in… (more)

Subjects/Keywords: lipofuscin; vision; autophagy; photoreceptor; retinal degeneration; neuronal ceroid lipofuscinosis; bio-metal

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APA (6th Edition):

von Eisenhart-Rothe, P. J. (2018). Impact of lipofuscin accumulation on retinal degeneration in the mouse model of the Neuronal Ceroid Lipofuscinosis variant CLN6. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/213191

Chicago Manual of Style (16th Edition):

von Eisenhart-Rothe, Philipp Johannes. “Impact of lipofuscin accumulation on retinal degeneration in the mouse model of the Neuronal Ceroid Lipofuscinosis variant CLN6.” 2018. Doctoral Dissertation, University of Melbourne. Accessed January 17, 2021. http://hdl.handle.net/11343/213191.

MLA Handbook (7th Edition):

von Eisenhart-Rothe, Philipp Johannes. “Impact of lipofuscin accumulation on retinal degeneration in the mouse model of the Neuronal Ceroid Lipofuscinosis variant CLN6.” 2018. Web. 17 Jan 2021.

Vancouver:

von Eisenhart-Rothe PJ. Impact of lipofuscin accumulation on retinal degeneration in the mouse model of the Neuronal Ceroid Lipofuscinosis variant CLN6. [Internet] [Doctoral dissertation]. University of Melbourne; 2018. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/11343/213191.

Council of Science Editors:

von Eisenhart-Rothe PJ. Impact of lipofuscin accumulation on retinal degeneration in the mouse model of the Neuronal Ceroid Lipofuscinosis variant CLN6. [Doctoral Dissertation]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/213191


University of Arizona

4. Imler, Elliot. A Drosophila Model of Autosomal Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis (ANCL/CLN4) Links Toxicity to CSP Activity .

Degree: 2016, University of Arizona

 Autosomal dominant adult onset neuronal ceroid lipofuscinoses (ANCL/CLN4) is a rare neurodegenerative disorder caused by mutations in the human gene DNAJC5 which encodes cysteine string… (more)

Subjects/Keywords: Drosophila; Neuronal Ceroid Lipofuscinosis; Neuroscience; Cysteine String Protein

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APA (6th Edition):

Imler, E. (2016). A Drosophila Model of Autosomal Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis (ANCL/CLN4) Links Toxicity to CSP Activity . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/621895

Chicago Manual of Style (16th Edition):

Imler, Elliot. “A Drosophila Model of Autosomal Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis (ANCL/CLN4) Links Toxicity to CSP Activity .” 2016. Doctoral Dissertation, University of Arizona. Accessed January 17, 2021. http://hdl.handle.net/10150/621895.

MLA Handbook (7th Edition):

Imler, Elliot. “A Drosophila Model of Autosomal Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis (ANCL/CLN4) Links Toxicity to CSP Activity .” 2016. Web. 17 Jan 2021.

Vancouver:

Imler E. A Drosophila Model of Autosomal Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis (ANCL/CLN4) Links Toxicity to CSP Activity . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10150/621895.

Council of Science Editors:

Imler E. A Drosophila Model of Autosomal Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis (ANCL/CLN4) Links Toxicity to CSP Activity . [Doctoral Dissertation]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/621895


Kansas State University

5. De Silva, Weerakonda Arachchige Bhagya Nilukshi. A study of neuronal ceroid lipofuscinosis proteins CLN5 and CLN8.

Degree: MS, Biochemistry and Molecular Biophysics Interdepartmental Program, 2015, Kansas State University

Neuronal ceroid lipofuscinoses (NCLs) are a group of neurodegenerative lysosomal storage disorders which is the most frequent group of inherited neurodegenerative disorders that affect children… (more)

Subjects/Keywords: Lysosomal storage disorder; Neuronal ceroid lipofuscinosis; CLN5; CLN8

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APA (6th Edition):

De Silva, W. A. B. N. (2015). A study of neuronal ceroid lipofuscinosis proteins CLN5 and CLN8. (Masters Thesis). Kansas State University. Retrieved from http://hdl.handle.net/2097/35749

Chicago Manual of Style (16th Edition):

De Silva, Weerakonda Arachchige Bhagya Nilukshi. “A study of neuronal ceroid lipofuscinosis proteins CLN5 and CLN8.” 2015. Masters Thesis, Kansas State University. Accessed January 17, 2021. http://hdl.handle.net/2097/35749.

MLA Handbook (7th Edition):

De Silva, Weerakonda Arachchige Bhagya Nilukshi. “A study of neuronal ceroid lipofuscinosis proteins CLN5 and CLN8.” 2015. Web. 17 Jan 2021.

Vancouver:

De Silva WABN. A study of neuronal ceroid lipofuscinosis proteins CLN5 and CLN8. [Internet] [Masters thesis]. Kansas State University; 2015. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/2097/35749.

Council of Science Editors:

De Silva WABN. A study of neuronal ceroid lipofuscinosis proteins CLN5 and CLN8. [Masters Thesis]. Kansas State University; 2015. Available from: http://hdl.handle.net/2097/35749


Massey University

6. Martinus, Ryan Dennis. Biochemical studies on animal models of ceroid-lipofuscinoses : a thesis presented in partial fulfilment of the requirements for the degree of Doctor in Philosophy in Veterinary Pathology, Massey University .

Degree: 1990, Massey University

 The ceroid-lipofuscinoses are recessively inherited lysosomal storage diseases of children and animals, characterised by brain and retinal atrophy and the accumulation of lipopigment in a… (more)

Subjects/Keywords: Neuronal ceroid-lipofuscinosis; Animal models

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APA (6th Edition):

Martinus, R. D. (1990). Biochemical studies on animal models of ceroid-lipofuscinoses : a thesis presented in partial fulfilment of the requirements for the degree of Doctor in Philosophy in Veterinary Pathology, Massey University . (Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/3295

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):

Martinus, Ryan Dennis. “Biochemical studies on animal models of ceroid-lipofuscinoses : a thesis presented in partial fulfilment of the requirements for the degree of Doctor in Philosophy in Veterinary Pathology, Massey University .” 1990. Thesis, Massey University. Accessed January 17, 2021. http://hdl.handle.net/10179/3295.

