Knoblach S - Search Results

1

Extracellular microRNA signature in chronic kidney disease.

Muralidharan J, Ramezani A, Hubal M, Knoblach S, Shrivastav S, Karandish S, Scott R, Maxwell N, Ozturk S, Beddhu S, Kopp JB, Raj DS. Muralidharan J, et al. Among authors: knoblach s. Am J Physiol Renal Physiol. 2017 Jun 1;312(6):F982-F991. doi: 10.1152/ajprenal.00569.2016. Epub 2017 Jan 11. Am J Physiol Renal Physiol. 2017. PMID: 28077372 Free PMC article.

2

Circulating and urinary microRNA profile in focal segmental glomerulosclerosis: a pilot study.

Ramezani A, Devaney JM, Cohen S, Wing MR, Scott R, Knoblach S, Singhal R, Howard L, Kopp JB, Raj DS. Ramezani A, et al. Among authors: knoblach s. Eur J Clin Invest. 2015 Apr;45(4):394-404. doi: 10.1111/eci.12420. Eur J Clin Invest. 2015. PMID: 25682967 Free PMC article.

3

Novel Association of miR-451 with the Incidence of TEVG Stenosis in a Murine Model.

Hibino N, Best CA, Engle A, Ghimbovschi S, Knoblach S, Nath DS, Ishibashi N, Jonas RA. Hibino N, et al. Among authors: knoblach s. Tissue Eng Part A. 2016 Jan;22(1-2):75-82. doi: 10.1089/ten.TEA.2014.0664. Epub 2015 Dec 17. Tissue Eng Part A. 2016. PMID: 26573748 Free PMC article.

4

Gene expression profiling of experimental traumatic spinal cord injury as a function of distance from impact site and injury severity.

De Biase A, Knoblach SM, Di Giovanni S, Fan C, Molon A, Hoffman EP, Faden AI. De Biase A, et al. Among authors: knoblach sm. Physiol Genomics. 2005 Aug 11;22(3):368-81. doi: 10.1152/physiolgenomics.00081.2005. Epub 2005 Jun 7. Physiol Genomics. 2005. PMID: 15942019 Free article.

5

SRY-box containing gene 17 regulates the Wnt/β-catenin signaling pathway in oligodendrocyte progenitor cells.

Chew LJ, Shen W, Ming X, Senatorov VV Jr, Chen HL, Cheng Y, Hong E, Knoblach S, Gallo V. Chew LJ, et al. Among authors: knoblach s. J Neurosci. 2011 Sep 28;31(39):13921-35. doi: 10.1523/JNEUROSCI.3343-11.2011. J Neurosci. 2011. PMID: 21957254 Free PMC article.

6

Dysferlin deficiency shows compensatory induction of Rab27A/Slp2a that may contribute to inflammatory onset.

Kesari A, Fukuda M, Knoblach S, Bashir R, Nader GA, Rao D, Nagaraju K, Hoffman EP. Kesari A, et al. Among authors: knoblach s. Am J Pathol. 2008 Nov;173(5):1476-87. doi: 10.2353/ajpath.2008.080098. Epub 2008 Oct 2. Am J Pathol. 2008. PMID: 18832576 Free PMC article.

7

Characterization of dysferlin deficient SJL/J mice to assess preclinical drug efficacy: fasudil exacerbates muscle disease phenotype.

Rayavarapu S, Van der Meulen JH, Gordish-Dressman H, Hoffman EP, Nagaraju K, Knoblach SM. Rayavarapu S, et al. Among authors: knoblach sm. PLoS One. 2010 Sep 24;5(9):e12981. doi: 10.1371/journal.pone.0012981. PLoS One. 2010. PMID: 20886045 Free PMC article.

8

PAC1R Genotype to Phenotype Correlations in Autism Spectrum Disorder.

Goodrich M, Armour AC, Panchapakesan K, You X, Devaney J, Knoblach S, Sullivan CAW, Herrero MJ, Gupta AR, Vaidya CJ, Kenworthy L, Corbin JG. Goodrich M, et al. Among authors: knoblach s. Autism Res. 2019 Feb;12(2):200-211. doi: 10.1002/aur.2051. Epub 2018 Dec 17. Autism Res. 2019. PMID: 30556326 Free PMC article.

9

Global gene expression profiling in R155H knock-in murine model of VCP disease.

Nalbandian A, Ghimbovschi S, Wang Z, Knoblach S, Llewellyn KJ, Vesa J, Hoffman EP, Kimonis VE. Nalbandian A, et al. Among authors: knoblach s. Clin Transl Sci. 2015 Feb;8(1):8-16. doi: 10.1111/cts.12241. Epub 2014 Nov 12. Clin Transl Sci. 2015. PMID: 25388089 Free PMC article.

10

Specification of select hypothalamic circuits and innate behaviors by the embryonic patterning gene dbx1.

Sokolowski K, Esumi S, Hirata T, Kamal Y, Tran T, Lam A, Oboti L, Brighthaupt SC, Zaghlula M, Martinez J, Ghimbovschi S, Knoblach S, Pierani A, Tamamaki N, Shah NM, Jones KS, Corbin JG. Sokolowski K, et al. Among authors: knoblach s. Neuron. 2015 Apr 22;86(2):403-16. doi: 10.1016/j.neuron.2015.03.022. Epub 2015 Apr 9. Neuron. 2015. PMID: 25864637 Free PMC article.

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