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Items: 27

1.

A Microbe Associated with Sleep Revealed by a Novel Systems Genetic Analysis of the Microbiome in Collaborative Cross Mice.

Bubier JA, Philip VM, Quince C, Campbell J, Zhou Y, Vishnivetskaya T, Duvvuru S, Blair RH, Ndukum J, Donohue KD, Foster CM, Mellert DJ, Weinstock G, Culiat CT, O'Hara BF, Palumbo AV, Podar M, Chesler EJ.

Genetics. 2020 Mar;214(3):719-733. doi: 10.1534/genetics.119.303013. Epub 2020 Jan 2.

2.

Neural EGFL like 1 as a potential pro-chondrogenic, anti-inflammatory dual-functional disease-modifying osteoarthritis drug.

Li C, Zheng Z, Ha P, Jiang W, Berthiaume EA, Lee S, Mills Z, Pan H, Chen EC, Jiang J, Culiat CT, Zhang X, Ting K, Soo C.

Biomaterials. 2020 Jan;226:119541. doi: 10.1016/j.biomaterials.2019.119541. Epub 2019 Oct 12.

PMID:
31634652
3.

Neural EGFL-Like 1 Regulates Cartilage Maturation through Runt-Related Transcription Factor 3-Mediated Indian Hedgehog Signaling.

Li C, Zheng Z, Jiang J, Jiang W, Lee K, Berthiaume EA, Chen EC, Culiat CT, Zhou YH, Zhang X, Ting K, Soo C.

Am J Pathol. 2018 Feb;188(2):392-403. doi: 10.1016/j.ajpath.2017.09.020. Epub 2017 Nov 11.

4.

NELL-1 induces Sca-1+ mesenchymal progenitor cell expansion in models of bone maintenance and repair.

James AW, Shen J, Tsuei R, Nguyen A, Khadarian K, Meyers CA, Pan HC, Li W, Kwak JH, Asatrian G, Culiat CT, Lee M, Ting K, Zhang X, Soo C.

JCI Insight. 2017 Jun 15;2(12). pii: 92573. doi: 10.1172/jci.insight.92573. eCollection 2017 Jun 15.

5.

Neural EGFL-Like 1 Is a Downstream Regulator of Runt-Related Transcription Factor 2 in Chondrogenic Differentiation and Maturation.

Li C, Jiang J, Zheng Z, Lee KS, Zhou Y, Chen E, Culiat CT, Qiao Y, Chen X, Ting K, Zhang X, Soo C.

Am J Pathol. 2017 May;187(5):963-972. doi: 10.1016/j.ajpath.2016.12.026. Epub 2017 Mar 14.

6.

NELL-1 in the treatment of osteoporotic bone loss.

James AW, Shen J, Zhang X, Asatrian G, Goyal R, Kwak JH, Jiang L, Bengs B, Culiat CT, Turner AS, Seim Iii HB, Wu BM, Lyons K, Adams JS, Ting K, Soo C.

Nat Commun. 2015 Jun 17;6:7362. doi: 10.1038/ncomms8362.

7.

Human NELL1 protein augments constructive tissue remodeling with biologic scaffolds.

Turner NJ, Londono R, Dearth CL, Culiat CT, Badylak SF.

Cells Tissues Organs. 2013;198(4):249-65. doi: 10.1159/000356491. Epub 2013 Dec 7.

PMID:
24335144
8.

Calvarial cleidocraniodysplasia-like defects with ENU-induced Nell-1 deficiency.

Zhang X, Ting K, Pathmanathan D, Ko T, Chen W, Chen F, Lee H, James AW, Siu RK, Shen J, Culiat CT, Soo C.

J Craniofac Surg. 2012 Jan;23(1):61-6. doi: 10.1097/SCS.0b013e318240c8c4.

9.

NELL-1, an osteoinductive factor, is a direct transcriptional target of Osterix.

Chen F, Zhang X, Sun S, Zara JN, Zou X, Chiu R, Culiat CT, Ting K, Soo C.

PLoS One. 2011;6(9):e24638. doi: 10.1371/journal.pone.0024638. Epub 2011 Sep 13.

10.

Genetic analysis in the Collaborative Cross breeding population.

Philip VM, Sokoloff G, Ackert-Bicknell CL, Striz M, Branstetter L, Beckmann MA, Spence JS, Jackson BL, Galloway LD, Barker P, Wymore AM, Hunsicker PR, Durtschi DC, Shaw GS, Shinpock S, Manly KF, Miller DR, Donohue KD, Culiat CT, Churchill GA, Lariviere WR, Palmer AA, O'Hara BF, Voy BH, Chesler EJ.

Genome Res. 2011 Aug;21(8):1223-38. doi: 10.1101/gr.113886.110. Epub 2011 Jul 6.

11.

Nfatc2 is a primary response gene of Nell-1 regulating chondrogenesis in ATDC5 cells.

Chen W, Zhang X, Siu RK, Chen F, Shen J, Zara JN, Culiat CT, Tetradis S, Ting K, Soo C.

J Bone Miner Res. 2011 Jun;26(6):1230-41. doi: 10.1002/jbmr.314.

12.

Nell-1, a key functional mediator of Runx2, partially rescues calvarial defects in Runx2(+/-) mice.

Zhang X, Ting K, Bessette CM, Culiat CT, Sung SJ, Lee H, Chen F, Shen J, Wang JJ, Kuroda S, Soo C.

