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

Year Number of Results
1927 1
1935 2
1938 1
1939 1
1945 2
1946 4
1947 2
1949 4
1951 2
1952 1
1953 2
1954 2
1955 2
1956 4
1957 3
1958 1
1959 1
1961 1
1962 1
1964 1
1965 1
1966 1
1967 2
1968 1
1969 2
1970 2
1971 1
1973 2
1974 1
1975 4
1976 1
1977 2
1978 1
1980 1
1981 1
1985 1
1987 1
1989 1
1990 1
1993 3
1995 3
1998 1
2000 1
2001 1
2005 3
2006 1
2007 2
2008 2
2009 1
2010 2
2011 3
2012 2
2013 2
2014 5
2015 6
2016 2
2017 2
2018 6
2019 4
2020 4
2021 4
Text availability
Article attribute
Article type
Publication date

Search Results

117 results
Results by year
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Page 1
mTORC1 Activation Requires DRAM-1 by Facilitating Lysosomal Amino Acid Efflux.
Beaumatin F, O'Prey J, Barthet VJA, Zunino B, Parvy JP, Bachmann AM, O'Prey M, Kania E, Gonzalez PS, Macintosh R, Lao LY, Nixon C, Lopez J, Long JS, Tait SWG, Ryan KM. Beaumatin F, et al. Among authors: macintosh r. Mol Cell. 2019 Oct 3;76(1):163-176.e8. doi: 10.1016/j.molcel.2019.07.021. Epub 2019 Sep 3. Mol Cell. 2019. PMID: 31492633 Free PMC article.
De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-Progressive Neurocognitive Syndrome.
Palmer EE, Hong S, Al Zahrani F, Hashem MO, Aleisa FA, Ahmed HMJ, Kandula T, Macintosh R, Minoche AE, Puttick C, Gayevskiy V, Drew AP, Cowley MJ, Dinger M, Rosenfeld JA, Xiao R, Cho MT, Yakubu SF, Henderson LB, Guillen Sacoto MJ, Begtrup A, Hamad M, Shinawi M, Andrews MV, Jones MC, Lindstrom K, Bristol RE, Kayani S, Snyder M, Villanueva MM, Schteinschnaider A, Faivre L, Thauvin C, Vitobello A, Roscioli T, Kirk EP, Bye A, Merzaban J, Jaremko Ł, Jaremko M, Sachdev RK, Alkuraya FS, Arold ST. Palmer EE, et al. Among authors: macintosh r. Am J Hum Genet. 2019 Mar 7;104(3):542-552. doi: 10.1016/j.ajhg.2019.01.013. Epub 2019 Feb 28. Am J Hum Genet. 2019. PMID: 30827498 Free PMC article.
A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures.
Gennarino VA, Palmer EE, McDonell LM, Wang L, Adamski CJ, Koire A, See L, Chen CA, Schaaf CP, Rosenfeld JA, Panzer JA, Moog U, Hao S, Bye A, Kirk EP, Stankiewicz P, Breman AM, McBride A, Kandula T, Dubbs HA, Macintosh R, Cardamone M, Zhu Y, Ying K, Dias KR, Cho MT, Henderson LB, Baskin B, Morris P, Tao J, Cowley MJ, Dinger ME, Roscioli T, Caluseriu O, Suchowersky O, Sachdev RK, Lichtarge O, Tang J, Boycott KM, Holder JL Jr, Zoghbi HY. Gennarino VA, et al. Among authors: macintosh r. Cell. 2018 Feb 22;172(5):924-936.e11. doi: 10.1016/j.cell.2018.02.006. Cell. 2018. PMID: 29474920 Free PMC article.
SAAD.
Macintosh R. Macintosh R. SAAD Dig. 1976 Apr;3(2):30-35. SAAD Dig. 1976. PMID: 1064994 No abstract available.
Autophagy in tumour cell death.
Macintosh RL, Ryan KM. Macintosh RL, et al. Semin Cancer Biol. 2013 Oct;23(5):344-51. doi: 10.1016/j.semcancer.2013.05.006. Epub 2013 Jun 14. Semin Cancer Biol. 2013. PMID: 23774296 Review.
RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial Features.
Palmer EE, Carroll R, Shaw M, Kumar R, Minoche AE, Leffler M, Murray L, Macintosh R, Wright D, Troedson C, McKenzie F, Townshend S, Ward M, Nawaz U, Ravine A, Runke CK, Thorland EC, Hummel M, Foulds N, Pichon O, Isidor B, Le Caignec C, Demeer B, Andrieux J, Albarazi SH, Bye A, Sachdev R, Kirk EP, Cowley MJ, Field M, Gecz J. Palmer EE, et al. Among authors: macintosh r. Am J Hum Genet. 2020 Dec 3;107(6):1157-1169. doi: 10.1016/j.ajhg.2020.10.005. Epub 2020 Nov 6. Am J Hum Genet. 2020. PMID: 33159883 Free PMC article.
Le Morte d'Arthur: A Commentary on Hugo L. Obwegeser.
MacIntosh RB. MacIntosh RB. J Oral Maxillofac Surg. 2018 Jan;76(1):6-7. doi: 10.1016/j.joms.2017.09.024. Epub 2017 Oct 13. J Oral Maxillofac Surg. 2018. PMID: 29080405 No abstract available.
117 results
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