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Items: 1 to 50 of 57

1.

The regulatory landscape of a core maize domestication module controlling bud dormancy and growth repression.

Dong Z, Xiao Y, Govindarajulu R, Feil R, Siddoway ML, Nielsen T, Lunn JE, Hawkins J, Whipple C, Chuck G.

Nat Commun. 2019 Aug 23;10(1):3810. doi: 10.1038/s41467-019-11774-w.

2.

Understanding Grass Domestication through Maize Mutants.

Dong Z, Alexander M, Chuck G.

Trends Genet. 2019 Feb;35(2):118-128. doi: 10.1016/j.tig.2018.10.007. Epub 2018 Nov 30. Review.

PMID:
30509788
3.

Early-life events associated with first-lactation performance in pasture-based dairy herds.

Chuck GM, Mansell PD, Stevenson MA, Izzo MM.

J Dairy Sci. 2018 Apr;101(4):3488-3500. doi: 10.3168/jds.2017-12626. Epub 2018 Feb 13.

4.

Factors affecting colostrum quality in Australian pasture-based dairy herds.

Chuck GM, Mansell PD, Stevenson MA, Izzo MM.

Aust Vet J. 2017 Nov;95(11):421-426. doi: 10.1111/avj.12643.

PMID:
29076220
5.

Ideal crop plant architecture is mediated by tassels replace upper ears1, a BTB/POZ ankyrin repeat gene directly targeted by TEOSINTE BRANCHED1.

Dong Z, Li W, Unger-Wallace E, Yang J, Vollbrecht E, Chuck G.

Proc Natl Acad Sci U S A. 2017 Oct 10;114(41):E8656-E8664. doi: 10.1073/pnas.1714960114. Epub 2017 Sep 27.

6.

microRNA172 plays a crucial role in wheat spike morphogenesis and grain threshability.

Debernardi JM, Lin H, Chuck G, Faris JD, Dubcovsky J.

Development. 2017 Jun 1;144(11):1966-1975. doi: 10.1242/dev.146399. Epub 2017 Apr 28.

7.

Maize SBP-box transcription factors unbranched2 and unbranched3 affect yield traits by regulating the rate of lateral primordia initiation.

Chuck GS, Brown PJ, Meeley R, Hake S.

Proc Natl Acad Sci U S A. 2014 Dec 30;111(52):18775-80. doi: 10.1073/pnas.1407401112. Epub 2014 Dec 15.

8.
9.

Brassinosteroid control of sex determination in maize.

Hartwig T, Chuck GS, Fujioka S, Klempien A, Weizbauer R, Potluri DP, Choe S, Johal GS, Schulz B.

Proc Natl Acad Sci U S A. 2011 Dec 6;108(49):19814-9. doi: 10.1073/pnas.1108359108. Epub 2011 Nov 21.

10.

Overexpression of the maize Corngrass1 microRNA prevents flowering, improves digestibility, and increases starch content of switchgrass.

Chuck GS, Tobias C, Sun L, Kraemer F, Li C, Dibble D, Arora R, Bragg JN, Vogel JP, Singh S, Simmons BA, Pauly M, Hake S.

Proc Natl Acad Sci U S A. 2011 Oct 18;108(42):17550-5. doi: 10.1073/pnas.1113971108. Epub 2011 Oct 10. Erratum in: Proc Natl Acad Sci U S A. 2012 Jan 17;109(3):995.

11.

From organelle to organ: ZRIZI MATE-Type transporter is an organelle transporter that enhances organ initiation.

Burko Y, Geva Y, Refael-Cohen A, Shleizer-Burko S, Shani E, Berger Y, Halon E, Chuck G, Moshelion M, Ori N.

Plant Cell Physiol. 2011 Mar;52(3):518-27. doi: 10.1093/pcp/pcr007. Epub 2011 Jan 20.

PMID:
21257605
12.

The unique relationship between tsh4 and ra2 in patterning floral phytomers.

Chuck G, Bortiri E.

Plant Signal Behav. 2010 Aug;5(8):979-81. Epub 2010 Aug 1.

13.

The maize SBP-box transcription factor encoded by tasselsheath4 regulates bract development and the establishment of meristem boundaries.

Chuck G, Whipple C, Jackson D, Hake S.

Development. 2010 Apr;137(8):1243-50. doi: 10.1242/dev.048348. Epub 2010 Mar 10. Erratum in: Development. 2010 May;137(9):1585.

14.

Small RNAs going the distance during plant development.

Chuck G, O'Connor D.

Curr Opin Plant Biol. 2010 Feb;13(1):40-5. doi: 10.1016/j.pbi.2009.08.006. Epub 2009 Sep 30. Review.

PMID:
19796985
15.

Big impacts by small RNAs in plant development.