J Bone Miner Res. 2011 Apr;26(4):777-91. doi: 10.1002/jbmr.267.

13.

A targeted deleterious allele of the splicing factor SCNM1 in the mouse.

Howell VM, de Haan G, Bergren S, Jones JM, Culiat CT, Michaud EJ, Frankel WN, Meisler MH.

Genetics. 2008 Nov;180(3):1419-27. doi: 10.1534/genetics.108.094227. Epub 2008 Sep 14.

14.

The Collaborative Cross at Oak Ridge National Laboratory: developing a powerful resource for systems genetics.

Chesler EJ, Miller DR, Branstetter LR, Galloway LD, Jackson BL, Philip VM, Voy BH, Culiat CT, Threadgill DW, Williams RW, Churchill GA, Johnson DK, Manly KF.

Mamm Genome. 2008 Jun;19(6):382-9. doi: 10.1007/s00335-008-9135-8. Epub 2008 Aug 21.

15.

The near-naked hairless (Hr(N)) mutation disrupts hair formation but is not due to a mutation in the Hairless coding region.

Liu Y, Das S, Olszewski RE, Carpenter DA, Culiat CT, Sundberg JP, Soteropoulos P, Liu X, Doktycz MJ, Michaud EJ, Voy BH.

J Invest Dermatol. 2007 Jul;127(7):1605-14. Epub 2007 Mar 1.

16.

Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defects.

Desai J, Shannon ME, Johnson MD, Ruff DW, Hughes LA, Kerley MK, Carpenter DA, Johnson DK, Rinchik EM, Culiat CT.

Hum Mol Genet. 2006 Apr 15;15(8):1329-41. Epub 2006 Mar 14.

PMID:
16537572
17.

Functional and evolutionary analyses on expressed intronless genes in the mouse genome.

Sakharkar KR, Sakharkar MK, Culiat CT, Chow VT, Pervaiz S.

FEBS Lett. 2006 Feb 20;580(5):1472-8. Epub 2006 Jan 31.

18.

Efficient gene-driven germ-line point mutagenesis of C57BL/6J mice.

Michaud EJ, Culiat CT, Klebig ML, Barker PE, Cain KT, Carpenter DJ, Easter LL, Foster CM, Gardner AW, Guo ZY, Houser KJ, Hughes LA, Kerley MK, Liu Z, Olszewski RE, Pinn I, Shaw GD, Shinpock SG, Wymore AM, Rinchik EM, Johnson DK.

BMC Genomics. 2005 Nov 21;6:164.

19.

Identification of mutations from phenotype-driven ENU mutagenesis in mouse chromosome 7.

Culiat CT, Klebig ML, Liu Z, Monroe H, Stanford B, Desai J, Tandan S, Hughes L, Kerley MK, Carpenter DA, Johnson DK, Rinchik EM, Li Q.

Mamm Genome. 2005 Aug;16(8):555-66.

PMID:
16180137
20.

Heightened susceptibility to chronic gastritis, hyperplasia and metaplasia in Kcnq1 mutant mice.

Elso CM, Lu X, Culiat CT, Rutledge JC, Cacheiro NL, Generoso WM, Stubbs LJ.

Hum Mol Genet. 2004 Nov 15;13(22):2813-21. Epub 2004 Sep 22.

PMID:
15385447
21.

Integrated platform for detection of DNA sequence variants using capillary array electrophoresis.

Li Q, Liu Z, Monroe H, Culiat CT.

Electrophoresis. 2002 May;23(10):1499-511.

PMID:
12116161
22.

Point mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1.

Aponte JL, Sega GA, Hauser LJ, Dhar MS, Withrow CM, Carpenter DA, Rinchik EM, Culiat CT, Johnson DK.

Proc Natl Acad Sci U S A. 2001 Jan 16;98(2):641-5.

23.

Induced mouse chromosomal rearrangements as tools for identifying critical developmental genes and pathways.

Culiat CT, Carver EA, Walkowicz M, Rinchik EM, Cacheiro NL, Russell LB, Generoso WM, Stubbs L.

Reprod Toxicol. 1997 Mar-Jun;11(2-3):345-51. Review.

PMID:
9100310
24.

Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus.

Johnson DK, Stubbs LJ, Culiat CT, Montgomery CS, Russell LB, Rinchik EM.

Genetics. 1995 Dec;141(4):1563-71.

25.

Deficiency of the beta 3 subunit of the type A gamma-aminobutyric acid receptor causes cleft palate in mice.

Culiat CT, Stubbs LJ, Woychik RP, Russell LB, Johnson DK, Rinchik EM.

Nat Genet. 1995 Nov;11(3):344-6.

PMID:
7581464
26.

Phenotypic consequences of deletion of the gamma 3, alpha 5, or beta 3 subunit of the type A gamma-aminobutyric acid receptor in mice.

Culiat CT, Stubbs LJ, Montgomery CS, Russell LB, Rinchik EM.

Proc Natl Acad Sci U S A. 1994 Mar 29;91(7):2815-8.

27.

Concordance between isolated cleft palate in mice and alterations within a region including the gene encoding the beta 3 subunit of the type A gamma-aminobutyric acid receptor.

Culiat CT, Stubbs L, Nicholls RD, Montgomery CS, Russell LB, Johnson DK, Rinchik EM.

Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5105-9.

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