Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 97

1.

Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities.

Stewart M, Lau P, Banks G, Bains RS, Castroflorio E, Oliver PL, Dixon CL, Kruer MC, Kullmann DM, Acevedo-Arozena A, Wells SE, Corrochano S, Nolan PM.

Dis Model Mech. 2019 Jan 28. pii: dmm.036806. doi: 10.1242/dmm.036806. [Epub ahead of print]

2.

Differential roles for cryptochromes in the mammalian retinal clock.

Wong JCY, Smyllie NJ, Banks GT, Pothecary CA, Barnard AR, Maywood ES, Jagannath A, Hughes S, van der Horst GTJ, MacLaren RE, Hankins MW, Hastings MH, Nolan PM, Foster RG, Peirson SN.

FASEB J. 2018 Aug;32(8):4302-4314. doi: 10.1096/fj.201701165RR. Epub 2018 Mar 21.

3.

The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis.

Maggi S, Balzani E, Lassi G, Garcia-Garcia C, Plano A, Espinoza S, Mus L, Tinarelli F, Nolan PM, Gainetdinov RR, Balci F, Nieus T, Tucci V.

Sci Rep. 2017 Dec 19;7(1):17765. doi: 10.1038/s41598-017-18130-2.

4.

Disruption of the homeodomain transcription factor orthopedia homeobox (Otp) is associated with obesity and anxiety.

Moir L, Bochukova EG, Dumbell R, Banks G, Bains RS, Nolan PM, Scudamore C, Simon M, Watson KA, Keogh J, Henning E, Hendricks A, O'Rahilly S, Barroso I; UK10K consortium, Sullivan AE, Bersten DC, Whitelaw ML, Kirsch S, Bentley E, Farooqi IS, Cox RD.

Mol Metab. 2017 Nov;6(11):1419-1428. doi: 10.1016/j.molmet.2017.08.006. Epub 2017 Aug 24.

5.

Meta-analysis of transcriptomic datasets identifies genes enriched in the mammalian circadian pacemaker.

Brown LA, Williams J, Taylor L, Thomson RJ, Nolan PM, Foster RG, Peirson SN.

Nucleic Acids Res. 2017 Sep 29;45(17):9860-9873. doi: 10.1093/nar/gkx714.

6.

Inducible Knockout of Mouse Zfhx3 Emphasizes Its Key Role in Setting the Pace and Amplitude of the Adult Circadian Clock.

Wilcox AG, Vizor L, Parsons MJ, Banks G, Nolan PM.

J Biol Rhythms. 2017 Oct;32(5):433-443. doi: 10.1177/0748730417722631. Epub 2017 Aug 17.

7.

Phenotyping first-generation genome editing mutants: a new standard?

Teboul L, Murray SA, Nolan PM.

Mamm Genome. 2017 Aug;28(7-8):377-382. doi: 10.1007/s00335-017-9711-x. Epub 2017 Jul 29. Review.

8.

SNPs across time and space: population genomic signatures of founder events and epizootics in the House Finch (Haemorhous mexicanus).

Shultz AJ, Baker AJ, Hill GE, Nolan PM, Edwards SV.

Ecol Evol. 2016 Sep 28;6(20):7475-7489. doi: 10.1002/ece3.2444. eCollection 2016 Oct.

9.

Assessing mouse behaviour throughout the light/dark cycle using automated in-cage analysis tools.

Bains RS, Wells S, Sillito RR, Armstrong JD, Cater HL, Banks G, Nolan PM.

J Neurosci Methods. 2018 Apr 15;300:37-47. doi: 10.1016/j.jneumeth.2017.04.014. Epub 2017 Apr 26.

10.

A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies.

Banks G, Lassi G, Hoerder-Suabedissen A, Tinarelli F, Simon MM, Wilcox A, Lau P, Lawson TN, Johnson S, Rutman A, Sweeting M, Chesham JE, Barnard AR, Horner N, Westerberg H, Smith LB, Molnár Z, Hastings MH, Hirst RA, Tucci V, Nolan PM.