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

MLA Handbook (7th Edition):

Martinus, Ryan Dennis. “Biochemical studies on animal models of ceroid-lipofuscinoses : a thesis presented in partial fulfilment of the requirements for the degree of Doctor in Philosophy in Veterinary Pathology, Massey University .” 1990. Web. 17 Jan 2021.

Vancouver:

Martinus RD. Biochemical studies on animal models of ceroid-lipofuscinoses : a thesis presented in partial fulfilment of the requirements for the degree of Doctor in Philosophy in Veterinary Pathology, Massey University . [Internet] [Thesis]. Massey University; 1990. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10179/3295.

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

Council of Science Editors:

Martinus RD. Biochemical studies on animal models of ceroid-lipofuscinoses : a thesis presented in partial fulfilment of the requirements for the degree of Doctor in Philosophy in Veterinary Pathology, Massey University . [Thesis]. Massey University; 1990. Available from: http://hdl.handle.net/10179/3295

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


University of Sydney

7. Mohd Ismail, Izmira Farhana. Identification of a novel mutation in the CLN6 gene (CLN6) in South Hampshire sheep affected with Neuronal Ceroid Lipofuscinosis .

Degree: 2014, University of Sydney

Neuronal ceroid lipofuscinoses (NCL/Batten disease) are a group of fatal inherited neurodegenerative diseases that occur in many species including humans, sheep, dogs and cattle. Typical… (more)

Subjects/Keywords: Animal model; Neuronal ceroid lipofuscinosis; CLN6 gene; Sheep; Mutation; Neurodegenerative

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APA (6th Edition):

Mohd Ismail, I. F. (2014). Identification of a novel mutation in the CLN6 gene (CLN6) in South Hampshire sheep affected with Neuronal Ceroid Lipofuscinosis . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/14579

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):

Mohd Ismail, Izmira Farhana. “Identification of a novel mutation in the CLN6 gene (CLN6) in South Hampshire sheep affected with Neuronal Ceroid Lipofuscinosis .” 2014. Thesis, University of Sydney. Accessed January 17, 2021. http://hdl.handle.net/2123/14579.

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

MLA Handbook (7th Edition):

Mohd Ismail, Izmira Farhana. “Identification of a novel mutation in the CLN6 gene (CLN6) in South Hampshire sheep affected with Neuronal Ceroid Lipofuscinosis .” 2014. Web. 17 Jan 2021.

Vancouver:

Mohd Ismail IF. Identification of a novel mutation in the CLN6 gene (CLN6) in South Hampshire sheep affected with Neuronal Ceroid Lipofuscinosis . [Internet] [Thesis]. University of Sydney; 2014. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/2123/14579.

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

Council of Science Editors:

Mohd Ismail IF. Identification of a novel mutation in the CLN6 gene (CLN6) in South Hampshire sheep affected with Neuronal Ceroid Lipofuscinosis . [Thesis]. University of Sydney; 2014. Available from: http://hdl.handle.net/2123/14579

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


Massey University

8. Westlake, Valerie Jean. Ceroid-lipofuscinosis (Batten disease).

Degree: PhD, 1995, Massey University

 The ceroid-lipofuscinoses are a group of inherited neurodegenerative diseases occurring in human beings and animals. Histologically there is generalised accumulation of a fluorescent lipopigment within… (more)

Subjects/Keywords: Neuronal ceroid-lipofuscinosis; Neurodegenerative disorder; Ceroid-lipofuscinosis in sheep

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APA (6th Edition):

Westlake, V. J. (1995). Ceroid-lipofuscinosis (Batten disease). (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/2970

Chicago Manual of Style (16th Edition):

Westlake, Valerie Jean. “Ceroid-lipofuscinosis (Batten disease).” 1995. Doctoral Dissertation, Massey University. Accessed January 17, 2021. http://hdl.handle.net/10179/2970.

MLA Handbook (7th Edition):

Westlake, Valerie Jean. “Ceroid-lipofuscinosis (Batten disease).” 1995. Web. 17 Jan 2021.

Vancouver:

Westlake VJ. Ceroid-lipofuscinosis (Batten disease). [Internet] [Doctoral dissertation]. Massey University; 1995. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10179/2970.

Council of Science Editors:

Westlake VJ. Ceroid-lipofuscinosis (Batten disease). [Doctoral Dissertation]. Massey University; 1995. Available from: http://hdl.handle.net/10179/2970


Cornell University

9. Paushter, Daniel Harris. The roles of progranulin and TMEM106B in lysosomal physiology and neurodegenerative disease.

Degree: PhD, Comparative Biomedical Sciences, 2018, Cornell University

 Frontotemporal lobar degeneration (FTLD) is a devastating, clinically heterogeneous neurodegenerative disease that results in the progressive atrophy of the frontal and temporal lobes of the… (more)

Subjects/Keywords: Neuronal ceroid lipofuscinosis; Progranulin; TMEM106B; Lysosome; Cellular biology; Molecular biology; Frontotemporal lobar degeneration; Neurodegeneration

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APA (6th Edition):

Paushter, D. H. (2018). The roles of progranulin and TMEM106B in lysosomal physiology and neurodegenerative disease. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59371

Chicago Manual of Style (16th Edition):

Paushter, Daniel Harris. “The roles of progranulin and TMEM106B in lysosomal physiology and neurodegenerative disease.” 2018. Doctoral Dissertation, Cornell University. Accessed January 17, 2021. http://hdl.handle.net/1813/59371.

MLA Handbook (7th Edition):

Paushter, Daniel Harris. “The roles of progranulin and TMEM106B in lysosomal physiology and neurodegenerative disease.” 2018. Web. 17 Jan 2021.

Vancouver:

Paushter DH. The roles of progranulin and TMEM106B in lysosomal physiology and neurodegenerative disease. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1813/59371.

Council of Science Editors:

Paushter DH. The roles of progranulin and TMEM106B in lysosomal physiology and neurodegenerative disease. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59371


University of Missouri – Columbia

10. Tracy, Christopher J., 1988-. Ex vivo gene therapy for the preservation of retinal and central nervous system structure and function in a canine model of CLN2 neuronal ceroid lipofuscinosis.

