Výsledky vyhledávání - "Anju K, Philips"

Akademický článek

Music-listening regulates human microRNA expression

Autor: Preethy Sasidharan Nair, Pirre Raijas, Minna Ahvenainen, Anju K. Philips, Liisa Ukkola-Vuoti, Irma Järvelä

Publikováno v: Epigenetics, Vol 16, Iss 5, Pp 554-566 (2021)

Music-listening and performance have been shown to affect human gene expression. In order to further elucidate the biological basis of the effects of music on the human body, we studied the effects of music-listening on gene regulation by sequencing

Externí odkaz: https://doaj.org/article/6f64078925c7446485231d63622a7222

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Akademický článek

Music-performance regulates microRNAs in professional musicians

Autor: Preethy Sasidharan Nair, Tuire Kuusi, Minna Ahvenainen, Anju K. Philips, Irma Järvelä

Publikováno v: PeerJ, Vol 7, p e6660 (2019)

Musical training and performance require precise integration of multisensory and motor centres of the human brain and can be regarded as an epigenetic modifier of brain functions. Numerous studies have identified structural and functional differences

Externí odkaz: https://doaj.org/article/c2a886691063499fbbe078410abfde2e

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Akademický článek

The effect of listening to music on human transcriptome

Autor: Chakravarthi Kanduri, Pirre Raijas, Minna Ahvenainen, Anju K. Philips, Liisa Ukkola-Vuoti, Harri Lähdesmäki, Irma Järvelä

Publikováno v: PeerJ, Vol 3, p e830 (2015)

Although brain imaging studies have demonstrated that listening to music alters human brain structure and function, the molecular mechanisms mediating those effects remain unknown. With the advent of genomics and bioinformatics approaches, these effe

Externí odkaz: https://doaj.org/article/d593c626c7ef4aa1bca42d63d3f0a483

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Music-listening regulates human microRNA transcriptome

Autor: Minna Ahvenainen, Preethy Sasidharan Nair, Pirre Raijas, Anju K. Philips, Irma Järvelä, Liisa Ukkola-Vuoti

Here, we used microRNA sequencing to study the effect of 20 minutes of classical music-listening on the peripheral blood microRNA transcriptome in subjects characterized for musical aptitude and music education and compared it to a control study with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eee08d443ee64888389606973c436b8
https://doi.org/10.1101/599217

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Identification ofC12orf4as a gene for autosomal recessive intellectual disability

Autor: Heleen H. Arts, Teppo Varilo, Michele Pinelli, K.L.I. van Gassen, Christian Gilissen, Irma Järvelä, Ronald Roepman, Sergio Cocozza, Aki Mustonen, Giovanni Scala, S. Raza, Tuomo Määttä, Anju K. Philips, Ka Man Wu, Jukka S. Moilanen, C.I. de Bie

Publikováno v: Clinical Genetics. 91:100-105

Intellectual disability (ID) is a major health problem in our society. Genetic causes of ID remain unknown because of its vast heterogeneity. Here we report two Finnish families and one Dutch family with affected individuals presenting with mild to m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::17b550bfabac3540b7aa58981de60534
https://doi.org/10.1111/cge.12821

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Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population

Autor: Marc Abramowicz, Isabelle Pirson, Outi Kuismin, Hans van Bokhoven, Elisa Rahikkala, Arjan P.M. de Brouwer, Tuomo Määttä, Michaela K. Bode, Teppo Varilo, Kristiina Avela, Valérie Jacquemin, Anju K. Philips, Daniel L. Polla, Päivi Vieira, Jarmo Körkkö, Irma Järvelä, Mitja I. Kurki, Aarno Palotie, Thyrza Loman

Publikováno v: Eur J Hum Genet
European journal of human genetics

Intellectual disability (ID), megalencephaly, frontal predominant pachygyria, and seizures, previously called “thin” lissencephaly, are reported to be caused by recessive variants in CRADD. Among five families of different ethnicities identified,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::002d4f8dbeeaddc4e5a207eedcc465c0
https://pubmed.ncbi.nlm.nih.gov/31506600

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Music-performance regulates microRNAs in professional musicians

Autor: Irma Järvelä, Preethy Sasidharan Nair, Tuire Kuusi, Anju K. Philips, Minna Ahvenainen

Publikováno v: PeerJ
PeerJ, Vol 7, p e6660 (2019)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c667dbb7208de43378bad00d415d2be
https://pubmed.ncbi.nlm.nih.gov/30956902

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Identification of C12orf4 as a gene for autosomal recessive intellectual disability

Autor: Anju K Philips, Pinelli M, Ci, Bie, Mustonen A, Määttä T, Hh, Arts, Wu K, Roepman R, Js, Moilanen, Raza S, Varilo T, Scala G, Cocozza S, Gilissen C, Kl, Gassen, Järvelä I

Publikováno v: Clinical Genetics, 91, 1, pp. 100-105
Europe PubMed Central
Clinical Genetics, 91, 100-105
Clinical Genetics, 91(1), 100. Wiley-Blackwell

Contains fulltext : 169700.pdf (Publisher’s version ) (Closed access) Intellectual disability (ID) is a major health problem in our society. Genetic causes of ID remain unknown because of its vast heterogeneity. Here we report two Finnish families

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::018b7c0ed747049cc658a558594d7f84
https://hdl.handle.net/2066/169700

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