Dosage Compensation and Gene Expression of the X Chromosome in Sheep

Autor: Jingyue (Ellie) Duan, Kaleigh Flock, Nathanial Jue, Mingyuan Zhang, Amanda Jones, Sahar Al Seesi, Ion Mandoiu, Sambhu Pillai, Maria Hoffman, Rachel O’Neill, Steven Zinn, Kristen Govoni, Sarah Reed, Hesheng Jiang, Zongliang (Carl) Jiang, Xiuchun (Cindy) Tian

Publikováno v: G3: Genes, Genomes, Genetics, Vol 9, Iss 1, Pp 305-314 (2019)

Ohno’s hypothesis predicts that the expression of the single X chromosome in males needs compensatory upregulation to balance its dosage with that of the diploid autosomes. Additionally, X chromosome inactivation ensures that quadruple expression o

Externí odkaz: https://doaj.org/article/864b5ffcf0614b31a7f65df7c0eed917

Introducing the READY study:DHH young people’s well-being and self-determination

Autor: Alys Young, Francisco Espinoza, Claire Dodds, Garry Squires, Katherine Rogers, Helen Chilton, Rachel O’Neill

Publikováno v: Young, A, Espinoza, F, Dodds, C, Rogers, K, Squires, G, Chilton, H & O'Neill, R 2023, ' Introducing the READY study : DHH young people’s well-being and self-determination ', Journal of Deaf Studies and Deaf Education, vol. 28, no. 3, pp. 267-279 . https://doi.org/10.1093/deafed/enad002
Young, A, Espinoza, F, Dodds, C, Squires, G, Rogers, K, Chilton, H & O'Neill, R 2023, ' Introducing the READY study: DHH young people’s well-being and self-determination. ', The Journal of Deaf Studies and Deaf Education . https://doi.org/10.1093/deafed/enad002

READY is a self-report prospective longitudinal study of deaf and hard of hearing (DHH) young people aged 16 to 19 years on entry. Its overarching aim is to explore the risk and protective factors for successful transition to adulthood. This article

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab04ba5b9bc2b9a555c2029cf5f09138
https://www.pure.ed.ac.uk/ws/files/332523154/YoungEtalJDSDE2023IntroducingTheREADYstudy_published.pdf

Access, Disability and Mature Student Opinion on Academic Mathematics Supports

Autor: Ciarán Mac an Bhaird, Peter Mulligan, James O'Malley, Rachel O'Neill

Publikováno v: MSOR Connections. 20:19-25

In this paper we report on the main themes which emerged from analysis of a survey of students registered with the Access, Disability and Mature Student offices at Maynooth University. The survey focussed on the students’ experiences of mathematics

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::52f101a810f66e34ddae34f9f4c1915d
https://doi.org/10.21100/msor.v20i3.1288

Reading online in deaf and hearing young people:Do differences exist?

Autor: Wolfgang Mann, Rachel O’Neill, Freya Watkins, Robin L. Thompson

Publikováno v: Mann, W, O'Neill, R, Watkins, F & Thompson, R 2023, ' Reading online in deaf and hearing young people : Do differences exist? ', Deafness & Education International . https://doi.org/10.1080/14643154.2023.2207860

This pilot study explored effects of hearing loss on deaf children’s reading comprehension in an online context. Eighteen deaf secondary students, ages 12–14 years (11 with British Sign Language as their dominant language, seven with English as t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a7002abf48224da8215ee81f4191543
https://www.pure.ed.ac.uk/ws/files/345619075/MannEtalDEI2023ReadingOnlineInDeaf.pdf

The complete sequence of a human Y chromosome

Autor: Arang Rhie, Sergey Nurk, Monika Cechova, Savannah J. Hoyt, Dylan J. Taylor, Nicolas Altemose, Paul W. Hook, Sergey Koren, Mikko Rautiainen, Ivan A. Alexandrov, Jamie Allen, Mobin Asri, Andrey V. Bzikadze, Nae-Chyun Chen, Chen-Shan Chin, Mark Diekhans, Paul Flicek, Giulio Formenti, Arkarachai Fungtammasan, Carlos Garcia Giron, Erik Garrison, Ariel Gershman, Jennifer Gerton, Patrick G.S. Grady, Andrea Guarracino, Leanne Haggerty, Reza Halabian, Nancy F. Hansen, Robert Harris, Gabrielle A. Hartley, William T. Harvey, Marina Haukness, Jakob Heinz, Thibaut Hourlier, Robert M. Hubley, Sarah E. Hunt, Stephen Hwang, Miten Jain, Rupesh K. Kesharwani, Alexandra P. Lewis, Heng Li, Glennis A. Logsdon, Julian K. Lucas, Wojciech Makalowski, Christopher Markovic, Fergal J. Martin, Ann M. Mc Cartney, Rajiv C. McCoy, Jennifer McDaniel, Brandy M. McNulty, Paul Medvedev, Alla Mikheenko, Katherine M. Munson, Terence D. Murphy, Hugh E. Olsen, Nathan D. Olson, Luis F. Paulin, David Porubsky, Tamara Potapova, Fedor Ryabov, Steven L. Salzberg, Michael E.G. Sauria, Fritz J. Sedlazeck, Kishwar Shafin, Valery A. Shepelev, Alaina Shumate, Jessica M. Storer, Likhitha Surapaneni, Angela M. Taravella Oill, Françoise Thibaud-Nissen, Winston Timp, Marta Tomaszkiewicz, Mitchell R. Vollger, Brian P. Walenz, Allison C. Watwood, Matthias H. Weissensteiner, Aaron M. Wenger, Melissa A. Wilson, Samantha Zarate, Yiming Zhu, Justin M. Zook, Evan E. Eichler, Rachel O’Neill, Michael C. Schatz, Karen H. Miga, Kateryna D. Makova, Adam M. Phillippy

The human Y chromosome has been notoriously difficult to sequence and assemble because of its complex repeat structure including long palindromes, tandem repeats, and segmental duplications. As a result, more than half of the Y chromosome is missing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d38b477c2daccca72d1302cd2225927d
https://doi.org/10.1101/2022.12.01.518724