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Items: 1 to 50 of 261

1.

Complete Genome Sequences of Mycobacterium smegmatis Phages NihilNomen and Carlyle, Isolated in Las Vegas, Nevada.

Salisbury A, Doss R, Mehta A, Bhatti K, Dapra C, Huntsinger A, Rodriguez S, Yacek S, Sandberg R, Gildore A, Knudtson J, Tibayan F, Ohta T, Zafar N, Mercado G, Le A, Mekhaeel N, Willer J, Rodrich-Zuniga E, McFarland M, Regner K, Strong C, Tsourkas PK.

Microbiol Resour Announc. 2019 Sep 19;8(38). pii: e00677-19. doi: 10.1128/MRA.00677-19.

2.

Genetic variation across the human olfactory receptor repertoire alters odor perception.

Trimmer C, Keller A, Murphy NR, Snyder LL, Willer JR, Nagai MH, Katsanis N, Vosshall LB, Matsunami H, Mainland JD.

Proc Natl Acad Sci U S A. 2019 May 7;116(19):9475-9480. doi: 10.1073/pnas.1804106115. Epub 2019 Apr 30.

3.

Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion.

Spataro R, Kousi M, Farhan SMK, Willer JR, Ross JP, Dion PA, Rouleau GA, Daly MJ, Neale BM, La Bella V, Katsanis N.

Hum Genomics. 2019 Apr 16;13(1):19. doi: 10.1186/s40246-019-0203-9.

4.

Cytotoxic Properties of Damiana (Turnera diffusa) Extracts and Constituents and A Validated Quantitative UHPLC-DAD Assay.

Willer J, Jöhrer K, Greil R, Zidorn C, Çiçek SS.

Molecules. 2019 Feb 28;24(5). pii: E855. doi: 10.3390/molecules24050855.

5.

A population of descending tyraminergic/octopaminergic projection neurons of the insect deutocerebrum.

Kononenko NL, Hartfil S, Willer J, Ferch J, Wolfenberg H, Pflüger HJ.

J Comp Neurol. 2019 Apr 15;527(6):1027-1038. doi: 10.1002/cne.24583. Epub 2018 Dec 11.

PMID:
30444529
6.

Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome.

Helm BM, Willer JR, Sadeghpour A, Golzio C, Crouch E, Vergano SS, Katsanis N, Davis EE.

Hum Genomics. 2017 Jul 19;11(1):16. doi: 10.1186/s40246-017-0111-9.

7.

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
8.

Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome.

Ta-Shma A, Khan TN, Vivante A, Willer JR, Matak P, Jalas C, Pode-Shakked B, Salem Y, Anikster Y, Hildebrandt F, Katsanis N, Elpeleg O, Davis EE.

Am J Hum Genet. 2017 Apr 6;100(4):666-675. doi: 10.1016/j.ajhg.2017.02.007. Epub 2017 Mar 16.

9.

Systematic Functional Testing of Rare Variants: Contributions of CFI to Age-Related Macular Degeneration.

Tan PL, Garrett ME, Willer JR, Campochiaro PA, Campochiaro B, Zack DJ, Ashley-Koch AE, Katsanis N.

Invest Ophthalmol Vis Sci. 2017 Mar 1;58(3):1570-1576. doi: 10.1167/iovs.16-20867.

10.

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.

11.

N6-Methyladenosine in Flaviviridae Viral RNA Genomes Regulates Infection.

Gokhale NS, McIntyre ABR, McFadden MJ, Roder AE, Kennedy EM, Gandara JA, Hopcraft SE, Quicke KM, Vazquez C, Willer J, Ilkayeva OR, Law BA, Holley CL, Garcia-Blanco MA, Evans MJ, Suthar MS, Bradrick SS, Mason CE, Horner SM.

Cell Host Microbe. 2016 Nov 9;20(5):654-665. doi: 10.1016/j.chom.2016.09.015. Epub 2016 Oct 20.

12.

Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome.

Lindstrand A, Frangakis S, Carvalho CM, Richardson EB, McFadden KA, Willer JR, Pehlivan D, Liu P, Pediaditakis IL, Sabo A, Lewis RA, Banin E, Lupski JR, Davis EE, Katsanis N.

Am J Hum Genet. 2016 Aug 4;99(2):318-36. doi: 10.1016/j.ajhg.2015.04.023.

13.

