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Items: 1 to 50 of 53

1.

Spreading of perturbations in myosin group kinetics along actin filaments.

Balassy Z, Lauzon AM, Hilbert L.

Proc Natl Acad Sci U S A. 2019 Aug 27;116(35):17336-17344. doi: 10.1073/pnas.1904164116. Epub 2019 Aug 12.

PMID:
31405981
2.

Freezing in response to social threat: a replication.

Noordewier MK, Scheepers DT, Hilbert LP.

Psychol Res. 2019 Jun 10. doi: 10.1007/s00426-019-01203-4. [Epub ahead of print]

PMID:
31179521
3.

Publisher Correction: Evidence for mid-Holocene rice domestication in the Americas.

Hilbert L, Neves EG, Pugliese F, Whitney BS, Shock M, Veasey E, Zimpel CA, Iriarte J.

Nat Ecol Evol. 2019 Jan;3(1):135. doi: 10.1038/s41559-018-0774-1.

PMID:
30546128
4.

Referral and Diagnosis of Developmental Auditory Processing Disorder in a Large, United States Hospital-Based Audiology Service.

Moore DR, Sieswerda SL, Grainger MM, Bowling A, Smith N, Perdew A, Eichert S, Alston S, Hilbert LW, Summers L, Lin L, Hunter LL.

J Am Acad Audiol. 2018 May;29(5):364-377. doi: 10.3766/jaaa.16130.

PMID:
29708487
5.

Evidence for mid-Holocene rice domestication in the Americas.

Hilbert L, Neves EG, Pugliese F, Whitney BS, Shock M, Veasey E, Zimpel CA, Iriarte J.

Nat Ecol Evol. 2017 Nov;1(11):1693-1698. doi: 10.1038/s41559-017-0322-4. Epub 2017 Oct 9. Erratum in: Nat Ecol Evol. 2019 Jan;3(1):135.

PMID:
28993622
6.

A tunable refractive index matching medium for live imaging cells, tissues and model organisms.

Boothe T, Hilbert L, Heide M, Berninger L, Huttner WB, Zaburdaev V, Vastenhouw NL, Myers EW, Drechsel DN, Rink JC.

Elife. 2017 Jul 14;6. pii: e27240. doi: 10.7554/eLife.27240.

7.

Competition between histone and transcription factor binding regulates the onset of transcription in zebrafish embryos.

Joseph SR, Pálfy M, Hilbert L, Kumar M, Karschau J, Zaburdaev V, Shevchenko A, Vastenhouw NL.

Elife. 2017 Apr 20;6. pii: e23326. doi: 10.7554/eLife.23326.

8.

Computational study of synchrony in fields and microclusters of ephaptically coupled neurons.

Stacey RG, Hilbert L, Quail T.

J Neurophysiol. 2015 May 1;113(9):3229-41. doi: 10.1152/jn.00546.2014. Epub 2015 Feb 11.

9.

Phosphate and ADP differently inhibit coordinated smooth muscle myosin groups.

Hilbert L, Balassy Z, Zitouni NB, Mackey MC, Lauzon AM.

Biophys J. 2015 Feb 3;108(3):622-31. doi: 10.1016/j.bpj.2014.12.008.

10.

Molecular mechanical differences between isoforms of contractile actin in the presence of isoforms of smooth muscle tropomyosin.

Hilbert L, Bates G, Roman HN, Blumenthal JL, Zitouni NB, Sobieszek A, Mackey MC, Lauzon AM.

PLoS Comput Biol. 2013 Oct;9(10):e1003273. doi: 10.1371/journal.pcbi.1003273. Epub 2013 Oct 24.

11.

The kinetics of mechanically coupled myosins exhibit group size-dependent regimes.

Hilbert L, Cumarasamy S, Zitouni NB, Mackey MC, Lauzon AM.

Biophys J. 2013 Sep 17;105(6):1466-74. doi: 10.1016/j.bpj.2013.07.054.

12.

Unphosphorylated calponin enhances the binding force of unphosphorylated myosin to actin.

Roman HN, Zitouni NB, Kachmar L, Ijpma G, Hilbert L, Matusovsky O, Benedetti A, Sobieszek A, Lauzon AM.

Biochim Biophys Acta. 2013 Oct;1830(10):4634-41. doi: 10.1016/j.bbagen.2013.05.042. Epub 2013 Jun 6.

13.

Stress-induced hypermutation as a physical property of life, a force of natural selection and its role in four thought experiments.

Hilbert L.

Phys Biol. 2013 Apr;10(2):026001. doi: 10.1088/1478-3975/10/2/026001. Epub 2013 Feb 13.

PMID:
23406696
14.

Pre-power-stroke cross-bridges contribute to force transients during imposed shortening in isolated muscle fibers.

Minozzo FC, Hilbert L, Rassier DE.

