Access the latest scientific research and medical evidence related to Developmental Disabilities 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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163 Consensuses
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16075 Abstracts
Research
Cancer screening, prevention, and treatment in people with mental illness.
Weinstein Lara C, Stefancic Ana, Cunningham Amy T, Hurley Katelyn E, Cabassa Leopodo J ...
CA: a cancer journal for clinicians Vol 66(2)
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Date 31 Mar 2016
Research
Integrating behavioural health tracking in human genetics research.
Freimer Nelson B, Mohr David C
Nature reviews. Genetics Vol 20(3)
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Date 01 Mar 2019
Research
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.
Cell Vol 179(7)
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Date 12 Dec 2019
Research
Psychedelic Psychiatry's Brave New World.
Nutt David, Erritzoe David, Carhart-Harris Robin
Cell Vol 181(1)
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Date 02 Apr 2020
Research
TMCO1 Is an ER Ca(2+) Load-Activated Ca(2+) Channel.
Wang Qiao-Chu, Zheng Qiaoxia, Tan Haiyan, Zhang Bing, Li Xiaoling ...
Cell Vol 165(6)
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Date 02 Jun 2016
Research
β-Arrestin-Biased Allosteric Modulator of NTSR1 Selectively Attenuates Addictive Behaviors.
Slosky Lauren M, Bai Yushi, Toth Krisztian, Ray Caroline, Rochelle Lauren K ...
Cell Vol 181(6)
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Date 11 Jun 2020
Research
Modular Organization and Assembly of SWI/SNF Family Chromatin Remodeling Complexes.
Mashtalir Nazar, D'Avino Andrew R, Michel Brittany C, Luo Jie, Pan Joshua ...
Cell Vol 175(5)
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Date 15 Nov 2018
Research
A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures.
Gennarino Vincenzo A, Palmer Elizabeth E, McDonell Laura M, Wang Li, Adamski Carolyn J ...
Cell Vol 172(5)
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Date 22 Feb 2018
Research
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements.
Liu Pengfei, Erez Ayelet, Nagamani Sandesh C Sreenath, Dhar Shweta U, Kołodziejska Katarzyna E ...
Cell Vol 146(6)
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Date 16 Sep 2011
Research
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.
Tischfield Max A, Baris Hagit N, Wu Chen, Rudolph Guenther, Van Maldergem Lionel ...
Cell Vol 140(1)
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Date 08 Jan 2010
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