Safe long-term repeated disruption of the blood-brain barrier using an implantable ultrasound device: a multiparametric study in a primate model.

Horodyckid C, Canney M, Vignot A, Boisgard R, Drier A, Huberfeld G, François C, Prigent A, Santin MD, Adam C, Willer JC, Lafon C, Chapelon JY, Carpentier A.

J Neurosurg. 2017 Apr;126(4):1351-1361. doi: 10.3171/2016.3.JNS151635. Epub 2016 Jun 10.

PMID:
27285538
14.

An organelle-specific protein landscape identifies novel diseases and molecular mechanisms.

Boldt K, van Reeuwijk J, Lu Q, Koutroumpas K, Nguyen TM, Texier Y, van Beersum SE, Horn N, Willer JR, Mans DA, Dougherty G, Lamers IJ, Coene KL, Arts HH, Betts MJ, Beyer T, Bolat E, Gloeckner CJ, Haidari K, Hetterschijt L, Iaconis D, Jenkins D, Klose F, Knapp B, Latour B, Letteboer SJ, Marcelis CL, Mitic D, Morleo M, Oud MM, Riemersma M, Rix S, Terhal PA, Toedt G, van Dam TJ, de Vrieze E, Wissinger Y, Wu KM, Apic G, Beales PL, Blacque OE, Gibson TJ, Huynen MA, Katsanis N, Kremer H, Omran H, van Wijk E, Wolfrum U, Kepes F, Davis EE, Franco B, Giles RH, Ueffing M, Russell RB, Roepman R; UK10K Rare Diseases Group.

Nat Commun. 2016 May 13;7:11491. doi: 10.1038/ncomms11491.

15.

De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.

Burrage LC, Charng WL, Eldomery MK, Willer JR, Davis EE, Lugtenberg D, Zhu W, Leduc MS, Akdemir ZC, Azamian M, Zapata G, Hernandez PP, Schoots J, de Munnik SA, Roepman R, Pearring JN, Jhangiani S, Katsanis N, Vissers LE, Brunner HG, Beaudet AL, Rosenfeld JA, Muzny DM, Gibbs RA, Eng CM, Xia F, Lalani SR, Lupski JR, Bongers EM, Yang Y.

Am J Hum Genet. 2015 Dec 3;97(6):904-13. doi: 10.1016/j.ajhg.2015.11.006.

16.

Transient laminin beta 1a Induction Defines the Wound Epidermis during Zebrafish Fin Regeneration.

Chen CH, Merriman AF, Savage J, Willer J, Wahlig T, Katsanis N, Yin VP, Poss KD.

PLoS Genet. 2015 Aug 25;11(8):e1005437. doi: 10.1371/journal.pgen.1005437. eCollection 2015 Aug.

17.

Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy.

Gonzaga-Jauregui C, Harel T, Gambin T, Kousi M, Griffin LB, Francescatto L, Ozes B, Karaca E, Jhangiani SN, Bainbridge MN, Lawson KS, Pehlivan D, Okamoto Y, Withers M, Mancias P, Slavotinek A, Reitnauer PJ, Goksungur MT, Shy M, Crawford TO, Koenig M, Willer J, Flores BN, Pediaditrakis I, Us O, Wiszniewski W, Parman Y, Antonellis A, Muzny DM; Baylor-Hopkins Center for Mendelian Genomics, Katsanis N, Battaloglu E, Boerwinkle E, Gibbs RA, Lupski JR.

Cell Rep. 2015 Aug 18;12(7):1169-83. doi: 10.1016/j.celrep.2015.07.023. Epub 2015 Aug 6.

18.

pigk Mutation underlies macho behavior and affects Rohon-Beard cell excitability.

Carmean V, Yonkers MA, Tellez MB, Willer JR, Willer GB, Gregg RG, Geisler R, Neuhauss SC, Ribera AB.

J Neurophysiol. 2015 Aug;114(2):1146-57. doi: 10.1152/jn.00355.2015. Epub 2015 Jul 1.

19.

Epigenetic control of intestinal barrier function and inflammation in zebrafish.

Marjoram L, Alvers A, Deerhake ME, Bagwell J, Mankiewicz J, Cocchiaro JL, Beerman RW, Willer J, Sumigray KD, Katsanis N, Tobin DM, Rawls JF, Goll MG, Bagnat M.

Proc Natl Acad Sci U S A. 2015 Mar 3;112(9):2770-5. doi: 10.1073/pnas.1424089112. Epub 2015 Feb 17.

