Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1962 1
1968 1
1969 1
1970 2
1974 1
1975 5
1976 9
1977 5
1978 6
1979 7
1980 9
1981 11
1982 14
1983 20
1984 33
1985 35
1986 50
1987 51
1988 69
1989 58
1990 93
1991 126
1992 149
1993 157
1994 210
1995 243
1996 282
1997 362
1998 353
1999 413
2000 518
2001 580
2002 598
2003 681
2004 777
2005 819
2006 847
2007 952
2008 997
2009 1132
2010 1277
2011 1453
2012 1539
2013 1604
2014 1815
2015 1897
2016 2000
2017 2054
2018 2160
2019 2433
2020 3034
2021 3386
2022 3400
2023 3243
2024 1258

Text availability

Article attribute

Article type

Publication date

Search Results

38,213 results

Results by year

Filters applied: . Clear all
Page 1
Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications.
Chia R, Chiò A, Traynor BJ. Chia R, et al. Lancet Neurol. 2018 Jan;17(1):94-102. doi: 10.1016/S1474-4422(17)30401-5. Epub 2017 Nov 16. Lancet Neurol. 2018. PMID: 29154141 Free PMC article. Review.
Each of the seven novel genes code for proteins associated with one or more molecular pathways known to be involved in ALS. ...WHERE NEXT?: The identification of these seven novel genes has been important in unravelling the molecular mechanisms underly …
Each of the seven novel genes code for proteins associated with one or more molecular pathways known to be involved in ALS. .. …
The novel class of seven transmembrane segment inverted repeat carriers.
Chang YN, Geertsma ER. Chang YN, et al. Biol Chem. 2017 Feb 1;398(2):165-174. doi: 10.1515/hsz-2016-0254. Biol Chem. 2017. PMID: 27865089 Review.
While these families do not share any obvious sequence relationship, they are united by their unique and novel architecture. Each member of this structural class is organized into two structurally related halves of seven transmembrane segments each. ...
While these families do not share any obvious sequence relationship, they are united by their unique and novel architecture. Each mem …
Identification of seven novel HLA-C alleles.
Senoussi O, Dard C, Buhler S, Bardy B, Masson D. Senoussi O, et al. HLA. 2020 Jul;96(1):99-101. doi: 10.1111/tan.13890. Epub 2020 May 26. HLA. 2020. PMID: 32250040
Seven novel HLA-C alleles were detected using two next-generation sequencing technologies....
Seven novel HLA-C alleles were detected using two next-generation sequencing technologies....
Seven novel genetic variants in a North Indian cohort with classical homocystinuria.
Kaur R, Attri SV, Saini AG, Sankhyan N, Singh S, Faruq M, Ramprasad VL, Sharda S, Murugan S. Kaur R, et al. Sci Rep. 2020 Oct 14;10(1):17299. doi: 10.1038/s41598-020-73475-5. Sci Rep. 2020. PMID: 33057012 Free PMC article.
Sanger sequencing of the CBS gene confirmed 15 different pathogenic or likely pathogenic variants in 14 cases. Of these, seven variants were novel (three frameshift deletions, two nonsense, one missense, one splice site variant) and were predicted to be deleterious …
Sanger sequencing of the CBS gene confirmed 15 different pathogenic or likely pathogenic variants in 14 cases. Of these, seven varian …
Hepatic glycogen synthase (GYS2) deficiency: seven novel patients and seven novel variants.
Kamenets EA, Gusarova EA, Milovanova NV, Itkis YS, Strokova TV, Melikyan MA, Garyaeva IV, Rybkina IG, Nikitina NV, Zakharova EY. Kamenets EA, et al. JIMD Rep. 2020 Feb 25;53(1):39-44. doi: 10.1002/jmd2.12082. eCollection 2020 May. JIMD Rep. 2020. PMID: 32395408 Free PMC article.
Seven variants are novel.We present seven new GSD 0 patients with variable phenotypes. ...SYNOPSIS: Seven new patients with glycogen storage disease type 0 were found using next-generation sequencing and seven novel variants of GYS2 gene
