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Correction: Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons.
Runge K, Mathieu R, Bugeon S, Lafi S, Beurrier C, Sahu S, Schaller F, Loubat A, Herault L, Gaillard S, Pallesi-Pocachard E, Montheil A, Bosio A, Rosenfeld JA, Hudson E, Lindstrom K, Mercimek-Andrews S, Jeffries L, van Haeringen A, Vanakker O, Van Hecke A, Amrom D, Küry S, Ratner C, Jethva R, Gamble C, Jacq B, Fasano L, Santpere G, Lorente-Galdos B, Sestan N, Gelot A, Giacuzz S, Goebbels S, Represa A, Cardoso C, Cremer H, de Chevigny A. Runge K, et al. Among authors: hudson e. Mol Psychiatry. 2021 Dec;26(12):7852. doi: 10.1038/s41380-021-01234-7. Mol Psychiatry. 2021. PMID: 34282265 Free PMC article. No abstract available.
Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons.
Runge K, Mathieu R, Bugeon S, Lafi S, Beurrier C, Sahu S, Schaller F, Loubat A, Herault L, Gaillard S, Pallesi-Pocachard E, Montheil A, Bosio A, Rosenfeld JA, Hudson E, Lindstrom K, Mercimek-Andrews S, Jeffries L, van Haeringen A, Vanakker O, Van Hecke A, Amrom D, Küry S, Ratner C, Jethva R, Gamble C, Jacq B, Fasano L, Santpere G, Lorente-Galdos B, Sestan N, Gelot A, Giacuzz S, Goebbels S, Represa A, Cardoso C, Cremer H, de Chevigny A. Runge K, et al. Among authors: hudson e. Mol Psychiatry. 2021 Nov;26(11):6125-6148. doi: 10.1038/s41380-021-01179-x. Epub 2021 Jun 29. Mol Psychiatry. 2021. PMID: 34188164 Free PMC article.
C4B deficiency in two siblings with IgA nephropathy.
Wyatt RJ, Schneider PD, Alpers CE, Hudson EC, Julian BA. Wyatt RJ, et al. Among authors: hudson ec. Am J Kidney Dis. 1990 Jan;15(1):66-71. doi: 10.1016/s0272-6386(12)80594-4. Am J Kidney Dis. 1990. PMID: 2294735
Bf and C4 phenotypes in patients with psoriasis.
Wyatt RJ, Wang C, Hudson EC, Jones RM, Noah PW, Rosenberg EW. Wyatt RJ, et al. Among authors: hudson ec. Acta Derm Venereol Suppl (Stockh). 1989;146:211-3. Acta Derm Venereol Suppl (Stockh). 1989. PMID: 2609873
Complement phenotypes in patients with psoriasis.
Wyatt RJ, Wang C, Hudson EC, Jones RM, Noah PW, Rosenberg EW. Wyatt RJ, et al. Among authors: hudson ec. Hum Hered. 1989;39(6):327-32. doi: 10.1159/000153884. Hum Hered. 1989. PMID: 2613261
Complement activation in IgA nephropathy.
Wyatt RJ, Kanayama Y, Julian BA, Negoro N, Sugimoto S, Hudson EC, Curd JG. Wyatt RJ, et al. Among authors: hudson ec. Kidney Int. 1987 Apr;31(4):1019-23. doi: 10.1038/ki.1987.101. Kidney Int. 1987. PMID: 3586493 Free article.
Visium spatial transcriptomics and proteomics identifies novel hepatic cell populations and transcriptomic signatures of alcohol-associated hepatitis.
Gripshover TC, Treves RS, Rouchka EC, Chariker JH, Zheng S, Hudson E, Smith ML, Singal AK, McClain CJ, Hardesty JE. Gripshover TC, et al. Among authors: hudson e. Alcohol Clin Exp Res (Hoboken). 2024 Nov 26. doi: 10.1111/acer.15494. Online ahead of print. Alcohol Clin Exp Res (Hoboken). 2024. PMID: 39592394
516 results