Degree: 2016, University of Missouri – Columbia

 The neuronal ceroid lipofuscinoses (NCLs) are an inherited group of related lysosomal storage disorders. The NCLs are characterized in general by the accumulation of autofluorescent… (more)

Subjects/Keywords: Neuronal ceroid-lipofuscinosis  – Animal models; Gene therapy  – Research; Mesenchymal stem cells; Retinal degeneration

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APA (6th Edition):

Tracy, Christopher J., 1. (2016). Ex vivo gene therapy for the preservation of retinal and central nervous system structure and function in a canine model of CLN2 neuronal ceroid lipofuscinosis. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/56993

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):

Tracy, Christopher J., 1988-. “Ex vivo gene therapy for the preservation of retinal and central nervous system structure and function in a canine model of CLN2 neuronal ceroid lipofuscinosis.” 2016. Thesis, University of Missouri – Columbia. Accessed January 17, 2021. https://doi.org/10.32469/10355/56993.

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

MLA Handbook (7th Edition):

Tracy, Christopher J., 1988-. “Ex vivo gene therapy for the preservation of retinal and central nervous system structure and function in a canine model of CLN2 neuronal ceroid lipofuscinosis.” 2016. Web. 17 Jan 2021.

Vancouver:

Tracy, Christopher J. 1. Ex vivo gene therapy for the preservation of retinal and central nervous system structure and function in a canine model of CLN2 neuronal ceroid lipofuscinosis. [Internet] [Thesis]. University of Missouri – Columbia; 2016. [cited 2021 Jan 17]. Available from: https://doi.org/10.32469/10355/56993.

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

Council of Science Editors:

Tracy, Christopher J. 1. Ex vivo gene therapy for the preservation of retinal and central nervous system structure and function in a canine model of CLN2 neuronal ceroid lipofuscinosis. [Thesis]. University of Missouri – Columbia; 2016. Available from: https://doi.org/10.32469/10355/56993

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


Massey University

11. Graydon, Russell John. The retinal pathology of ovine ceroid-lipofuscinosis.

Degree: Master of Veterinary Science, 1984, Massey University

 Ovine ceriod-lipofuscinosis is an animal model of a rare genetic disease of man and some domestic animals. The disease is characterized by blindness idiocy and… (more)

Subjects/Keywords: Ovine ceriod-lipofuscinosis; Sheep diseases; Neuronal ceroid lipofuscinosis

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APA (6th Edition):

Graydon, R. J. (1984). The retinal pathology of ovine ceroid-lipofuscinosis. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/4845

Chicago Manual of Style (16th Edition):

Graydon, Russell John. “The retinal pathology of ovine ceroid-lipofuscinosis.” 1984. Masters Thesis, Massey University. Accessed January 17, 2021. http://hdl.handle.net/10179/4845.

MLA Handbook (7th Edition):

Graydon, Russell John. “The retinal pathology of ovine ceroid-lipofuscinosis.” 1984. Web. 17 Jan 2021.

Vancouver:

Graydon RJ. The retinal pathology of ovine ceroid-lipofuscinosis. [Internet] [Masters thesis]. Massey University; 1984. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10179/4845.

Council of Science Editors:

Graydon RJ. The retinal pathology of ovine ceroid-lipofuscinosis. [Masters Thesis]. Massey University; 1984. Available from: http://hdl.handle.net/10179/4845


Washington University in St. Louis

12. Shyng, Charles. Infantile Batten Disease: Effective Therapy and Novel Model.

Degree: PhD, Biology & Biomedical Sciences (Molecular Cell Biology), 2016, Washington University in St. Louis

  Infantile neuronal ceroid lipofuscinosis (INCL, Infantile Batten) is typically an early onset, neurodegenerative lysosomal storage disorder. INCL is caused by mutations to the gene… (more)

Subjects/Keywords: Gene Therapy; Infantile Batten Disease; Lysosomal Storage Disorder; Neuronal Ceroid Lipofuscinosis; Palmitoyl-protein thioesterase-1; Rare Disease

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APA (6th Edition):

Shyng, C. (2016). Infantile Batten Disease: Effective Therapy and Novel Model. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/896

Chicago Manual of Style (16th Edition):

Shyng, Charles. “Infantile Batten Disease: Effective Therapy and Novel Model.” 2016. Doctoral Dissertation, Washington University in St. Louis. Accessed January 17, 2021. https://openscholarship.wustl.edu/art_sci_etds/896.

MLA Handbook (7th Edition):

Shyng, Charles. “Infantile Batten Disease: Effective Therapy and Novel Model.” 2016. Web. 17 Jan 2021.

Vancouver:

Shyng C. Infantile Batten Disease: Effective Therapy and Novel Model. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2016. [cited 2021 Jan 17]. Available from: https://openscholarship.wustl.edu/art_sci_etds/896.

Council of Science Editors:

Shyng C. Infantile Batten Disease: Effective Therapy and Novel Model. [Doctoral Dissertation]. Washington University in St. Louis; 2016. Available from: https://openscholarship.wustl.edu/art_sci_etds/896


University of Missouri – Columbia

13. Awano, Tomoyuki. Three mutations that cause fifferent [i.e. different] forms of canine neuronal ceroid lipofuscinosis.

Degree: 2006, University of Missouri – Columbia

Neuronal ceroid-lipofuscinosis (NCL), also known as Battens disease, is really a group of inherited neurodegenerative diseases. A common feature of the ceroid lipofuscinoses is the… (more)

Subjects/Keywords: Dogs  – Diseases  – Genetic aspects; Neuronal ceroid-lipofuscinosis  – Genetic aspects

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APA (6th Edition):

Awano, T. (2006). Three mutations that cause fifferent [i.e. different] forms of canine neuronal ceroid lipofuscinosis. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/4592

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):

Awano, Tomoyuki. “Three mutations that cause fifferent [i.e. different] forms of canine neuronal ceroid lipofuscinosis.” 2006. Thesis, University of Missouri – Columbia. Accessed January 17, 2021. http://hdl.handle.net/10355/4592.

