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

Year Number of Results
1968 2
1973 1
1978 2
1981 1
1983 3
1984 1
1985 1
1986 2
1987 1
1988 2
1989 4
1991 3
1992 10
1993 4
1994 7
1995 8
1996 7
1997 7
1998 4
1999 11
2000 6
2001 9
2002 11
2003 5
2004 7
2005 13
2006 22
2007 21
2008 17
2009 14
2010 23
2011 28
2012 32
2013 64
2014 86
2015 102
2016 115
2017 130
2018 158
2019 188
2020 239
2021 300
2022 296
2023 313
2024 110

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2,167 results

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Page 1
Hypertension Pharmacological Treatment in Adults: A World Health Organization Guideline Executive Summary.
Al-Makki A, DiPette D, Whelton PK, Murad MH, Mustafa RA, Acharya S, Beheiry HM, Champagne B, Connell K, Cooney MT, Ezeigwe N, Gaziano TA, Gidio A, Lopez-Jaramillo P, Khan UI, Kumarapeli V, Moran AE, Silwimba MM, Rayner B, Sukonthasan A, Yu J, Saraffzadegan N, Reddy KS, Khan T. Al-Makki A, et al. Hypertension. 2022 Jan;79(1):293-301. doi: 10.1161/HYPERTENSIONAHA.121.18192. Epub 2021 Nov 15. Hypertension. 2022. PMID: 34775787 Free PMC article.
Antithrombotic Treatment for Stroke Prevention in Cervical Artery Dissection: The STOP-CAD Study.
Yaghi S, Shu L, Mandel D, Leon Guerrero CR, Henninger N, Muppa J, Affan M, Ul Haq Lodhi O, Heldner MR, Antonenko K, Seiffge D, Arnold M, Salehi Omran S, Crandall R, Lester E, Lopez Mena D, Arauz A, Nehme A, Boulanger M, Touze E, Sousa JA, Sargento-Freitas J, Barata V, Castro-Chaves P, Brito MT, Khan M, Mallick D, Rothstein A, Khazaal O, Kaufmann JE, Engelter ST, Traenka C, Aguiar de Sousa D, Soares M, Rosa S, Zhou LW, Gandhi P, Field TS, Mancini S, Metanis I, Leker RR, Pan K, Dantu V, Baumgartner K, Burton T, Von Rennenberg R, Nolte CH, Choi R, MacDonald J, Bavarsad Shahripour R, Guo X, Ghannam M, Almajali M, Samaniego EA, Sanchez S, Rioux B, Zine-Eddine F, Poppe A, Fonseca AC, Baptista MF, Cruz D, Romoli M, De Marco G, Longoni M, Keser Z, Griffin K, Kuohn L, Frontera J, Amar J, Giles J, Zedde M, Pascarella R, Grisendi I, Nzwalo H, Liebeskind DS, Molaie A, Cavalier A, Kam W, Mac Grory B, Al Kasab S, Anadani M, Kicielinski K, Eltatawy A, Chervak L, Chulluncuy-Rivas R, Aziz Y, Bakradze E, Tran TL, Rodrigo-Gisbert M, Requena M, Saleh Velez F, Ortiz Gracia J, Mudassani V, de Havenon A, Vishnu VY, Yaddanapudi S, Adams L, Browngoehl A, Ranasinghe T, Dunston R, Lynch Z, Penckofer M, Sieg… See abstract for full author list ➔ Yaghi S, et al. Stroke. 2024 Apr;55(4):908-918. doi: 10.1161/STROKEAHA.123.045731. Epub 2024 Feb 9. Stroke. 2024. PMID: 38335240 Free article.
Mucosal immunity.
Hanson LA, Ahlstedt S, Andersson B, Carlsson B, Cole MF, Cruz JR, Dahlgren U, Ericsson TH, Jalil F, Khan SR, Mellander L, Schneerson R, Edén CS, Söderström T, Wadsworth C. Hanson LA, et al. Ann N Y Acad Sci. 1983 Jun 30;409:1-21. doi: 10.1111/j.1749-6632.1983.tb26855.x. Ann N Y Acad Sci. 1983. PMID: 6191608 Review.
Erratum for Research Article "Whole-exome sequencing reveals germline-mutated small cell lung cancer subtype with favorable response to DNA repair-targeted therapies" by C. Tlemsani, N. Takahashi, L. Pongor, V. N. Rajapakse, M. Tyagi, X. Wen, G.-A. Fasaye, K. T. Schmidt, P. Desai, C. Kim, A. Rajan, S. Swift, L. Sciuto, R. Vilimas, S. Webb, S. Nichols, W. D. Figg, Y. Pommier, K. Calzone, S. M. Steinberg, J. S. Wei, U. Guha, C. E. Turner, J. Khan, A. Thomas.
[No authors listed] [No authors listed] Sci Transl Med. 2021 Oct 13;13(615):eabm6064. doi: 10.1126/scitranslmed.abm6064. Epub 2021 Oct 13. Sci Transl Med. 2021. PMID: 34644151 No abstract available.