20.

Feasibility study of dual-task-managing training to improve gait performance of older adults.

Wollesen B, Voelcker-Rehage C, Willer J, Zech A, Mattes K.

Aging Clin Exp Res. 2015 Aug;27(4):447-55. doi: 10.1007/s40520-014-0301-4. Epub 2015 Jan 3.

PMID:
25556156
21.

Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.

Balasubramanian R, Choi JH, Francescatto L, Willer J, Horton ER, Asimacopoulos EP, Stankovic KM, Plummer L, Buck CL, Quinton R, Nebesio TD, Mericq V, Merino PM, Meyer BF, Monies D, Gusella JF, Al Tassan N, Katsanis N, Crowley WF Jr.

Proc Natl Acad Sci U S A. 2014 Dec 16;111(50):17953-8. doi: 10.1073/pnas.1417438111. Epub 2014 Dec 3.

22.

A novel ribosomopathy caused by dysfunction of RPL10 disrupts neurodevelopment and causes X-linked microcephaly in humans.

Brooks SS, Wall AL, Golzio C, Reid DW, Kondyles A, Willer JR, Botti C, Nicchitta CV, Katsanis N, Davis EE.

Genetics. 2014 Oct;198(2):723-33. doi: 10.1534/genetics.114.168211.

23.

Recurrent CNVs and SNVs at the NPHP1 locus contribute pathogenic alleles to Bardet-Biedl syndrome.

Lindstrand A, Davis EE, Carvalho CM, Pehlivan D, Willer JR, Tsai IC, Ramanathan S, Zuppan C, Sabo A, Muzny D, Gibbs R, Liu P, Lewis RA, Banin E, Lupski JR, Clark R, Katsanis N.

Am J Hum Genet. 2014 May 1;94(5):745-54. doi: 10.1016/j.ajhg.2014.03.017. Epub 2014 Apr 17.

24.

Whole exome sequencing of a dominant retinitis pigmentosa family identifies a novel deletion in PRPF31.

Villanueva A, Willer JR, Bryois J, Dermitzakis ET, Katsanis N, Davis EE.

Invest Ophthalmol Vis Sci. 2014 Apr 7;55(4):2121-9. doi: 10.1167/iovs.13-13827.

25.

Elution profile analysis of SDS-induced subcomplexes by quantitative mass spectrometry.

Texier Y, Toedt G, Gorza M, Mans DA, van Reeuwijk J, Horn N, Willer J, Katsanis N, Roepman R, Gibson TJ, Ueffing M, Boldt K.

Mol Cell Proteomics. 2014 May;13(5):1382-91. doi: 10.1074/mcp.O113.033233. Epub 2014 Feb 21.

26.

Analgesic effects of dyspnoea: "Air hunger" does not inhibit the spinal nociception reflex in humans.

Morélot-Panzini C, Mayaux J, Hug F, Willer JC, Similowski T.

Respir Physiol Neurobiol. 2014 Jan 1;190:81-5. doi: 10.1016/j.resp.2013.09.012. Epub 2013 Oct 17.

PMID:
24140942
27.

Rapid identification of kidney cyst mutations by whole exome sequencing in zebrafish.

Ryan S, Willer J, Marjoram L, Bagwell J, Mankiewicz J, Leshchiner I, Goessling W, Bagnat M, Katsanis N.

Development. 2013 Nov;140(21):4445-51. doi: 10.1242/dev.101170.

28.

snow white, a zebrafish model of Hermansky-Pudlak Syndrome type 5.

Daly CM, Willer J, Gregg R, Gross JM.

Genetics. 2013 Oct;195(2):481-94. doi: 10.1534/genetics.113.154898. Epub 2013 Jul 26.

29.

Intravenous adenosine activates diffuse nociceptive inhibitory controls in humans.

Morélot-Panzini C, Corvol JC, Demoule A, Raux M, Fiamma MN, Willer JC, Similowski T.

J Appl Physiol (1985). 2013 Sep 1;115(5):697-703. doi: 10.1152/japplphysiol.00027.2013. Epub 2013 Jul 18.

30.

TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.

