Kunkel LM - Search Results

1

Concordance between gene expression in peripheral whole blood and colonic tissue in children with inflammatory bowel disease.

Palmer NP, Silvester JA, Lee JJ, Beam AL, Fried I, Valtchinov VI, Rahimov F, Kong SW, Ghodoussipour S, Hood HC, Bousvaros A, Grand RJ, Kunkel LM, Kohane IS. Palmer NP, et al. Among authors: kunkel lm. PLoS One. 2019 Oct 16;14(10):e0222952. doi: 10.1371/journal.pone.0222952. eCollection 2019. PLoS One. 2019. PMID: 31618209 Free PMC article.

2

Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders.

Kong SW, Collins CD, Shimizu-Motohashi Y, Holm IA, Campbell MG, Lee IH, Brewster SJ, Hanson E, Harris HK, Lowe KR, Saada A, Mora A, Madison K, Hundley R, Egan J, McCarthy J, Eran A, Galdzicki M, Rappaport L, Kunkel LM, Kohane IS. Kong SW, et al. Among authors: kunkel lm. PLoS One. 2012;7(12):e49475. doi: 10.1371/journal.pone.0049475. Epub 2012 Dec 5. PLoS One. 2012. PMID: 23227143 Free PMC article.

3

Peripheral blood gene expression signature differentiates children with autism from unaffected siblings.

Kong SW, Shimizu-Motohashi Y, Campbell MG, Lee IH, Collins CD, Brewster SJ, Holm IA, Rappaport L, Kohane IS, Kunkel LM. Kong SW, et al. Among authors: kunkel lm. Neurogenetics. 2013 May;14(2):143-52. doi: 10.1007/s10048-013-0363-z. Epub 2013 Apr 28. Neurogenetics. 2013. PMID: 23625158 Free PMC article.

4

Gene expression profiling of Duchenne muscular dystrophy skeletal muscle.

Haslett JN, Sanoudou D, Kho AT, Han M, Bennett RR, Kohane IS, Beggs AH, Kunkel LM. Haslett JN, et al. Among authors: kunkel lm. Neurogenetics. 2003 Aug;4(4):163-71. doi: 10.1007/s10048-003-0148-x. Epub 2003 Apr 16. Neurogenetics. 2003. PMID: 12698323

5

Transcriptome-scale similarities between mouse and human skeletal muscles with normal and myopathic phenotypes.

Kho AT, Kang PB, Kohane IS, Kunkel LM. Kho AT, et al. Among authors: kunkel lm. BMC Musculoskelet Disord. 2006 Mar 7;7:23. doi: 10.1186/1471-2474-7-23. BMC Musculoskelet Disord. 2006. PMID: 16522209 Free PMC article.

6

Gene expression profiling of skeletal muscles treated with a soluble activin type IIB receptor.

Rahimov F, King OD, Warsing LC, Powell RE, Emerson CP Jr, Kunkel LM, Wagner KR. Rahimov F, et al. Among authors: kunkel lm. Physiol Genomics. 2011 Apr 27;43(8):398-407. doi: 10.1152/physiolgenomics.00223.2010. Epub 2011 Jan 25. Physiol Genomics. 2011. PMID: 21266502 Free PMC article.

7

Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers.

Rahimov F, King OD, Leung DG, Bibat GM, Emerson CP Jr, Kunkel LM, Wagner KR. Rahimov F, et al. Among authors: kunkel lm. Proc Natl Acad Sci U S A. 2012 Oct 2;109(40):16234-9. doi: 10.1073/pnas.1209508109. Epub 2012 Sep 17. Proc Natl Acad Sci U S A. 2012. PMID: 22988124 Free PMC article.

8

The cell biology of disease: cellular and molecular mechanisms underlying muscular dystrophy.

Rahimov F, Kunkel LM. Rahimov F, et al. Among authors: kunkel lm. J Cell Biol. 2013 May 13;201(4):499-510. doi: 10.1083/jcb.201212142. J Cell Biol. 2013. PMID: 23671309 Free PMC article. Review.

9

Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis.

Kong SW, Sahin M, Collins CD, Wertz MH, Campbell MG, Leech JD, Krueger D, Bear MF, Kunkel LM, Kohane IS. Kong SW, et al. Among authors: kunkel lm. Mol Autism. 2014 Feb 24;5(1):16. doi: 10.1186/2040-2392-5-16. Mol Autism. 2014. PMID: 24564913 Free PMC article.

10

Molecular profiles of inflammatory myopathies.

Greenberg SA, Sanoudou D, Haslett JN, Kohane IS, Kunkel LM, Beggs AH, Amato AA. Greenberg SA, et al. Among authors: kunkel lm. Neurology. 2002 Oct 22;59(8):1170-82. doi: 10.1212/wnl.59.8.1170. Neurology. 2002. PMID: 12391344

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