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Page 1
Cosmic Ray Background Removal With Deep Neural Networks in SBND.
Acciarri R, Adams C, Andreopoulos C, Asaadi J, Babicz M, Backhouse C, Badgett W, Bagby L, Barker D, Basque V, Bazetto MCQ, Betancourt M, Bhanderi A, Bhat A, Bonifazi C, Brailsford D, Brandt AG, Brooks T, Carneiro MF, Chen Y, Chen H, Chisnall G, Crespo-Anadón JI, Cristaldo E, Cuesta C, de Icaza Astiz IL, De Roeck A, de Sá Pereira G, Del Tutto M, Di Benedetto V, Ereditato A, Evans JJ, Ezeribe AC, Fitzpatrick RS, Fleming BT, Foreman W, Franco D, Furic I, Furmanski AP, Gao S, Garcia-Gamez D, Frandini H, Ge G, Gil-Botella I, Gollapinni S, Goodwin O, Green P, Griffith WC, Guenette R, Guzowski P, Ham T, Henzerling J, Holin A, Howard B, Jones RS, Kalra D, Karagiorgi G, Kashur L, Ketchum W, Kim MJ, Kudryavtsev VA, Larkin J, Lay H, Lepetic I, Littlejohn BR, Louis WC, Machado AA, Malek M, Mardsen D, Mariani C, Marinho F, Mastbaum A, Mavrokoridis K, McConkey N, Meddage V, Méndez DP, Mettler T, Mistry K, Mogan A, Molina J, Mooney M, Mora L, Moura CA, Mousseau J, Navrer-Agasson A, Nicolas-Arnaldos FJ, Nowak JA, Palamara O, Pandey V, Pater J, Paulucci L, Pimentel VL, Psihas F, Putnam G, Qian X, Raguzin E, Ray H, Reggiani-Guzzo M, Rivera D, Roda M, Ross-Lonergan M, Scanavini G, Scarff A, S… See abstract for full author list ➔ Acciarri R, et al. Among authors: ham t. Front Artif Intell. 2021 Aug 24;4:649917. doi: 10.3389/frai.2021.649917. eCollection 2021. Front Artif Intell. 2021. PMID: 34505055 Free PMC article.
Detection of Fluorescent Protein Mechanical Switching in Cellulo.
Shoyer TC, Collins KL, Ham TR, Blanchard AT, Malavade JN, West JL, Hoffman BD. Shoyer TC, et al. Among authors: ham tr. bioRxiv [Preprint]. 2024 Jan 11:2024.01.10.575065. doi: 10.1101/2024.01.10.575065. bioRxiv. 2024. PMID: 38260589 Free PMC article. Preprint.
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease.
Claus LR, Chen C, Stallworth J, Turner JL, Slaats GG, Hawks AL, Mabillard H, Senum SR, Srikanth S, Flanagan-Steet H, Louie RJ, Silver J, Lerner-Ellis J, Morel C, Mighton C, Sleutels F, van Slegtenhorst M, van Ham T, Brooks AS, Dorresteijn EM, Barakat TS, Dahan K, Demoulin N, Goffin EJ, Olinger E; Genomics England Research Consortium; Larsen M, Hertz JM, Lilien MR, Obeidová L, Seeman T, Stone HK, Kerecuk L, Gurgu M, Yousef Yengej FA, Ammerlaan CME, Rookmaaker MB, Hanna C, Rogers RC, Duran K, Peters E, Sayer JA, van Haaften G, Harris PC, Ling K, Mason JM, van Eerde AM, Steet R. Claus LR, et al. Among authors: van ham t. Kidney Int. 2023 Nov;104(5):995-1007. doi: 10.1016/j.kint.2023.07.021. Epub 2023 Aug 19. Kidney Int. 2023. PMID: 37598857
Biallelic variants in FLII cause pediatric cardiomyopathy by disrupting cardiomyocyte cell adhesion and myofibril organization.
