Access the latest scientific research and medical evidence related to Phenylketonuria, Maternal treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 19 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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40866 Abstracts
Research
Using tandem mass spectrometry for metabolic disease screening among newborns. A report of a work group.
MMWR. Recommendations and reports : Morbidity and mortality weekly rep... Vol 50(RR-3)
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Date 13 Apr 2001
Research
Stress-Induced Metabolic Disorder in Peripheral CD4+ T Cells Leads to Anxiety-like Behavior.
Fan Ke-Qi, Li Yi-Yuan, Wang Hao-Li, Mao Xin-Tao, Guo Jin-Xin ...
Cell Vol 179(4)
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Date 31 Oct 2019
Research
Lipid-Associated Macrophages Control Metabolic Homeostasis in a Trem2-Dependent Manner.
Jaitin Diego Adhemar, Adlung Lorenz, Thaiss Christoph A, Weiner Assaf, Li Baoguo ...
Cell Vol 178(3)
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Date 25 Jul 2019
Research
A Compendium of Genetic Modifiers of Mitochondrial Dysfunction Reveals Intra-organelle Buffering.
To Tsz-Leung, Cuadros Alejandro M, Shah Hardik, Hung Wendy H W, Li Yang ...
Cell Vol 179(5)
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Date 14 Nov 2019
Research
A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection.
Casanova Jean-Laurent, Su Helen C
Cell Vol 181(6)
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Date 11 Jun 2020
Research
Diet-Induced Circadian Enhancer Remodeling Synchronizes Opposing Hepatic Lipid Metabolic Processes.
Guan Dongyin, Xiong Ying, Borck Patricia C, Jang Cholsoon, Doulias Paschalis-Thomas ...
Cell Vol 174(4)
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Date 09 Aug 2018
Research
Glia-to-Neuron Conversion by CRISPR-CasRx Alleviates Symptoms of Neurological Disease in Mice.
Zhou Haibo, Su Jinlin, Hu Xinde, Zhou Changyang, Li He ...
Cell Vol 181(3)
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Date 30 Apr 2020
Research
Chemical Hybridization of Glucagon and Thyroid Hormone Optimizes Therapeutic Impact for Metabolic Disease.
Finan Brian, Clemmensen Christoffer, Zhu Zhimeng, Stemmer Kerstin, Gauthier Karine ...
Cell Vol 167(3)
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Date 20 Oct 2016
Research
Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.
Cross N C, Tolan D R, Cox T M
Cell Vol 53(6)
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Date 17 Jun 1988
Research
Expression of cDNA encoding the human "protective protein" associated with lysosomal beta-galactosidase and neuraminidase: homology to yeast proteases...
Galjart N J, Gillemans N, Harris A, van der Horst G T, Verheijen F W ...
Cell Vol 54(6)
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Date 09 Sep 1988
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