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

Year Number of Results
1962 2
1963 4
1964 4
1965 1
1976 1
1981 1
1983 2
1986 21
1987 68
1988 92
1989 123
1990 135
1991 219
1992 262
1993 324
1994 328
1995 348
1996 344
1997 310
1998 343
1999 339
2000 334
2001 321
2002 275
2003 286
2004 249
2005 233
2006 269
2007 242
2008 245
2009 221
2010 206
2011 241
2012 231
2013 184
2014 188
2015 179
2016 154
2017 110
2018 103
2019 38
2020 2
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7,204 results
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Page 1
Naxos disease: from the origin to today
Li GL, et al. Orphanet J Rare Dis 2018 - Review. PMID 29747658 Free PMC article.
The identification of the responsible first gene on chromosome 17, and its product plakoglobin as the responsible protein for Naxos disease proved to be a milestone in the study of ARVD, which opened a new field of research. ...
The identification of the responsible first gene on chromosome 17, and its product plakoglobin as the responsible protein for Naxos d …
Heterozygous deletion of chromosome 17p renders prostate cancer vulnerable to inhibition of RNA polymerase II.
Li Y, et al. Nat Commun 2018. PMID 30349055 Free PMC article.
Heterozygous deletion of chromosome 17p (17p) is one of the most frequent genomic events in human cancers. Beyond the tumor suppressor TP53, the POLR2A gene encoding the catalytic subunit of RNA polymerase II (RNAP2) is also included in a ~20-megabase deletion region of 17p in 63% of metastatic castration-resistant prostate cancer (CRPC). ...
Heterozygous deletion of chromosome 17p (17p) is one of the most frequent genomic events in human cancers. Beyond the tumor suppresso …
Human artificial chromosomes containing chromosome 17 alphoid DNA maintain an active centromere in murine cells but are not stable.
Alazami AM, et al. Genomics 2004. PMID 15081114
Human artificial chromosomes (HACs) are autonomous molecules that can function and segregate as normal chromosomes in human cells. ...Artificial chromosomes containing mouse centromeric sequences may be required for better stability and maintenance in murine cells....
Human artificial chromosomes (HACs) are autonomous molecules that can function and segregate as normal chromosomes in human ce …
Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrum.
Natacci F, et al. Eur J Paediatr Neurol 2016. PMID 26565673
A comparison of clinical manifestations between deletion and duplication syndromes of the chromosome regione is provided....
A comparison of clinical manifestations between deletion and duplication syndromes of the chromosome regione is provided....
Structure and Protein Interaction-Based Gene Ontology Annotations Reveal Likely Functions of Uncharacterized Proteins on Human Chromosome 17.
Zhang C, et al. J Proteome Res 2018. PMID 30265558 Free PMC article.
As a case study, the pipeline was applied to all 66 PE1 proteins with unknown or insufficiently specific function (uPE1) on human chromosome 17 as of neXtProt 2017-07-01. Benchmark testing on a control set of 100 well-characterized proteins randomly selected from the same chromosome shows high Gene Ontology (GO) term prediction accuracies of 0.69, 0.57, and 0.67 for molecular function (MF), biological process (BP), and cellular component (CC), respectively. ...
As a case study, the pipeline was applied to all 66 PE1 proteins with unknown or insufficiently specific function (uPE1) on human chromos
Localization of the human erbB-2 gene on normal and rearranged chromosomes 17 to bands q12-21.32.
Popescu NC, et al. Genomics 1989. PMID 2565881
In situ hybridization of chromosomes derived from fibroblasts carrying a constitutional 15;17t(q22.3;q11.21) translocation showed that the erbB-2 gene was relocated on the rearranged chromosome 15. These results as well as grain localization on prophase chromosomes locate the erbB-2 gene at 17q12-q21.32. This localization may facilitate the search for human malignancies with chromosome changes involving the erbB-2 gene....
In situ hybridization of chromosomes derived from fibroblasts carrying a constitutional 15;17t(q22.3;q11.21) translocation showed tha …
Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion
Clissold RL, et al. Clin Epigenetics 2018. PMID 30021660 Free PMC article.
Disease-associated mutations fall into two categories: HNF1B intragenic mutations and a 1.3 Mb deletion at chromosome 17q12. ...
Disease-associated mutations fall into two categories: HNF1B intragenic mutations and a 1.3 Mb deletion at chromosome 17q12. ...
Novel agents in chronic lymphocytic leukemia
Lamanna N and O'Brien S. Hematology Am Soc Hematol Educ Program 2016 - Review. PMID 27913472 Free PMC article.
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