Chuck G, Candela H, Hake S.

Curr Opin Plant Biol. 2009 Feb;12(1):81-6. doi: 10.1016/j.pbi.2008.09.008. Epub 2008 Nov 6. Review.

PMID:
18980858
16.

Floral meristem initiation and meristem cell fate are regulated by the maize AP2 genes ids1 and sid1.

Chuck G, Meeley R, Hake S.

Development. 2008 Sep;135(18):3013-9. doi: 10.1242/dev.024273. Epub 2008 Aug 13.

17.

Screening of male patients with autism spectrum disorder for creatine transporter deficiency.

Newmeyer A, deGrauw T, Clark J, Chuck G, Salomons G.

Neuropediatrics. 2007 Dec;38(6):310-2. doi: 10.1055/s-2008-1065353.

PMID:
18461508
18.

Sirolimus for angiomyolipoma in tuberous sclerosis complex or lymphangioleiomyomatosis.

Bissler JJ, McCormack FX, Young LR, Elwing JM, Chuck G, Leonard JM, Schmithorst VJ, Laor T, Brody AS, Bean J, Salisbury S, Franz DN.

N Engl J Med. 2008 Jan 10;358(2):140-51. doi: 10.1056/NEJMoa063564.

19.

The maize tasselseed4 microRNA controls sex determination and meristem cell fate by targeting Tasselseed6/indeterminate spikelet1.

Chuck G, Meeley R, Irish E, Sakai H, Hake S.

Nat Genet. 2007 Dec;39(12):1517-21. Epub 2007 Nov 18.

PMID:
18026103
20.

The heterochronic maize mutant Corngrass1 results from overexpression of a tandem microRNA.

Chuck G, Cigan AM, Saeteurn K, Hake S.

Nat Genet. 2007 Apr;39(4):544-9. Epub 2007 Mar 18.

PMID:
17369828
21.

Levetiracetam as adjunctive antiepileptic therapy for patients with tuberous sclerosis complex: a retrospective open-label trial.

Collins JJ, Tudor C, Leonard JM, Chuck G, Franz DN.

J Child Neurol. 2006 Jan;21(1):53-7.

PMID:
16551454
22.

Rapamycin causes regression of astrocytomas in tuberous sclerosis complex.

Franz DN, Leonard J, Tudor C, Chuck G, Care M, Sethuraman G, Dinopoulos A, Thomas G, Crone KR.

Ann Neurol. 2006 Mar;59(3):490-8.

PMID:
16453317
23.

ramosa2 encodes a LATERAL ORGAN BOUNDARY domain protein that determines the fate of stem cells in branch meristems of maize.

Bortiri E, Chuck G, Vollbrecht E, Rocheford T, Martienssen R, Hake S.

Plant Cell. 2006 Mar;18(3):574-85. Epub 2006 Jan 6.

24.

Glycine decarboxylase mutations: a distinctive phenotype of nonketotic hyperglycinemia in adults.

Dinopoulos A, Kure S, Chuck G, Sato K, Gilbert DL, Matsubara Y, Degrauw T.

Neurology. 2005 Apr 12;64(7):1255-7.

PMID:
15824356
25.

Regulation of developmental transitions.

Chuck G, Hake S.

Curr Opin Plant Biol. 2005 Feb;8(1):67-70.

PMID:
15653402
26.

Presence of normal creatine in the muscle of a patient with a mutation in the creatine transporter: a case study.

Pyne-Geithman GJ, deGrauw TJ, Cecil KM, Chuck G, Lyons MA, Ishida Y, Clark JF.

Mol Cell Biochem. 2004 Jul;262(1-2):35-9.

PMID:
15532707
27.

Congenital creatine transporter deficiency.

deGrauw TJ, Salomons GS, Cecil KM, Chuck G, Newmeyer A, Schapiro MB, Jakobs C.

Neuropediatrics. 2002 Oct;33(5):232-8.

PMID:
12536364
28.

The control of spikelet meristem identity by the branched silkless1 gene in maize.

Chuck G, Muszynski M, Kellogg E, Hake S, Schmidt RJ.

Science. 2002 Nov 8;298(5596):1238-41.

29.

KNAT1 and ERECTA regulate inflorescence architecture in Arabidopsis.

Douglas SJ, Chuck G, Dengler RE, Pelecanda L, Riggs CD.

Plant Cell. 2002 Mar;14(3):547-58.

30.

Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle.

Bissler JJ, Tsoras M, Göring HH, Hug P, Chuck G, Tombragel E, McGraw C, Schlotman J, Ralston MA, Hug G.

Lab Invest. 2002 Mar;82(3):335-44.

PMID:
11896212
31.

