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pro vyhledávání: '"Kelly A. Jackson"'
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Autor:
Ronald W. Wolff, Chia-Li Wang
Publikováno v:
Advances in Applied Probability. 53:463-483
In open Kelly and Jackson networks, servers are assigned to individual stations, serving customers only where they are assigned. We investigate the performance of modified networks where servers cooperate. A server who would be idle at the assigned s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::307043f1500fae03101965f39cc8dee1
https://doi.org/10.1017/apr.2020.63
https://doi.org/10.1017/apr.2020.63
Autor:
BATAILLE, ROBERT R.
Publikováno v:
The Papers of the Bibliographical Society of America, 1985 Dec 01. 79(4), 523-527.
Externí odkaz:
https://www.jstor.org/stable/24303683
Autor:
Don R Kelly
Publikováno v:
Social Work. 67:197-198
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fd1360966a21449f62502e705269ead
https://doi.org/10.1093/sw/swac006
https://doi.org/10.1093/sw/swac006
Autor:
Isaac See, Kelly A. Jackson, Rebecca Byram, Nadege Charles Toney, Cheri Grigg, Shelley S. Magill
Publikováno v:
Emerging Infectious Diseases, Vol 30, Iss 6, Pp 1302-1302 (2024)
Externí odkaz:
https://doaj.org/article/95670d330a334cf997be40b28e69c29f
In this book, Jackson and Samuels draw from their own research and direct practice with multiracial individuals and families, and also a rich interdisciplinary science and theory base, to share their model of multiracial cultural attunement. Core to
Autor:
Yue Huang, Rajesh Sharma, Annette Feigenbaum, Chung Lee, Inderneel Sahai, Rossana Sanchez Russo, Juanita Neira, Susan Sklower Brooks, Kelly E. Jackson, Derek Wong, Stephen Cederbaum, Felicitas L. Lacbawan, Charles M. Rowland, Pranoot Tanpaiboon, Denise Salazar
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 27, Iss , Pp 100735- (2021)
Arginase deficiency is a rare inborn error of metabolism that interrupts the final step of the urea cycle. Untreated individuals often present with episodic hyperammonemia, developmental delay, cognitive impairment, and spasticity in early childhood.
Externí odkaz:
https://doaj.org/article/3bd6b55f70134d4d897f63c7b81b6687
Autor:
Julie L. Self, Amanda Conrad, Steven Stroika, Alikeh Jackson, Laura Whitlock, Kelly A. Jackson, Jennifer Beal, Allison Wellman, Marianne K. Fatica, Sally Bidol, Paula Pennell Huth, Meghan Hamel, Kristyn Franklin, Lorelee Tschetter, Christine Kopko, Penelope Kirsch, Matthew E. Wise, Colin Basler
Publikováno v:
Emerging Infectious Diseases, Vol 25, Iss 8, Pp 1461-1468 (2019)
We investigated an outbreak of listeriosis detected by whole-genome multilocus sequence typing and associated with packaged leafy green salads. Nineteen cases were identified in the United States during July 5, 2015–January 31, 2016; isolates from
Externí odkaz:
https://doaj.org/article/8a267381995b45a9b7f75e536ca530d8
Autor:
Brothers, Amy A. Lemke, Michelle L. Thompson, Emily C. Gimpel, Katelyn C. McNamara, Carla A. Rich, Candice R. Finnila, Meagan E. Cochran, James M. J. Lawlor, Kelly M. East, Kevin M. Bowling, Donald R. Latner, Susan M. Hiatt, Michelle D. Amaral, Whitley V. Kelley, Veronica Greve, David E. Gray, Stephanie A. Felker, Hannah Meddaugh, Ashley Cannon, Amanda Luedecke, Kelly E. Jackson, Laura G. Hendon, Hillary M. Janani, Marla Johnston, Lee Ann Merin, Sarah L. Deans, Carly Tuura, Trent Hughes, Heather Williams, Kelly Laborde, Matthew B. Neu, Jessica Patrick-Esteve, Anna C. E. Hurst, Brian M. Kirmse, Renate Savich, Steven B. Spedale, Sara J. Knight, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper, Kyle B.
Publikováno v:
Journal of Personalized Medicine; Volume 13; Issue 7; Pages: 1026
Background: It is critical to understand the wide-ranging clinical and non-clinical effects of genome sequencing (GS) for parents in the NICU context. We assessed parents’ experiences with GS as a first-line diagnostic tool for infants with suspect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::657740f79eb9a508fdaea4a4ed6566e0
Publikováno v:
International Journal of Neonatal Screening, Vol 7, Iss 3, p 48 (2021)
Homocystinuria, caused by cystathionine β-synthase deficiency, is a rare inherited disorder involving metabolism of methionine. Impaired synthesis of cystathionine leads to accumulation of homocysteine that affects several organ systems leading to a
Externí odkaz:
https://doaj.org/article/231d66fe2c064d35898141adc9445170