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Results by year

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

Year Number of Results
1963 1
1966 2
1967 4
1968 2
1969 3
1970 3
1972 2
1973 5
1974 4
1975 5
1976 1
1977 2
1979 4
1980 3
1981 3
1982 3
1983 3
1984 2
1985 4
1986 3
1987 8
1988 2
1990 5
1991 3
1993 2
1994 4
1995 6
1996 4
1997 6
1998 4
1999 10
2000 3
2001 5
2002 4
2003 8
2004 8
2005 9
2006 18
2007 19
2008 13
2009 26
2010 25
2011 23
2012 16
2013 15
2014 14
2015 23
2016 23
2017 15
2018 21
2019 11
2020 20
2021 15
2022 17
2023 26
2024 7

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459 results

Results by year

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Page 1
Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis.
Mohassel P, Donkervoort S, Lone MA, Nalls M, Gable K, Gupta SD, Foley AR, Hu Y, Saute JAM, Moreira AL, Kok F, Introna A, Logroscino G, Grunseich C, Nickolls AR, Pourshafie N, Neuhaus SB, Saade D, Gangfuß A, Kölbel H, Piccus Z, Le Pichon CE, Fiorillo C, Ly CV, Töpf A, Brady L, Specht S, Zidell A, Pedro H, Mittelmann E, Thomas FP, Chao KR, Konersman CG, Cho MT, Brandt T, Straub V, Connolly AM, Schara U, Roos A, Tarnopolsky M, Höke A, Brown RH, Lee CH, Hornemann T, Dunn TM, Bönnemann CG. Mohassel P, et al. Among authors: gupta sd. Nat Med. 2021 Jul;27(7):1197-1204. doi: 10.1038/s41591-021-01346-1. Epub 2021 May 31. Nat Med. 2021. PMID: 34059824 Free PMC article.
SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia.
Srivastava S, Shaked HM, Gable K, Gupta SD, Pan X, Somashekarappa N, Han G, Mohassel P, Gotkine M, Doney E, Goldenberg P, Tan QKG, Gong Y, Kleinstiver B, Wishart B, Cope H, Pires CB, Stutzman H, Spillmann RC; Undiagnosed Disease Network; Sadjadi R, Elpeleg O, Lee CH, Bellen HJ, Edvardson S, Eichler F, Dunn TM. Srivastava S, et al. Among authors: gupta sd. Brain. 2023 Apr 19;146(4):1420-1435. doi: 10.1093/brain/awac460. Brain. 2023. PMID: 36718090 Free PMC article.
Structural insights into the regulation of human serine palmitoyltransferase complexes.
Wang Y, Niu Y, Zhang Z, Gable K, Gupta SD, Somashekarappa N, Han G, Zhao H, Myasnikov AG, Kalathur RC, Dunn TM, Lee CH. Wang Y, et al. Among authors: gupta sd. Nat Struct Mol Biol. 2021 Mar;28(3):240-248. doi: 10.1038/s41594-020-00551-9. Epub 2021 Feb 8. Nat Struct Mol Biol. 2021. PMID: 33558761 Free PMC article.
Recurrent de novo SPTLC2 variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis.
Syeda SB, Lone MA, Mohassel P, Donkervoort S, Munot P, França MC Jr, Galarza-Brito JE, Eckenweiler M, Asamoah A, Gable K, Majumdar A, Schumann A, Gupta SD, Lakhotia A, Shieh PB, Foley AR, Jackson KE, Chao KR, Winder TL, Catapano F, Feng L, Kirschner J, Muntoni F, Dunn TM, Hornemann T, Bönnemann CG. Syeda SB, et al. Among authors: gupta sd. J Neurol Neurosurg Psychiatry. 2024 Jan 11;95(2):103-113. doi: 10.1136/jnnp-2023-332132. J Neurol Neurosurg Psychiatry. 2024. PMID: 38041679 Free PMC article.
Interpretation of ileal biopsies.
Das P, Gahlot GP, Mehta R, Gupta SD. Das P, et al. Among authors: gupta sd. Indian J Pathol Microbiol. 2015 Apr-Jun;58(2):146-53. doi: 10.4103/0377-4929.155302. Indian J Pathol Microbiol. 2015. PMID: 25885124 Review.
Nonfamilial cherubism.
Trivedi A, Gupta SD, Sharma S, Mehta R. Trivedi A, et al. Among authors: gupta sd. J Indian Soc Pedod Prev Dent. 2013 Jan-Mar;31(1):43-7. doi: 10.4103/0970-4388.112408. J Indian Soc Pedod Prev Dent. 2013. PMID: 23727742
459 results