Zobrazeno 1 - 10
of 142
pro vyhledávání: '"Genetics and Heredity"'
Autor:
Selin ÖZKAN KOTİLOĞLU, Dilek KAYA AKYÜZLÜ, Gizem DÜZGÜN, Mustafa DANIŞMAN, Ece AĞTAŞ ERTAN, İnci ÖZGÜR İLHAN
Publikováno v:
Volume: 22, Issue: 6 1245-1255
Afyon Kocatepe Üniversitesi Fen Ve Mühendislik Bilimleri Dergisi
Afyon Kocatepe Üniversitesi Fen Ve Mühendislik Bilimleri Dergisi
Çağımızın ciddi sorunlardan biri olan alkol bağımlılığı, genetik, çevresel, kültürel, gelişimsel ve nörobiyolojik faktörlerin etkisiyle ortaya çıkmaktadır. Son yıllarda yeme davranışı nörobiyolojisi ile bağımlılık yapan m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa01f551ba16f8ceb85a79a3acac227d
https://doi.org/10.35414/akufemubid.1137753
https://doi.org/10.35414/akufemubid.1137753
Autor:
Sylvan C. Baca, Cassandra Singler, Soumya Zacharia, Ji-Heui Seo, Tunc Morova, Faraz Hach, Yi Ding, Tommer Schwarz, Chia-Chi Flora Huang, Jacob Anderson, André P. Fay, Cynthia Kalita, Stefan Groha, Mark M. Pomerantz, Victoria Wang, Simon Linder, Christopher J. Sweeney, Wilbert Zwart, Nathan A. Lack, Bogdan Pasaniuc, David Y. Takeda, Alexander Gusev, Matthew L. Freedman
Publikováno v:
Nature genetics, vol 54, iss 9
Nat Genet
Nature Genetics, 54(9), 1364-1375. Nature Publishing Group
Nature Genetics
Nat Genet
Nature Genetics, 54(9), 1364-1375. Nature Publishing Group
Nature Genetics
Many genetic variants affect disease risk by altering context-dependent gene regulation. Such variants are difficult to study mechanistically using current methods that link genetic variation to steady-state gene expression levels, such as expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f31adbbbe58ce2977ca25659cb2381f9
https://doi.org/10.1038/s41588-022-01168-y
https://doi.org/10.1038/s41588-022-01168-y
Autor:
KANABE, Belan, ÖZASLAN, Mehmet
Publikováno v:
Volume: 3, Issue: 3 20-26
Zeugma Biological Science
Zeugma Biological Science
Recurrent abortion is multifactorial involving clinical and biological risk factors. Evidence addressed the relationship of inherited thrombophilia with repeated pregnancy abortion and other serious pregnancy complications. However, the relation betw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f374a8ebac4ec45ba562f66a3d11bad
https://doi.org/10.55549/zbs.1167427
https://doi.org/10.55549/zbs.1167427
Autor:
Darko Nedovic
Publikováno v:
Journal of Epidemiology, Vol 26, Iss 8, Pp 399-404 (2016)
The STrengthening the REporting of Genetic Association studies (STREGA) statement was based on the STrengthening the REporting of OBservational studies in Epidemiology (STROBE) statement, and it was published in 2009 in order to improve the reporti
Externí odkaz:
https://doaj.org/article/abb1fa6b10344436b9eb5e0b0e64d818
Autor:
Ahmad Al Khleifat, Alfredo Iacoangeli, Joke J. F. A. van Vugt, Harry Bowles, Matthieu Moisse, Ramona A. J. Zwamborn, Rick A. A. van der Spek, Aleksey Shatunov, Johnathan Cooper-Knock, Simon Topp, Ross Byrne, Cinzia Gellera, Victoria López, Ashley R. Jones, Sarah Opie-Martin, Atay Vural, Yolanda Campos, Wouter van Rheenen, Brendan Kenna, Kristel R. Van Eijk, Kevin Kenna, Markus Weber, Bradley Smith, Isabella Fogh, Vincenzo Silani, Karen E. Morrison, Richard Dobson, Michael A. van Es, Russell L. McLaughlin, Patrick Vourc’h, Adriano Chio, Philippe Corcia, Mamede de Carvalho, Marc Gotkine, Monica P. Panades, Jesus S. Mora, Pamela J. Shaw, John E. Landers, Jonathan D. Glass, Christopher E. Shaw, Nazli Basak, Orla Hardiman, Wim Robberecht, Philip Van Damme, Leonard H. van den Berg, Jan H. Veldink, Ammar Al-Chalabi
