Browning MF - Search Results

1

Macroautophagy is defective in mucolipin-1-deficient mouse neurons.

Curcio-Morelli C, Charles FA, Micsenyi MC, Cao Y, Venugopal B, Browning MF, Dobrenis K, Cotman SL, Walkley SU, Slaugenhaupt SA. Curcio-Morelli C, et al. Among authors: browning mf. Neurobiol Dis. 2010 Nov;40(2):370-7. doi: 10.1016/j.nbd.2010.06.010. Epub 2010 Jun 28. Neurobiol Dis. 2010. PMID: 20600908 Free PMC article.

2

Neurologic, gastric, and opthalmologic pathologies in a murine model of mucolipidosis type IV.

Venugopal B, Browning MF, Curcio-Morelli C, Varro A, Michaud N, Nanthakumar N, Walkley SU, Pickel J, Slaugenhaupt SA. Venugopal B, et al. Among authors: browning mf. Am J Hum Genet. 2007 Nov;81(5):1070-83. doi: 10.1086/521954. Epub 2007 Oct 2. Am J Hum Genet. 2007. PMID: 17924347 Free PMC article.

3

Functional multimerization of mucolipin channel proteins.

Curcio-Morelli C, Zhang P, Venugopal B, Charles FA, Browning MF, Cantiello HF, Slaugenhaupt SA. Curcio-Morelli C, et al. Among authors: browning mf. J Cell Physiol. 2010 Feb;222(2):328-35. doi: 10.1002/jcp.21956. J Cell Physiol. 2010. PMID: 19885840

4

Normal acylcarnitine levels during confirmation of abnormal newborn screening in long-chain fatty acid oxidation defects.

Browning MF, Larson C, Strauss A, Marsden DL. Browning MF, et al. J Inherit Metab Dis. 2005;28(4):545-50. doi: 10.1007/s10545-005-0545-4. J Inherit Metab Dis. 2005. PMID: 15902557

5

A novel mutation in JARID1C/SMCX in a patient with autism spectrum disorder (ASD).

Adegbola A, Gao H, Sommer S, Browning M. Adegbola A, et al. Am J Med Genet A. 2008 Feb 15;146A(4):505-11. doi: 10.1002/ajmg.a.32142. Am J Med Genet A. 2008. PMID: 18203167

6

Fetal fatty acid oxidation defects and maternal liver disease in pregnancy.

Browning MF, Levy HL, Wilkins-Haug LE, Larson C, Shih VE. Browning MF, et al. Obstet Gynecol. 2006 Jan;107(1):115-20. doi: 10.1097/01.AOG.0000191297.47183.bd. Obstet Gynecol. 2006. PMID: 16394048

7

An evidence development process for newborn screening.

Perrin JM, Knapp AA, Browning MF, Comeau AM, Green NS, Lipstein EA, Metterville DR, Prosser L, Queally D, Kemper AR. Perrin JM, et al. Among authors: browning mf. Genet Med. 2010 Mar;12(3):131-4. doi: 10.1097/GIM.0b013e3181d28eb1. Genet Med. 2010. PMID: 20154629 Free article. Review. No abstract available.

8

Systematic evidence review of newborn screening and treatment of severe combined immunodeficiency.

Lipstein EA, Vorono S, Browning MF, Green NS, Kemper AR, Knapp AA, Prosser LA, Perrin JM. Lipstein EA, et al. Among authors: browning mf. Pediatrics. 2010 May;125(5):e1226-35. doi: 10.1542/peds.2009-1567. Epub 2010 Apr 19. Pediatrics. 2010. PMID: 20403930 Review.

9

Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay.

Wiśniowiecka-Kowalnik B, Nesteruk M, Peters SU, Xia Z, Cooper ML, Savage S, Amato RS, Bader P, Browning MF, Haun CL, Duda AW 3rd, Cheung SW, Stankiewicz P. Wiśniowiecka-Kowalnik B, et al. Among authors: browning mf. Am J Med Genet B Neuropsychiatr Genet. 2010 Jul;153B(5):983-93. doi: 10.1002/ajmg.b.31064. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20162629

10

Parents' decision-making in newborn screening: opinions, choices, and information needs.

Lipstein EA, Nabi E, Perrin JM, Luff D, Browning MF, Kuhlthau KA. Lipstein EA, et al. Among authors: browning mf. Pediatrics. 2010 Oct;126(4):696-704. doi: 10.1542/peds.2010-0217. Epub 2010 Sep 13. Pediatrics. 2010. PMID: 20837593

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