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Items: 1 to 50 of 175

1.

Identification of the determinants of incomplete vaccination in Australian children.

Lim C, Currie GE, Waddington CS, Wu Y, Setijo S, Leask J, Marsh JA, Snelling TL.

Vaccine X. 2019 Jan 29;1:100010. doi: 10.1016/j.jvacx.2019.100010. eCollection 2019 Apr 11.

2.

Ligand Binding Site Structure Shapes Folding, Assembly and Degradation of Homomeric Protein Complexes.

Abrusán G, Marsh JA.

J Mol Biol. 2019 Jul 12. pii: S0022-2836(19)30443-7. doi: 10.1016/j.jmb.2019.07.014. [Epub ahead of print]

3.

The role of protein complexes in human genetic disease.

Bergendahl LT, Gerasimavicius L, Miles J, Macdonald L, Wells JN, Welburn JPI, Marsh JA.

Protein Sci. 2019 Aug;28(8):1400-1411. doi: 10.1002/pro.3667. Epub 2019 Jul 1. Review.

PMID:
31219644
4.

Evolution of protein interfaces in multimers and fibrils.

Zabel WJ, Hagner KP, Livesey BJ, Marsh JA, Setayeshgar S, Lynch M, Higgs PG.

J Chem Phys. 2019 Jun 14;150(22):225102. doi: 10.1063/1.5086042.

5.

Protein aggregation mediates stoichiometry of protein complexes in aneuploid cells.

Brennan CM, Vaites LP, Wells JN, Santaguida S, Paulo JA, Storchova Z, Harper JW, Marsh JA, Amon A.

Genes Dev. 2019 Aug 1;33(15-16):1031-1047. doi: 10.1101/gad.327494.119. Epub 2019 Jun 13.

PMID:
31196865
6.

Ligands and Receptors with Broad Binding Capabilities Have Common Structural Characteristics: An Antibiotic Design Perspective.

Abrusán G, Marsh JA.

J Med Chem. 2019 Jun 25. doi: 10.1021/acs.jmedchem.9b00220. [Epub ahead of print]

PMID:
31188598
7.

Biallelic variants in DNA2 cause microcephalic primordial dwarfism.

Tarnauskaitė Ž, Bicknell LS, Marsh JA, Murray JE, Parry DA, Logan CV, Bober MB, de Silva DC, Duker AL, Sillence D, Wise C, Jackson AP, Murina O, Reijns MAM.

Hum Mutat. 2019 Aug;40(8):1063-1070. doi: 10.1002/humu.23776. Epub 2019 Jun 23.

PMID:
31045292
8.

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors.

