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Items: 1 to 20 of 40

1.

Epigenetic deregulation of GATA3 in neuroblastoma is associated with increased GATA3 protein expression and with poor outcomes.

Almutairi B, Charlet J, Dallosso AR, Szemes M, Etchevers HC, Malik KTA, Brown KW.

Sci Rep. 2019 Dec 12;9(1):18934. doi: 10.1038/s41598-019-55382-6.

2.

A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation.

Jaouadi H, Chehida AB, Kraoua L, Etchevers HC, Argiro L, Kasdallah N, Blibech S, Delague V, Lévy N, Tebib N, Mrad R, Abdelhak S, Benkhalifa R, Zaffran S.

Genet Res (Camb). 2019 Apr 29;101:e6. doi: 10.1017/S0016672319000041.

3.

The diverse neural crest: from embryology to human pathology.

Etchevers HC, Dupin E, Le Douarin NM.

Development. 2019 Mar 11;146(5). pii: dev169821. doi: 10.1242/dev.169821. Review.

4.

Macrophage-Derived IL1β and TNFα Regulate Arginine Metabolism in Neuroblastoma.

Fultang L, Gamble LD, Gneo L, Berry AM, Egan SA, De Bie F, Yogev O, Eden GL, Booth S, Brownhill S, Vardon A, McConville CM, Cheng PN, Norris MD, Etchevers HC, Murray J, Ziegler DS, Chesler L, Schmidt R, Burchill SA, Haber M, De Santo C, Mussai F.

Cancer Res. 2019 Feb 1;79(3):611-624. doi: 10.1158/0008-5472.CAN-18-2139. Epub 2018 Dec 13.

5.

Ectopic expression of Hoxb1 induces cardiac and craniofacial malformations.

Zaffran S, Odelin G, Stefanovic S, Lescroart F, Etchevers HC.

Genesis. 2018 Jun;56(6-7):e23221. doi: 10.1002/dvg.23221.

PMID:
30134070
6.

The hedgehog pathway and ocular developmental anomalies.

Cavodeassi F, Creuzet S, Etchevers HC.

Hum Genet. 2019 Sep;138(8-9):917-936. doi: 10.1007/s00439-018-1918-8. Epub 2018 Aug 2. Review.

7.

Reduced H3K27me3 Expression is Common in Nodular Melanomas of Childhood Associated With Congenital Melanocytic Nevi But Not in Proliferative Nodules.

Macagno N, Etchevers HC, Malissen N, Rome A, Hesse S, Mallet S, Degardin N, Gaudy C.

Am J Surg Pathol. 2018 May;42(5):701-704. doi: 10.1097/PAS.0000000000001026. No abstract available.

PMID:
29369061
8.

Widespread dynamic and pleiotropic expression of the melanocortin-1-receptor (MC1R) system is conserved across chick, mouse and human embryonic development.

Thomas AC, Heux P, Santos C, Arulvasan W, Solanky N, Carey ME, Gerrelli D, Kinsler VA, Etchevers HC.

Birth Defects Res. 2018 Mar 15;110(5):443-455. doi: 10.1002/bdr2.1183. Epub 2018 Jan 8.

9.

Giant congenital melanocytic nevus with vascular malformation and epidermal cysts associated with a somatic activating mutation in BRAF.

Etchevers HC, Rose C, Kahle B, Vorbringer H, Fina F, Heux P, Berger I, Schwarz B, Zaffran S, Macagno N, Krengel S.

Pigment Cell Melanoma Res. 2018 May;31(3):437-441. doi: 10.1111/pcmr.12685. Epub 2018 Jan 29.

PMID:
29316280
10.

Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries.

Boeva V, Louis-Brennetot C, Peltier A, Durand S, Pierre-Eugène C, Raynal V, Etchevers HC, Thomas S, Lermine A, Daudigeos-Dubus E, Geoerger B, Orth MF, Grünewald TGP, Diaz E, Ducos B, Surdez D, Carcaboso AM, Medvedeva I, Deller T, Combaret V, Lapouble E, Pierron G, Grossetête-Lalami S, Baulande S, Schleiermacher G, Barillot E, Rohrer H, Delattre O, Janoueix-Lerosey I.

Nat Genet. 2017 Sep;49(9):1408-1413. doi: 10.1038/ng.3921. Epub 2017 Jul 24.

PMID:
28740262
11.

Genome-wide DNA methylation analysis identifies MEGF10 as a novel epigenetically repressed candidate tumor suppressor gene in neuroblastoma.