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

MLA Handbook (7th Edition):

Awano, Tomoyuki. “Three mutations that cause fifferent [i.e. different] forms of canine neuronal ceroid lipofuscinosis.” 2006. Web. 17 Jan 2021.

Vancouver:

Awano T. Three mutations that cause fifferent [i.e. different] forms of canine neuronal ceroid lipofuscinosis. [Internet] [Thesis]. University of Missouri – Columbia; 2006. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10355/4592.

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

Council of Science Editors:

Awano T. Three mutations that cause fifferent [i.e. different] forms of canine neuronal ceroid lipofuscinosis. [Thesis]. University of Missouri – Columbia; 2006. Available from: http://hdl.handle.net/10355/4592

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


Leiden University

14. Voer, de, G. The cln-3 genes of Caenorhabditis elegans: making C. elegans models for Juvenile Neuronal Ceroid Lipofuscinosis.

Degree: 2008, Leiden University

 The most common neurodegenerative genetic childhood disease, juvenile neuronal ceroid lipofuscinosis (JNCL), is a lysosomal storage disorder that is caused by mutations in the CLN3… (more)

Subjects/Keywords: Batten disease; Caenorhabditis elegans; CLN3; JNCL; Lysosome; Neuronal Ceroid Lipofuscinosis; Batten disease; Caenorhabditis elegans; CLN3; JNCL; Lysosome; Neuronal Ceroid Lipofuscinosis

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APA (6th Edition):

Voer, de, G. (2008). The cln-3 genes of Caenorhabditis elegans: making C. elegans models for Juvenile Neuronal Ceroid Lipofuscinosis. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/12840

Chicago Manual of Style (16th Edition):

Voer, de, G. “The cln-3 genes of Caenorhabditis elegans: making C. elegans models for Juvenile Neuronal Ceroid Lipofuscinosis.” 2008. Doctoral Dissertation, Leiden University. Accessed January 17, 2021. http://hdl.handle.net/1887/12840.

MLA Handbook (7th Edition):

Voer, de, G. “The cln-3 genes of Caenorhabditis elegans: making C. elegans models for Juvenile Neuronal Ceroid Lipofuscinosis.” 2008. Web. 17 Jan 2021.

Vancouver:

Voer, de G. The cln-3 genes of Caenorhabditis elegans: making C. elegans models for Juvenile Neuronal Ceroid Lipofuscinosis. [Internet] [Doctoral dissertation]. Leiden University; 2008. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1887/12840.

Council of Science Editors:

Voer, de G. The cln-3 genes of Caenorhabditis elegans: making C. elegans models for Juvenile Neuronal Ceroid Lipofuscinosis. [Doctoral Dissertation]. Leiden University; 2008. Available from: http://hdl.handle.net/1887/12840


University of Otago

15. Neverman, Nicole Jayne. Prenatal Synaptic Pathology and Correction in CLN6 Ovine Neuronal Ceroid Lipofuscinosis .

Degree: University of Otago

 The neuronal ceroid lipofuscinoses (NCL, Batten disease) are a group of severe autosomal recessive and incurable childhood lysosomal storage disorders (LSD). They have a combined… (more)

Subjects/Keywords: NCL; Ovine; Neuronal; Neuronal Ceroid Lipofuscinosis; Batten Disease; Cell Culture

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

APA (6th Edition):

Neverman, N. J. (n.d.). Prenatal Synaptic Pathology and Correction in CLN6 Ovine Neuronal Ceroid Lipofuscinosis . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/5721

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

Chicago Manual of Style (16th Edition):

Neverman, Nicole Jayne. “Prenatal Synaptic Pathology and Correction in CLN6 Ovine Neuronal Ceroid Lipofuscinosis .” Doctoral Dissertation, University of Otago. Accessed January 17, 2021. http://hdl.handle.net/10523/5721.

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

MLA Handbook (7th Edition):

Neverman, Nicole Jayne. “Prenatal Synaptic Pathology and Correction in CLN6 Ovine Neuronal Ceroid Lipofuscinosis .” Web. 17 Jan 2021.

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

Vancouver:

Neverman NJ. Prenatal Synaptic Pathology and Correction in CLN6 Ovine Neuronal Ceroid Lipofuscinosis . [Internet] [Doctoral dissertation]. University of Otago; [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10523/5721.

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

Council of Science Editors:

Neverman NJ. Prenatal Synaptic Pathology and Correction in CLN6 Ovine Neuronal Ceroid Lipofuscinosis . [Doctoral Dissertation]. University of Otago; Available from: http://hdl.handle.net/10523/5721

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


Lincoln University

16. Barry, Lucy A. Neuroinflammation and defining gene therapy approaches for ovine CLN6 Batten disease.

Degree: 2011, Lincoln University

 The neuronal ceroid lipofuscinoses (NCLs, Batten disease) are a group of fatal inherited childhood diseases which result in severe cortical atrophy, blindness, seizures, and the… (more)

Subjects/Keywords: chimeras; neurogenesis; inflammation; sheep; microglia; Batten disease; neuronal ceroid lipofuscinosis; neural stem cells; cytokines; neurodegeneration; gene therapy; lysosomal storage disorder; animal model

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APA (6th Edition):

Barry, L. A. (2011). Neuroinflammation and defining gene therapy approaches for ovine CLN6 Batten disease. (Thesis). Lincoln University. Retrieved from http://hdl.handle.net/10182/3940

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):

Barry, Lucy A. “Neuroinflammation and defining gene therapy approaches for ovine CLN6 Batten disease.” 2011. Thesis, Lincoln University. Accessed January 17, 2021. http://hdl.handle.net/10182/3940.

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

MLA Handbook (7th Edition):

Barry, Lucy A. “Neuroinflammation and defining gene therapy approaches for ovine CLN6 Batten disease.” 2011. Web. 17 Jan 2021.

Vancouver:

Barry LA. Neuroinflammation and defining gene therapy approaches for ovine CLN6 Batten disease. [Internet] [Thesis]. Lincoln University; 2011. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10182/3940.

