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Items: 20

1.

Response to Letter to the Editor: IGSF1 Deficiency Results in Human and Murine Somatotrope Neurosecretory Hyperfunction.

Joustra SD, Roelfsema F, Paul van Trotsenburg AS, Schneider HJ, Kosilek RP, Kroon HM, Logan JG, Butterfield NC, Zhou X, Toufaily C, Bak B, Turgeon MO, Brûlé E, Steyn FJ, Gurnell M, Koulouri O, Le Tissier P, Fontanaud P, Bassett JHD, Williams GR, Oostdijk W, Wit JM, Pereira AM, Biermasz NR, Bernard DJ, Schoenmakers N.

J Clin Endocrinol Metab. 2020 Mar 24. pii: dgaa147. doi: 10.1210/clinem/dgaa147. [Epub ahead of print] No abstract available.

PMID:
32211768
2.

IGSF1 Deficiency Results in Human and Murine Somatotrope Neurosecretory Hyperfunction.

Joustra SD, Roelfsema F, van Trotsenburg ASP, Schneider HJ, Kosilek RP, Kroon HM, Logan JG, Butterfield NC, Zhou X, Toufaily C, Bak B, Turgeon MO, Brûlé E, Steyn FJ, Gurnell M, Koulouri O, Le Tissier P, Fontanaud P, Duncan Bassett JH, Williams GR, Oostdijk W, Wit JM, Pereira AM, Biermasz NR, Bernard DJ, Schoenmakers N.

J Clin Endocrinol Metab. 2020 Mar 1;105(3). pii: dgz093. doi: 10.1210/clinem/dgz093.

3.

PYY is a negative regulator of bone mass and strength.

Leitch VD, Brassill MJ, Rahman S, Butterfield NC, Ma P, Logan JG, Boyde A, Evans H, Croucher PI, Batterham RL, Williams GR, Bassett JHD.

Bone. 2019 Oct;127:427-435. doi: 10.1016/j.bone.2019.07.011. Epub 2019 Jul 12.

4.

Author Correction: An atlas of genetic influences on osteoporosis in humans and mice.

Morris JA, Kemp JP, Youlten SE, Laurent L, Logan JG, Chai RC, Vulpescu NA, Forgetta V, Kleinman A, Mohanty ST, Sergio CM, Quinn J, Nguyen-Yamamoto L, Luco AL, Vijay J, Simon MM, Pramatarova A, Medina-Gomez C, Trajanoska K, Ghirardello EJ, Butterfield NC, Curry KF, Leitch VD, Sparkes PC, Adoum AT, Mannan NS, Komla-Ebri DSK, Pollard AS, Dewhurst HF, Hassall TAD, Beltejar MG; 23andMe Research Team, Adams DJ, Vaillancourt SM, Kaptoge S, Baldock P, Cooper C, Reeve J, Ntzani EE, Evangelou E, Ohlsson C, Karasik D, Rivadeneira F, Kiel DP, Tobias JH, Gregson CL, Harvey NC, Grundberg E, Goltzman D, Adams DJ, Lelliott CJ, Hinds DA, Ackert-Bicknell CL, Hsu YH, Maurano MT, Croucher PI, Williams GR, Bassett JHD, Evans DM, Richards JB.

Nat Genet. 2019 May;51(5):920. doi: 10.1038/s41588-019-0415-x.

PMID:
30988516
5.

Genetic and Pharmacological Targeting of Transcriptional Repression in Resistance to Thyroid Hormone Alpha.

Freudenthal B, Shetty S, Butterfield NC, Logan JG, Han CR, Zhu X, Astapova I, Hollenberg AN, Cheng SY, Bassett JHD, Williams GR.

Thyroid. 2019 May;29(5):726-734. doi: 10.1089/thy.2018.0399. Epub 2019 Mar 14.

6.

Quantitative X-Ray Imaging of Mouse Bone by Faxitron.

Butterfield NC, Logan JG, Waung J, Williams GR, Bassett JHD.

Methods Mol Biol. 2019;1914:559-569. doi: 10.1007/978-1-4939-8997-3_30.

PMID:
30729486
7.

Slc20a2, Encoding the Phosphate Transporter PiT2, Is an Important Genetic Determinant of Bone Quality and Strength.

Beck-Cormier S, Lelliott CJ, Logan JG, Lafont DT, Merametdjian L, Leitch VD, Butterfield NC, Protheroe HJ, Croucher PI, Baldock PA, Gaultier-Lintia A, Maugars Y, Nicolas G, Banse C, Normant S, Magne N, Gérardin E, Bon N, Sourice S, Guicheux J, Beck L, Williams GR, Bassett JHD.

J Bone Miner Res. 2019 Jun;34(6):1101-1114. doi: 10.1002/jbmr.3691. Epub 2019 Mar 19.

8.

An atlas of genetic influences on osteoporosis in humans and mice.

Morris JA, Kemp JP, Youlten SE, Laurent L, Logan JG, Chai RC, Vulpescu NA, Forgetta V, Kleinman A, Mohanty ST, Sergio CM, Quinn J, Nguyen-Yamamoto L, Luco AL, Vijay J, Simon MM, Pramatarova A, Medina-Gomez C, Trajanoska K, Ghirardello EJ, Butterfield NC, Curry KF, Leitch VD, Sparkes PC, Adoum AT, Mannan NS, Komla-Ebri DSK, Pollard AS, Dewhurst HF, Hassall TAD, Beltejar MG; 23andMe Research Team, Adams DJ, Vaillancourt SM, Kaptoge S, Baldock P, Cooper C, Reeve J, Ntzani EE, Evangelou E, Ohlsson C, Karasik D, Rivadeneira F, Kiel DP, Tobias JH, Gregson CL, Harvey NC, Grundberg E, Goltzman D, Adams DJ, Lelliott CJ, Hinds DA, Ackert-Bicknell CL, Hsu YH, Maurano MT, Croucher PI, Williams GR, Bassett JHD, Evans DM, Richards JB.