Wiszniewski W, Hunter JV, Hanchard NA, Willer JR, Shaw C, Tian Q, Illner A, Wang X, Cheung SW, Patel A, Campbell IM, Gelowani V, Hixson P, Ester AR, Azamian MS, Potocki L, Zapata G, Hernandez PP, Ramocki MB, Santos-Cortez RL, Wang G, York MK, Justice MJ, Chu ZD, Bader PI, Omo-Griffith L, Madduri NS, Scharer G, Crawford HP, Yanatatsaneejit P, Eifert A, Kerr J, Bacino CA, Franklin AI, Goin-Kochel RP, Simpson G, Immken L, Haque ME, Stosic M, Williams MD, Morgan TM, Pruthi S, Omary R, Boyadjiev SA, Win KK, Thida A, Hurles M, Hibberd ML, Khor CC, Van Vinh Chau N, Gallagher TE, Mutirangura A, Stankiewicz P, Beaudet AL, Maletic-Savatic M, Rosenfeld JA, Shaffer LG, Davis EE, Belmont JW, Dunstan S, Simmons CP, Bonnen PE, Leal SM, Katsanis N, Lupski JR, Lalani SR.

Am J Hum Genet. 2013 Aug 8;93(2):197-210. doi: 10.1016/j.ajhg.2013.05.027. Epub 2013 Jun 27. Erratum in: Am J Hum Genet. 2013 Aug 8;93(2):405.

31.

Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes SEDT.

Davis EE, Savage JH, Willer JR, Jiang YH, Angrist M, Androutsopoulos A, Katsanis N.

Clin Genet. 2014 Apr;85(4):359-64. doi: 10.1111/cge.12189. Epub 2013 Jun 5.

PMID:
23656395
32.

Next-generation sequencing of the human olfactory receptors.

Mainland JD, Willer JR, Matsunami H, Katsanis N.

Methods Mol Biol. 2013;1003:133-47. doi: 10.1007/978-1-62703-377-0_10.

PMID:
23585039
33.

KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.

Golzio C, Willer J, Talkowski ME, Oh EC, Taniguchi Y, Jacquemont S, Reymond A, Sun M, Sawa A, Gusella JF, Kamiya A, Beckmann JS, Katsanis N.

Nature. 2012 May 16;485(7398):363-7. doi: 10.1038/nature11091.

34.

TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone.

Huang L, Szymanska K, Jensen VL, Janecke AR, Innes AM, Davis EE, Frosk P, Li C, Willer JR, Chodirker BN, Greenberg CR, McLeod DR, Bernier FP, Chudley AE, Müller T, Shboul M, Logan CV, Loucks CM, Beaulieu CL, Bowie RV, Bell SM, Adkins J, Zuniga FI, Ross KD, Wang J, Ban MR, Becker C, Nürnberg P, Douglas S, Craft CM, Akimenko MA, Hegele RA, Ober C, Utermann G, Bolz HJ, Bulman DE, Katsanis N, Blacque OE, Doherty D, Parboosingh JS, Leroux MR, Johnson CA, Boycott KM.

Am J Hum Genet. 2011 Dec 9;89(6):713-30. doi: 10.1016/j.ajhg.2011.11.005.

35.

Maternal topoisomerase II alpha, not topoisomerase II beta, enables embryonic development of zebrafish top2a-/- mutants.

Sapetto-Rebow B, McLoughlin SC, O'Shea LC, O'Leary O, Willer JR, Alvarez Y, Collery R, O'Sullivan J, Van Eeden F, Hensey C, Kennedy BN.

BMC Dev Biol. 2011 Nov 23;11:71. doi: 10.1186/1471-213X-11-71.

36.

Impact of dental implant length on early failure rates: a meta-analysis of observational studies.

Pommer B, Frantal S, Willer J, Posch M, Watzek G, Tepper G.

J Clin Periodontol. 2011 Sep;38(9):856-63. doi: 10.1111/j.1600-051X.2011.01750.x. Epub 2011 Jul 3. Review.

PMID:
21722154
37.

Loss of Lrp2 in zebrafish disrupts pronephric tubular clearance but not forebrain development.

Kur E, Christa A, Veth KN, Gajera CR, Andrade-Navarro MA, Zhang J, Willer JR, Gregg RG, Abdelilah-Seyfried S, Bachmann S, Link BA, Hammes A, Willnow TE.

Dev Dyn. 2011 Jun;240(6):1567-77. doi: 10.1002/dvdy.22624. Epub 2011 Mar 31.

38.
39.

Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma.