Mol Psychiatry. 2018 Mar;23(3):713-722. doi: 10.1038/mp.2017.54. Epub 2017 Apr 4.

11.

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.

Potter PK, Bowl MR, Jeyarajan P, Wisby L, Blease A, Goldsworthy ME, Simon MM, Greenaway S, Michel V, Barnard A, Aguilar C, Agnew T, Banks G, Blake A, Chessum L, Dorning J, Falcone S, Goosey L, Harris S, Haynes A, Heise I, Hillier R, Hough T, Hoslin A, Hutchison M, King R, Kumar S, Lad HV, Law G, MacLaren RE, Morse S, Nicol T, Parker A, Pickford K, Sethi S, Starbuck B, Stelma F, Cheeseman M, Cross SH, Foster RG, Jackson IJ, Peirson SN, Thakker RV, Vincent T, Scudamore C, Wells S, El-Amraoui A, Petit C, Acevedo-Arozena A, Nolan PM, Cox R, Mallon AM, Brown SD.

Nat Commun. 2016 Aug 18;7:12444. doi: 10.1038/ncomms12444.

12.

Analysis of Individual Mouse Activity in Group Housed Animals of Different Inbred Strains using a Novel Automated Home Cage Analysis System.

Bains RS, Cater HL, Sillito RR, Chartsias A, Sneddon D, Concas D, Keskivali-Bond P, Lukins TC, Wells S, Acevedo Arozena A, Nolan PM, Armstrong JD.

Front Behav Neurosci. 2016 Jun 10;10:106. doi: 10.3389/fnbeh.2016.00106. eCollection 2016.

13.

The Zfhx3-Mediated Axis Regulates Sleep and Interval Timing in Mice.

Balzani E, Lassi G, Maggi S, Sethi S, Parsons MJ, Simon M, Nolan PM, Tucci V.

Cell Rep. 2016 Jul 19;16(3):615-21. doi: 10.1016/j.celrep.2016.06.017. Epub 2016 Jun 30.

14.

Melanopsin Regulates Both Sleep-Promoting and Arousal-Promoting Responses to Light.

Pilorz V, Tam SK, Hughes S, Pothecary CA, Jagannath A, Hankins MW, Bannerman DM, Lightman SL, Vyazovskiy VV, Nolan PM, Foster RG, Peirson SN.

PLoS Biol. 2016 Jun 8;14(6):e1002482. doi: 10.1371/journal.pbio.1002482. eCollection 2016 Jun.

15.

Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy.

Madeo M, Stewart M, Sun Y, Sahir N, Wiethoff S, Chandrasekar I, Yarrow A, Rosenfeld JA, Yang Y, Cordeiro D, McCormick EM, Muraresku CC, Jepperson TN, McBeth LJ, Seidahmed MZ, El Khashab HY, Hamad M, Azzedine H, Clark K, Corrochano S, Wells S, Elting MW, Weiss MM, Burn S, Myers A, Landsverk M, Crotwell PL, Waisfisz Q, Wolf NI, Nolan PM, Padilla-Lopez S, Houlden H, Lifton R, Mane S, Singh BB, Falk MJ, Mercimek-Mahmutoglu S, Bilguvar K, Salih MA, Acevedo-Arozena A, Kruer MC.

Am J Hum Genet. 2016 Jun 2;98(6):1249-1255. doi: 10.1016/j.ajhg.2016.04.008. Epub 2016 May 26.

16.

Reciprocal interactions between circadian clocks and aging.

Banks G, Nolan PM, Peirson SN.

Mamm Genome. 2016 Aug;27(7-8):332-40. doi: 10.1007/s00335-016-9639-6. Epub 2016 May 2. Review.

17.

Early doors (Edo) mutant mouse reveals the importance of period 2 (PER2) PAS domain structure for circadian pacemaking.

Militi S, Maywood ES, Sandate CR, Chesham JE, Barnard AR, Parsons MJ, Vibert JL, Joynson GM, Partch CL, Hastings MH, Nolan PM.