Nat Genet. 2019 Feb;51(2):258-266. doi: 10.1038/s41588-018-0302-x. Epub 2018 Dec 31. Erratum in: Nat Genet. 2019 May;51(5):920.

9.

Type 2 deiodinase polymorphism causes ER stress and hypothyroidism in the brain.

Jo S, Fonseca TL, Bocco BMLC, Fernandes GW, McAninch EA, Bolin AP, Da Conceição RR, Werneck-de-Castro JP, Ignacio DL, Egri P, Németh D, Fekete C, Bernardi MM, Leitch VD, Mannan NS, Curry KF, Butterfield NC, Bassett JHD, Williams GR, Gereben B, Ribeiro MO, Bianco AC.

J Clin Invest. 2019 Jan 2;129(1):230-245. doi: 10.1172/JCI123176. Epub 2018 Dec 3.

10.

Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.

Kemp JP, Morris JA, Medina-Gomez C, Forgetta V, Warrington NM, Youlten SE, Zheng J, Gregson CL, Grundberg E, Trajanoska K, Logan JG, Pollard AS, Sparkes PC, Ghirardello EJ, Allen R, Leitch VD, Butterfield NC, Komla-Ebri D, Adoum AT, Curry KF, White JK, Kussy F, Greenlaw KM, Xu C, Harvey NC, Cooper C, Adams DJ, Greenwood CMT, Maurano MT, Kaptoge S, Rivadeneira F, Tobias JH, Croucher PI, Ackert-Bicknell CL, Bassett JHD, Williams GR, Richards JB, Evans DM.

Nat Genet. 2017 Oct;49(10):1468-1475. doi: 10.1038/ng.3949. Epub 2017 Sep 4.

11.

Pitx1 determines characteristic hindlimb morphologies in cartilage micromass culture.

Butterfield NC, Qian C, Logan MPO.

PLoS One. 2017 Jul 26;12(7):e0180453. doi: 10.1371/journal.pone.0180453. eCollection 2017.

12.

Tbx5 Buffers Inherent Left/Right Asymmetry Ensuring Symmetric Forelimb Formation.

Sulaiman FA, Nishimoto S, Murphy GR, Kucharska A, Butterfield NC, Newbury-Ecob R, Logan MP.

PLoS Genet. 2016 Dec 19;12(12):e1006521. doi: 10.1371/journal.pgen.1006521. eCollection 2016 Dec.

13.

Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies.

Ashe A, Butterfield NC, Town L, Courtney AD, Cooper AN, Ferguson C, Barry R, Olsson F, Liem KF Jr, Parton RG, Wainwright BJ, Anderson KV, Whitelaw E, Wicking C.

Hum Mol Genet. 2012 Apr 15;21(8):1808-23. doi: 10.1093/hmg/ddr613. Epub 2012 Jan 6.

14.

The molecular regulation of vertebrate limb patterning.

Butterfield NC, McGlinn E, Wicking C.

Curr Top Dev Biol. 2010;90:319-41. doi: 10.1016/S0070-2153(10)90009-4.

PMID:
20691854
15.

Inactivation of Patched1 in the mouse limb has novel inhibitory effects on the chondrogenic program.

Bruce SJ, Butterfield NC, Metzis V, Town L, McGlinn E, Wicking C.

J Biol Chem. 2010 Sep 3;285(36):27967-81. doi: 10.1074/jbc.M109.091785. Epub 2010 Jun 24.

16.

The metalloendopeptidase gene Pitrm1 is regulated by hedgehog signaling in the developing mouse limb and is expressed in muscle progenitors.

Town L, McGlinn E, Fiorenza S, Metzis V, Butterfield NC, Richman JM, Wicking C.

Dev Dyn. 2009 Dec;238(12):3175-84. doi: 10.1002/dvdy.22126.

17.

Patched 1 is a crucial determinant of asymmetry and digit number in the vertebrate limb.

Butterfield NC, Metzis V, McGlinn E, Bruce SJ, Wainwright BJ, Wicking C.

Development. 2009 Oct;136(20):3515-24. doi: 10.1242/dev.037507.

18.

A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development.

Ashe A, Morgan DK, Whitelaw NC, Bruxner TJ, Vickaryous NK, Cox LL, Butterfield NC, Wicking C, Blewitt ME, Wilkins SJ, Anderson GJ, Cox TC, Whitelaw E.

Genome Biol. 2008;9(12):R182. doi: 10.1186/gb-2008-9-12-r182. Epub 2008 Dec 19.

19.

Expression of the NET family member Zfp503 is regulated by hedgehog and BMP signaling in the limb.

McGlinn E, Richman JM, Metzis V, Town L, Butterfield NC, Wainwright BJ, Wicking C.

Dev Dyn. 2008 Apr;237(4):1172-82. doi: 10.1002/dvdy.21508.

20.

Identification and analysis of novel genes expressed in the mouse embryonic facial primordia.

Bennetts JS, Fowles LF, Butterfield NC, Berkman JL, Teasdale RD, Simpson F, Wicking C.

Front Biosci. 2006 Sep 1;11:2631-46.

PMID:
16720340

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