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

Year Number of Results
1839 1
1841 1
1842 1
1848 2
1851 1
1858 3
1859 3
1861 3
1863 1
1864 4
1868 2
1872 1
1873 2
1874 4
1875 5
1876 2
1878 1
1879 1
1880 2
1881 3
1882 1
1888 2
1889 2
1890 1
1891 4
1892 7
1893 1
1894 2
1895 2
1896 1
1897 6
1898 4
1899 1
1900 8
1901 10
1902 5
1903 2
1904 2
1905 1
1906 3
1907 3
1908 11
1910 5
1911 3
1912 4
1913 4
1914 1
1915 1
1916 3
1917 2
1919 1
1923 1
1925 1
1928 1
1930 1
1935 1
1937 1
1938 1
1939 2
1941 1
1943 2
1945 1
1946 1
1947 6
1948 1
1949 5
1950 4
1951 5
1952 4
1953 6
1954 6
1955 2
1956 9
1957 3
1958 7
1959 3
1960 2
1961 6
1962 12
1963 14
1964 13
1965 15
1966 19
1967 19
1968 28
1969 36
1970 28
1971 24
1972 21
1973 28
1974 35
1975 66
1976 71
1977 75
1978 72
1979 85
1980 109
1981 121
1982 111
1983 176
1984 163
1985 205
1986 230
1987 697
1988 1272
1989 1356
1990 1577
1991 1661
1992 1628
1993 1762
1994 1921
1995 1978
1996 2005
1997 2066
1998 2072
1999 2290
2000 2813
2001 3140
2002 3460
2003 4061
2004 4758
2005 5358
2006 5869
2007 6435
2008 6832
2009 6960
2010 7533
2011 8096
2012 9102
2013 9522
2014 12009
2015 13939
2016 15462
2017 17015
2018 18136
2019 18900
2020 21755
2021 23448
2022 22526
2023 21837
2024 7596

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267,033 results

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The following term was not found in PubMed: 002816.1
Page 1
Identification and bioinformatics analysis of lncRNAs in serum of patients with ankylosing spondylitis.
Kou J, Bie Y, Liu M, Wang L, Liu X, Sun Y, Zheng X. Kou J, et al. BMC Musculoskelet Disord. 2024 Apr 15;25(1):291. doi: 10.1186/s12891-024-07396-z. BMC Musculoskelet Disord. 2024. PMID: 38622662
METHODS: We used high-throughput whole-transcriptome sequencing to generate sequencing data from three patients with AS and three normal controls (NC). Then, we performed bioinformatics analyses to identify the functional and biological processes associated with differenti …
METHODS: We used high-throughput whole-transcriptome sequencing to generate sequencing data from three patients with AS and three normal con …
Individualism, collectivism and conformity in nine countries: Relations with parenting and child adjustment.
Gorla L, Rothenberg WA, Lansford JE, Yotanyamaneewong S, Alampay LP, Al-Hassan SM, Bacchini D, Bornstein MH, Breiner K, Chang L, Deater-Deckard K, Di Giunta L, Dodge KA, Gurdal S, Junla D, Oburu P, Pastorelli C, Santona A, Skinner AT, Sorbring E, Steinberg L, Uribe Tirado LM. Gorla L, et al. Int J Psychol. 2024 Apr 15. doi: 10.1002/ijop.13130. Online ahead of print. Int J Psychol. 2024. PMID: 38622493
Detection of Residual Peritoneal Metastases Following Cytoreductive Surgery Using Pegsitacianine, a pH-Sensitive Imaging Agent: Final Results from a Phase II Study.
Wagner P, Levine EA, Kim AC, Shen P, Fleming ND, Westin SN, Berry LK, Karakousis GC, Tanyi JL, Olson MT, Madajewski B, Ostrander B, Krishnan K, Balch CM, Bartlett DL. Wagner P, et al. Ann Surg Oncol. 2024 Apr 15. doi: 10.1245/s10434-024-15165-4. Online ahead of print. Ann Surg Oncol. 2024. PMID: 38622456
Developmental characteristics and accuracy of autism screening among two-year-old toddlers in the ECHO program.
Shuster CL, Brennan PA, Carter BS, Check J, D'Sa V, Graff JC, Helderman J, Hofheimer JA, Joseph RM, Murphy LE, O'Connor TG, O'Shea TM, Pievsky M, Sheinkopf SJ, Shuffrey LC, Smith LM, Wu PC, Lester BM; program collaborators for Environmental influences on Child Health Outcomes. Shuster CL, et al. Pediatr Res. 2024 Apr 15. doi: 10.1038/s41390-024-03193-5. Online ahead of print. Pediatr Res. 2024. PMID: 38622260
Novel mutation leading to splice donor loss in a conserved site of DMD gene causes Duchenne muscular dystrophy with cryptorchidism.
Chen J, Jia Y, Zhong J, Zhang K, Dai H, He G, Li F, Zeng L, Fan C, Xu H. Chen J, et al. J Med Genet. 2024 Apr 15:jmg-2024-109896. doi: 10.1136/jmg-2024-109896. Online ahead of print. J Med Genet. 2024. PMID: 38621993
CRISPR-Cas9 mouse modelling of a splice donor loss variant in DMD (NC_000023.11:g.32454661C>G), which resides in a conserved site across vertebrates, replicated bilateral cryptorchidism phenotypes, confirmed by MRI at 4 and 10 weeks. ...
CRISPR-Cas9 mouse modelling of a splice donor loss variant in DMD (NC_000023.11:g.32454661C>G), which resides in a conserved site …
267,033 results
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