Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Marie A. Johnson"'
Autor:
Oluwaseun Akinyele, Anushe Munir, Marie A. Johnson, Megan S. Perez, Yuan Gao, Jackson R. Foley, Ashley Nwafor, Yijen Wu, Tracy Murray-Stewart, Robert A. Casero, Hülya Bayir, Dwi U. Kemaladewi
Publikováno v:
Disease Models & Mechanisms, Vol 17, Iss 6 (2024)
Externí odkaz:
https://doaj.org/article/97fb027069a74c2b824600638dca6afa
Autor:
Erik A. Koppes, Bethany K. Redel, Marie A. Johnson, Kristen J. Skvorak, Lina Ghaloul-Gonzalez, Megan E. Yates, Dale W. Lewis, Susanne M. Gollin, Yijen L. Wu, Shawn E. Christ, Martine Yerle, Angela Leshinski, Lee D. Spate, Joshua A. Benne, Stephanie L. Murphy, Melissa S. Samuel, Eric M. Walters, Sarah A. Hansen, Kevin D. Wells, Uta Lichter-Konecki, Robert A. Wagner, Joseph T. Newsome, Steven F. Dobrowolski, Jerry Vockley, Randall S. Prather, Robert D. Nicholls
Publikováno v:
JCI Insight, Vol 5, Iss 20 (2020)
Phenylalanine hydroxylase–deficient (PAH-deficient) phenylketonuria (PKU) results in systemic hyperphenylalaninemia, leading to neurotoxicity with severe developmental disabilities. Dietary phenylalanine (Phe) restriction prevents the most deleteri
Externí odkaz:
https://doaj.org/article/25a4c7bc5404441d96bc2b097f4c68db
Autor:
Annie I. Arockiaraj, Marie A. Johnson, Anushe Munir, Prasanna Ekambaram, Peter C. Lucas, Linda M. McAllister-Lucas, Dwi U. Kemaladewi
Publikováno v:
bioRxiv
Merosin-deficient congenital muscular dystrophy (MDC1A) is an autosomal recessive disorder caused by mutations in theLAMA2gene, resulting in a defective form of the extracellular matrix protein laminin-α2 (LAMA2). Individuals diagnosed with MDC1A ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2241a8f65f106bd521de37ad12bae115
https://europepmc.org/articles/PMC10028808/
https://europepmc.org/articles/PMC10028808/
Publikováno v:
Irish Educational Studies. 41:41-49
Autor:
Oluwaseun Akinyele, Anushe Munir, Marie A. Johnson, Megan S. Perez, Yuan Gao, Jackson R. Foley, Yijen Wu, Tracy Murray-Stewart, Robert A. Casero, Hulya Bayir, Dwi U. Kemaladewi
Polyamines (putrescine, spermidine, and spermine) are essential molecules for normal cellular functions and are subject to strict metabolic regulation. Mutations in the gene encoding spermine synthase (SMS) lead to accumulation of spermidine in an X-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::220b21781725b8fb6141b99c12da29a3
https://doi.org/10.1101/2023.01.15.524155
https://doi.org/10.1101/2023.01.15.524155
Publikováno v:
European Journal of Physiotherapy. 24:119-128
Objective: Breast cancer survivors who are physically active have lower recurrence and all-cause mortality. Breast cancer survivors often struggle to initiate and maintain physically active lifestyles. Barriers include psychosocial, environmental, an
Autor:
Erik A. Koppes, Marie A. Johnson, James J. Moresco, Patrizia Luppi, Dale W. Lewis, Donna B. Stolz, Jolene K. Diedrich, John R. Yates, Ronald C. Wek, Simon C. Watkins, Susanne M. Gollin, Hyun Jung Park, Peter Drain, Robert D. Nicholls
Prader-Willi syndrome (PWS) is a multisystem disorder with neurobehavioral, metabolic, and hormonal phenotypes, caused by loss of expression of a paternally-expressed imprinted gene cluster. Prior evidence from a PWS mouse model identified abnormal p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12173a833835d312e7baabd24c65a6d6
https://doi.org/10.1101/2021.12.16.473032
https://doi.org/10.1101/2021.12.16.473032
Autor:
Robert Wagner, Kevin D. Wells, Steven F. Dobrowolski, Susanne M. Gollin, Robert D. Nicholls, Yijen L. Wu, Marie A. Johnson, Eric M. Walters, Erik A. Koppes, Sarah A. Hansen, M Yerle, Shawn E. Christ, Dale W. Lewis, Melissa Samuel, Joseph T. Newsome, Kristen J. Skvorak, Megan E. Yates, Lina Ghaloul-Gonzalez, Randall S. Prather, Uta Lichter-Konecki, Stephanie L. Murphy, Lee D. Spate, Joshua A. Benne, Jerry Vockley, Bethany K. Redel, Angela Leshinski
Publikováno v:
JCI Insight
JCI Insight, American Society for Clinical Investigation, 2020, 5 (20), ⟨10.1172/jci.insight.141523⟩
JCI Insight, Vol 5, Iss 20 (2020)
JCI Insight, American Society for Clinical Investigation, 2020, 5 (20), ⟨10.1172/jci.insight.141523⟩
JCI Insight, Vol 5, Iss 20 (2020)
Phenylalanine hydroxylase–deficient (PAH-deficient) phenylketonuria (PKU) results in systemic hyperphenylalaninemia, leading to neurotoxicity with severe developmental disabilities. Dietary phenylalanine (Phe) restriction prevents the most deleteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85254df3b5697eb1b6ace05dcedc976c
https://hal.inrae.fr/hal-03158896
https://hal.inrae.fr/hal-03158896
Publikováno v:
American Journal of Dance Therapy. 38:437-454
This is the first published timeline to chronicle historical facts regarding the American Dance Therapy Association (ADTA). The timeline begins in 1964 when early strategic discussions to start an association were held, including the formation of a s