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

Year Number of Results
1818 2
1819 1
1822 1
1837 1
1838 1
1857 2
1881 1
1898 1
1915 1
1926 1
1928 1
1932 1
1935 1
1942 2
1945 1
1950 1
1956 1
1958 1
1961 1
1964 1
1966 3
1967 1
1968 1
1969 2
1971 1
1972 3
1973 4
1974 1
1975 9
1976 6
1977 4
1978 6
1979 18
1980 12
1981 17
1982 13
1983 26
1984 21
1985 21
1986 24
1987 27
1988 16
1989 23
1990 18
1991 29
1992 19
1993 28
1994 30
1995 24
1996 34
1997 29
1998 32
1999 25
2000 37
2001 39
2002 51
2003 50
2004 49
2005 63
2006 70
2007 77
2008 107
2009 104
2010 113
2011 90
2012 98
2013 99
2014 123
2015 168
2016 187
2017 207
2018 182
2019 144
2020 147
2021 162
2022 147
2023 140
2024 106

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3,067 results

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Page 1
Changing children's eating behaviour - A review of experimental research.
DeCosta P, Møller P, Frøst MB, Olsen A. DeCosta P, et al. Appetite. 2017 Jun 1;113:327-357. doi: 10.1016/j.appet.2017.03.004. Epub 2017 Mar 9. Appetite. 2017. PMID: 28286164 Free article. Review.
Medline and Cab abstract (Ovid) and Web of Science (Thomson Reuters) were used to identify the experimental studies. A total of 120 experimental studies were identified and they are presented grouped within these 11 topics; parental control, reward, social facilitation, co …
Medline and Cab abstract (Ovid) and Web of Science (Thomson Reuters) were used to identify the experimental studies. A total of 120 e …
Rothmund-Thomson syndrome, a disorder far from solved.
Martins DJ, Di Lazzaro Filho R, Bertola DR, Hoch NC. Martins DJ, et al. Front Aging. 2023 Nov 10;4:1296409. doi: 10.3389/fragi.2023.1296409. eCollection 2023. Front Aging. 2023. PMID: 38021400 Free PMC article. Review.
Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder characterized by a range of clinical symptoms, including poikiloderma, juvenile cataracts, short stature, sparse hair, eyebrows/eyelashes, nail dysplasia, and skeletal abnormalities. While classically a …
Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder characterized by a range of clinical symptoms, including poiki …
Expression of concern relating to: D. Poldermans, E. Boersma, J. J. Bax, I. R. Thomson, B. Paelinck, L. L. M. van de Ven, M. G. Scheffer, G. Trocino, C. Vigna, H. F. Baars, H. van Urk, J. R. T. C. Roelandt, for the Dutch Echocardiographic Cardiac Risk Evaluation Applying Stress Echocardiography Study Group. 'Bisoprolol reduces cardiac death and myocardial infarction in high-risk patients as long as 2 years after successful major vascular surgery'.
[No authors listed] [No authors listed] Eur Heart J. 2015 Mar 7;36(10):633. doi: 10.1093/eurheartj/ehu397. Epub 2014 Sep 18. Eur Heart J. 2015. PMID: 25234008 No abstract available.
The upgrade of the Thomson scattering system for measurement on the C-2/C-2U devices.
Zhai K, Schindler T, Kinley J, Deng B, Thompson MC. Zhai K, et al. Rev Sci Instrum. 2016 Nov;87(11):11D602. doi: 10.1063/1.4955496. Rev Sci Instrum. 2016. PMID: 27910634
The C-2/C-2U Thomson scattering system has been substantially upgraded during the latter phase of C-2/C-2U program. A Rayleigh channel has been added to each of the three polychromators of the C-2/C-2U Thomson scattering sys …
The C-2/C-2U Thomson scattering system has been substantially upgraded during the latter phase of C-2/C-2 …
Expression and immune function of tenascin-C.
Udalova IA, Ruhmann M, Thomson SJ, Midwood KS. Udalova IA, et al. Crit Rev Immunol. 2011;31(2):115-45. doi: 10.1615/critrevimmunol.v31.i2.30. Crit Rev Immunol. 2011. PMID: 21542790 Review.
Persistent tenascin-C expression is associated with pathologies such as chronic, non-healing wounds, autoimmune diseases, cancer, and fibrotic diseases. We discuss the myriad roles that this multifunctional molecule plays during the immune response, with a focus on how tis …
Persistent tenascin-C expression is associated with pathologies such as chronic, non-healing wounds, autoimmune diseases, cancer, and …
Microgrewiapine C: Asymmetric Synthesis, Spectroscopic Data, and Configuration Assignment.
Davies SG, Fletcher AM, Roberts PM, Taylor CE, Thomson JE. Davies SG, et al. J Nat Prod. 2022 Jul 22;85(7):1872-1879. doi: 10.1021/acs.jnatprod.2c00183. Epub 2022 Jun 30. J Nat Prod. 2022. PMID: 35771599 Free PMC article.
The first asymmetric synthesis of microgrewiapine C, a piperidine alkaloid isolated from Microcos paniculata, is reported. This synthesis prompted correction of the (1)H and (13)C NMR data for the natural sample of the alkaloid, which was achieved by reanalysis of t …
The first asymmetric synthesis of microgrewiapine C, a piperidine alkaloid isolated from Microcos paniculata, is reported. This synth …
Biallelic variants in CRIPT cause a Rothmund-Thomson-like syndrome with increased cellular senescence.
Averdunk L, Huetzen MA, Moreno-Andrés D, Kalb R, McKee S, Hsieh TC, Seibt A, Schouwink M, Lalani S, Faqeih EA, Brunet T, Boor P, Neveling K, Hoischen A, Hildebrandt B, Graf E, Lu L, Jin W, Schaper J, Omer JA, Demaret T, Fleischer N, Schindler D, Krawitz P, Mayatepek E, Wieczorek D, Wang LL, Antonin W, Jachimowicz RD, von Felbert V, Distelmaier F. Averdunk L, et al. Genet Med. 2023 Jul;25(7):100836. doi: 10.1016/j.gim.2023.100836. Epub 2023 Mar 31. Genet Med. 2023. PMID: 37013901 Free article.
PURPOSE: Rothmund-Thomson syndrome (RTS) is characterized by poikiloderma, sparse hair, small stature, skeletal defects, cancer, and cataracts, resembling features of premature aging. ...RECQL4- and CRIPT-deficient fibroblasts showed an unremarkable mitotic progression and …
PURPOSE: Rothmund-Thomson syndrome (RTS) is characterized by poikiloderma, sparse hair, small stature, skeletal defects, cancer, and …
A Chinese patient with Rothmund-Thomson syndrome.
Zeng J, Li J, Liu Y, Liang R, Wang L, Zhou Q, Sun J, Liu Z, Wang WJ, Zhu S. Zeng J, et al. Mol Genet Genomic Med. 2024 Jan;12(1):e2347. doi: 10.1002/mgg3.2347. Epub 2023 Dec 22. Mol Genet Genomic Med. 2024. PMID: 38131666 Free PMC article.
INTRODUCTION: Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder that has been reported in all ethnicities, with several identifiable pathogenic variants. ...RESULTS: After analyzing the WGS data, we found a heterozygous nonsense mutation c.2752G …
INTRODUCTION: Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder that has been reported in all ethnicities, with …
3,067 results