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-8 (2022)
npj Genomic Medicine
Al Khleifat, A, Iacoangeli, A, van Vugt, J J F A, Bowles, H, Moisse, M, Zwamborn, R A J, van der Spek, R A A, Shatunov, A, Cooper-Knock, J, Topp, S, Byrne, R, Gellera, C, López, V, Jones, A R, Opie-Martin, S, Vural, A, Campos, Y, van Rheenen, W, Kenna, B, Van Eijk, K R, Kenna, K, Weber, M, Smith, B, Fogh, I, Silani, V, Morrison, K E, Dobson, R, van Es, M A, McLaughlin, R L, Vourc'h, P, Chio, A, Corcia, P, de Carvalho, M, Gotkine, M, Panades, M P, Mora, J S, Shaw, P J, Landers, J E, Glass, J D, Shaw, C E, Basak, N, Hardiman, O, Robberecht, W, Van Damme, P, van den Berg, L H, Veldink, J H & Al-Chalabi, A 2022, ' Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis ', NPJ Genomic Medicine, vol. 7, no. 1, 8 . https://doi.org/10.1038/s41525-021-00267-9
Dipòsit Digital de la UB
Universidad de Barcelona
NPJ Genomic Medicine
npj Genomic Medicine
Al Khleifat, A, Iacoangeli, A, van Vugt, J J F A, Bowles, H, Moisse, M, Zwamborn, R A J, van der Spek, R A A, Shatunov, A, Cooper-Knock, J, Topp, S, Byrne, R, Gellera, C, López, V, Jones, A R, Opie-Martin, S, Vural, A, Campos, Y, van Rheenen, W, Kenna, B, Van Eijk, K R, Kenna, K, Weber, M, Smith, B, Fogh, I, Silani, V, Morrison, K E, Dobson, R, van Es, M A, McLaughlin, R L, Vourc'h, P, Chio, A, Corcia, P, de Carvalho, M, Gotkine, M, Panades, M P, Mora, J S, Shaw, P J, Landers, J E, Glass, J D, Shaw, C E, Basak, N, Hardiman, O, Robberecht, W, Van Damme, P, van den Berg, L H, Veldink, J H & Al-Chalabi, A 2022, ' Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis ', NPJ Genomic Medicine, vol. 7, no. 1, 8 . https://doi.org/10.1038/s41525-021-00267-9
Dipòsit Digital de la UB
Universidad de Barcelona
NPJ Genomic Medicine
© The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ed582d2f280d0aca61a78bfda7e338e
https://doaj.org/article/2c1accb04c5e475dbe0325f3e155c28c
https://doaj.org/article/2c1accb04c5e475dbe0325f3e155c28c
Autor:
TARTIK, Musa
Publikováno v:
Trakya University Journal of Natural Sciences
Although genetic material is vertically transferred between generations via sexual or asexual reproduction, similarities in some chromosome and gene parts of unrelated organisms provide important clues for another way of transfer. The mobility of gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a836709a0f030f1da408e0f06b65f27c
https://doi.org/10.23902/trkjnat.1171052
https://doi.org/10.23902/trkjnat.1171052
Autor:
Franziska Paul, Calista Ng, Umar Bin Mohamad Sahari, Shahriar Nafissi, Yalda Nilipoor, Ali Reza Tavasoli, Carine Bonnard, Pui-Mun Wong, Nasrinsadat Nabavizadeh, Umut Altunoğlu, Mehrdad A Estiar, Charles B Majoie, Hane Lee, Stanley F Nelson, Ziv Gan-Or, Guy A Rouleau, Paul P Van Veldhoven, Rami Massie, Raoul C Hennekam, Ariana Kariminejad, Bruno Reversade
