The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing
Primary ovarian insufficiency (POI) is a frequently occurring pathology, leading to infertility. Genetic anomalies have been described in POI and mutations in numerous genes have been definitively related to the pathogenesis of the disease. Some studies based on next generation sequencing (NGS) have...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2018
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/22605
- Acceso en línea:
- https://doi.org/10.1016/j.mce.2017.07.021
https://repository.urosario.edu.co/handle/10336/22605
- Palabra clave:
- Gene expression
Gene mutation
Human
Massively parallel sequencing
Meiosis
Next generation sequencing
Nonhuman
Ovary follicle development
Ovulation
Pathogenesis
Premature ovarian failure
Priority journal
Review
Sequence analysis
Sex determination
Female
Genetics
High throughput sequencing
Metabolism
Ovary follicle
Premature ovarian failure
Procedures
Sex determination process
Female
High-throughput nucleotide sequencing
Humans
Meiosis
Ovarian follicle
Ovulation
Primary ovarian insufficiency
Sex determination processes
Female infertility
Molecular aetiology
Next generation sequencing
Primary ovarian insufficiency
- Rights
- License
- Abierto (Texto Completo)
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f27097fd-56db-4d27-91ed-7ffc57f6a046-12020-05-25T23:57:06Z2020-05-25T23:57:06Z2018Primary ovarian insufficiency (POI) is a frequently occurring pathology, leading to infertility. Genetic anomalies have been described in POI and mutations in numerous genes have been definitively related to the pathogenesis of the disease. Some studies based on next generation sequencing (NGS) have been successfully undertaken as they have led to identify new mutations associated with POI aetiology. The purpose of this review is to present the most relevant molecules involved in diverse complex pathways, which may contribute towards POI. The main genes participating in bipotential gonad formation, sex determination, meiosis, folliculogenesis and ovulation are described to enable understanding how they may be considered putative candidates involved in POI. Considerations regarding NGS technical aspects such as design and data interpretation are mentioned. Successful NGS initiatives used for POI studying and future challenges are also discussed. © 2017 Elsevier B.V.application/pdfhttps://doi.org/10.1016/j.mce.2017.07.0213037207https://repository.urosario.edu.co/handle/10336/22605engElsevier Ireland Ltd180170Molecular and Cellular EndocrinologyVol. 460Molecular and Cellular Endocrinology, ISSN:3037207, Vol.460,(2018); pp. 170-180https://www.scopus.com/inward/record.uri?eid=2-s2.0-85025838278&doi=10.1016%2fj.mce.2017.07.021&partnerID=40&md5=279ced63f83ca6e682a36982b5fda24cAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURGene expressionGene mutationHumanMassively parallel sequencingMeiosisNext generation sequencingNonhumanOvary follicle developmentOvulationPathogenesisPremature ovarian failurePriority journalReviewSequence analysisSex determinationFemaleGeneticsHigh throughput sequencingMetabolismOvary folliclePremature ovarian failureProceduresSex determination processFemaleHigh-throughput nucleotide sequencingHumansMeiosisOvarian follicleOvulationPrimary ovarian insufficiencySex determination processesFemale infertilityMolecular aetiologyNext generation sequencingPrimary ovarian insufficiencyThe molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencingarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Laissue P.ORIGINAL1-s2-0-S0303720717303945-main.pdfapplication/pdf387692https://repository.urosario.edu.co/bitstreams/972fea9b-d7de-437f-aa40-b218386d499c/download0e16da5a587ee305a7e202903256247aMD51TEXT1-s2-0-S0303720717303945-main.pdf.txt1-s2-0-S0303720717303945-main.pdf.txtExtracted texttext/plain91190https://repository.urosario.edu.co/bitstreams/d711bbd0-51d8-44ba-9c96-fd1ed79dfdc7/download780e17cedcee739a674b0b70e9d21bc4MD52THUMBNAIL1-s2-0-S0303720717303945-main.pdf.jpg1-s2-0-S0303720717303945-main.pdf.jpgGenerated Thumbnailimage/jpeg4414https://repository.urosario.edu.co/bitstreams/4b0feacc-70a6-412e-9ba6-515fe6e82eb9/download8b63d7050eef581a60ba9ad8986e5dc5MD5310336/22605oai:repository.urosario.edu.co:10336/226052022-05-02 07:37:20.558081https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing |
title |
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing |
spellingShingle |
