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Results by year

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

Year Number of Results
1849 1
1874 2
1875 1
1898 1
1924 1
1926 2
1927 1
1928 2
1929 3
1931 3
1932 3
1933 4
1934 2
1937 1
1942 1
1943 1
1944 1
1946 1
1947 2
1950 2
1952 1
1953 4
1954 1
1955 3
1956 1
1958 1
1959 1
1961 2
1962 3
1963 1
1964 4
1965 1
1966 7
1967 2
1968 4
1969 6
1970 5
1971 5
1972 6
1973 5
1974 2
1975 9
1976 10
1977 16
1978 15
1979 17
1980 12
1981 10
1982 12
1983 17
1984 22
1985 15
1986 21
1987 33
1988 45
1989 44
1990 58
1991 48
1992 52
1993 59
1994 64
1995 70
1996 64
1997 55
1998 73
1999 96
2000 79
2001 117
2002 115
2003 137
2004 133
2005 159
2006 157
2007 186
2008 180
2009 170
2010 203
2011 215
2012 253
2013 284
2014 389
2015 534
2016 589
2017 604
2018 748
2019 766
2020 747
2021 867
2022 851
2023 806
2024 403

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9,672 results

Results by year

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Page 1
Emerging structural insights into C-type glycosyltransferases.
Alexander JAN, Locher KP. Alexander JAN, et al. Curr Opin Struct Biol. 2023 Apr;79:102547. doi: 10.1016/j.sbi.2023.102547. Epub 2023 Feb 22. Curr Opin Struct Biol. 2023. PMID: 36827761 Free article. Review.
Glycosyltransferases of the C superfamily (GT-Cs) are enzymes found in all domains of life. ...Until recently, GT-Cs were thought to share a conserved structural module of 7 transmembrane helices; however, recently determined GT-C structures revealed novel folds. He …
Glycosyltransferases of the C superfamily (GT-Cs) are enzymes found in all domains of life. ...Until recently, GT-Cs were thought to …
S3-Leitlinie: Diagnostik und Therapie des hepatozellulären Karzinoms.
Sabrina V, Michael B, Jörg A, Peter B, Wolf B, Susanne B, Thomas B, Frank D, Matthias E, Markus F, Christian F, Paul F, Andreas G, Eleni G, Martin G, Elke H, Thomas H, Ralf-Thorsten H, Wolf-Peter H, Peter H, Achim K, Gabi K, Jürgen K, David K, Frank L, Hauke L, Thomas L, Philipp L, Andreas M, Alexander M, Oliver M, Silvio N, Huu Phuc N, Johann O, Karl-Jürgen O, Philipp P, Kerstin P, Philippe P, Thorsten P, Mathias P, Ruben P, Jürgen P, Jutta R, Peter R, Johanna R, Ulrike R, Elke R, Barbara S, Peter S, Irene S, Andreas S, Dietrich VS, Daniel S, Marianne S, Alexander S, Andreas S, Nadine S, Christian S, Andrea T, Anne T, Jörg T, Ingo VT, Reina T, Arndt V, Thomas V, Hilke V, Frank W, Oliver W, Heiner W, Henning W, Dane W, Christian W, Marcus-Alexander W, Peter G, Nisar M. Sabrina V, et al. Z Gastroenterol. 2022 Jan;60(1):e56-e130. doi: 10.1055/a-1589-7568. Epub 2022 Jan 18. Z Gastroenterol. 2022. PMID: 35042248 Free article. German. No abstract available.
S3-Leitlinie: Diagnostik und Therapie des hepatozellulären Karzinoms – Kurzversion 2.00 – Juni 2021, AWMF-Registernummer: 032-053OL.