Neurodegenerative and functional signatures of the cerebellar cortex in m.3243A > G patients.
Haast RAM, De Coo IFM, Ivanov D, Khan AR, Jansen JFA, Smeets HJM, Uludağ K. Haast RAM, et al. Brain Commun. 2022 Feb 3;4(1):fcac024. doi: 10.1093/braincomms/fcac024. eCollection 2022. Brain Commun. 2022. PMID: 35187487 Free PMC article.
Mutations of the mitochondrial DNA are an important cause of inherited diseases that can severely affect the tissue's homeostasis and integrity. The m.3243A > G mutation is the most commonly observed across mitochondrial disorders and is linked to multisystemic c …
Mutations of the mitochondrial DNA are an important cause of inherited diseases that can severely affect the tissue's homeostasis and integr …
Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy.
Khan NA, Govindaraj P, Jyothi V, Meena AK, Thangaraj K. Khan NA, et al. Mol Vis. 2013 Jun 11;19:1282-9. Print 2013. Mol Vis. 2013. PMID: 23805034 Free PMC article.
RESULTS: We observed the existence of double pathogenic mutations (m.11778G>A and m.1555A>G) in two Indian LHON families, who are from different haplogroup backgrounds (M5a and U2e1), with different clinical penetrance of the disease (visual impairment) …
RESULTS: We observed the existence of double pathogenic mutations (m.11778G>A and m.1555A>G) in two Indian LHON f …
Investigation on synthesis of ternary g-C(3)N(4)/ZnO-W/M nanocomposites integrated heterojunction II as efficient photocatalyst for environmental applications.
Malik M, Len T, Luque R, Osman SM, Paone E, Khan MI, Wattoo MA, Jamshaid M, Anum A, Rehman AU. Malik M, et al. Environ Res. 2023 Jan 15;217:114621. doi: 10.1016/j.envres.2022.114621. Epub 2022 Nov 5. Environ Res. 2023. PMID: 36347396
Here in, we successfully synthesized a vigorous photocatalysts comprising of g-C(3)N(4) and doped ZnO-W/M (M = Co, Ce, Yb, Sm) by co-precipitation followed by metals doping via calcination approach. ...The SEM images reveal an agglomerated morphology and EDS …
Here in, we successfully synthesized a vigorous photocatalysts comprising of g-C(3)N(4) and doped ZnO-W/M (M = Co, Ce, …
The G-M-N motif determines ion selectivity in the yeast magnesium channel Mrs2p.
Sponder G, Svidová S, Khan MB, Kolisek M, Schweyen RJ, Carugo O, Djinović-Carugo K. Sponder G, et al. Metallomics. 2013 Jun;5(6):745-52. doi: 10.1039/c3mt20201a. Metallomics. 2013. PMID: 23686104
The highly conserved G-M-N motif of the CorA-Mrs2-Alr1 family of Mg(2+) channels has been shown to be essential for Mg(2+) transport. We performed random mutagenesis of the G-M-N sequence of Saccharomyces cerevisiae Mrs2p in an unbiased genetic screen. …
The highly conserved G-M-N motif of the CorA-Mrs2-Alr1 family of Mg(2+) channels has been shown to be essential for Mg(2+) tra …
CD82 controls CpG-dependent TLR9 signaling.
Khan NS, Lukason DP, Feliu M, Ward RA, Lord AK, Reedy JL, Ramirez-Ortiz ZG, Tam JM, Kasperkovitz PV, Negoro PE, Vyas TD, Xu S, Brinkmann MM, Acharaya M, Artavanis-Tsakonas K, Frickel EM, Becker CE, Dagher Z, Kim YM, Latz E, Ploegh HL, Mansour MK, Miranti CK, Levitz SM, Vyas JM. Khan NS, et al. FASEB J. 2019 Nov;33(11):12500-12514. doi: 10.1096/fj.201901547R. Epub 2019 Aug 13. FASEB J. 2019. PMID: 31408613 Free PMC article.
L., Ramirez-Ortiz, Z. G., Tam, J. M., Kasperkovitz, P. V., Negoro, P. E., Vyas, T. D., Xu, S., Brinkmann, M. M., Acharaya, M., Artavanis-Tsakonas, K., Frickel, E.-M., Becker, C. ...
L., Ramirez-Ortiz, Z. G., Tam, J. M., Kasperkovitz, P. V., Negoro, P. E., Vyas, T. D., Xu, S., Brinkmann, M. M., …
2,167 results