Warrington NM, Beaumont RN, Horikoshi M, Day FR, Helgeland Ø, Laurin C, Bacelis J, Peng S, Hao K, Feenstra B, Wood AR, Mahajan A, Tyrrell J, Robertson NR, Rayner NW, Qiao Z, Moen GH, Vaudel M, Marsit CJ, Chen J, Nodzenski M, Schnurr TM, Zafarmand MH, Bradfield JP, Grarup N, Kooijman MN, Li-Gao R, Geller F, Ahluwalia TS, Paternoster L, Rueedi R, Huikari V, Hottenga JJ, Lyytikäinen LP, Cavadino A, Metrustry S, Cousminer DL, Wu Y, Thiering E, Wang CA, Have CT, Vilor-Tejedor N, Joshi PK, Painter JN, Ntalla I, Myhre R, Pitkänen N, van Leeuwen EM, Joro R, Lagou V, Richmond RC, Espinosa A, Barton SJ, Inskip HM, Holloway JW, Santa-Marina L, Estivill X, Ang W, Marsh JA, Reichetzeder C, Marullo L, Hocher B, Lunetta KL, Murabito JM, Relton CL, Kogevinas M, Chatzi L, Allard C, Bouchard L, Hivert MF, Zhang G, Muglia LJ, Heikkinen J; EGG Consortium, Morgen CS, van Kampen AHC, van Schaik BDC, Mentch FD, Langenberg C, Luan J, Scott RA, Zhao JH, Hemani G, Ring SM, Bennett AJ, Gaulton KJ, Fernandez-Tajes J, van Zuydam NR, Medina-Gomez C, de Haan HG, Rosendaal FR, Kutalik Z, Marques-Vidal P, Das S, Willemsen G, Mbarek H, Müller-Nurasyid M, Standl M, Appel EVR, Fonvig CE, Trier C, van Beijsterveldt CEM, Murcia M, Bustamante M, Bonas-Guarch S, Hougaard DM, Mercader JM, Linneberg A, Schraut KE, Lind PA, Medland SE, Shields BM, Knight BA, Chai JF, Panoutsopoulou K, Bartels M, Sánchez F, Stokholm J, Torrents D, Vinding RK, Willems SM, Atalay M, Chawes BL, Kovacs P, Prokopenko I, Tuke MA, Yaghootkar H, Ruth KS, Jones SE, Loh PR, Murray A, Weedon MN, Tönjes A, Stumvoll M, Michaelsen KF, Eloranta AM, Lakka TA, van Duijn CM, Kiess W, Körner A, Niinikoski H, Pahkala K, Raitakari OT, Jacobsson B, Zeggini E, Dedoussis GV, Teo YY, Saw SM, Montgomery GW, Campbell H, Wilson JF, Vrijkotte TGM, Vrijheid M, de Geus EJCN, Hayes MG, Kadarmideen HN, Holm JC, Beilin LJ, Pennell CE, Heinrich J, Adair LS, Borja JB, Mohlke KL, Eriksson JG, Widén EE, Hattersley AT, Spector TD, Kähönen M, Viikari JS, Lehtimäki T, Boomsma DI, Sebert S, Vollenweider P, Sørensen TIA, Bisgaard H, Bønnelykke K, Murray JC, Melbye M, Nohr EA, Mook-Kanamori DO, Rivadeneira F, Hofman A, Felix JF, Jaddoe VWV, Hansen T, Pisinger C, Vaag AA, Pedersen O, Uitterlinden AG, Järvelin MR, Power C, Hyppönen E, Scholtens DM, Lowe WL Jr, Davey Smith G, Timpson NJ, Morris AP, Wareham NJ, Hakonarson H, Grant SFA, Frayling TM, Lawlor DA, Njølstad PR, Johansson S, Ong KK, McCarthy MI, Perry JRB, Evans DM, Freathy RM.

Nat Genet. 2019 May;51(5):804-814. doi: 10.1038/s41588-019-0403-1. Epub 2019 May 1.

PMID:
31043758
9.

Ligand-Binding-Site Structure Shapes Allosteric Signal Transduction and the Evolution of Allostery in Protein Complexes.

Abrusán G, Marsh JA.

Mol Biol Evol. 2019 Aug 1;36(8):1711-1727. doi: 10.1093/molbev/msz093.

10.

Trial Refresh: A Case for an Adaptive Platform Trial for Pulmonary Exacerbations of Cystic Fibrosis.

Schultz A, Marsh JA, Saville BR, Norman R, Middleton PG, Greville HW, Bellgard MI, Berry SM, Snelling T.

Front Pharmacol. 2019 Mar 28;10:301. doi: 10.3389/fphar.2019.00301. eCollection 2019. Review.

11.

Intrinsic lipid binding activity of ATG16L1 supports efficient membrane anchoring and autophagy.

Dudley LJ, Cabodevilla AG, Makar AN, Sztacho M, Michelberger T, Marsh JA, Houston DR, Martens S, Jiang X, Gammoh N.

EMBO J. 2019 May 2;38(9). pii: e100554. doi: 10.15252/embj.2018100554. Epub 2019 Apr 1.

12.

Research Note: Adaptive trials.

Marsh JA, Schultz A, Saville BR, Berry SM, Snelling TL.

J Physiother. 2019 Apr;65(2):113-116. doi: 10.1016/j.jphys.2019.02.004. Epub 2019 Mar 26. No abstract available.

13.

Exploring wearable sensors as an alternative to marker-based motion capture in the pitching delivery.

Boddy KJ, Marsh JA, Caravan A, Lindley KE, Scheffey JO, O'Connell ME.

PeerJ. 2019 Jan 24;7:e6365. doi: 10.7717/peerj.6365. eCollection 2019.

14.

Motivational factors in makerspaces: a mixed methods study of elementary school students' situational interest, self-efficacy, and achievement emotions.

Vongkulluksn VW, Matewos AM, Sinatra GM, Marsh JA.

Int J STEM Educ. 2018;5(1):43. doi: 10.1186/s40594-018-0129-0. Epub 2018 Nov 30.