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing Gene expression Gene mutation Human Massively parallel sequencing Meiosis Next generation sequencing Nonhuman Ovary follicle development Ovulation Pathogenesis Premature ovarian failure Priority journal Review Sequence analysis Sex determination Female Genetics High throughput sequencing Metabolism Ovary follicle Premature ovarian failure Procedures Sex determination process Female High-throughput nucleotide sequencing Humans Meiosis Ovarian follicle Ovulation Primary ovarian insufficiency Sex determination processes Female infertility Molecular aetiology Next generation sequencing Primary ovarian insufficiency |
title_short |
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing |
title_full |
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing |
title_fullStr |
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing |
title_full_unstemmed |
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing |
title_sort |
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing |
dc.subject.keyword.spa.fl_str_mv |
Gene expression Gene mutation Human Massively parallel sequencing Meiosis Next generation sequencing Nonhuman Ovary follicle development Ovulation Pathogenesis Premature ovarian failure Priority journal Review Sequence analysis Sex determination Female Genetics High throughput sequencing Metabolism Ovary follicle Premature ovarian failure Procedures Sex determination process Female High-throughput nucleotide sequencing Humans Meiosis Ovarian follicle Ovulation Primary ovarian insufficiency Sex determination processes Female infertility Molecular aetiology Next generation sequencing Primary ovarian insufficiency |
topic |
Gene expression Gene mutation Human Massively parallel sequencing Meiosis Next generation sequencing Nonhuman Ovary follicle development Ovulation Pathogenesis Premature ovarian failure Priority journal Review Sequence analysis Sex determination Female Genetics High throughput sequencing Metabolism Ovary follicle Premature ovarian failure Procedures Sex determination process Female High-throughput nucleotide sequencing Humans Meiosis Ovarian follicle Ovulation Primary ovarian insufficiency Sex determination processes Female infertility Molecular aetiology Next generation sequencing Primary ovarian insufficiency |
description |
Primary ovarian insufficiency (POI) is a frequently occurring pathology, leading to infertility. Genetic anomalies have been described in POI and mutations in numerous genes have been definitively related to the pathogenesis of the disease. Some studies based on next generation sequencing (NGS) have been successfully undertaken as they have led to identify new mutations associated with POI aetiology. The purpose of this review is to present the most relevant molecules involved in diverse complex pathways, which may contribute towards POI. The main genes participating in bipotential gonad formation, sex determination, meiosis, folliculogenesis and ovulation are described to enable understanding how they may be considered putative candidates involved in POI. Considerations regarding NGS technical aspects such as design and data interpretation are mentioned. Successful NGS initiatives used for POI studying and future challenges are also discussed. © 2017 Elsevier B.V. |
publishDate |
2018 |
dc.date.created.spa.fl_str_mv |
2018 |
dc.date.accessioned.none.fl_str_mv |
2020-05-25T23:57:06Z |
dc.date.available.none.fl_str_mv |
2020-05-25T23:57:06Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1016/j.mce.2017.07.021 |
dc.identifier.issn.none.fl_str_mv |
3037207 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/22605 |
url |
https://doi.org/10.1016/j.mce.2017.07.021 https://repository.urosario.edu.co/handle/10336/22605 |
identifier_str_mv |
3037207 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
180 |
dc.relation.citationStartPage.none.fl_str_mv |
170 |
dc.relation.citationTitle.none.fl_str_mv |
Molecular and Cellular Endocrinology |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 460 |
dc.relation.ispartof.spa.fl_str_mv |
Molecular and Cellular Endocrinology, ISSN:3037207, Vol.460,(2018); pp. 170-180 |
dc.relation.uri.spa.fl_str_mv |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85025838278&doi=10.1016%2fj.mce.2017.07.021&partnerID=40&md5=279ced63f83ca6e682a36982b5fda24c |
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http://purl.org/coar/access_right/c_abf2 |
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Abierto (Texto Completo) |
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Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
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application/pdf |
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Elsevier Ireland Ltd |
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Universidad del Rosario |
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