Seven variants are novel.We present seven new GSD 0 patients with variable phenotypes. ...SYNOPSIS: Seven new pa
Seven novel mutations of ADAR in multi-ethnic pedigrees with dyschromatosis symmetrica hereditaria in China.
Wang P, Yu S, Liu J, Zhang D, Kang X. Wang P, et al. Mol Genet Genomic Med. 2019 Oct;7(10):e00905. doi: 10.1002/mgg3.905. Epub 2019 Aug 18. Mol Genet Genomic Med. 2019. PMID: 31423758 Free PMC article.
The ADEAMc domain may be a hot spot of ADAR mutations among patients with DSH. RESULTS: Seven novel mutations were identified in seven multi-ethnic pedigrees: c.497delA(p.Arg105fs), c.3352C>T(p.Gln1058*) and c.3722delT(p.Ser1181fs) were found in three Uygu …
The ADEAMc domain may be a hot spot of ADAR mutations among patients with DSH. RESULTS: Seven novel mutations were identified …
Novel Molecular Approaches in Heart Failure: Seven Trans-Membrane Receptors Signaling in the Heart and Circulating Blood Leukocytes.
Schiattarella GG, Magliulo F, Cattaneo F, Gargiulo G, Sannino A, Franzone A, Oliveti M, Perrino C, Trimarco B, Esposito G. Schiattarella GG, et al. Front Cardiovasc Med. 2015 Mar 16;2:13. doi: 10.3389/fcvm.2015.00013. eCollection 2015. Front Cardiovasc Med. 2015. PMID: 26664885 Free PMC article. Review.
A complex network of signaling pathways have been involved in the development and progression of cardiac dysfunction. In this review, we summarize the pivotal role of seven trans-membrane receptors (7TMRs), also called G-protein-coupled receptors (GPCRs), in HF. ...
A complex network of signaling pathways have been involved in the development and progression of cardiac dysfunction. In this review, we sum …
Seven myths of memory.
Clayton NS, Wilkins C. Clayton NS, et al. Behav Processes. 2018 Jul;152:3-9. doi: 10.1016/j.beproc.2017.12.018. Epub 2017 Dec 24. Behav Processes. 2018. PMID: 29278777 Review.
In this paper we highlight seven myths about memory, which centre around the fact that memories, as we experience them, are not only about the past, they are also prospective. ...We refer to 'The Moustachio Quartet', a series of novels, which highlight themes and id …
In this paper we highlight seven myths about memory, which centre around the fact that memories, as we experience them, are not only …
Fungi: outstanding source of novel chemical scaffolds.
Liu Z, Zhao JY, Sun SF, Li Y, Liu YB. Liu Z, et al. J Asian Nat Prod Res. 2020 Feb;22(2):99-120. doi: 10.1080/10286020.2018.1488833. Epub 2018 Jul 26. J Asian Nat Prod Res. 2020. PMID: 30047298 Review.
A large number of remarkable studies on the secondary metabolites of fungi have been conducted in recent years. This review gives an overview of one hundred and sixty-seven molecules with novel skeletons and their bioactivities that have been reported in seventy-nin …
A large number of remarkable studies on the secondary metabolites of fungi have been conducted in recent years. This review gives an overvie …
Seven Novel and Three Known Mutations in FOXL2 in 10 Chinese Families with Blepharophimosis Syndrome.
Lin B, Zeng B, Zhao J, Xu T, Wang Y, Hu B, Li F, Zhao Q, Liu R, Liu J, Chen JM, Huang D, Wang Y. Lin B, et al. Curr Mol Med. 2018;18(3):152-159. doi: 10.2174/1566524018666180907162619. Curr Mol Med. 2018. PMID: 30198434
Ten mutations were identified in ten of the twenty-six families. Among these, seven were novel mutations. These included the six truncating mutations, p.Glu69*, p.Gly256Glyfs*14, p.Ala14Serfs*135, p.Pro333Profs*200, p.Pro290Leufs*70, and p.Pro157Profs*91, and one mi …
Ten mutations were identified in ten of the twenty-six families. Among these, seven were novel mutations. These included the s …
38,213 results
You have reached the last available page of results. Please see the User Guide for more information.