PLoS One. 2012;7(1):e29356. doi: 10.1371/journal.pone.0029356. Epub 2012 Jan 5.

15.

Small delay, big waves: a minimal delayed negative feedback model captures Escherichia coli single cell SOS kinetics.

Hilbert L, Albrecht D, Mackey MC.

Mol Biosyst. 2011 Sep;7(9):2599-607. doi: 10.1039/c1mb05122a. Epub 2011 Jun 23.

PMID:
21701705
16.

Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study.

Eikenboom J, Hilbert L, Ribba AS, Hommais A, Habart D, Messenger S, Al-Buhairan A, Guilliatt A, Lester W, Mazurier C, Meyer D, Fressinaud E, Budde U, Will K, Schneppenheim R, Obser T, Marggraf O, Eckert E, Castaman G, Rodeghiero F, Federici AB, Batlle J, Goudemand J, Ingerslev J, Lethagen S, Hill F, Peake I, Goodeve A.

J Thromb Haemost. 2009 Aug;7(8):1304-12. doi: 10.1111/j.1538-7836.2009.03486.x. Epub 2009 Jun 30.

17.

Silver-palladium surfaces inhibit biofilm formation.

Chiang WC, Schroll C, Hilbert LR, Møller P, Tolker-Nielsen T.

Appl Environ Microbiol. 2009 Mar;75(6):1674-8. doi: 10.1128/AEM.02274-08. Epub 2009 Jan 16.

18.

Nickel-containing coins: a health risk for nickel-sensitive individuals?

Jellesen MS, Hilbert LR, Menné T, Møller P.

Br J Dermatol. 2006 Dec;155(6):1301-2. No abstract available.

PMID:
17107412
19.

Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide.

Hilbert L, Nurden P, Caron C, Nurden AT, Goudemand J, Meyer D, Fressinaud E, Mazurier C; INSERM Network on Molecular Abnormalities in von Willebrand Disease.

Thromb Haemost. 2006 Sep;96(3):290-4.

PMID:
16953269
21.

GJB2 mutations and additional disabilities in a pediatric cochlear implant population.

Wiley S, Choo D, Meinzen-Derr J, Hilbert L, Greinwald J.

Int J Pediatr Otorhinolaryngol. 2006 Mar;70(3):493-500. Epub 2005 Sep 9.

PMID:
16154643
22.

Type 2N von Willebrand disease.

Mazurier C, Hilbert L.

Curr Hematol Rep. 2005 Sep;4(5):350-8.

PMID:
16131435
23.

First identification and expression of a type 2N von Willebrand disease mutation (E1078K) located in exon 25 of von Willebrand factor gene.

Hilbert L, D'Oiron R, Fressinaud E, Meyer D, Mazurier C; INSERM Network on Molecular Abnormalities in von Willebrand Disease.

J Thromb Haemost. 2004 Dec;2(12):2271-3. No abstract available.

24.

Expression of two type 2N von Willebrand disease mutations identified in exon 18 of von Willebrand factor gene.

Hilbert L, Jorieux S, Fontenay-Roupie M, Guicheteau M, Fressinaud E, Meyer D, Mazurier C; INSERM Network on Molecular Abnormalities in von Willebrand Disease.

Br J Haematol. 2004 Oct;127(2):184-9. Review.

PMID:
15461624
25.

A new candidate mutation, G1629R, in a patient with type 2A von Willebrand's disease: basic mechanisms and clinical implications.

Hilbert L, Federici AB, Baronciani L, Dallagiovanna S, Mazurier C.

Haematologica. 2004 Sep;89(9):1128-33.

26.

In vitro study of a triple-secured von Willebrand factor concentrate.

Mazurier C, Poulle M, Samor B, Hilbert L, Chtourou S.

Vox Sang. 2004 Feb;86(2):100-4.

PMID:
15023178
27.

Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European study.

Federici AB, Mazurier C, Berntorp E, Lee CA, Scharrer I, Goudemand J, Lethagen S, Nitu I, Ludwig G, Hilbert L, Mannucci PM.

Blood. 2004 Mar 15;103(6):2032-8. Epub 2003 Nov 20.

28.

Two novel mutations, Q1053H and C1060R, located in the D3 domain of von Willebrand factor, are responsible for decreased FVIII-binding capacity.

Hilbert L, Jorieux S, Proulle V, Favier R, Goudemand J, Parquet A, Meyer D, Fressinaud E, Mazurier C; INSERM Network on Molecular Abnormalities in von Willebrand Disease.

Br J Haematol. 2003 Feb;120(4):627-32.

PMID:
12588349
29.

Snack consumption and waste by preschool children served "cute" versus regular snacks.

Branen L, Fletcher J, Hilbert L.

J Nutr Educ Behav. 2002 Sep-Oct;34(5):279-82.

