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Year Number of Results
1993 4
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2001 2264
2002 45
2003 22
2004 24
2005 19
2006 19
2007 28
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The following term was not found in PubMed: Dev.15
Page 1
Complete genome sequence of Salmonella enterica serovar Typhimurium LT2.
McClelland M, Sanderson KE, Spieth J, Clifton SW, Latreille P, Courtney L, Porwollik S, Ali J, Dante M, Du F, Hou S, Layman D, Leonard S, Nguyen C, Scott K, Holmes A, Grewal N, Mulvaney E, Ryan E, Sun H, Florea L, Miller W, Stoneking T, Nhan M, Waterston R, Wilson RK. McClelland M, et al. Nature. 2001 Oct 25;413(6858):852-6. doi: 10.1038/35101614. Nature. 2001. PMID: 11677609
Here we sequenced the 4,857-kilobase (kb) chromosome and 94-kb virulence plasmid of S. typhimurium strain LT2. The distribution of close homologues of S. typhimurium LT2 genes in eight related enterobacteria was determined using previously completed genomes of three relate …
Here we sequenced the 4,857-kilobase (kb) chromosome and 94-kb virulence plasmid of S. typhimurium strain LT2. The distribution of close hom …
Somatic activation of the K-ras oncogene causes early onset lung cancer in mice.
Johnson L, Mercer K, Greenbaum D, Bronson RT, Crowley D, Tuveson DA, Jacks T. Johnson L, et al. Nature. 2001 Apr 26;410(6832):1111-6. doi: 10.1038/35074129. Nature. 2001. PMID: 11323676
About 30% of human tumours carry ras gene mutations. Of the three genes in this family (composed of K-ras, N-ras and H-ras), K-ras is the most frequently mutated member in human tumours, including adenocarcinomas of the pancreas ( approximately 70-90% incidence), colon ( a …
About 30% of human tumours carry ras gene mutations. Of the three genes in this family (composed of K-ras, N-ras and H-ras), K-ras is …
Roberts-SC phocomelia syndrome.
Maheshwari A, Kumar P, Dutta S, Narang A. Maheshwari A, et al. Indian J Pediatr. 2001 Jun;68(6):557-9. doi: 10.1007/BF02723253. Indian J Pediatr. 2001. PMID: 11450388 Review.
The phenotypic features match those described in the Roberts-SC phocomelia syndrome. A literature review revealed that 50% of these patients have chromosomal defects and antenatal detection is possible on ultrasound and by chromosome analysis of the amniocytes....
The phenotypic features match those described in the Roberts-SC phocomelia syndrome. A literature review revealed that 50% of these p …
Skewed X inactivation in X-linked disorders.
Van den Veyver IB. Van den Veyver IB. Semin Reprod Med. 2001 Jun;19(2):183-91. doi: 10.1055/s-2001-15398. Semin Reprod Med. 2001. PMID: 11480916 Review.
X chromosome inactivation is a process by which the dosage of proteins transcribed from genes on the X chromosome is equalized between males (XY) and females (XX) through the silencing of most genes on one of the two X chromosomes in females. Although the choice of …
X chromosome inactivation is a process by which the dosage of proteins transcribed from genes on the X chromosome is equalized betwee …
Recent advances in hereditary spastic paraplegia.
Tallaksen CM, Dürr A, Brice A. Tallaksen CM, et al. Curr Opin Neurol. 2001 Aug;14(4):457-63. doi: 10.1097/00019052-200108000-00005. Curr Opin Neurol. 2001. PMID: 11470961 Review.
The genes that encode L1 and PLP were the first to be identified in HSP disorders. ...The discovery of new genes should hopefully help to clarify the pathophysiology of these disorders....
The genes that encode L1 and PLP were the first to be identified in HSP disorders. ...The discovery of new genes should hopefu …
The DFNA10 phenotype.
De Leenheer EM, Huygen PL, Wayne S, Smith RJ, Cremers CW. De Leenheer EM, et al. Ann Otol Rhinol Laryngol. 2001 Sep;110(9):861-6. doi: 10.1177/000348940111000910. Ann Otol Rhinol Laryngol. 2001. PMID: 11558763
Cross-sectional analysis of air conduction threshold-on-age data from all available last-visit audiograms (linear regression analysis, age over 15 years) showed progression of hearing loss at a rate of 0.6 dB/y over all frequencies, with a flat to gently sloping age-corrected thr …
Cross-sectional analysis of air conduction threshold-on-age data from all available last-visit audiograms (linear regression analysis, age o …
Genomic organization of the mammalian MHC.
Kumánovics A, Takada T, Lindahl KF. Kumánovics A, et al. Annu Rev Immunol. 2003;21:629-57. doi: 10.1146/annurev.immunol.21.090501.080116. Epub 2001 Dec 19. Annu Rev Immunol. 2003. PMID: 12500978 Review.
The Human Genome Project transformed the quest of more than 50 years to understand the major histocompatibility complex (Mhc). ...The Mhc is a mosaic of stretches formed by conserved and nonconserved genes. Surprisingly, of the approximately 3.6-Mb Mhc, the stretche …
The Human Genome Project transformed the quest of more than 50 years to understand the major histocompatibility complex (Mhc). ...The …
Caveolin-1, a putative tumour suppressor gene.
Razani B, Schlegel A, Liu J, Lisanti MP. Razani B, et al. Biochem Soc Trans. 2001 Aug;29(Pt 4):494-9. doi: 10.1042/bst0290494. Biochem Soc Trans. 2001. PMID: 11498016 Review.
Caveolae ('little caves') are plasma membrane specializations of 50-100 nm in diameter, and the caveolins are structural proteins used by cells to form caveolae. ...
Caveolae ('little caves') are plasma membrane specializations of 50-100 nm in diameter, and the caveolins are structural proteins use …
The human genome structure and organization.
Makałowski W. Makałowski W. Acta Biochim Pol. 2001;48(3):587-98. Acta Biochim Pol. 2001. PMID: 11833767 Free article. Review.
Despite the fact that the nucleotide sequence of all chromosomes is established, the organisation of nuclear genome put still questions: for example: the exact number of genes encoded by the human genome is still unknown giving estimations from 30 to 150 thousand genes
Despite the fact that the nucleotide sequence of all chromosomes is established, the organisation of nuclear genome put still questions: for …
Molecular genetics of small cell lung carcinoma.
Wistuba II, Gazdar AF, Minna JD. Wistuba II, et al. Semin Oncol. 2001 Apr;28(2 Suppl 4):3-13. Semin Oncol. 2001. PMID: 11479891 Review.
The most frequent genetic abnormalities involve tumor suppressor genes (TSGs). The TSG p53 is mutated in more than 90% of SCLCs and more than 50% of NSCLCs; the retinoblastoma TSG is inactivated in over 90% of SCLC but only 15% of NSCLCs, and p16, the other componen …
The most frequent genetic abnormalities involve tumor suppressor genes (TSGs). The TSG p53 is mutated in more than 90% of SCLCs and m …
2,581 results