Proc Natl Acad Sci U S A. 2016 Mar 8;113(10):2756-61. doi: 10.1073/pnas.1517549113. Epub 2016 Feb 22.

18.

The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven Axis.

Parsons MJ, Brancaccio M, Sethi S, Maywood ES, Satija R, Edwards JK, Jagannath A, Couch Y, Finelli MJ, Smyllie NJ, Esapa C, Butler R, Barnard AR, Chesham JE, Saito S, Joynson G, Wells S, Foster RG, Oliver PL, Simon MM, Mallon AM, Hastings MH, Nolan PM.

Cell. 2015 Jul 30;162(3):607-21. doi: 10.1016/j.cell.2015.06.060.

19.

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.

de Angelis MH, Nicholson G, Selloum M, White J, Morgan H, Ramirez-Solis R, Sorg T, Wells S, Fuchs H, Fray M, Adams DJ, Adams NC, Adler T, Aguilar-Pimentel A, Ali-Hadji D, Amann G, André P, Atkins S, Auburtin A, Ayadi A, Becker J, Becker L, Bedu E, Bekeredjian R, Birling MC, Blake A, Bottomley J, Bowl M, Brault V, Busch DH, Bussell JN, Calzada-Wack J, Cater H, Champy MF, Charles P, Chevalier C, Chiani F, Codner GF, Combe R, Cox R, Dalloneau E, Dierich A, Di Fenza A, Doe B, Duchon A, Eickelberg O, Esapa CT, El Fertak L, Feigel T, Emelyanova I, Estabel J, Favor J, Flenniken A, Gambadoro A, Garrett L, Gates H, Gerdin AK, Gkoutos G, Greenaway S, Glasl L, Goetz P, Da Cruz IG, Götz A, Graw J, Guimond A, Hans W, Hicks G, Hölter SM, Höfler H, Hancock JM, Hoehndorf R, Hough T, Houghton R, Hurt A, Ivandic B, Jacobs H, Jacquot S, Jones N, Karp NA, Katus HA, Kitchen S, Klein-Rodewald T, Klingenspor M, Klopstock T, Lalanne V, Leblanc S, Lengger C, le Marchand E, Ludwig T, Lux A, McKerlie C, Maier H, Mandel JL, Marschall S, Mark M, Melvin DG, Meziane H, Micklich K, Mittelhauser C, Monassier L, Moulaert D, Muller S, Naton B, Neff F, Nolan PM, Nutter LM, Ollert M, Pavlovic G, Pellegata NS, Peter E, Petit-Demoulière B, Pickard A, Podrini C, Potter P, Pouilly L, Puk O, Richardson D, Rousseau S, Quintanilla-Fend L, Quwailid MM, Racz I, Rathkolb B, Riet F, Rossant J, Roux M, Rozman J, Ryder E, Salisbury J, Santos L, Schäble KH, Schiller E, Schrewe A, Schulz H, Steinkamp R, Simon M, Stewart M, Stöger C, Stöger T, Sun M, Sunter D, Teboul L, Tilly I, Tocchini-Valentini GP, Tost M, Treise I, Vasseur L, Velot E, Vogt-Weisenhorn D, Wagner C, Walling A, Weber B, Wendling O, Westerberg H, Willershäuser M, Wolf E, Wolter A, Wood J, Wurst W, Yildirim AÖ, Zeh R, Zimmer A, Zimprich A; EUMODIC Consortium, Holmes C, Steel KP, Herault Y, Gailus-Durner V, Mallon AM, Brown SD.

Nat Genet. 2015 Sep;47(9):969-978. doi: 10.1038/ng.3360. Epub 2015 Jul 27.

20.

A twin and molecular genetics study of sleep paralysis and associated factors.

Denis D, French CC, Rowe R, Zavos HM, Nolan PM, Parsons MJ, Gregory AM.

J Sleep Res. 2015 Aug;24(4):438-46. doi: 10.1111/jsr.12282. Epub 2015 Feb 9.

21.

Social jetlag, obesity and metabolic disorder: investigation in a cohort study.