PMID:
12559064
30.

Clinical and audiological features in auditory neuropathy.

Madden C, Rutter M, Hilbert L, Greinwald JH Jr, Choo DI.

Arch Otolaryngol Head Neck Surg. 2002 Sep;128(9):1026-30.

PMID:
12220206
31.

Identification of a new type 2M von Willebrand disease mutation also at position 1324 of von Willebrand factor.

Hilbert L, Fressinaud E, Ribba AS, Meyer D, Mazurier C; INSERM network on molecular abnormalities in von Willebrand disease.

Thromb Haemost. 2002 Apr;87(4):635-40.

PMID:
12008946
32.
33.

Pediatric cochlear implantation in auditory neuropathy.

Madden C, Hilbert L, Rutter M, Greinwald J, Choo D.

Otol Neurotol. 2002 Mar;23(2):163-8.

PMID:
11875345
34.

Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet function.

Meyer D, Fressinaud E, Hilbert L, Ribba AS, Lavergne JM, Mazurier C.

Best Pract Res Clin Haematol. 2001 Jun;14(2):349-64. Review.

PMID:
11686104
35.

Type 2N von Willebrand disease: clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology.

Mazurier C, Goudemand J, Hilbert L, Caron C, Fressinaud E, Meyer D.

Best Pract Res Clin Haematol. 2001 Jun;14(2):337-47. Review.

PMID:
11686103
36.

A standard nomenclature for von Willebrand factor gene mutations and polymorphisms. On behalf of the ISTH SSC Subcommittee on von Willebrand factor.

Goodeve AC, Eikenboom JC, Ginsburg D, Hilbert L, Mazurier C, Peake IR, Sadler JE, Rodeghiero F; ISTH SSC Subcommittee on von Willebrand factor.

Thromb Haemost. 2001 May;85(5):929-31.

PMID:
11372690
37.
38.

Type 2M vWD resulting from a lysine deletion within a four lysine residue repeat in the A1 loop of von Willebrand factor.

Hilbert L, Jenkins PV, Gaucher C, Meriane E, Collins PW, Pasi KJ, Mazurier C.

Thromb Haemost. 2000 Aug;84(2):188-94.

PMID:
10959688
39.

Identification of new type 2B von Willebrand disease mutations: Arg543Gln, Arg545Pro and Arg578Leu.

Hilbert L, Gaucher C, Abgrall JF, Parquet A, Trzeciak C, Mazurier C.

Br J Haematol. 1998 Dec;103(3):877-84.

PMID:
9858249
41.

Gene defects in 150 unrelated French cases with type 2 von Willebrand disease: from the patient to the gene. INSERM Network on Molecular Abnormalities in von Willebrand Disease.

Meyer D, Fressinaud E, Gaucher C, Lavergne JM, Hilbert L, Ribba AS, Jorieux S, Mazurier C.

Thromb Haemost. 1997 Jul;78(1):451-6. Review.

PMID:
9198195
42.

The prevalence of non-viable pregnancy at 10-13 weeks of gestation.

Pandya PP, Snijders RJ, Psara N, Hilbert L, Nicolaides KH.

Ultrasound Obstet Gynecol. 1996 Mar;7(3):170-3.

43.
45.

Chromosomal defects and outcome in 1015 fetuses with increased nuchal translucency.

Pandya PP, Kondylios A, Hilbert L, Snijders RJ, Nicolaides KH.

Ultrasound Obstet Gynecol. 1995 Jan;5(1):15-9.

46.

Leu 697-->Val mutation in mature von Willebrand factor is responsible for type IIB von Willebrand disease.

Hilbert L, Gaucher C, de Romeuf C, Horellou MH, Vink T, Mazurier C.

Blood. 1994 Mar 15;83(6):1542-50.

47.

Helium-cooled balloon-borne infrared experiment for measurements of stratospheric trace gas emissions.

Rippel H, Hilbert L, Jarisch M, Kampf D, Offermann D, Schneider R.

Appl Opt. 1987 Aug 1;26(15):3097-102. doi: 10.1364/AO.26.003097.

PMID:
20490015
48.

Cervical and lumbopelvic traction. To stretch or not to stretch.

Kekosz VN, Hilbert L, Tepperman PS.

Postgrad Med. 1986 Dec;80(8):187-94.

PMID:
2947056
49.

Rehabilitation medicine. Its time has come.

Soric R, Hilbert L, Tepperman PS.

Postgrad Med. 1985 Jun;77(8):13-4, 18. No abstract available.

PMID:
3158888
50.

Reflex sympathetic dystrophy in hemiplegia.

Tepperman PS, Greyson ND, Hilbert L, Jimenez J, Williams JI.

Arch Phys Med Rehabil. 1984 Aug;65(8):442-7.

PMID:
6466074

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