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

Year Number of Results
1952 1
1954 1
1964 1
1972 2
1975 2
1976 3
1977 2
1978 1
1979 1
1980 2
1981 3
1982 2
1983 6
1984 10
1985 10
1986 11
1987 20
1988 35
1989 37
1990 31
1991 36
1992 47
1993 54
1994 54
1995 48
1996 62
1997 71
1998 74
1999 117
2000 104
2001 111
2002 132
2003 130
2004 131
2005 164
2006 190
2007 168
2008 203
2009 191
2010 181
2011 200
2012 213
2013 235
2014 360
2015 423
2016 409
2017 405
2018 383
2019 375
2020 318
2021 252
2022 209
2023 199
2024 74

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5,812 results

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Page 1
Showing results for marie rodent
Search for Marie Grodent instead (1 results)
What constitutes the prefrontal cortex?
Carlén M. Carlén M. Science. 2017 Oct 27;358(6362):478-482. doi: 10.1126/science.aan8868. Science. 2017. PMID: 29074767 Review.
TGFbeta4 alleviates the phenotype of Charcot-Marie-Tooth disease type 1A.
Jeon H, Jang SY, Kwak G, Yi YW, You MH, Park NY, Jo JH, Yang JW, Jang HJ, Jeong SY, Moon SK, Doo HM, Nahm M, Kim D, Chang JW, Choi BO, Hong YB. Jeon H, et al. Brain. 2023 Sep 1;146(9):3608-3615. doi: 10.1093/brain/awad147. Brain. 2023. PMID: 37143322
The duplication of the peripheral myelin protein 22 (PMP22) gene causes a demyelinating type of neuropathy, commonly known as Charcot-Marie-Tooth disease type 1A (CMT1A). Development of effective drugs for CMT1A still remains as an unmet medical need. ...
The duplication of the peripheral myelin protein 22 (PMP22) gene causes a demyelinating type of neuropathy, commonly known as Charcot-Mar
tRNA overexpression rescues peripheral neuropathy caused by mutations in tRNA synthetase.
Zuko A, Mallik M, Thompson R, Spaulding EL, Wienand AR, Been M, Tadenev ALD, van Bakel N, Sijlmans C, Santos LA, Bussmann J, Catinozzi M, Das S, Kulshrestha D, Burgess RW, Ignatova Z, Storkebaum E. Zuko A, et al. Science. 2021 Sep 3;373(6559):1161-1166. doi: 10.1126/science.abb3356. Epub 2021 Sep 1. Science. 2021. PMID: 34516840 Free PMC article.
Heterozygous mutations in six transfer RNA (tRNA) synthetase genes cause Charcot-Marie-Tooth (CMT) peripheral neuropathy. CMT mutant tRNA synthetases inhibit protein synthesis by an unknown mechanism. ...
Heterozygous mutations in six transfer RNA (tRNA) synthetase genes cause Charcot-Marie-Tooth (CMT) peripheral neuropathy. CMT mutant …
Charcot-Marie-Tooth 2F (Hsp27 mutations): A review.
Schwartz NU. Schwartz NU. Neurobiol Dis. 2019 Oct;130:104505. doi: 10.1016/j.nbd.2019.104505. Epub 2019 Jun 15. Neurobiol Dis. 2019. PMID: 31212070 Review.
Charcot-Marie-Tooth disease is a commonly inherited form of neuropathy. Although named over 100 years ago, identification of subtypes of Charcot-Marie-Tooth has rapidly expanded in the preceding decades with the advancement of genetic sequencing, including type 2F ( …
Charcot-Marie-Tooth disease is a commonly inherited form of neuropathy. Although named over 100 years ago, identification of subtypes …
Understanding neuromyotonia.
Vincent A. Vincent A. Muscle Nerve. 2000 May;23(5):655-7. doi: 10.1002/(sici)1097-4598(200005)23:5<655::aid-mus1>3.0.co;2-e. Muscle Nerve. 2000. PMID: 10797387 Review. No abstract available.
Regulation of the Methylation and Expression Levels of the BMPR2 Gene by SIN3a as a Novel Therapeutic Mechanism in Pulmonary Arterial Hypertension.
Bisserier M, Mathiyalagan P, Zhang S, Elmastour F, Dorfmüller P, Humbert M, David G, Tarzami S, Weber T, Perros F, Sassi Y, Sahoo S, Hadri L. Bisserier M, et al. Circulation. 2021 Jul 6;144(1):52-73. doi: 10.1161/CIRCULATIONAHA.120.047978. Epub 2021 Jun 3. Circulation. 2021. PMID: 34078089 Free PMC article.
It is interesting that we detected a dysregulation of SIN3 expression in patients and in rodent models, which is strongly associated with decreased BMPR2 expression. ...Last, we identified intratracheal delivery of adeno-associated virus serotype human SIN3a to be a benefi …
It is interesting that we detected a dysregulation of SIN3 expression in patients and in rodent models, which is strongly associated …
Acute stress induces long-term metabolic, functional, and structural remodeling of the heart.
Yoganathan T, Perez-Liva M, Balvay D, Le Gall M, Lallemand A, Certain A, Autret G, Mokrani Y, Guillonneau F, Bruce J, Nguyen V, Gencer U, Schmitt A, Lager F, Guilbert T, Bruneval P, Vilar J, Maissa N, Mousseaux E, Viel T, Renault G, Kachenoura N, Tavitian B. Yoganathan T, et al. Nat Commun. 2023 Jun 28;14(1):3835. doi: 10.1038/s41467-023-39590-3. Nat Commun. 2023. PMID: 37380648 Free PMC article.
Takotsubo was initially considered spontaneously reversible, but epidemiological studies revealed significant long-term morbidity and mortality, the reason for which is unknown. Here, we show in a female rodent model that a single pharmacological challenge creates a stress …
Takotsubo was initially considered spontaneously reversible, but epidemiological studies revealed significant long-term morbidity and mortal …
Rodent models of pheochromocytoma, parallels in rodent and human tumorigenesis.
Lussey-Lepoutre C, Buffet A, Morin A, Goncalves J, Favier J. Lussey-Lepoutre C, et al. Cell Tissue Res. 2018 May;372(2):379-392. doi: 10.1007/s00441-018-2797-y. Epub 2018 Feb 9. Cell Tissue Res. 2018. PMID: 29427052 Review.
Among them, only cluster 2-related predisposed models have been successful but grafted models are however available to study cluster 1-related tumors. In this review, we present an overview of existing rodent models targeting predisposition genes involved or not in human p …
Among them, only cluster 2-related predisposed models have been successful but grafted models are however available to study cluster 1-relat …
Humans: the ultimate animal models.
Reilly MM, Rossor AM. Reilly MM, et al. J Neurol Neurosurg Psychiatry. 2020 Nov;91(11):1132-1136. doi: 10.1136/jnnp-2020-323016. Epub 2020 Aug 7. J Neurol Neurosurg Psychiatry. 2020. PMID: 32769113 Free PMC article. Review. No abstract available.
5,812 results