15.

Effects of a six-week weighted-implement throwing program on baseball pitching velocity, kinematics, arm stress, and arm range of motion.

Marsh JA, Wagshol MI, Boddy KJ, O'Connell ME, Briend SJ, Lindley KE, Caravan A.

PeerJ. 2018 Nov 23;6:e6003. doi: 10.7717/peerj.6003. eCollection 2018.

16.

Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions.

Heyn P, Logan CV, Fluteau A, Challis RC, Auchynnikava T, Martin CA, Marsh JA, Taglini F, Kilanowski F, Parry DA, Cormier-Daire V, Fong CT, Gibson K, Hwa V, Ibáñez L, Robertson SP, Sebastiani G, Rappsilber J, Allshire RC, Reijns MAM, Dauber A, Sproul D, Jackson AP.

Nat Genet. 2019 Jan;51(1):96-105. doi: 10.1038/s41588-018-0274-x. Epub 2018 Nov 26.

17.

Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function.

Findlay AS, Carter RN, Starbuck B, McKie L, Nováková K, Budd PS, Keighren MA, Marsh JA, Cross SH, Simon MM, Potter PK, Morton NM, Jackson IJ.

Dis Model Mech. 2018 Dec 18;11(12). pii: dmm036426. doi: 10.1242/dmm.036426.

18.

A Graph-Based Approach for Detecting Sequence Homology in Highly Diverged Repeat Protein Families.

Wells JN, Marsh JA.

Methods Mol Biol. 2019;1851:251-261. doi: 10.1007/978-1-4939-8736-8_13.

PMID:
30298401
19.

Ascertaining infectious disease burden through primary care clinic attendance among young Aboriginal children living in four remote communities in Western Australia.

Hendrickx D, Bowen AC, Marsh JA, Carapetis JR, Walker R.

PLoS One. 2018 Sep 17;13(9):e0203684. doi: 10.1371/journal.pone.0203684. eCollection 2018.

20.

Editorial overview: Sequences and topology: Dynamic sequences and topologies of proteins.

Marsh JA, Teichmann SA.

Curr Opin Struct Biol. 2018 Jun;50:vii-viii. doi: 10.1016/j.sbi.2018.07.005. No abstract available.

PMID:
30080482
21.

Interrogation of Mammalian Protein Complex Structure, Function, and Membership Using Genome-Scale Fitness Screens.

Pan J, Meyers RM, Michel BC, Mashtalir N, Sizemore AE, Wells JN, Cassel SH, Vazquez F, Weir BA, Hahn WC, Marsh JA, Tsherniak A, Kadoch C.

Cell Syst. 2018 May 23;6(5):555-568.e7. doi: 10.1016/j.cels.2018.04.011. Epub 2018 May 16.

22.

The influence of incomplete case ascertainment on measures of vaccine efficacy.

Wu Y, Marsh JA, McBryde ES, Snelling TL.

Vaccine. 2018 May 17;36(21):2946-2952. doi: 10.1016/j.vaccine.2018.04.046. Epub 2018 Apr 23.

PMID:
29699788
23.

Computational Modelling of Protein Complex Structure and Assembly.

Wells JN, Bergendahl LT, Marsh JA.

Methods Mol Biol. 2018;1764:347-356. doi: 10.1007/978-1-4939-7759-8_22.

PMID:
29605926
24.

Experimental Characterization of Protein Complex Structure, Dynamics, and Assembly.

Wells JN, Marsh JA.

Methods Mol Biol. 2018;1764:3-27. doi: 10.1007/978-1-4939-7759-8_1. Review.

PMID:
29605905
25.

Ligand Binding Site Structure Influences the Evolution of Protein Complex Function and Topology.

Abrusán G, Marsh JA.

Cell Rep. 2018 Mar 20;22(12):3265-3276. doi: 10.1016/j.celrep.2018.02.085.

26.

Cotranslational protein assembly imposes evolutionary constraints on homomeric proteins.

Natan E, Endoh T, Haim-Vilmovsky L, Flock T, Chalancon G, Hopper JTS, Kintses B, Horvath P, Daruka L, Fekete G, Pál C, Papp B, Oszi E, Magyar Z, Marsh JA, Elcock AH, Babu MM, Robinson CV, Sugimoto N, Teichmann SA.

