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

Year Number of Results
1946 1
1947 1
1948 3
1954 2
1956 3
1957 1
1958 1
1959 2
1961 2
1962 1
1964 1
1965 1
1967 2
1968 2
1969 1
1971 5
1972 4
1973 11
1974 5
1975 11
1976 4
1977 3
1978 1
1979 3
1980 1
1981 1
1982 3
1983 4
1984 8
1985 3
1986 3
1988 8
1990 9
1991 6
1992 9
1993 9
1994 8
1995 6
1996 10
1997 16
1998 15
1999 13
2000 15
2001 13
2002 4
2003 14
2004 17
2005 16
2006 8
2007 9
2008 11
2009 13
2010 18
2011 12
2012 22
2013 24
2014 38
2015 41
2016 31
2017 22
2018 28
2019 32
2020 2
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540 results
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Page 1
Identifying cell populations with scRNASeq
Andrews TS and Hemberg M. Mol Aspects Med 2018 - Review. PMID 28712804 Free article.
Gain-of-function IKBKB mutation causes human combined immune deficiency
Cardinez C, et al. J Exp Med 2018. Among authors: Andrews TD. PMID 30337470 Free PMC article.
Whole exome sequencing in two cohorts of such patients identified a novel heterozygous de novo IKBKB missense mutation (c.607G>A) in two separate kindreds in whom probands presented with immune dysregulation, combined T and B cell deficiency, inflammation, and epithelial defects. ...IKK2(V203I) results in enhanced NF-κB signaling, as well as T and B cell functional defects. IKK2(V203) is a highly conserved residue, and to prove causation, we generated an accurate mouse model by introducing the precise orthologous codon change in Ikbkb using CRISPR/Cas9. ...
Whole exome sequencing in two cohorts of such patients identified a novel heterozygous de novo IKBKB missense mutation (c.607G>A) in two …
540 results
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