Pulmonary cysts consistent with lymphangioleiomyomatosis are common in women with tuberous sclerosis: genetic and radiographic analysis.

McCormack F, Brody A, Meyer C, Leonard J, Chuck G, Dabora S, Sethuraman G, Colby TV, Kwiatkowski DJ, Franz DN.

Chest. 2002 Mar;121(3 Suppl):61S. No abstract available.

PMID:
11893688
32.

Anticoagulant effects on plasma coenzyme Q(10) estimated by HPLC with coulometric detection.

Tang PH, Miles MV, Steele P, DeGrauw A, Chuck G, Schroer L, Pesce A.

Clin Chim Acta. 2002 Apr;318(1-2):127-31.

PMID:
11880122
33.

Mutational and radiographic analysis of pulmonary disease consistent with lymphangioleiomyomatosis and micronodular pneumocyte hyperplasia in women with tuberous sclerosis.

Franz DN, Brody A, Meyer C, Leonard J, Chuck G, Dabora S, Sethuraman G, Colby TV, Kwiatkowski DJ, McCormack FX.

Am J Respir Crit Care Med. 2001 Aug 15;164(4):661-8.

PMID:
11520734
34.

Irreversible brain creatine deficiency with elevated serum and urine creatine: a creatine transporter defect?

Cecil KM, Salomons GS, Ball WS Jr, Wong B, Chuck G, Verhoeven NM, Jakobs C, DeGrauw TJ.

Ann Neurol. 2001 Mar;49(3):401-4.

PMID:
11261517
35.

Mechanisms that control knox gene expression in the Arabidopsis shoot.

Ori N, Eshed Y, Chuck G, Bowman JL, Hake S.

Development. 2000 Dec;127(24):5523-32.

36.
37.

Biochemical and molecular analysis in a patient with the severe form of Hunter syndrome after bone marrow transplantation.

Li P, Thompson JN, Hug G, Huffman P, Chuck G.

Am J Med Genet. 1996 Sep 6;64(4):531-5.

PMID:
8870917
38.
39.

Homeobox genes in the functioning of plant meristems.

Hake S, Char BR, Chuck G, Foster T, Long J, Jackson D.

Philos Trans R Soc Lond B Biol Sci. 1995 Oct 30;350(1331):45-51. Review.

PMID:
8577849
40.

Weanling and adult rats differ in fatty acid and carnitine metabolism during sepsis.

Linz DN, Garcia VF, Arya G, Hug G, Tombragel E, Landrigan E, Chuck G, Tsoras M, Ryan M, Ziegler MM.

J Pediatr Surg. 1995 Jul;30(7):959-65; discussion 966.

PMID:
7472953
41.

Tagging and Cloning of a Petunia Flower Color Gene with the Maize Transposable Element Activator.

Chuck G, Robbins T, Nijjar C, Ralston E, Courtney-Gutterson N, Dooner HK.

Plant Cell. 1993 Apr;5(4):371-378.

42.

Chorionic villus ultrastructure in type II glycogen storage disease (Pompe's disease)

Hug G, Chuck G, Chen YT, Kay HH, Bossen EH.

N Engl J Med. 1991 Jan 31;324(5):342-3. No abstract available.

PMID:
1986298
44.

Rapid prenatal diagnosis of glycogen-storage disease type II by electron microscopy of uncultured amniotic-fluid cells.

Hug G, Soukup S, Ryan M, Chuck G.

N Engl J Med. 1984 Apr 19;310(16):1018-22.

PMID:
6369132
45.

Membranoproliferative glomerulonephritis and alpha 1-antitrypsin deficiency in children.

Strife CF, Hug G, Chuck G, McAdams AJ, Davis CA, Kline JJ.

Pediatrics. 1983 Jan;71(1):88-92.

PMID:
6600289
46.

A study of the relationship of alpha 1-antitrypsin phenotype to the occurrence and severity of juvenile rheumatoid arthritis.

Crowe WE, Hug G, Chuck G, Knapp DS, Levinson JE.

Arthritis Rheum. 1982 Aug;25(8):1010-2. No abstract available.

PMID:
6981415
47.
48.

Pi Wfinneytown: a new alpha1-antitrypsin allele in an American Negro family.

Hug G, Chuck G, McGill M.

Hum Hered. 1982;32(4):280-4. No abstract available.

PMID:
6982220
49.

PiPclifton: a new alpha 1-antitrypsin allele in an American Negro family.

Hug G, Chuck G, Fagerhol MK.

J Med Genet. 1981 Feb;18(1):43-5. No abstract available.

50.

PiZpratt: a new alpha 1-antitrypsin allele in an American Negro family.

Hug G, Chuck G, Bowles B, Fagerhol MK.

Hum Genet. 1980;56(1):107-10.

PMID:
6970715

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