Baker EK - Search Results

1

The cyclophilin homolog ninaA is required in the secretory pathway.

Colley NJ, Baker EK, Stamnes MA, Zuker CS. Colley NJ, et al. Among authors: baker ek. Cell. 1991 Oct 18;67(2):255-63. doi: 10.1016/0092-8674(91)90177-z. Cell. 1991. PMID: 1913822

2

The cyclophilin homolog NinaA functions as a chaperone, forming a stable complex in vivo with its protein target rhodopsin.

Baker EK, Colley NJ, Zuker CS. Baker EK, et al. EMBO J. 1994 Oct 17;13(20):4886-95. EMBO J. 1994. PMID: 7957056 Free PMC article.

3

Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration.

Colley NJ, Cassill JA, Baker EK, Zuker CS. Colley NJ, et al. Among authors: baker ek. Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):3070-4. doi: 10.1073/pnas.92.7.3070. Proc Natl Acad Sci U S A. 1995. PMID: 7708777 Free PMC article.

4

Genetic dissection of cyclophilin function. Saturation mutagenesis of the Drosophila cyclophilin homolog ninaA.

Ondek B, Hardy RW, Baker EK, Stamnes MA, Shieh BH, Zuker CS. Ondek B, et al. Among authors: baker ek. J Biol Chem. 1992 Aug 15;267(23):16460-6. J Biol Chem. 1992. PMID: 1644830

5

A mutation in the alpha subunit of the platelet integrin alphaIIbbeta3 identifies a novel region important for ligand binding.

Tozer EC, Baker EK, Ginsberg MH, Loftus JC. Tozer EC, et al. Among authors: baker ek. Blood. 1999 Feb 1;93(3):918-24. Blood. 1999. PMID: 9920841

6

A genetic analysis of integrin function: Glanzmann thrombasthenia in vitro.

Baker EK, Tozer EC, Pfaff M, Shattil SJ, Loftus JC, Ginsberg MH. Baker EK, et al. Proc Natl Acad Sci U S A. 1997 Mar 4;94(5):1973-8. doi: 10.1073/pnas.94.5.1973. Proc Natl Acad Sci U S A. 1997. PMID: 9050889 Free PMC article.

7

The characterization of distinct populations of murine skeletal cells that have different roles in B lymphopoiesis.

Green AC, Tjin G, Lee SC, Chalk AM, Straszkowski L, Kwang D, Baker EK, Quach JM, Kimura T, Wu J, Purton LE. Green AC, et al. Among authors: baker ek. Blood. 2021 Mar 30:blood.2020005865. doi: 10.1182/blood.2020005865. Online ahead of print. Blood. 2021. PMID: 33786586

8

Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.

Jarmolowicz AI, Baker EK, Bartlett E, Francis D, Ling L, Gamage D, Delatycki MB, Godler DE. Jarmolowicz AI, et al. Among authors: baker ek. Am J Med Genet A. 2021 May;185(5):1498-1503. doi: 10.1002/ajmg.a.62106. Epub 2021 Feb 5. Am J Med Genet A. 2021. PMID: 33544979

9

A protocol for cell therapy infusion in neonates.

Baker EK, Wallace EM, Davis PG, Malhotra A, Jacobs SE, Hooper SB, Lim R. Baker EK, et al. Stem Cells Transl Med. 2021 May;10(5):773-780. doi: 10.1002/sctm.20-0281. Epub 2021 Jan 6. Stem Cells Transl Med. 2021. PMID: 33405397 Free article.

10

Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders.

Baker EK, Butler MG, Hartin SN, Ling L, Bui M, Francis D, Rogers C, Field MJ, Slee J, Gamage D, Amor DJ, Godler DE. Baker EK, et al. Transl Psychiatry. 2020 Oct 29;10(1):362. doi: 10.1038/s41398-020-01034-7. Transl Psychiatry. 2020. PMID: 33116122 Free PMC article.

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