Parsons MJ, Moffitt TE, Gregory AM, Goldman-Mellor S, Nolan PM, Poulton R, Caspi A.

Int J Obes (Lond). 2015 May;39(5):842-8. doi: 10.1038/ijo.2014.201. Epub 2014 Dec 22.

22.

Sleep-like behavior and 24-h rhythm disruption in the Tc1 mouse model of Down syndrome.

Heise I, Fisher SP, Banks GT, Wells S, Peirson SN, Foster RG, Nolan PM.

Genes Brain Behav. 2015 Feb;14(2):209-16. doi: 10.1111/gbb.12198. Epub 2015 Feb 16.

23.

A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity.

Joyce PI, Mcgoldrick P, Saccon RA, Weber W, Fratta P, West SJ, Zhu N, Carter S, Phatak V, Stewart M, Simon M, Kumar S, Heise I, Bros-Facer V, Dick J, Corrochano S, Stanford MJ, Luong TV, Nolan PM, Meyer T, Brandner S, Bennett DL, Ozdinler PH, Greensmith L, Fisher EM, Acevedo-Arozena A.

Hum Mol Genet. 2015 Apr 1;24(7):1883-97. doi: 10.1093/hmg/ddu605. Epub 2014 Dec 2.

24.

Song characteristics track bill morphology along a gradient of urbanization in house finches (Haemorhous mexicanus).

Giraudeau M, Nolan PM, Black CE, Earl SR, Hasegawa M, McGraw KJ.

Front Zool. 2014 Nov 12;11(1):83. doi: 10.1186/s12983-014-0083-8. eCollection 2014.

25.

Genetic background influences age-related decline in visual and nonvisual retinal responses, circadian rhythms, and sleep.

Banks G, Heise I, Starbuck B, Osborne T, Wisby L, Potter P, Jackson IJ, Foster RG, Peirson SN, Nolan PM.

Neurobiol Aging. 2015 Jan;36(1):380-93. doi: 10.1016/j.neurobiolaging.2014.07.040. Epub 2014 Aug 2.

26.

Polymorphisms in the circadian expressed genes PER3 and ARNTL2 are associated with diurnal preference and GNβ3 with sleep measures.

Parsons MJ, Lester KJ, Barclay NL, Archer SN, Nolan PM, Eley TC, Gregory AM.

J Sleep Res. 2014 Oct;23(5):595-604. doi: 10.1111/jsr.12144. Epub 2014 Mar 17.

27.

Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features.

Tucci V, Kleefstra T, Hardy A, Heise I, Maggi S, Willemsen MH, Hilton H, Esapa C, Simon M, Buenavista MT, McGuffin LJ, Vizor L, Dodero L, Tsaftaris S, Romero R, Nillesen WN, Vissers LE, Kempers MJ, Vulto-van Silfhout AT, Iqbal Z, Orlando M, Maccione A, Lassi G, Farisello P, Contestabile A, Tinarelli F, Nieus T, Raimondi A, Greco B, Cantatore D, Gasparini L, Berdondini L, Bifone A, Gozzi A, Wells S, Nolan PM.

J Clin Invest. 2014 Apr;124(4):1468-82. doi: 10.1172/JCI70372. Epub 2014 Mar 10.

28.

Cognitive assessment of mice strains heterozygous for cell-adhesion genes reveals strain-specific alterations in timing.

Gallistel CR, Tucci V, Nolan PM, Schachner M, Jakovcevski I, Kheifets A, Barboza L.

Philos Trans R Soc Lond B Biol Sci. 2014 Jan 20;369(1637):20120464. doi: 10.1098/rstb.2012.0464. Print 2014 Mar 5.

29.

Early motor deficits in mouse disease models are reliably uncovered using an automated home-cage wheel-running system: a cross-laboratory validation.

Mandillo S, Heise I, Garbugino L, Tocchini-Valentini GP, Giuliani A, Wells S, Nolan PM.

Dis Model Mech. 2014 Mar;7(3):397-407. doi: 10.1242/dmm.013946. Epub 2014 Jan 13.

30.