Nat Struct Mol Biol. 2018 Mar;25(3):279-288. doi: 10.1038/s41594-018-0029-5. Epub 2018 Feb 12.

27.

The NICE-GUT trial protocol: a randomised, placebo controlled trial of oral nitazoxanide for the empiric treatment of acute gastroenteritis among Australian Aboriginal children.

Waddington CS, McLeod C, Morris P, Bowen A, Naunton M, Carapetis J, Grimwood K, Robins-Browne R, Kirkwood CD, Baird R, Green D, Andrews R, Fearon D, Francis J, Marsh JA, Snelling T.

BMJ Open. 2018 Feb 1;8(2):e019632. doi: 10.1136/bmjopen-2017-019632.

28.

Protocol for Pertussis Immunisation and Food Allergy (PIFA): a case-control study of the association between pertussis vaccination in infancy and the risk of IgE-mediated food allergy among Australian children.

Estcourt MJ, Marsh JA, Campbell DE, Gold MS, Allen KJ, Richmond P, Waddington CS, Snelling TL.

BMJ Open. 2018 Jan 31;8(1):e020232. doi: 10.1136/bmjopen-2017-020232.

29.

Characterization of a novel RP2-OSTF1 interaction and its implication for actin remodelling.

Lyraki R, Lokaj M, Soares DC, Little A, Vermeren M, Marsh JA, Wittinghofer A, Hurd T.

J Cell Sci. 2018 Feb 20;131(4). pii: jcs211748. doi: 10.1242/jcs.211748.

30.

Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics.

Beaumont RN, Warrington NM, Cavadino A, Tyrrell J, Nodzenski M, Horikoshi M, Geller F, Myhre R, Richmond RC, Paternoster L, Bradfield JP, Kreiner-Møller E, Huikari V, Metrustry S, Lunetta KL, Painter JN, Hottenga JJ, Allard C, Barton SJ, Espinosa A, Marsh JA, Potter C, Zhang G, Ang W, Berry DJ, Bouchard L, Das S; Early Growth Genetics (EGG) Consortium, Hakonarson H, Heikkinen J, Helgeland Ø, Hocher B, Hofman A, Inskip HM, Jones SE, Kogevinas M, Lind PA, Marullo L, Medland SE, Murray A, Murray JC, Njølstad PR, Nohr EA, Reichetzeder C, Ring SM, Ruth KS, Santa-Marina L, Scholtens DM, Sebert S, Sengpiel V, Tuke MA, Vaudel M, Weedon MN, Willemsen G, Wood AR, Yaghootkar H, Muglia LJ, Bartels M, Relton CL, Pennell CE, Chatzi L, Estivill X, Holloway JW, Boomsma DI, Montgomery GW, Murabito JM, Spector TD, Power C, Järvelin MR, Bisgaard H, Grant SFA, Sørensen TIA, Jaddoe VW, Jacobsson B, Melbye M, McCarthy MI, Hattersley AT, Hayes MG, Frayling TM, Hivert MF, Felix JF, Hyppönen E, Lowe WL Jr, Evans DM, Lawlor DA, Feenstra B, Freathy RM.

Hum Mol Genet. 2018 Feb 15;27(4):742-756. doi: 10.1093/hmg/ddx429.

31.

The genetic basis and evolution of red blood cell sickling in deer.

Esin A, Bergendahl LT, Savolainen V, Marsh JA, Warnecke T.

Nat Ecol Evol. 2018 Feb;2(2):367-376. doi: 10.1038/s41559-017-0420-3. Epub 2017 Dec 18.

32.

Microfluidic Separation Coupled to Mass Spectrometry for Quantification of Peanut Allergens in a Complex Food Matrix.

Sayers RL, Gethings LA, Lee V, Balasundaram A, Johnson PE, Marsh JA, Wallace A, Brown H, Rogers A, Langridge JI, Mills ENC.

J Proteome Res. 2018 Jan 5;17(1):647-655. doi: 10.1021/acs.jproteome.7b00714. Epub 2017 Nov 21.

PMID:
29083186
33.

ER stress-induced aggresome trafficking of HtrA1 protects against proteotoxicity.

Gerhardt MJ, Marsh JA, Morrison M, Kazlauskas A, Khadka A, Rosenkranz S, DeAngelis MM, Saint-Geniez M, Jacobo SMP.

J Mol Cell Biol. 2017 Dec 1;9(6):533. doi: 10.1093/jmcb/mjx040. No abstract available.

