Mutations in the HFE gene can be associated with increased lung disease severity in cystic fibrosis.
Gene. 2019.
PMID: 30291871
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Table representation of search results timeline featuring number of search results per year.
| Year | Number of Results |
|---|---|
| 1956 | 1 |
| 1957 | 1 |
| 1959 | 2 |
| 1960 | 1 |
| 1965 | 1 |
| 1967 | 6 |
| 1968 | 3 |
| 1970 | 6 |
| 1971 | 7 |
| 1972 | 6 |
| 1973 | 7 |
| 1974 | 5 |
| 1975 | 10 |
| 1976 | 13 |
| 1977 | 14 |
| 1978 | 27 |
| 1979 | 17 |
| 1980 | 28 |
| 1981 | 35 |
| 1982 | 37 |
| 1983 | 38 |
| 1984 | 35 |
| 1985 | 48 |
| 1986 | 51 |
| 1987 | 55 |
| 1988 | 67 |
| 1989 | 77 |
| 1990 | 90 |
| 1991 | 97 |
| 1992 | 95 |
| 1993 | 135 |
| 1994 | 109 |
| 1995 | 139 |
| 1996 | 116 |
| 1997 | 117 |
| 1998 | 153 |
| 1999 | 143 |
| 2000 | 165 |
| 2001 | 172 |
| 2002 | 209 |
| 2003 | 159 |
| 2004 | 219 |
| 2005 | 269 |
| 2006 | 253 |
| 2007 | 271 |
| 2008 | 251 |
| 2009 | 255 |
| 2010 | 286 |
| 2011 | 334 |
| 2012 | 352 |
| 2013 | 351 |
| 2014 | 359 |
| 2015 | 346 |
| 2016 | 336 |
| 2017 | 337 |
| 2018 | 342 |
| 2019 | 346 |
| 2020 | 378 |
| 2021 | 379 |
| 2022 | 271 |
| 2023 | 297 |
| 2024 | 129 |
Search Results
8,096 results
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Citations
37
articles
found by citation matching
Next generation sequencing as a useful tool in the diagnostics of mosaicism in Alport syndrome.
Gene. 2013.
PMID: 23732293
Search results
Page 1
Intrachromosomal Recombination in Yeast.
Methods Mol Biol. 2021;2153:193-200. doi: 10.1007/978-1-0716-0644-5_14.
Methods Mol Biol. 2021.
PMID: 32840781
This chapter describes commonly used types of reporters where a gene is duplicated as direct repeats and both copies are mutated with different mutations, rendering the cell defective for the gene and auxotrophic for the gene product. Recombination between th …
This chapter describes commonly used types of reporters where a gene is duplicated as direct repeats and both copies are mutated with …
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders.
Genome Med. 2020 Mar 17;12(1):28. doi: 10.1186/s13073-020-00725-6.
Genome Med. 2020.
PMID: 32183904
Free PMC article.
We developed a gene family de novo enrichment framework that identified 43 exome-wide enriched gene families including 98 de novo variant carrying genes in NDD patients of which 28 represent novel candidate genes for NDD which are brain expressed and u …
We developed a gene family de novo enrichment framework that identified 43 exome-wide enriched gene families including 98 de n …
Tumour suppressor genes.
J Cell Sci Suppl. 1988;10:171-80. doi: 10.1242/jcs.1988.supplement_10.13.
J Cell Sci Suppl. 1988.
PMID: 3077935
Review.
Such tumour suppressor genes will probably turn out to be as, if not more, diversified as the oncogenes. Consideration of both kinds of genes may reveal common or interrelated functional properties....
Such tumour suppressor genes will probably turn out to be as, if not more, diversified as the oncogenes. Consideration of both kinds …
Evolutionary aspects of cancer resistance.
Semin Cancer Biol. 2014 Apr;25:10-4. doi: 10.1016/j.semcancer.2014.01.001. Epub 2014 Jan 15.
Semin Cancer Biol. 2014.
PMID: 24440448
Review.
The inhibitory capacity of the fibroblast differs depending on the site of origin, and is also different between normal and cancer derived stroma cells. Preliminary gene analysis points to major differences in gene expression in between inhibitory and non-inhibitory …
The inhibitory capacity of the fibroblast differs depending on the site of origin, and is also different between normal and cancer derived s …
Identifying modules of cooperating cancer drivers.
Mol Syst Biol. 2021 Mar;17(3):e9810. doi: 10.15252/msb.20209810.
Mol Syst Biol. 2021.
PMID: 33769711
Free PMC article.
How Do I Report Genes in a Paper?
Mov Disord Clin Pract. 2024 May;11(5):594-597. doi: 10.1002/mdc3.13984. Epub 2024 Mar 12.
Mov Disord Clin Pract. 2024.
PMID: 38469948
Free PMC article.
Review.
Genetic testing, including whole genome, whole exome, and other next-generation sequencing technologies, has evolved vastly in the past decade. With this, the number of identified genes and genetic variants is constantly increasing. Although a variety of databases and onli …
Genetic testing, including whole genome, whole exome, and other next-generation sequencing technologies, has evolved vastly in the past deca …
The tomato cis-prenyltransferase gene family.
Plant J. 2013 Feb;73(4):640-52. doi: 10.1111/tpj.12063. Epub 2012 Dec 31.
Plant J. 2013.
PMID: 23134568
Free article.
Six of the SlCPT genes encode proteins with N-terminal targeting sequences, which, when fused to GFP, mediated GFP transport to the plastids of Arabidopsis protoplasts. ...RNAi-mediated suppression of NDPS1 led to a large decrease in beta-phellandrene (which is produced fr …
Six of the SlCPT genes encode proteins with N-terminal targeting sequences, which, when fused to GFP, mediated GFP transport to the p …
Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting.
Clin Pharmacol Ther. 2016 Feb;99(2):172-85. doi: 10.1002/cpt.280. Epub 2015 Nov 20.
Clin Pharmacol Ther. 2016.
PMID: 26479518
Free PMC article.
Review.
In addition, PGx analysis may detect different sets of variants for each gene, which can affect interpretation of results. This practice has caused confusion and may thereby impede the adoption of clinical PGx testing. ...
In addition, PGx analysis may detect different sets of variants for each gene, which can affect interpretation of results. This pract …
Gene therapy for inherited disorders of haematopoietic cells.
Hematol J. 2004;5(2):103-11. doi: 10.1038/sj.thj.6200366.
Hematol J. 2004.
PMID: 15048059
Review.
Over the last decade, the majority of inborn errors of haematopoiesis has been elucidated on a molecular level. For some of these diseases, gene transfer into transplantable cells offers new therapeutic perspectives. ...Promises with respect to the potential impact of g …
Over the last decade, the majority of inborn errors of haematopoiesis has been elucidated on a molecular level. For some of these diseases, …
TransFind--predicting transcriptional regulators for gene sets.
Nucleic Acids Res. 2010 Jul;38(Web Server issue):W275-80. doi: 10.1093/nar/gkq438. Epub 2010 May 28.
Nucleic Acids Res. 2010.
PMID: 20511592
Free PMC article.
The analysis of putative transcription factor binding sites in promoter regions of coregulated genes allows to infer the transcription factors that underlie observed changes in gene expression. ...
The analysis of putative transcription factor binding sites in promoter regions of coregulated genes allows to infer the transcriptio …
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