Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Alissa M, Hulstrand"'
Publikováno v:
Vector borne and zoonotic diseases (Larchmont, N.Y.). 22(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9cabf6c360df85b75e7bb7cf16508b1c
https://pubmed.ncbi.nlm.nih.gov/36322883
https://pubmed.ncbi.nlm.nih.gov/36322883
Publikováno v:
Vector-Borne and Zoonotic Diseases. 22:582-583
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e584bea9d01b199e63bb10de14761a7f
https://doi.org/10.1089/vbz.2022.0055
https://doi.org/10.1089/vbz.2022.0055
Autor:
Adam S. Gunnelson, Sharon E. Anthony, Jonathan G. Martin, Leigh Ramon, Paula Spaeth Anich, Michaela Jurewicz, Erik R. Olson, Michaela R. Carlson, V. M. Sadagopa Ramanujam, Alissa M. Hulstrand, Allison M Kohler, Lindsay Sears
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Scientific Reports
Scientific Reports
Biofluorescence has been detected in several nocturnal-crepuscular organisms from invertebrates to birds and mammals. Biofluorescence in mammals has been detected across the phylogeny, including the monotreme duck-billed platypus (Ornithorhyncus anat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::461405cee75a4a4e722c3348b212f079
https://doaj.org/article/85b0a97d308a4154b79ffab1d76967af
https://doaj.org/article/85b0a97d308a4154b79ffab1d76967af
Autor:
Alissa M. Hulstrand, Jeffrey C. Murray, J. Robert Manak, Robert A. Cornell, Lisa A. Lansdon, Douglas W. Houston, Abby Long, Rachel B. Brouillette, M. Adela Mansilla, Aline Petrin, Benjamin W. Darbro, Jennifer Standley
Publikováno v:
Genetics. 208:283-296
Orofacial clefts are one of the most common birth defects, affecting 1–2 per 1000 births, and have a complex etiology. High-resolution array-based comparative genomic hybridization has increased the ability to detect copy number variants (CNVs) tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8713d29ba88b897f6f94c1fd7e6969f0
https://doi.org/10.1534/genetics.117.300535
https://doi.org/10.1534/genetics.117.300535
Autor:
Lisa A, Lansdon, Benjamin W, Darbro, Aline L, Petrin, Alissa M, Hulstrand, Jennifer M, Standley, Rachel B, Brouillette, Abby, Long, M Adela, Mansilla, Robert A, Cornell, Jeffrey C, Murray, Douglas W, Houston, J Robert, Manak
Publikováno v:
Genetics. 208(1)
Orofacial clefts are one of the most common birth defects, affecting 1–2 per 1000 births, and have a complex etiology. High-resolution array-based comparative genomic hybridization has increased the ability to detect copy number variants (CNVs) tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::97a35b6d3eb9240a41c8b47227279310
https://pubmed.ncbi.nlm.nih.gov/29162626
https://pubmed.ncbi.nlm.nih.gov/29162626
Publikováno v:
Developmental Biology. 382:385-399
Fibroblast growth factor (FGF) signaling is required for numerous aspects of neural development, including neural induction, CNS patterning and neurogenesis. The ability of FGFs to activate Ras/MAPK signaling is thought to be critical for these funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38192d9b45c0296f9b9c60fa7ccb6282
https://doi.org/10.1016/j.ydbio.2013.08.020
https://doi.org/10.1016/j.ydbio.2013.08.020
Publikováno v:
Molecular Biology and Evolution. 24:2827-2841
Spo11 is a meiotic protein of fundamental importance as it is a conserved meiosis-specific transesterase required for meiotic recombination initiation in fungi, animals, and plants. Spo11 is homologous to the archaebacterial topoisomerase VIA (Top6A)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f1f0fb351c065b6984549446a7e07fb
https://doi.org/10.1093/molbev/msm217
https://doi.org/10.1093/molbev/msm217
Autor:
J. Robert Manak, Abby Long, Douglas W. Houston, Christina A. Gurnett, Matthew Hakeman, Jason M. Dierdorff, Lakshmi Muthuswamy, Robert A. Cornell, Kit Sing Au, Hope Northrup, Alissa M. Hulstrand, Alexander G. Bassuk, Christina K. Yung, Rachel B. Brouillette, Tiffany L. Smith, Riley Boland
Neural tube defects (NTDs) are common birth defects of complex etiology. Family and population-based studies have confirmed a genetic component to NTDs. However, despite more than three decades of research, the genes involved in human NTDs remain lar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e103ee03f01b0a9cb82ffbe1ad30530
https://europepmc.org/articles/PMC3578410/
https://europepmc.org/articles/PMC3578410/
Publikováno v:
Methods in Molecular Biology ISBN: 9781617799914
The ability to inhibit the activity of maternally stored gene products in Xenopus has led to numerous insights into early developmental mechanisms. Oocytes can be cultured and manipulated in vitro and then implanted into the body cavity of a host fem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9191f6bddf7f276109624aca5de8a2a0
https://doi.org/10.1007/978-1-61779-992-1_10
https://doi.org/10.1007/978-1-61779-992-1_10
Publikováno v:
Developmental Biology. 356(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbc70f2a8d53d4a0d3b154578becba64