PMID:
29040612
34.

ER stress-induced aggresome trafficking of HtrA1 protects against proteotoxicity.

Gerhardt MJ, Marsh JA, Morrison M, Kazlauskas A, Khadka A, Rosenkranz S, DeAngelis MM, Saint-Geniez M, Jacobo SMP.

J Mol Cell Biol. 2017 Dec 1;9(6):516-532. doi: 10.1093/jmcb/mjx024. Erratum in: J Mol Cell Biol. 2017 Dec 1;9(6):533.

35.

Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degeneration.

Stanton CM, Borooah S, Drake C, Marsh JA, Campbell S, Lennon A, Soares DC, Vallabh NA, Sahni J, Cideciyan AV, Dhillon B, Vitart V, Jacobson SG, Wright AF, Hayward C.

Sci Rep. 2017 Sep 22;7(1):12147. doi: 10.1038/s41598-017-11898-3.

36.

Functional determinants of protein assembly into homomeric complexes.

Bergendahl LT, Marsh JA.

Sci Rep. 2017 Jul 10;7(1):4932. doi: 10.1038/s41598-017-05084-8.

37.

Social media in nurse education: Utilization and E-professionalism.

Duke VJA, Anstey A, Carter S, Gosse N, Hutchens KM, Marsh JA.

Nurse Educ Today. 2017 Oct;57:8-13. doi: 10.1016/j.nedt.2017.06.009. Epub 2017 Jun 24.

PMID:
28683342
38.

Regular exercise improves the well-being of parents of children with cancer.

Halliday GC, Miles GCP, Marsh JA, Kotecha RS, Alessandri AJ.

Pediatr Blood Cancer. 2017 Dec;64(12). doi: 10.1002/pbc.26668. Epub 2017 Jun 19.

PMID:
28627013
39.

Signalling assemblies: the odds of symmetry.

Maksay G, Marsh JA.

Biochem Soc Trans. 2017 Jun 15;45(3):599-611. doi: 10.1042/BST20170009. Review.

PMID:
28620024
40.

Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Shaw ND, Brand H, Kupchinsky ZA, Bengani H, Plummer L, Jones TI, Erdin S, Williamson KA, Rainger J, Stortchevoi A, Samocha K, Currall BB, Dunican DS, Collins RL, Willer JR, Lek A, Lek M, Nassan M, Pereira S, Kammin T, Lucente D, Silva A, Seabra CM, Chiang C, An Y, Ansari M, Rainger JK, Joss S, Smith JC, Lippincott MF, Singh SS, Patel N, Jing JW, Law JR, Ferraro N, Verloes A, Rauch A, Steindl K, Zweier M, Scheer I, Sato D, Okamoto N, Jacobsen C, Tryggestad J, Chernausek S, Schimmenti LA, Brasseur B, Cesaretti C, García-Ortiz JE, Buitrago TP, Silva OP, Hoffman JD, Mühlbauer W, Ruprecht KW, Loeys BL, Shino M, Kaindl AM, Cho CH, Morton CC, Meehan RR, van Heyningen V, Liao EC, Balasubramanian R, Hall JE, Seminara SB, Macarthur D, Moore SA, Yoshiura KI, Gusella JF, Marsh JA, Graham JM Jr, Lin AE, Katsanis N, Jones PL, Crowley WF Jr, Davis EE, FitzPatrick DR, Talkowski ME.

Nat Genet. 2017 May 26;49(6):969. doi: 10.1038/ng0617-969c. No abstract available.

PMID:
28546579
41.

Evolution of condensin and cohesin complexes driven by replacement of Kite by Hawk proteins.

Wells JN, Gligoris TG, Nasmyth KA, Marsh JA.

Curr Biol. 2017 Jan 9;27(1):R17-R18. doi: 10.1016/j.cub.2016.11.050.

42.

