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Developmental Dynamics : an Official Publication of the American Association of Anatomists|March 19, 2024
Disruption of Fuz in mouse embryos generates hypoplastic hindbrain development and reduced cranial nerve gangliaCarlo Donato Caiaffa, Yogeshwari S Ambekar, Manmohan Singh, et al.
The Journal of Clinical Investigation|May 17, 2016
Inhibition of SHP2 ameliorates the pathogenesis of systemic lupus erythematosusJianxun Wang, Masayuki Mizui, Li-Fan Zeng, et al.
British Journal of Pharmacology|February 25, 2003
Characterization of the anticonvulsant profile and enantioselective pharmacokinetics of the chiral valproylamide propylisopropyl acetamide in rodentsNina Isoherranen, Boris Yagen, José H Woodhead, et al.
Frontiers in Genetics|December 10, 2021
<i>Wnt1</i> Lineage Specific Deletion of <i>Gpr161</i> Results in Embryonic Midbrain Malformation and Failure of Craniofacial Skeletal DevelopmentSung-Eun Kim, Karla Robles-Lopez, Xuanye Cao, et al.
Nature Genetics|October 3, 1999
Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic developmentJ A Piedrahita, B Oetama, G D Bennett, et al.
BMC Genomics|April 11, 2008
Microarray analysis of E9.5 reduced folate carrier (RFC1; Slc19a1) knockout embryos reveals altered expression of genes in the cubilin-megalin multiligand endocytic receptor complexJanee Gelineau-van Waes, Joyce R Maddox, Lynette M Smith, et al.
American Journal of Medical Genetics|April 17, 1998
Lack of association between mutations in the folate receptor-alpha gene and spina bifidaR C Barber, G M Shaw, E J Lammer, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 11, 2009
Genetic or nutritional disorders in homocysteine or folate metabolism increase protein N-homocysteinylation in miceHieronim Jakubowski, Joanna Perla-Kaján, Richard H Finnell, et al.
Cerebrovascular Diseases Extra|October 17, 2019
Infarct Patterns in Patients with Atherosclerotic Vertebrobasilar Disease in Relation to HemodynamicsJoanna D Schaafsma, Frank L Silver, Scott E Kasner, et al.
Clinical Science (London, England : 1979)|November 1, 2016
Genetic analysis of rare coding mutations of <i>CELSR1-3</i> in congenital heart and neural tube defects in Chinese peopleXiaojin Qiao, Yahui Liu, Peiqiang Li, et al.
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