Veth KN, Willer JR, Collery RF, Gray MP, Willer GB, Wagner DS, Mullins MC, Udvadia AJ, Smith RS, John SW, Gregg RG, Link BA.

PLoS Genet. 2011 Feb;7(2):e1001310. doi: 10.1371/journal.pgen.1001310. Epub 2011 Feb 17.

40.

Upper leg conduction time distinguishes demyelinating neuropathies.

Maccabee PJ, Eberle LP, Stein IA, Willer JA, Lipitz ME, Kula RW, Marx T, Muntean EV, Amassian VE.

Muscle Nerve. 2011 Apr;43(4):518-30. doi: 10.1002/mus.21909. Epub 2011 Feb 11.

PMID:
21319166
41.

rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNA.

Haud N, Kara F, Diekmann S, Henneke M, Willer JR, Hillwig MS, Gregg RG, Macintosh GC, Gärtner J, Alia A, Hurlstone AF.

Proc Natl Acad Sci U S A. 2011 Jan 18;108(3):1099-103. doi: 10.1073/pnas.1009811107. Epub 2011 Jan 3.

42.

Neural and synaptic defects in slytherin, a zebrafish model for human congenital disorders of glycosylation.

Song Y, Willer JR, Scherer PC, Panzer JA, Kugath A, Skordalakes E, Gregg RG, Willer GB, Balice-Gordon RJ.

PLoS One. 2010 Oct 29;5(10):e13743. doi: 10.1371/journal.pone.0013743.

43.

Muscle contractions guide rohon-beard peripheral sensory axons.

Paulus JD, Willer GB, Willer JR, Gregg RG, Halloran MC.

J Neurosci. 2009 Oct 21;29(42):13190-201. doi: 10.1523/JNEUROSCI.2179-09.2009.

44.

Facial nerve decompression for idiopathic Bell's palsy: report of 13 cases and literature review.

Bodénez C, Bernat I, Willer JC, Barré P, Lamas G, Tankéré F.

J Laryngol Otol. 2010 Mar;124(3):272-8. doi: 10.1017/S0022215109991265. Epub 2009 Oct 2. Review.

PMID:
19796438
45.

Are patients with schizophrenia insensitive to pain? A reconsideration of the question.

Bonnot O, Anderson GM, Cohen D, Willer JC, Tordjman S.

Clin J Pain. 2009 Mar-Apr;25(3):244-52. doi: 10.1097/AJP.0b013e318192be97. Review.

PMID:
19333176
46.

Influence of prefrontal target region on the efficacy of repetitive transcranial magnetic stimulation in patients with medication-resistant depression: a [(18)F]-fluorodeoxyglucose PET and MRI study.

Paillère Martinot ML, Galinowski A, Ringuenet D, Gallarda T, Lefaucheur JP, Bellivier F, Picq C, Bruguière P, Mangin JF, Rivière D, Willer JC, Falissard B, Leboyer M, Olié JP, Artiges E, Martinot JL.

Int J Neuropsychopharmacol. 2010 Feb;13(1):45-59. doi: 10.1017/S146114570900008X. Epub 2009 Mar 9.

PMID:
19267956
47.

Motor neuron disorders: novel electrophysiologic approach (MUFDEC protocol).

Wang FC, Le Forestier N, Gérard P, Willer JC, Meininger V, Dive D, de Noordhout AM, Bouche P.

Suppl Clin Neurophysiol. 2009;60:143-52. No abstract available.

PMID:
20715376
48.

[Congenital insensitivity to pain].

Danziger N, Willer JC.

Rev Neurol (Paris). 2009 Feb;165(2):129-36. doi: 10.1016/j.neurol.2008.05.003. Epub 2008 Jul 9. Review. French.

PMID:
18808773
49.

[Electrophysiology: mismatch negativity and prognosis of coma].

Chausson N, Wassouf A, Pegado F, Willer JC, Naccache L.

Rev Neurol (Paris). 2008 Mar;164 Spec No 1:F34-5. Review. French. No abstract available.

PMID:
18680818
50.

Zebrafish blowout provides genetic evidence for Patched1-mediated negative regulation of Hedgehog signaling within the proximal optic vesicle of the vertebrate eye.

Lee J, Willer JR, Willer GB, Smith K, Gregg RG, Gross JM.

Dev Biol. 2008 Jul 1;319(1):10-22. doi: 10.1016/j.ydbio.2008.03.035. Epub 2008 Apr 4.

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