Sabrina V, Michael B, Jörg A, Peter B, Wolf B, Susanne B, Thomas B, Frank D, Matthias E, Markus F, Christian F, Paul F, Andreas G, Eleni G, Martin G, Elke H, Thomas H, Ralf-Thorsten H, Wolf-Peter H, Peter H, Achim K, Gabi K, Jürgen K, David K, Frank L, Hauke L, Thomas L, Philipp L, Andreas M, Alexander M, Oliver M, Silvio N, Huu Phuc N, Johann O, Karl-Jürgen O, Philipp P, Kerstin P, Philippe P, Thorsten P, Mathias P, Ruben P, Jürgen P, Jutta R, Peter R, Johanna R, Ulrike R, Elke R, Barbara S, Peter S, Irene S, Andreas S, Dietrich VS, Daniel S, Marianne S, Alexander S, Andreas S, Nadine S, Christian S, Andrea T, Anne T, Jörg T, Ingo VT, Reina T, Arndt V, Thomas V, Hilke V, Frank W, Oliver W, Heiner W, Henning W, Dane W, Christian W, Marcus-Alexander W, Peter G, Nisar M. Sabrina V, et al. Z Gastroenterol. 2022 Jan;60(1):81-107. doi: 10.1055/a-1589-7520. Epub 2022 Jan 18. Z Gastroenterol. 2022. PMID: 35042249 Free article. German. No abstract available.
Implantable Cardioverter-Defibrillator-Cybersecurity.
Alexander B, Neira V, Campbell D, Crystal E, Simpson C, Enriquez A, Chacko S, Abdollah H, Redfearn D, Baranchuk A. Alexander B, et al. Circ Arrhythm Electrophysiol. 2020 Mar;13(3):e008261. doi: 10.1161/CIRCEP.119.008261. Epub 2020 Feb 11. Circ Arrhythm Electrophysiol. 2020. PMID: 32078370 No abstract available.
Biographical Feature: Alexander C. Sonnenwirth, Ph.D.
Onderdonk AB. Onderdonk AB. J Clin Microbiol. 2016 May;54(5):1183-5. doi: 10.1128/JCM.00263-16. Epub 2016 Feb 17. J Clin Microbiol. 2016. PMID: 26888903 Free PMC article. No abstract available.
Immunoglobulin G-dependent inhibition of inflammatory bone remodeling requires pattern recognition receptor Dectin-1.
Seeling M, Pöhnl M, Kara S, Horstmann N, Riemer C, Wöhner M, Liang C, Brückner C, Eiring P, Werner A, Biburger M, Altmann L, Schneider M, Amon L, Lehmann CHK, Lee S, Kunz M, Dudziak D, Schett G, Bäuerle T, Lux A, Tuckermann J, Vögtle T, Nieswandt B, Sauer M, Böckmann RA, Nimmerjahn F. Seeling M, et al. Immunity. 2023 May 9;56(5):1046-1063.e7. doi: 10.1016/j.immuni.2023.02.019. Epub 2023 Mar 21. Immunity. 2023. PMID: 36948194 Free article.
Type I Alexander disease: Update and validation of the clinical evolution-based classification.
Vaia Y, Mura E, Tonduti D. Vaia Y, et al. Mol Genet Metab. 2023 Mar;138(3):107540. doi: 10.1016/j.ymgme.2023.107540. Epub 2023 Feb 10. Mol Genet Metab. 2023. PMID: 36804850 Review.
BACKGROUND AND OBJECTIVES: Alexander disease (AxD) is a rare progressive leukodystrophy caused by autosomal dominant mutations in the Glial Fibrillary Acidic Protein (GFAP) gene. ...
BACKGROUND AND OBJECTIVES: Alexander disease (AxD) is a rare progressive leukodystrophy caused by autosomal dominant mutations in the …
Adult-onset Alexander disease among patients of Jewish Syrian descent.
Anis S, Fay-Karmon T, Lassman S, Shbat F, Lesman-Segev O, Mor N, Barel O, Dominissini D, Chorin O, Pras E, Greenbaum L, Hassin-Baer S. Anis S, et al. Neurogenetics. 2023 Oct;24(4):303-310. doi: 10.1007/s10048-023-00732-w. Epub 2023 Sep 2. Neurogenetics. 2023. PMID: 37658208
Alexander disease (AxD) is a rare autosomal dominant leukodystrophy caused by heterozygous mutations in the glial fibrillary acid protein (GFAP) gene. ...Five patients (4 females) were diagnosed with adult-onset AxD due to the heterozygous mutation c.219G > A, p. …
Alexander disease (AxD) is a rare autosomal dominant leukodystrophy caused by heterozygous mutations in the glial fibrillary acid pro …
9,672 results