PubMed for id: 462555

Year	Number of Results
1976	1
1983	1
1984	1
1988	1
1993	1
1995	1
2000	1
2008	1
2011	4
2012	1
2014	1
2015	1
2016	3
2017	1
2019	1
2021	1
2024	0

1

Dihydrofolate reductase deficiency due to a homozygous DHFR mutation causes megaloblastic anemia and cerebral folate deficiency leading to severe neurologic disease.

Cario H, Smith DE, Blom H, Blau N, Bode H, Holzmann K, Pannicke U, Hopfner KP, Rump EM, Ayric Z, Kohne E, Debatin KM, Smulders Y, Schwarz K. Cario H, et al. Am J Hum Genet. 2011 Feb 11;88(2):226-31. doi: 10.1016/j.ajhg.2011.01.007. Am J Hum Genet. 2011. PMID: 21310277 Free PMC article.

2

Identification and characterization of an inborn error of metabolism caused by dihydrofolate reductase deficiency.

Banka S, Blom HJ, Walter J, Aziz M, Urquhart J, Clouthier CM, Rice GI, de Brouwer AP, Hilton E, Vassallo G, Will A, Smith DE, Smulders YM, Wevers RA, Steinfeld R, Heales S, Crow YJ, Pelletier JN, Jones S, Newman WG. Banka S, et al. Am J Hum Genet. 2011 Feb 11;88(2):216-25. doi: 10.1016/j.ajhg.2011.01.004. Am J Hum Genet. 2011. PMID: 21310276 Free PMC article.

3

Conditional dihydrofolate reductase deficiency due to transposon Tn5tac1 insertion downstream from the folA gene in Escherichia coli.

Neuwald AF, Krishnan BR, Ahrweiler PM, Frieden C, Berg DE. Neuwald AF, et al. Gene. 1993 Mar 15;125(1):69-73. doi: 10.1016/0378-1119(93)90747-q. Gene. 1993. PMID: 8383626

4

Dihydrofolate reductase deficiency causing megaloblastic anemia in two families.

Tauro GP, Danks DM, Rowe PB, Van der Weyden MB, Schwarz MA, Collins VL, Neal BW. Tauro GP, et al. N Engl J Med. 1976 Feb 26;294(9):466-70. doi: 10.1056/NEJM197602262940903. N Engl J Med. 1976. PMID: 1060915

5

Targeting MicroRNA-192-5p, a Downstream Effector of NOXs (NADPH Oxidases), Reverses Endothelial DHFR (Dihydrofolate Reductase) Deficiency to Attenuate Abdominal Aortic Aneurysm Formation.

Huang K, Narumi T, Zhang Y, Li Q, Murugesan P, Wu Y, Liu NM, Cai H. Huang K, et al. Hypertension. 2021 Aug;78(2):282-293. doi: 10.1161/HYPERTENSIONAHA.120.15070. Epub 2021 Jun 28. Hypertension. 2021. PMID: 34176283 Free PMC article.

6

NOX isoforms in the development of abdominal aortic aneurysm.

Siu KL, Li Q, Zhang Y, Guo J, Youn JY, Du J, Cai H. Siu KL, et al. Redox Biol. 2017 Apr;11:118-125. doi: 10.1016/j.redox.2016.11.002. Epub 2016 Nov 19. Redox Biol. 2017. PMID: 27912196 Free PMC article.

7

Update and new concepts in vitamin responsive disorders of folate transport and metabolism.

Watkins D, Rosenblatt DS. Watkins D, et al. J Inherit Metab Dis. 2012 Jul;35(4):665-70. doi: 10.1007/s10545-011-9418-1. Epub 2011 Nov 23. J Inherit Metab Dis. 2012. PMID: 22108709 Review.

8

Supplementation of serum free media with HT is not sufficient to restore growth properties of DHFR-/- cells in fed-batch processes - Implications for designing novel CHO-based expression platforms.

Florin L, Lipske C, Becker E, Kaufmann H. Florin L, et al. J Biotechnol. 2011 Apr 10;152(4):189-93. doi: 10.1016/j.jbiotec.2011.02.002. Epub 2011 Feb 21. J Biotechnol. 2011. PMID: 21345355

9

Identification of Cryptosporidium parvum dihydrofolate reductase inhibitors by complementation in Saccharomyces cerevisiae.

Brophy VH, Vasquez J, Nelson RG, Forney JR, Rosowsky A, Sibley CH. Brophy VH, et al. Antimicrob Agents Chemother. 2000 Apr;44(4):1019-28. doi: 10.1128/AAC.44.4.1019-1028.2000. Antimicrob Agents Chemother. 2000. PMID: 10722506 Free PMC article.

10

Congenital errors of folate metabolism.

Zittoun J. Zittoun J. Baillieres Clin Haematol. 1995 Sep;8(3):603-16. doi: 10.1016/s0950-3536(05)80222-7. Baillieres Clin Haematol. 1995. PMID: 8534963 Review.

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