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

Council of Science Editors:

Barry LA. Neuroinflammation and defining gene therapy approaches for ovine CLN6 Batten disease. [Thesis]. Lincoln University; 2011. Available from: http://hdl.handle.net/10182/3940

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


Lincoln University

17. Chen, Zhe (Jarol). A molecular dissection of neuroinflammation in ovine Batten disease.

Degree: 2016, Lincoln University

 Batten disease (Neuronal ceroid lipofuscinosis, NCL) is a group of devastating neurodegenerative diseases that affect children, caused by mutations in a number of genes, but… (more)

Subjects/Keywords: Batten disease; lysosomal storage disorder; neuronal ceroid lipofuscinosis; sheep; neuroinflammatory cascade; neurodegeneration; oxidative stress; Animal Model; 110904 Neurology and Neuromuscular Diseases; 060410 Neurogenetics

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APA (6th Edition):

Chen, Z. (. (2016). A molecular dissection of neuroinflammation in ovine Batten disease. (Thesis). Lincoln University. Retrieved from http://hdl.handle.net/10182/7191

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):

Chen, Zhe (Jarol). “A molecular dissection of neuroinflammation in ovine Batten disease.” 2016. Thesis, Lincoln University. Accessed January 17, 2021. http://hdl.handle.net/10182/7191.

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

MLA Handbook (7th Edition):

Chen, Zhe (Jarol). “A molecular dissection of neuroinflammation in ovine Batten disease.” 2016. Web. 17 Jan 2021.

Vancouver:

Chen Z(. A molecular dissection of neuroinflammation in ovine Batten disease. [Internet] [Thesis]. Lincoln University; 2016. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10182/7191.

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

Council of Science Editors:

Chen Z(. A molecular dissection of neuroinflammation in ovine Batten disease. [Thesis]. Lincoln University; 2016. Available from: http://hdl.handle.net/10182/7191

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


Lincoln University

18. Mitchell, Nadia. Longitudinal studies and the development of gene therapy for ovine neuronal ceroid lipofuscinoses.

Degree: 2016, Lincoln University

 The neuronal ceroid lipofuscinoses (NCLs, Batten disease) are a group of fatal inherited lysosomal storage diseases characterised by progressive neurodegeneration, cortical atrophy, and blindness. Currently… (more)

Subjects/Keywords: Batten disease; neuronal ceroid lipofuscinosis; lysosomal storage disorder; animal models; sheep; brain; neurodegeneration; neuroinflammation; neurogenesis; gene therapy; vector; adeno-associated virus; lentivirus; transduction; 1109 Neurosciences; 070709 Veterinary Pathology

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APA (6th Edition):

Mitchell, N. (2016). Longitudinal studies and the development of gene therapy for ovine neuronal ceroid lipofuscinoses. (Thesis). Lincoln University. Retrieved from http://hdl.handle.net/10182/7237

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):

Mitchell, Nadia. “Longitudinal studies and the development of gene therapy for ovine neuronal ceroid lipofuscinoses.” 2016. Thesis, Lincoln University. Accessed January 17, 2021. http://hdl.handle.net/10182/7237.

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

MLA Handbook (7th Edition):

Mitchell, Nadia. “Longitudinal studies and the development of gene therapy for ovine neuronal ceroid lipofuscinoses.” 2016. Web. 17 Jan 2021.

Vancouver:

Mitchell N. Longitudinal studies and the development of gene therapy for ovine neuronal ceroid lipofuscinoses. [Internet] [Thesis]. Lincoln University; 2016. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10182/7237.

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

Council of Science Editors:

Mitchell N. Longitudinal studies and the development of gene therapy for ovine neuronal ceroid lipofuscinoses. [Thesis]. Lincoln University; 2016. Available from: http://hdl.handle.net/10182/7237

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


Lincoln University

19. Xu, Janet Boyu. Cell biology and biochemical studies of ovine batten disease.

Degree: 2018, Lincoln University

 The neuronal ceroid lipofuscinoses (NCLs, Batten disease) are a group of fatal inherited neurodegenerative lysosomal storage diseases of humans, which result in severe cortical atrophy,… (more)

Subjects/Keywords: Batten disease; neuronal ceroid lipofuscinosis; lysosomal storage disease; animal models; sheep; brain; CLN5; CLN6; proteins; antibodies; 060108 Protein Trafficking; 070709 Veterinary Pathology; 110903 Central Nervous System

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APA (6th Edition):

Xu, J. B. (2018). Cell biology and biochemical studies of ovine batten disease. (Thesis). Lincoln University. Retrieved from http://hdl.handle.net/10182/10185

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):

Xu, Janet Boyu. “Cell biology and biochemical studies of ovine batten disease.” 2018. Thesis, Lincoln University. Accessed January 17, 2021. http://hdl.handle.net/10182/10185.

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

MLA Handbook (7th Edition):

Xu, Janet Boyu. “Cell biology and biochemical studies of ovine batten disease.” 2018. Web. 17 Jan 2021.

Vancouver:

Xu JB. Cell biology and biochemical studies of ovine batten disease. [Internet] [Thesis]. Lincoln University; 2018. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10182/10185.

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

Council of Science Editors:

Xu JB. Cell biology and biochemical studies of ovine batten disease. [Thesis]. Lincoln University; 2018. Available from: http://hdl.handle.net/10182/10185

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


University of Texas Southwestern Medical Center

20. Cho, Steve Kyungrae. Examination of Abnormal Dolichol Metabolism in Infantile Batten Disease Caused by Palmitoyl Protein Thioesterase-1 (PPT1) Deficiency.

Degree: 2004, University of Texas Southwestern Medical Center

 The neuronal ceroid lipofuscinosis (NCLs, also known collectively as Batten disease) are a group of lysosomal storage disorders characterized by the accumulation of autofluorescent storage… (more)

Subjects/Keywords: Lysosomal Storage Diseases; Dolichol; Neuronal Ceroid Lipofuscinosis, Infantile; Lipid Metabolism

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APA (6th Edition):

Cho, S. K. (2004). Examination of Abnormal Dolichol Metabolism in Infantile Batten Disease Caused by Palmitoyl Protein Thioesterase-1 (PPT1) Deficiency. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/363

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):

Cho, Steve Kyungrae. “Examination of Abnormal Dolichol Metabolism in Infantile Batten Disease Caused by Palmitoyl Protein Thioesterase-1 (PPT1) Deficiency.” 2004. Thesis, University of Texas Southwestern Medical Center. Accessed January 17, 2021. http://hdl.handle.net/2152.5/363.

