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Year Number of Results
1979 1
1983 1
1985 1
1986 2
1987 2
1988 2
1989 6
1990 8
1991 10
1992 7
1993 9
1994 12
1995 12
1996 18
1997 31
1998 25
1999 31
2000 44
2001 42
2002 69
2003 64
2004 120
2005 128
2006 154
2007 165
2008 203
2009 232
2010 260
2011 205
2012 289
2013 302
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2017 382
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2023 769
2024 840
2025 277

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7,954 results

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Page 1
Single-cell RNA-seq reveals dynamic, random monoallelic gene expression in mammalian cells.
Deng Q, Ramsköld D, Reinius B, Sandberg R. Deng Q, et al. Science. 2014 Jan 10;343(6167):193-6. doi: 10.1126/science.1245316. Science. 2014. PMID: 24408435
Our allelic expression analysis also demonstrates the de novo inactivation of the paternal X chromosome. We conclude that independent and stochastic allelic transcription generates abundant random monoallelic expression in the mammalian cell....
Our allelic expression analysis also demonstrates the de novo inactivation of the paternal X chromosome. We conclude that independent …
Channelopathies in fragile X syndrome.
Deng PY, Klyachko VA. Deng PY, et al. Nat Rev Neurosci. 2021 May;22(5):275-289. doi: 10.1038/s41583-021-00445-9. Epub 2021 Apr 7. Nat Rev Neurosci. 2021. PMID: 33828309 Free PMC article. Review.
Fragile X syndrome (FXS) is the most common inherited form of intellectual disability and the leading monogenic cause of autism. The condition stems from loss of fragile X mental retardation protein (FMRP), which regulates a wide range of ion channels via translatio …
Fragile X syndrome (FXS) is the most common inherited form of intellectual disability and the leading monogenic cause of autism. The …
X chromosome regulation: diverse patterns in development, tissues and disease.
Deng X, Berletch JB, Nguyen DK, Disteche CM. Deng X, et al. Nat Rev Genet. 2014 Jun;15(6):367-78. doi: 10.1038/nrg3687. Epub 2014 Apr 15. Nat Rev Genet. 2014. PMID: 24733023 Free PMC article. Review.
Genes on the mammalian X chromosome are present in one copy in males and two copies in females. The complex mechanisms that regulate the X chromosome lead to evolutionary and physiological variability in gene expression between species, the sexes, individuals, devel …
Genes on the mammalian X chromosome are present in one copy in males and two copies in females. The complex mechanisms that regulate …
Uremic Leontiasis Ossea.
Lakhani DA, Deng F. Lakhani DA, et al. Radiology. 2024 May;311(2):e233506. doi: 10.1148/radiol.233506. Radiology. 2024. PMID: 38805734 No abstract available.
Intracranial Dermoid Cyst.
Lakhani DA, Morris MO, Deng F. Lakhani DA, et al. Radiology. 2024 Apr;311(1):e232952. doi: 10.1148/radiol.232952. Radiology. 2024. PMID: 38687215 No abstract available.
Features and futures of X-ray free-electron lasers.
Huang N, Deng H, Liu B, Wang D, Zhao Z. Huang N, et al. Innovation (Camb). 2021 Mar 17;2(2):100097. doi: 10.1016/j.xinn.2021.100097. eCollection 2021 May 28. Innovation (Camb). 2021. PMID: 34557749 Free PMC article. Review.
Linear accelerator-based free-electron lasers (FELs) are the leading source of fully coherent X-rays with ultra-high peak powers and ultra-short pulse lengths. Current X-ray FEL facilities have proved their worth as useful tools for diverse scientific applications. …
Linear accelerator-based free-electron lasers (FELs) are the leading source of fully coherent X-rays with ultra-high peak powers and …
Transmission X-ray microscopy-based three-dimensional XANES imaging.
Gao R, Zhang L, Tao F, Wang J, Du G, Xiao T, Deng B. Gao R, et al. Analyst. 2024 Aug 19;149(17):4506-4513. doi: 10.1039/d4an00705k. Analyst. 2024. PMID: 39051769
Full-field transmission X-ray microscopy (TXM) in conjunction with X-ray absorption near edge structure (XANES) spectroscopy provides two-dimensional (2D) or three-dimensional (3D) morphological and chemical-specific information within samples at the tens of nanomet …
Full-field transmission X-ray microscopy (TXM) in conjunction with X-ray absorption near edge structure (XANES) spectroscopy p …
Genetics, molecular biology, and phenotypes of x-linked epilepsy.
Deng H, Zheng W, Song Z. Deng H, et al. Mol Neurobiol. 2014 Jun;49(3):1166-80. doi: 10.1007/s12035-013-8589-1. Epub 2013 Nov 22. Mol Neurobiol. 2014. PMID: 24258407 Review.
Comparing to the phenotype of epilepsy caused by mutation of single gene on an autosome, the phenotype of X-linked epilepsy is more complex. X-linked epilepsy usually manifests as part of a syndrome or epileptic encephalopathy, and the variability of clinical manife …
Comparing to the phenotype of epilepsy caused by mutation of single gene on an autosome, the phenotype of X-linked epilepsy is more c …
Gerbode Defect Type 2.
Deng J, Xie J. Deng J, et al. Radiology. 2023 Aug;308(2):e230478. doi: 10.1148/radiol.230478. Radiology. 2023. PMID: 37526544 No abstract available.
Commentary on: Zhuo Y, Wang X, Wu J, Zhang S, Deng H, Liu W, et al. Simultaneous quantitative determination of amphetamines, opiates, ketamine, cocaine and metabolites in human hair: application to forensic cases of drug abuse. J Forensic Sci doi: 10.1111/1556-4029.14179. Epub 2019 Sep 9.
Hu J, Zheng N, Liang M. Hu J, et al. J Forensic Sci. 2020 Mar;65(2):664. doi: 10.1111/1556-4029.14225. Epub 2019 Oct 25. J Forensic Sci. 2020. PMID: 31651991 No abstract available.
7,954 results