Replication of Genome-Wide Association Studies (GWAS) loci for sleep in the British G1219 cohort.

Parsons MJ, Lester KJ, Barclay NL, Nolan PM, Eley TC, Gregory AM.

Am J Med Genet B Neuropsychiatr Genet. 2013 Jul;162B(5):431-8. doi: 10.1002/ajmg.b.32106.

PMID:
23780892
31.

Distinct and separable roles for endogenous CRY1 and CRY2 within the circadian molecular clockwork of the suprachiasmatic nucleus, as revealed by the Fbxl3(Afh) mutation.

Anand SN, Maywood ES, Chesham JE, Joynson G, Banks GT, Hastings MH, Nolan PM.

J Neurosci. 2013 Apr 24;33(17):7145-53. doi: 10.1523/JNEUROSCI.4950-12.2013.

32.

Clusterin regulates β-amyloid toxicity via Dickkopf-1-driven induction of the wnt-PCP-JNK pathway.

Killick R, Ribe EM, Al-Shawi R, Malik B, Hooper C, Fernandes C, Dobson R, Nolan PM, Lourdusamy A, Furney S, Lin K, Breen G, Wroe R, To AW, Leroy K, Causevic M, Usardi A, Robinson M, Noble W, Williamson R, Lunnon K, Kellie S, Reynolds CH, Bazenet C, Hodges A, Brion JP, Stephenson J, Simons JP, Lovestone S.

Mol Psychiatry. 2014 Jan;19(1):88-98. doi: 10.1038/mp.2012.163. Epub 2012 Nov 20.

33.

Retinal ganglion cell topography and spatial resolving power in penguins.

Coimbra JP, Nolan PM, Collin SP, Hart NS.

Brain Behav Evol. 2012;80(4):254-68. doi: 10.1159/000341901. Epub 2012 Oct 2.

34.

Generation of mouse mutants as tools in dissecting the molecular clock.

Anand SN, Edwards JK, Nolan PM.

Prog Brain Res. 2012;199:247-65. doi: 10.1016/B978-0-444-59427-3.00015-0.

PMID:
22877670
35.

Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours.

Keers R, Pedroso I, Breen G, Aitchison KJ, Nolan PM, Cichon S, Nöthen MM, Rietschel M, Schalkwyk LC, Fernandes C.

PLoS One. 2012;7(6):e38263. doi: 10.1371/journal.pone.0038263. Epub 2012 Jun 15.

36.

Tuning the period of the mammalian circadian clock: additive and independent effects of CK1εTau and Fbxl3Afh mutations on mouse circadian behavior and molecular pacemaking.

Maywood ES, Chesham JE, Meng QJ, Nolan PM, Loudon AS, Hastings MH.

J Neurosci. 2011 Jan 26;31(4):1539-44. doi: 10.1523/JNEUROSCI.4107-10.2011.

37.

Stringent requirement of a proper level of canonical WNT signalling activity for head formation in mouse embryo.

Fossat N, Jones V, Khoo PL, Bogani D, Hardy A, Steiner K, Mukhopadhyay M, Westphal H, Nolan PM, Arkell R, Tam PP.

Development. 2011 Feb;138(4):667-76. doi: 10.1242/dev.052803. Epub 2011 Jan 12.

38.

Assessment of Circadian and Light-Entrainable Parameters in Mice Using Wheel-Running Activity.

Banks GT, Nolan PM.

Curr Protoc Mouse Biol. 2011 Sep 1;1(3):369-81. doi: 10.1002/9780470942390.mo110123.

PMID:
26068996
39.

Overexpression of Fto leads to increased food intake and results in obesity.

Church C, Moir L, McMurray F, Girard C, Banks GT, Teboul L, Wells S, Brüning JC, Nolan PM, Ashcroft FM, Cox RD.

Nat Genet. 2010 Dec;42(12):1086-92. doi: 10.1038/ng.713. Epub 2010 Nov 14.

40.

An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy.

