Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Alison L. Lane"'
Autor:
Amanda R. Jensen, Alison L. Lane, Brianna A. Werner, Sallie E. McLees, Tessa S. Fletcher, Richard E. Frye
Publikováno v:
Molecular Diagnosis & Therapy. 26:483-495
Autism spectrum disorder is an increasingly prevalent neurodevelopmental disorder in the world today, with an estimated 2% of the population being affected in the USA. A major complicating factor in diagnosing, treating, and understanding autism spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa8803dd6d09eaaa4d61d13136eb54ef
https://doi.org/10.1007/s40291-022-00600-7
https://doi.org/10.1007/s40291-022-00600-7
Autor:
Ahmad K. Almekkawi, Marwa W. AlJardali, Hicham M. Daadaa, Alison L. Lane, Ashley R. Worner, Mohammad A. Karim, Adrienne C. Scheck, Richard E. Frye
Publikováno v:
Journal of personalized medicine. 12(10)
Neural tube defects (NTDs) are congenital abnormalities in the central nervous system. The exact etiology of NTDs is still not determined, but several genetic and epigenetic factors have been studied. Folate supplementation during gestation is recomm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e9e3fb373d72928d1ea0b22d0308c45
https://pubmed.ncbi.nlm.nih.gov/36294748
https://pubmed.ncbi.nlm.nih.gov/36294748
Autor:
Brianna A, Werner, Patrick J, McCarty, Alison L, Lane, Indrapal, Singh, Mohammad A, Karim, Shannon, Rose, Richard E, Frye
Publikováno v:
Am J Transl Res
Objectives: Bioenergetic measurements in peripheral blood mononuclear cells (PBMCs) using high-throughput respirometry is a promising minimally invasive approach to studying mitochondrial function in humans. However, optimal methods for collecting PB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d0c8740b7bd4ded278997531996331de
https://pubmed.ncbi.nlm.nih.gov/35422946
https://pubmed.ncbi.nlm.nih.gov/35422946
Autor:
James S. Wainscoat, Luke R Holmes, Alison L Lane, Lesley F Drynan, Jillian L. Barlow, Silvia Lorenzo-Abalde, Alan J. Warren, Richard Pannell, See Heng Wong, Helen E. Jolin, Jacqueline Boultwood, Andrew N. J. McKenzie, Duncan R. Hewett, Angela J Middleton
Publikováno v:
Nature medicine
The identification of the genes associated with chromosomal translocation breakpoints has fundamentally changed understanding of the molecular basis of hematological malignancies. By contrast, the study of chromosomal deletions has been hampered by t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2624f154f731dffcc515adf006ef7491
https://doi.org/10.1038/nm.2063
https://doi.org/10.1038/nm.2063