Ruijmbeek CW, Housley F, Idrees H, Housley MP, Pestel J, Keller L, Lai JK, der Linde HCV, Willemsen R, Piesker J, Al-Hassnan ZN, Almesned A, Dalinghaus M, den Bersselaar LMV, van Slegtenhorst MA, Tessadori F, Bakkers J, van Ham TJ, Stainier DY, Verhagen JM, Reischauer S. Ruijmbeek CW, et al. Among authors: van ham tj. JCI Insight. 2023 Sep 8;8(17):e168247. doi: 10.1172/jci.insight.168247. JCI Insight. 2023. PMID: 37561591 Free PMC article.
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model.
Deng R, Medico-Salsench E, Nikoncuk A, Ramakrishnan R, Lanko K, Kühn NA, van der Linde HC, Lor-Zade S, Albuainain F, Shi Y, Yousefi S, Capo I, van den Herik EM, van Slegtenhorst M, van Minkelen R, Geeven G, Mulder MT, Ruijter GJG, Lütjohann D, Jacobs EH, Houlden H, Pagnamenta AT, Metcalfe K, Jackson A, Banka S, De Simone L, Schwaede A, Kuntz N, Palculict TB, Abbas S, Umair M, AlMuhaizea M, Colak D, AlQudairy H, Alsagob M, Pereira C, Trunzo R, Karageorgou V, Bertoli-Avella AM, Bauer P, Bouman A, Hoefsloot LH, van Ham TJ, Issa M, Zaki MS, Gleeson JG, Willemsen R, Kaya N, Arold ST, Maroofian R, Sanderson LE, Barakat TS. Deng R, et al. Among authors: van ham tj. Acta Neuropathol. 2023 Aug;146(2):353-368. doi: 10.1007/s00401-023-02579-9. Epub 2023 Apr 29. Acta Neuropathol. 2023. PMID: 37119330 Free PMC article.
SMPD4 regulates mitotic nuclear envelope dynamics and its loss causes microcephaly and diabetes.
Smits DJ, Schot R, Krusy N, Wiegmann K, Utermöhlen O, Mulder MT, den Hoedt S, Yoon G, Deshwar AR, Kresge C, Pletcher B, van Mook M, Ferreira MS, Poot RA, Slotman JA, Kremers GJ, Ahmad A, Albash B, Bastaki L, Marafi D, Dekker J, van Ham TJ, Nguyen L, Mancini GMS. Smits DJ, et al. Among authors: van ham tj. Brain. 2023 Aug 1;146(8):3528-3541. doi: 10.1093/brain/awad033. Brain. 2023. PMID: 36732302 Free PMC article.
Web-accessible application for identifying pathogenic transcripts with RNA-seq: Increased sensitivity in diagnosis of neurodevelopmental disorders.
Dekker J, Schot R, Bongaerts M, de Valk WG, van Veghel-Plandsoen MM, Monfils K, Douben H, Elfferich P, Kasteleijn E, van Unen LMA, Geeven G, Saris JJ, van Ierland Y, Verheijen FW, van der Sterre MLT, Sadeghi Niaraki F, Smits DJ, Huidekoper HH, Williams M, Wilke M, Verhoeven VJM, Joosten M, Kievit AJA, van de Laar IMBH, Hoefsloot LH, Hoogeveen-Westerveld M, Nellist M, Mancini GMS, van Ham TJ. Dekker J, et al. Among authors: van ham tj. Am J Hum Genet. 2023 Feb 2;110(2):251-272. doi: 10.1016/j.ajhg.2022.12.015. Epub 2023 Jan 19. Am J Hum Genet. 2023. PMID: 36669495 Free PMC article.
Myelination generates aberrant ultrastructure that is resolved by microglia.
Djannatian M, Radha S, Weikert U, Safaiyan S, Wrede C, Deichsel C, Kislinger G, Rhomberg A, Ruhwedel T, Campbell DS, van Ham T, Schmid B, Hegermann J, Möbius W, Schifferer M, Simons M. Djannatian M, et al. Among authors: van ham t. J Cell Biol. 2023 Mar 6;222(3):e202204010. doi: 10.1083/jcb.202204010. Epub 2023 Jan 13. J Cell Biol. 2023. PMID: 36637807 Free PMC article.
180 results