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

MLA Handbook (7th Edition):

Cho, Steve Kyungrae. “Examination of Abnormal Dolichol Metabolism in Infantile Batten Disease Caused by Palmitoyl Protein Thioesterase-1 (PPT1) Deficiency.” 2004. Web. 17 Jan 2021.

Vancouver:

Cho SK. Examination of Abnormal Dolichol Metabolism in Infantile Batten Disease Caused by Palmitoyl Protein Thioesterase-1 (PPT1) Deficiency. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2004. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/2152.5/363.

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

Council of Science Editors:

Cho SK. Examination of Abnormal Dolichol Metabolism in Infantile Batten Disease Caused by Palmitoyl Protein Thioesterase-1 (PPT1) Deficiency. [Thesis]. University of Texas Southwestern Medical Center; 2004. Available from: http://hdl.handle.net/2152.5/363

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

21. Nijssen, Peter C.G. Autosomal dominant adult neuronal ceroid lipofuscinosis.

Degree: 2011, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

this thesis investigates a family with autosomal dominant neuronal ceroid lipofuscinosis, with chapters on clinical neurology, neuropathology, neurogenetics, neurophysiology, auditory and visual aspects.

Subjects/Keywords: Clinical neurology; Dementia. epilepsy; Electroencephalography; Lipofuscinosis; Movement disorders; Neurodegenerative diseases; Neurogenetics; Neuronal ceroid lipofuscinosis; Neuropathology; Parry disease; Clinical neurology; Dementia. epilepsy; Electroencephalography; Lipofuscinosis; Movement disorders; Neurodegenerative diseases; Neurogenetics; Neuronal ceroid lipofuscinosis; Neuropathology; Parry disease

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APA (6th Edition):

Nijssen, P. C. G. (2011). Autosomal dominant adult neuronal ceroid lipofuscinosis. (Doctoral Dissertation). Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/16344

Chicago Manual of Style (16th Edition):

Nijssen, Peter C G. “Autosomal dominant adult neuronal ceroid lipofuscinosis.” 2011. Doctoral Dissertation, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed January 17, 2021. http://hdl.handle.net/1887/16344.

MLA Handbook (7th Edition):

Nijssen, Peter C G. “Autosomal dominant adult neuronal ceroid lipofuscinosis.” 2011. Web. 17 Jan 2021.

Vancouver:

Nijssen PCG. Autosomal dominant adult neuronal ceroid lipofuscinosis. [Internet] [Doctoral dissertation]. Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2011. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1887/16344.

Council of Science Editors:

Nijssen PCG. Autosomal dominant adult neuronal ceroid lipofuscinosis. [Doctoral Dissertation]. Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2011. Available from: http://hdl.handle.net/1887/16344


University of Missouri – Columbia

22. Sanders, Douglas N., 1973-. Autologous bone marrow-derived mesenchymal stem cell transplantation as a therapy for neuronal ceroid lipofuscinosis.

Degree: PhD, 2007, University of Missouri – Columbia

 The Neuronal Ceroid Lipofuscinoses (NCLs) are a group of rare genetic diseases characterized by neurodegeneration and accumulation of autofluorescent lysosomal storage bodies in numerous cell… (more)

Subjects/Keywords: Neuronal ceroid-lipofuscinosis  – Treatment; Stem cells  – Transplantation; Bone marrow cells; Autotransplantation; Diseases  – Animal models

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APA (6th Edition):

Sanders, Douglas N., 1. (2007). Autologous bone marrow-derived mesenchymal stem cell transplantation as a therapy for neuronal ceroid lipofuscinosis. (Doctoral Dissertation). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/4830

Chicago Manual of Style (16th Edition):

Sanders, Douglas N., 1973-. “Autologous bone marrow-derived mesenchymal stem cell transplantation as a therapy for neuronal ceroid lipofuscinosis.” 2007. Doctoral Dissertation, University of Missouri – Columbia. Accessed January 17, 2021. http://hdl.handle.net/10355/4830.

MLA Handbook (7th Edition):

Sanders, Douglas N., 1973-. “Autologous bone marrow-derived mesenchymal stem cell transplantation as a therapy for neuronal ceroid lipofuscinosis.” 2007. Web. 17 Jan 2021.

Vancouver:

Sanders, Douglas N. 1. Autologous bone marrow-derived mesenchymal stem cell transplantation as a therapy for neuronal ceroid lipofuscinosis. [Internet] [Doctoral dissertation]. University of Missouri – Columbia; 2007. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10355/4830.

Council of Science Editors:

Sanders, Douglas N. 1. Autologous bone marrow-derived mesenchymal stem cell transplantation as a therapy for neuronal ceroid lipofuscinosis. [Doctoral Dissertation]. University of Missouri – Columbia; 2007. Available from: http://hdl.handle.net/10355/4830

23. Moharir, Akshay. Role of N-glycosylation in trafficking and stability of human CLN5.

Degree: MS, Division of Biology, 2012, Kansas State University

Neuronal Ceroid Lipofuscinoses (NCLs) are a group of lysosomal storage diseases that are characterized by accumulating autofluorescent lipopigments in cells. NCLs are a form of… (more)

Subjects/Keywords: CLN5; Neuronal Ceroid Lipofuscinosis (NCL); N-glycosylation; Biology (0306); Cellular Biology (0379)

…LSDs (including Neuronal ceroid lipofuscinosis or NCL). Yeast cells that are… …R, Jackson M, Anderson G, Green E, Mole SE 2007 Adult neuronal ceroid lipofuscinosis… …thioesterase gene causing infantile neuronal ceroid lipofuscinosis. Nature 376:584-587 62. Jarvela I… …White R 1991 Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the… …enzyme and disturbed cellular routing in infantile neuronal ceroid lipofuscinosis. EMBO J 15… 

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APA (6th Edition):

Moharir, A. (2012). Role of N-glycosylation in trafficking and stability of human CLN5. (Masters Thesis). Kansas State University. Retrieved from http://hdl.handle.net/2097/14143

Chicago Manual of Style (16th Edition):

Moharir, Akshay. “Role of N-glycosylation in trafficking and stability of human CLN5.” 2012. Masters Thesis, Kansas State University. Accessed January 17, 2021. http://hdl.handle.net/2097/14143.