Charlet J, Tomari A, Dallosso AR, Szemes M, Kaselova M, Curry TJ, Almutairi B, Etchevers HC, McConville C, Malik KT, Brown KW.

Mol Carcinog. 2017 Apr;56(4):1290-1301. doi: 10.1002/mc.22591. Epub 2016 Nov 29.

12.

Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network.

Chassaing N, Davis EE, McKnight KL, Niederriter AR, Causse A, David V, Desmaison A, Lamarre S, Vincent-Delorme C, Pasquier L, Coubes C, Lacombe D, Rossi M, Dufier JL, Dollfus H, Kaplan J, Katsanis N, Etchevers HC, Faguer S, Calvas P.

Genome Res. 2016 Apr;26(4):474-85. doi: 10.1101/gr.196048.115. Epub 2016 Feb 18.

13.

Cardiac outflow morphogenesis depends on effects of retinoic acid signaling on multiple cell lineages.

El Robrini N, Etchevers HC, Ryckebüsch L, Faure E, Eudes N, Niederreither K, Zaffran S, Bertrand N.

Dev Dyn. 2016 Mar;245(3):388-401. doi: 10.1002/dvdy.24357. Epub 2015 Oct 28.

14.

Hiding in plain sight: molecular genetics applied to giant congenital melanocytic nevi.

Etchevers HC.

J Invest Dermatol. 2014 Apr;134(4):879-882. doi: 10.1038/jid.2013.531.

15.

A subpopulation of smooth muscle cells, derived from melanocyte-competent precursors, prevents patent ductus arteriosus.

Yajima I, Colombo S, Puig I, Champeval D, Kumasaka M, Belloir E, Bonaventure J, Mark M, Yamamoto H, Taketo MM, Choquet P, Etchevers HC, Beermann F, Delmas V, Monassier L, Larue L.

PLoS One. 2013;8(1):e53183. doi: 10.1371/journal.pone.0053183. Epub 2013 Jan 31.

16.

Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE).

Krupp DR, Xu PT, Thomas S, Dellinger A, Etchevers HC, Vekemans M, Gilbert JR, Speer MC, Ashley-Koch AE, Gregory SG; National Birth Defects Prevention Study.

Birth Defects Res A Clin Mol Teratol. 2012 Sep;94(9):683-92. doi: 10.1002/bdra.23040. Epub 2012 Jul 18.

17.

OTX2 mutations contribute to the otocephaly-dysgnathia complex.

Chassaing N, Sorrentino S, Davis EE, Martin-Coignard D, Iacovelli A, Paznekas W, Webb BD, Faye-Petersen O, Encha-Razavi F, Lequeux L, Vigouroux A, Yesilyurt A, Boyadjiev SA, Kayserili H, Loget P, Carles D, Sergi C, Puvabanditsin S, Chen CP, Etchevers HC, Katsanis N, Mercer CL, Calvas P, Jabs EW.

J Med Genet. 2012 Jun;49(6):373-9. doi: 10.1136/jmedgenet-2012-100892. Epub 2012 May 10.

PMID:
22577225
18.

ISL1 directly regulates FGF10 transcription during human cardiac outflow formation.

Golzio C, Havis E, Daubas P, Nuel G, Babarit C, Munnich A, Vekemans M, Zaffran S, Lyonnet S, Etchevers HC.

PLoS One. 2012;7(1):e30677. doi: 10.1371/journal.pone.0030677. Epub 2012 Jan 27.

19.

CLMP is required for intestinal development, and loss-of-function mutations cause congenital short-bowel syndrome.

Van Der Werf CS, Wabbersen TD, Hsiao NH, Paredes J, Etchevers HC, Kroisel PM, Tibboel D, Babarit C, Schreiber RA, Hoffenberg EJ, Vekemans M, Zeder SL, Ceccherini I, Lyonnet S, Ribeiro AS, Seruca R, Te Meerman GJ, van Ijzendoorn SC, Shepherd IT, Verheij JB, Hofstra RM.

Gastroenterology. 2012 Mar;142(3):453-462.e3. doi: 10.1053/j.gastro.2011.11.038. Epub 2011 Dec 7.

PMID:
22155368
20.

Meeting report from the 2011 International Expert Meeting on Large Congenital Melanocytic Nevi and Neurocutaneous Melanocytosis, Tübingen.

Krengel S, Breuninger H, Beckwith M, Etchevers HC.

Pigment Cell Melanoma Res. 2011 Aug;24(4):E1-6. doi: 10.1111/j.1755-148X.2011.00875.x. Epub 2011 Jul 4. No abstract available.

PMID:
21672181

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