Publikováno v:
Human Molecular Genetics, 31(21), 3729-3740. Oxford University Press
Paul, F, Ng, C, Mohamad Sahari, U B, Nafissi, S, Nilipoor, Y, Tavasoli, A R, Bonnard, C, Wong, P-M, Nabavizadeh, N, Altunoğlu, U, Estiar, M A, Majoie, C B, Lee, H, Nelson, S F, Gan-Or, Z, Rouleau, G A, van Veldhoven, P P, Massie, R, Hennekam, R C, Kariminejad, A & Reversade, B 2022, ' RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, causing a distinct Mendelian disorder ', Human Molecular Genetics, vol. 31, no. 21, pp. 3729-3740 . https://doi.org/10.1093/hmg/ddac120
Human molecular genetics
Human molecular genetics, 31(21), 3729-3740. Oxford University Press
Paul, F, Ng, C, Mohamad Sahari, U B, Nafissi, S, Nilipoor, Y, Tavasoli, A R, Bonnard, C, Wong, P-M, Nabavizadeh, N, Altunoğlu, U, Estiar, M A, Majoie, C B, Lee, H, Nelson, S F, Gan-Or, Z, Rouleau, G A, van Veldhoven, P P, Massie, R, Hennekam, R C, Kariminejad, A & Reversade, B 2022, ' RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, causing a distinct Mendelian disorder ', Human Molecular Genetics, vol. 31, no. 21, pp. 3729-3740 . https://doi.org/10.1093/hmg/ddac120
Human molecular genetics
Human molecular genetics, 31(21), 3729-3740. Oxford University Press
Rabenosyn (RBSN) is a conserved endosomal protein necessary for regulating internalized cargo. Here, we present clinical, genetic, cellular and biochemical evidence that two distinct RBSN missense variants are responsible for a novel Mendelian disord
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2b1dd1a7a9fd8d470fb2eff3d0d9131
https://research.vumc.nl/en/publications/0515c80a-a981-4e73-b15c-fb3d70568012
https://research.vumc.nl/en/publications/0515c80a-a981-4e73-b15c-fb3d70568012
Autor:
F.O'rinova Z.Abduraxmanova
In this state, the development of pedagogical competence and the improvement of education and skills, personal and professional qualities of the pedagogue, and the creative approach to the pedagogue are discussed. Tvorcheskie kachestva uchitelya. Inn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa8d4b8e62f81c3aa371c58a52c8038e
Re‐emergence and diversification of a specialized antennal lobe morphology in ithomiine butterflies*
Publikováno v:
Evolution
Morris, B J, Couto, A, Aydin, A & Montgomery, S H 2021, ' Re-emergence and diversification of a specialised antennal lobe morphology in ithomiine butterflies ', Evolution, vol. 75, no. 12, pp. 3191-3202 . https://doi.org/10.1111/evo.14324
Morris, B J, Couto, A, Aydin, A & Montgomery, S H 2021, ' Re-emergence and diversification of a specialised antennal lobe morphology in ithomiine butterflies ', Evolution, vol. 75, no. 12, pp. 3191-3202 . https://doi.org/10.1111/evo.14324
How an organism's sensory system functions is central to how it navigates its environment. The insect olfactory system is a prominent model for investigating how ecological factors impact sensory reception and processing. Notably, work in Lepidoptera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5daa7425d9c4f7b9cbb32672a61dfed9
https://doi.org/10.1111/evo.14324
https://doi.org/10.1111/evo.14324