Achilli F, Bros-Facer V, Williams HP, Banks GT, AlQatari M, Chia R, Tucci V, Groves M, Nickols CD, Seburn KL, Kendall R, Cader MZ, Talbot K, van Minnen J, Burgess RW, Brandner S, Martin JE, Koltzenburg M, Greensmith L, Nolan PM, Fisher EM.

Dis Model Mech. 2009 Jul-Aug;2(7-8):359-73. doi: 10.1242/dmm.002527. Epub 2009 May 26.

41.

A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice.

Becker EB, Oliver PL, Glitsch MD, Banks GT, Achilli F, Hardy A, Nolan PM, Fisher EM, Davies KE.

Proc Natl Acad Sci U S A. 2009 Apr 21;106(16):6706-11. doi: 10.1073/pnas.0810599106. Epub 2009 Apr 7.

42.

Clocks go forward: progress in the molecular genetic analysis of rhythmic behaviour.

Nolan PM, Parsons MJ.

Mamm Genome. 2009 Feb;20(2):67-70. doi: 10.1007/s00335-008-9166-1. Epub 2009 Jan 15. Review.

PMID:
19145460
43.

Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse.

Tsipouri V, Curtin JA, Nolan PM, Vizor L, Parsons CA, Clapham CM, Latham ID, Rooke LJ, Martin JE, Peters J, Hunter AJ, Rogers D, Rastan S, Brown SD, Fisher EM, Spurr NK, Gray IC.

Comp Funct Genomics. 2004;5(2):123-7. doi: 10.1002/cfg.382.

44.

When clocks go bad: neurobehavioural consequences of disrupted circadian timing.

Barnard AR, Nolan PM.

PLoS Genet. 2008 May 30;4(5):e1000040. doi: 10.1371/journal.pgen.1000040. Review.

45.

Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study.

Mandillo S, Tucci V, Hölter SM, Meziane H, Banchaabouchi MA, Kallnik M, Lad HV, Nolan PM, Ouagazzal AM, Coghill EL, Gale K, Golini E, Jacquot S, Krezel W, Parker A, Riet F, Schneider I, Marazziti D, Auwerx J, Brown SD, Chambon P, Rosenthal N, Tocchini-Valentini G, Wurst W.

Physiol Genomics. 2008 Aug 15;34(3):243-55. doi: 10.1152/physiolgenomics.90207.2008. Epub 2008 May 27. Erratum in: Physiol Genomics. 2010 Feb,40(3):217.

46.

Genetic and molecular analysis of the central and peripheral circadian clockwork of mice.

Maywood ES, O'Neill JS, Reddy AB, Chesham JE, Prosser HM, Kyriacou CP, Godinho SI, Nolan PM, Hastings MH.

Cold Spring Harb Symp Quant Biol. 2007;72:85-94. doi: 10.1101/sqb.2007.72.005. Review.

PMID:
18419265
47.

Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.

Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SD, Nolan PM, Pääbo S, Channon KM, Costa RM, Eilers J, Ehret G, Rawlins JN, Fisher SE.

Curr Biol. 2008 Mar 11;18(5):354-62. doi: 10.1016/j.cub.2008.01.060.

48.

A description of unique fluorescent yellow pigments in penguin feathers.

McGraw KJ, Toomey MB, Nolan PM, Morehouse NI, Massaro M, Jouventin P.

Pigment Cell Res. 2007 Aug;20(4):301-4. No abstract available.

PMID:
17630963
49.

Reaching and grasping phenotypes in the mouse (Mus musculus): a characterization of inbred strains and mutant lines.

Tucci V, Achilli F, Blanco G, Lad HV, Wells S, Godinho S, Nolan PM.

Neuroscience. 2007 Jul 13;147(3):573-82. Epub 2007 Jun 15.

PMID:
17574766
50.

Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2.

Hough TA, Polewski M, Johnson K, Cheeseman M, Nolan PM, Vizor L, Rastan S, Boyde A, Pritzker K, Hunter AJ, Fisher EM, Terkeltaub R, Brown SD.

J Bone Miner Res. 2007 Sep;22(9):1397-407.

Supplemental Content

Loading ...
Support Center