MLA Handbook (7th Edition):

Moharir, Akshay. “Role of N-glycosylation in trafficking and stability of human CLN5.” 2012. Web. 17 Jan 2021.

Vancouver:

Moharir A. Role of N-glycosylation in trafficking and stability of human CLN5. [Internet] [Masters thesis]. Kansas State University; 2012. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/2097/14143.

Council of Science Editors:

Moharir A. Role of N-glycosylation in trafficking and stability of human CLN5. [Masters Thesis]. Kansas State University; 2012. Available from: http://hdl.handle.net/2097/14143

24. Song, Wensi. Modulating the Lysosome-Autophagy System to Restore Homeostasis in in vitro Model Systems of Lysosomal Storage Disorders.

Degree: PhD, Engineering, 2014, Rice University

 The protein quality control system is a complex network that promotes the folding and trafficking of newly synthesized proteins and regulates the degradation of misfolded… (more)

Subjects/Keywords: lysosomes; lysosomal storage diseases; Gaucher's disease; glucocerebrosidase; autophagy; TFEB; ceroid lipopigment; cyclodextrin; neuronal ceroid lipofuscinosis; cerium oxide nanoparticle; ceria nanoparticle; nanoceria; polystyrene nanoparticle

…chaperone therapy HexA β-hexosaminidase A NCL neuronal ceroid lipofuscinosis LINCL late… …infantile neuronal ceroid lipofuscinosis TPP1 tripeptidyl peptidase UPS ubiquitin-proteasome… …LSDs. 1.2.3. Neuronal Ceroid Lipofuscinosis Neuronal ceroid lipofuscinoses (NCLs)… …neuronal ceroid lipofuscinosis (LINCL) is associated with deficiency of Tripeptidyl… …storage disorders (39), such as neuronal ceroid lipofuscinoses (40)… 

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APA (6th Edition):

Song, W. (2014). Modulating the Lysosome-Autophagy System to Restore Homeostasis in in vitro Model Systems of Lysosomal Storage Disorders. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/88163

Chicago Manual of Style (16th Edition):

Song, Wensi. “Modulating the Lysosome-Autophagy System to Restore Homeostasis in in vitro Model Systems of Lysosomal Storage Disorders.” 2014. Doctoral Dissertation, Rice University. Accessed January 17, 2021. http://hdl.handle.net/1911/88163.

MLA Handbook (7th Edition):

Song, Wensi. “Modulating the Lysosome-Autophagy System to Restore Homeostasis in in vitro Model Systems of Lysosomal Storage Disorders.” 2014. Web. 17 Jan 2021.

Vancouver:

Song W. Modulating the Lysosome-Autophagy System to Restore Homeostasis in in vitro Model Systems of Lysosomal Storage Disorders. [Internet] [Doctoral dissertation]. Rice University; 2014. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1911/88163.

Council of Science Editors:

Song W. Modulating the Lysosome-Autophagy System to Restore Homeostasis in in vitro Model Systems of Lysosomal Storage Disorders. [Doctoral Dissertation]. Rice University; 2014. Available from: http://hdl.handle.net/1911/88163


Université de Montréal

25. Jules, Felix. Fonction de la protéine Ceroid lipofuscinosis neuronal 5 (CLN5) dans le tri et le recyclage à l’endosome.

Degree: 2015, Université de Montréal

Subjects/Keywords: Cln5; Rab7; Retromer; Sortilin; Endosome; Lysosome; MPR; CLN3; Lipidation; prenylation; palmitoylation; Céroïde-lipofuscinose neuronale; Neuronal ceroid-lipofuscinosis; Recepteur de tri vers le lysosome; Lysosomal sorting receptor; Chemistry - Biochemistry / Chimie - Biochimie (UMI : 0487)

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APA (6th Edition):

Jules, F. (2015). Fonction de la protéine Ceroid lipofuscinosis neuronal 5 (CLN5) dans le tri et le recyclage à l’endosome. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/13029

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):

Jules, Felix. “Fonction de la protéine Ceroid lipofuscinosis neuronal 5 (CLN5) dans le tri et le recyclage à l’endosome.” 2015. Thesis, Université de Montréal. Accessed January 17, 2021. http://hdl.handle.net/1866/13029.

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

MLA Handbook (7th Edition):

Jules, Felix. “Fonction de la protéine Ceroid lipofuscinosis neuronal 5 (CLN5) dans le tri et le recyclage à l’endosome.” 2015. Web. 17 Jan 2021.

Vancouver:

Jules F. Fonction de la protéine Ceroid lipofuscinosis neuronal 5 (CLN5) dans le tri et le recyclage à l’endosome. [Internet] [Thesis]. Université de Montréal; 2015. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1866/13029.

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

Council of Science Editors:

Jules F. Fonction de la protéine Ceroid lipofuscinosis neuronal 5 (CLN5) dans le tri et le recyclage à l’endosome. [Thesis]. Université de Montréal; 2015. Available from: http://hdl.handle.net/1866/13029

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


University of Otago

26. Partridge, Madison. Voluntary oral dosing of cannabidiol for the treatment of Batten Disease .

Degree: University of Otago

 Batten disease, or NCL (neuronal ceroid lipofuscinosis), is a collection of 13 pathologically similar, genetically distinct, autosomal recessive, neurodegenerative lysosomal storage diseases. Primarily affecting children… (more)

Subjects/Keywords: neuronal ceroid lipofuscinosis; cannabidiol; cln6; nclf; cbd; Battens; neurodegenerative; Batten disease; voluntary oral dosing; nNOS; GFAP; CD68; DCX; jelly; 10 mg/kg CBD; 25 mg/kg CBD; CBD

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APA (6th Edition):

Partridge, M. (n.d.). Voluntary oral dosing of cannabidiol for the treatment of Batten Disease . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/7648

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

Chicago Manual of Style (16th Edition):

Partridge, Madison. “Voluntary oral dosing of cannabidiol for the treatment of Batten Disease .” Masters Thesis, University of Otago. Accessed January 17, 2021. http://hdl.handle.net/10523/7648.