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Shaw ND, Brand H, Kupchinsky ZA, Bengani H, Plummer L, Jones TI, Erdin S, Williamson KA, Rainger J, Stortchevoi A, Samocha K, Currall BB, Dunican DS, Collins RL, Willer JR, Lek A, Lek M, Nassan M, Pereira S, Kammin T, Lucente D, Silva A, Seabra CM, Chiang C, An Y, Ansari M, Rainger JK, Joss S, Smith JC, Lippincott MF, Singh SS, Patel N, Jing JW, Law JR, Ferraro N, Verloes A, Rauch A, Steindl K, Zweier M, Scheer I, Sato D, Okamoto N, Jacobsen C, Tryggestad J, Chernausek S, Schimmenti LA, Brasseur B, Cesaretti C, García-Ortiz JE, Buitrago TP, Silva OP, Hoffman JD, Mühlbauer W, Ruprecht KW, Loeys BL, Shino M, Kaindl AM, Cho CH, Morton CC, Meehan RR, van Heyningen V, Liao EC, Balasubramanian R, Hall JE, Seminara SB, Macarthur D, Moore SA, Yoshiura KI, Gusella JF, Marsh JA, Graham JM Jr, Lin AE, Katsanis N, Jones PL, Crowley WF Jr, Davis EE, FitzPatrick DR, Talkowski ME.

Nat Genet. 2017 Feb;49(2):238-248. doi: 10.1038/ng.3743. Epub 2017 Jan 9. Erratum in: Nat Genet. 2017 May 26;49(6):969.

43.

Regulation, evolution and consequences of cotranslational protein complex assembly.

Natan E, Wells JN, Teichmann SA, Marsh JA.

Curr Opin Struct Biol. 2017 Feb;42:90-97. doi: 10.1016/j.sbi.2016.11.023. Epub 2016 Dec 12. Review.

44.

Alpha Helices Are More Robust to Mutations than Beta Strands.

Abrusán G, Marsh JA.

PLoS Comput Biol. 2016 Dec 9;12(12):e1005242. doi: 10.1371/journal.pcbi.1005242. eCollection 2016 Dec.

45.

Parental pre-pregnancy BMI is a dominant early-life risk factor influencing BMI of offspring in adulthood.

Rath SR, Marsh JA, Newnham JP, Zhu K, Atkinson HC, Mountain J, Oddy WH, Hughes IP, Harris M, Leong GM, Cotterill AM, Sly PD, Pennell CE, Choong CS.

Obes Sci Pract. 2016 Mar;2(1):48-57. Epub 2016 Feb 19.

46.

Kinetic Analysis of Protein Stability Reveals Age-Dependent Degradation.

McShane E, Sin C, Zauber H, Wells JN, Donnelly N, Wang X, Hou J, Chen W, Storchova Z, Marsh JA, Valleriani A, Selbach M.

Cell. 2016 Oct 20;167(3):803-815.e21. doi: 10.1016/j.cell.2016.09.015. Epub 2016 Oct 6.

47.

Effects of maternal dietary egg intake during early lactation on human milk ovalbumin concentration: a randomized controlled trial.

Metcalfe JR, Marsh JA, D'Vaz N, Geddes DT, Lai CT, Prescott SL, Palmer DJ.

Clin Exp Allergy. 2016 Dec;46(12):1605-1613. doi: 10.1111/cea.12806. Epub 2016 Oct 7.

48.

Structural Determinants of Sleeping Beauty Transposase Activity.

Abrusán G, Yant SR, Szilágyi A, Marsh JA, Mátés L, Izsvák Z, Barabás O, Ivics Z.

Mol Ther. 2016 Aug;24(8):1369-77. doi: 10.1038/mt.2016.110. Epub 2016 Jun 6.

49.

A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect.

McEntagart M, Williamson KA, Rainger JK, Wheeler A, Seawright A, De Baere E, Verdin H, Bergendahl LT, Quigley A, Rainger J, Dixit A, Sarkar A, López Laso E, Sanchez-Carpintero R, Barrio J, Bitoun P, Prescott T, Riise R, McKee S, Cook J, McKie L, Ceulemans B, Meire F, Temple IK, Prieur F, Williams J, Clouston P, Németh AH, Banka S, Bengani H, Handley M, Freyer E, Ross A; DDD Study, van Heyningen V, Marsh JA, Elmslie F, FitzPatrick DR.

Am J Hum Genet. 2016 May 5;98(5):981-992. doi: 10.1016/j.ajhg.2016.03.018. Epub 2016 Apr 21.

50.

Operon Gene Order Is Optimized for Ordered Protein Complex Assembly.

Wells JN, Bergendahl LT, Marsh JA.

Cell Rep. 2016 Feb 2;14(4):679-685. doi: 10.1016/j.celrep.2015.12.085. Epub 2016 Jan 21.

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