The CLN3 gene and protein: What we know. Issue 12 (30th September 2019)
- Record Type:
- Journal Article
- Title:
- The CLN3 gene and protein: What we know. Issue 12 (30th September 2019)
- Main Title:
- The CLN3 gene and protein: What we know
- Authors:
- Mirza, Myriam
Vainshtein, Anna
DiRonza, Alberto
Chandrachud, Uma
Haslett, Luke J.
Palmieri, Michela
Storch, Stephan
Groh, Janos
Dobzinski, Niv
Napolitano, Gennaro
Schmidtke, Carolin
Kerkovich, Danielle M. - Abstract:
- Abstract: Background: One of the most important steps taken by Beyond Batten Disease Foundation in our quest to cure juvenile Batten (CLN3) disease is to understand the State of the Science. We believe that a strong understanding of where we are in our experimental understanding of the CLN3 gene, its regulation, gene product, protein structure, tissue distribution, biomarker use, and pathological responses to its deficiency, lays the groundwork for determining therapeutic action plans. Objectives: To present an unbiased comprehensive reference tool of the experimental understanding of the CLN3 gene and gene product of the same name. Methods: BBDF compiled all of the available CLN3 gene and protein data from biological databases, repositories of federally and privately funded projects, patent and trademark offices, science and technology journals, industrial drug and pipeline reports as well as clinical trial reports and with painstaking precision, validated the information together with experts in Batten disease, lysosomal storage disease, lysosome/endosome biology. Results: The finished product is an indexed review of the CLN3 gene and protein which is not limited in page size or number of references, references all available primary experiments, and does not draw conclusions for the reader. Conclusions: Revisiting the experimental history of a target gene and its product ensures that inaccuracies and contradictions come to light, long‐held beliefs and assumptions continueAbstract: Background: One of the most important steps taken by Beyond Batten Disease Foundation in our quest to cure juvenile Batten (CLN3) disease is to understand the State of the Science. We believe that a strong understanding of where we are in our experimental understanding of the CLN3 gene, its regulation, gene product, protein structure, tissue distribution, biomarker use, and pathological responses to its deficiency, lays the groundwork for determining therapeutic action plans. Objectives: To present an unbiased comprehensive reference tool of the experimental understanding of the CLN3 gene and gene product of the same name. Methods: BBDF compiled all of the available CLN3 gene and protein data from biological databases, repositories of federally and privately funded projects, patent and trademark offices, science and technology journals, industrial drug and pipeline reports as well as clinical trial reports and with painstaking precision, validated the information together with experts in Batten disease, lysosomal storage disease, lysosome/endosome biology. Results: The finished product is an indexed review of the CLN3 gene and protein which is not limited in page size or number of references, references all available primary experiments, and does not draw conclusions for the reader. Conclusions: Revisiting the experimental history of a target gene and its product ensures that inaccuracies and contradictions come to light, long‐held beliefs and assumptions continue to be challenged, and information that was previously deemed inconsequential gets a second look. Compiling the information into one manuscript with all appropriate primary references provides quick clues to which studies have been completed under which conditions and what information has been reported. This compendium does not seek to replace original articles or subtopic reviews but provides an historical roadmap to completed works. Abstract : The CLN3 gene, its regulation, gene product, CLN3 protein structure, tissue distribution, biomarker use, and pathological responses to its deficiency. … (more)
- Is Part Of:
- Molecular genetics & genomic medicine. Volume 7:Issue 12(2019)
- Journal:
- Molecular genetics & genomic medicine
- Issue:
- Volume 7:Issue 12(2019)
- Issue Display:
- Volume 7, Issue 12 (2019)
- Year:
- 2019
- Volume:
- 7
- Issue:
- 12
- Issue Sort Value:
- 2019-0007-0012-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2019-09-30
- Subjects:
- Batten -- CLN3 -- JNCL -- juvenile Batten -- neuronal ceroid lipofuscinosis
Medical genetics -- Periodicals
Genomics -- Periodicals
616.042 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2324-9269 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mgg3.859 ↗
- Languages:
- English
- ISSNs:
- 2324-9269
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12465.xml