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

MLA Handbook (7th Edition):

Partridge, Madison. “Voluntary oral dosing of cannabidiol for the treatment of Batten Disease .” Web. 17 Jan 2021.

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

Vancouver:

Partridge M. Voluntary oral dosing of cannabidiol for the treatment of Batten Disease . [Internet] [Masters thesis]. University of Otago; [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10523/7648.

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

Council of Science Editors:

Partridge M. Voluntary oral dosing of cannabidiol for the treatment of Batten Disease . [Masters Thesis]. University of Otago; Available from: http://hdl.handle.net/10523/7648

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

27. Pérez Poyato, María del Socorro. Espectro clínico-mutacional y estudios de correlación genotipo-fenotipo en la población española afectada de lipofuscinosis neuronal ceroidea.

Degree: 2012, Universitat de Barcelona

Neuronal ceroid lipofuscinosis (NCLs) is one of the most common groups of progressive neurodegenerative diseases in childhood. Eight disease genes causing NCL in childhood have… (more)

Subjects/Keywords: Malalties neurodegeneratives; Enfermedades neurodegenerativas; Lipofuscinosis neuronal ceroidea (LNCs); Lipofuscinosi neuronal ceroidea (LNCs); Espectro clínico-mutacional; Espectre clínic-mutacional; Correlación genotipo-fenotipo; Correlació genotip-fenotip; Algoritmo diagnóstico; Algoritme diagnòstic; Neuronal ceroid lipofuscinosis (NCLs); Progressive neurodegenerative diseases; Diagnostic algorithm; Correlation genotype-phenotype; Ciències de la Salut; 616.8

…Forma infantil de lipofuscinosis neuronal ceroidea: seguimiento y valoración clínica de una… …españoles .…77 3. Forma juvenil de lipofuscinosis neuronal ceroidea: descripción del curso… …lipofuscinosis neuronal ceroidea .107 5. Protocolo de estudio para las lipofuscinosis neuronal… …Localización de las proteínas en las lipofuscinosis neuronal ceroidea…....6 x Tabla 1… …lipofuscinosis neuronal ceroidea ….. ...12 x Tabla 2. Resumen de la nueva y antigua nomenclatura… 

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APA (6th Edition):

Pérez Poyato, M. d. S. (2012). Espectro clínico-mutacional y estudios de correlación genotipo-fenotipo en la población española afectada de lipofuscinosis neuronal ceroidea. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/84123

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):

Pérez Poyato, María del Socorro. “Espectro clínico-mutacional y estudios de correlación genotipo-fenotipo en la población española afectada de lipofuscinosis neuronal ceroidea.” 2012. Thesis, Universitat de Barcelona. Accessed January 17, 2021. http://hdl.handle.net/10803/84123.

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

MLA Handbook (7th Edition):

Pérez Poyato, María del Socorro. “Espectro clínico-mutacional y estudios de correlación genotipo-fenotipo en la población española afectada de lipofuscinosis neuronal ceroidea.” 2012. Web. 17 Jan 2021.

Vancouver:

Pérez Poyato MdS. Espectro clínico-mutacional y estudios de correlación genotipo-fenotipo en la población española afectada de lipofuscinosis neuronal ceroidea. [Internet] [Thesis]. Universitat de Barcelona; 2012. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/10803/84123.

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

Council of Science Editors:

Pérez Poyato MdS. Espectro clínico-mutacional y estudios de correlación genotipo-fenotipo en la población española afectada de lipofuscinosis neuronal ceroidea. [Thesis]. Universitat de Barcelona; 2012. Available from: http://hdl.handle.net/10803/84123

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

28. Cadieux-Dion, Maxime. Utilisation du séquençage à haut débit dans l’identification des gènes prédisposant à l’épilepsie et aux syndromes neurocutanés.

Degree: 2017, Université de Montréal

Subjects/Keywords: génétique; séquençage à haut débit; syndrome de Kufs; céroïde-lipofuscinose neuronal (NCL); syndrome de Giroux-Barbeau; ataxie spinocérébelleuse (SCA); érythrokératodermie variabilis (EKV); analyse de liaison; diagnostic génétique; étude de famille; épilepsie; epilepsy; genetic; family study; high throughput sequencing; Kufs disease; Giroux-Barbeau syndrome; neuronal ceroid lipofuscinosis (NCL); spinocerebellar ataxia (SCA); erythrokeratodermia variabilis (EKV); linkage analysis; genetic diagnosis; Biology - Genetics / Biologie - Génétique (UMI : 0369)

…iv Annexe 4 : Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs… …crise. En effet, les crises généralisées « prennent origine dans un réseau neuronal et… 

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

APA (6th Edition):

Cadieux-Dion, M. (2017). Utilisation du séquençage à haut débit dans l’identification des gènes prédisposant à l’épilepsie et aux syndromes neurocutanés. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/18378

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):

Cadieux-Dion, Maxime. “Utilisation du séquençage à haut débit dans l’identification des gènes prédisposant à l’épilepsie et aux syndromes neurocutanés.” 2017. Thesis, Université de Montréal. Accessed January 17, 2021. http://hdl.handle.net/1866/18378.

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

MLA Handbook (7th Edition):

Cadieux-Dion, Maxime. “Utilisation du séquençage à haut débit dans l’identification des gènes prédisposant à l’épilepsie et aux syndromes neurocutanés.” 2017. Web. 17 Jan 2021.

Vancouver:

Cadieux-Dion M. Utilisation du séquençage à haut débit dans l’identification des gènes prédisposant à l’épilepsie et aux syndromes neurocutanés. [Internet] [Thesis]. Université de Montréal; 2017. [cited 2021 Jan 17]. Available from: http://hdl.handle.net/1866/18378.

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

Council of Science Editors:

Cadieux-Dion M. Utilisation du séquençage à haut débit dans l’identification des gènes prédisposant à l’épilepsie et aux syndromes neurocutanés. [Thesis]. Université de Montréal; 2017. Available from: http://hdl.handle.net/1866/18378

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

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