Rosenblatt DS - Search Results

1

Sacrificial Cobalt-Carbon Bond Homolysis in Coenzyme B₁₂ as a Cofactor Conservation Strategy.

Campanello GC, Ruetz M, Dodge GJ, Gouda H, Gupta A, Twahir UT, Killian MM, Watkins D, Rosenblatt DS, Brunold TC, Warncke K, Smith JL, Banerjee R. Campanello GC, et al. Among authors: rosenblatt ds. J Am Chem Soc. 2018 Oct 17;140(41):13205-13208. doi: 10.1021/jacs.8b08659. Epub 2018 Oct 8. J Am Chem Soc. 2018. PMID: 30282455 Free PMC article.

2

Lessons in biology from patients with inborn errors of vitamin B12 metabolism.

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Biochimie. 2013 May;95(5):1019-22. doi: 10.1016/j.biochi.2013.01.013. Epub 2013 Feb 10. Biochimie. 2013. PMID: 23402785 Review.

3

Allosteric Regulation of Oligomerization by a B₁₂ Trafficking G-Protein Is Corrupted in Methylmalonic Aciduria.

Ruetz M, Campanello GC, McDevitt L, Yokom AL, Yadav PK, Watkins D, Rosenblatt DS, Ohi MD, Southworth DR, Banerjee R. Ruetz M, et al. Among authors: rosenblatt ds. Cell Chem Biol. 2019 Jul 18;26(7):960-969.e4. doi: 10.1016/j.chembiol.2019.03.014. Epub 2019 May 2. Cell Chem Biol. 2019. PMID: 31056463 Free PMC article.

4

Inborn errors of cobalamin absorption and metabolism.

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Am J Med Genet C Semin Med Genet. 2011 Feb 15;157C(1):33-44. doi: 10.1002/ajmg.c.30288. Epub 2011 Feb 10. Am J Med Genet C Semin Med Genet. 2011. PMID: 21312325

5

Immunodeficiency and inborn disorders of vitamin B12 and folate metabolism.

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Curr Opin Clin Nutr Metab Care. 2020 Jul;23(4):241-246. doi: 10.1097/MCO.0000000000000668. Curr Opin Clin Nutr Metab Care. 2020. PMID: 32412981 Review.

6

Inherited defects of cobalamin metabolism.

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Vitam Horm. 2022;119:355-376. doi: 10.1016/bs.vh.2022.01.010. Epub 2022 Feb 21. Vitam Horm. 2022. PMID: 35337626

7

High resolution melting analysis of the MMAB gene in cblB patients and in those with undiagnosed methylmalonic aciduria.

Illson ML, Dempsey-Nunez L, Kent J, Huang Q, Brebner A, Raff ML, Watkins D, Gilfix BM, Wittwer CT, Rosenblatt DS. Illson ML, et al. Among authors: rosenblatt ds. Mol Genet Metab. 2013 Sep-Oct;110(1-2):86-9. doi: 10.1016/j.ymgme.2013.04.020. Epub 2013 May 4. Mol Genet Metab. 2013. PMID: 23707710

8

Lessons in biology from patients with inherited disorders of vitamin B12 and folate metabolism.

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Biochimie. 2016 Jul;126:3-5. doi: 10.1016/j.biochi.2016.05.001. Epub 2016 May 6. Biochimie. 2016. PMID: 27163846

9

Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity.

Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Am J Med Genet. 1989 Nov;34(3):427-34. doi: 10.1002/ajmg.1320340320. Am J Med Genet. 1989. PMID: 2688421 Review.

10

Complementation studies in the cblA class of inborn error of cobalamin metabolism: evidence for interallelic complementation and for a new complementation class (cblH).

Watkins D, Matiaszuk N, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. J Med Genet. 2000 Jul;37(7):510-3. doi: 10.1136/jmg.37.7.510. J Med Genet. 2000. PMID: 10882753 Free PMC article.

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