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Items: 1 to 20 of 53

1.

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.

Fachal L, Aschard H, Beesley J, Barnes DR, Allen J, Kar S, Pooley KA, Dennis J, Michailidou K, Turman C, Soucy P, Lemaçon A, Lush M, Tyrer JP, Ghoussaini M, Moradi Marjaneh M, Jiang X, Agata S, Aittomäki K, Alonso MR, Andrulis IL, Anton-Culver H, Antonenkova NN, Arason A, Arndt V, Aronson KJ, Arun BK, Auber B, Auer PL, Azzollini J, Balmaña J, Barkardottir RB, Barrowdale D, Beeghly-Fadiel A, Benitez J, Bermisheva M, Białkowska K, Blanco AM, Blomqvist C, Blot W, Bogdanova NV, Bojesen SE, Bolla MK, Bonanni B, Borg A, Bosse K, Brauch H, Brenner H, Briceno I, Brock IW, Brooks-Wilson A, Brüning T, Burwinkel B, Buys SS, Cai Q, Caldés T, Caligo MA, Camp NJ, Campbell I, Canzian F, Carroll JS, Carter BD, Castelao JE, Chiquette J, Christiansen H, Chung WK, Claes KBM, Clarke CL; GEMO Study Collaborators; EMBRACE Collaborators, Collée JM, Cornelissen S, Couch FJ, Cox A, Cross SS, Cybulski C, Czene K, Daly MB, de la Hoya M, Devilee P, Diez O, Ding YC, Dite GS, Domchek SM, Dörk T, Dos-Santos-Silva I, Droit A, Dubois S, Dumont M, Duran M, Durcan L, Dwek M, Eccles DM, Engel C, Eriksson M, Evans DG, Fasching PA, Fletcher O, Floris G, Flyger H, Foretova L, Foulkes WD, Friedman E, Fritschi L, Frost D, Gabrielson M, Gago-Dominguez M, Gambino G, Ganz PA, Gapstur SM, Garber J, García-Sáenz JA, Gaudet MM, Georgoulias V, Giles GG, Glendon G, Godwin AK, Goldberg MS, Goldgar DE, González-Neira A, Tibiletti MG, Greene MH, Grip M, Gronwald J, Grundy A, Guénel P, Hahnen E, Haiman CA, Håkansson N, Hall P, Hamann U, Harrington PA, Hartikainen JM, Hartman M, He W, Healey CS, Heemskerk-Gerritsen BAM, Heyworth J, Hillemanns P, Hogervorst FBL, Hollestelle A, Hooning MJ, Hopper JL, Howell A, Huang G, Hulick PJ, Imyanitov EN; KConFab Investigators; HEBON Investigators; ABCTB Investigators, Isaacs C, Iwasaki M, Jager A, Jakimovska M, Jakubowska A, James PA, Janavicius R, Jankowitz RC, John EM, Johnson N, Jones ME, Jukkola-Vuorinen A, Jung A, Kaaks R, Kang D, Kapoor PM, Karlan BY, Keeman R, Kerin MJ, Khusnutdinova E, Kiiski JI, Kirk J, Kitahara CM, Ko YD, Konstantopoulou I, Kosma VM, Koutros S, Kubelka-Sabit K, Kwong A, Kyriacou K, Laitman Y, Lambrechts D, Lee E, Leslie G, Lester J, Lesueur F, Lindblom A, Lo WY, Long J, Lophatananon A, Loud JT, Lubiński J, MacInnis RJ, Maishman T, Makalic E, Mannermaa A, Manoochehri M, Manoukian S, Margolin S, Martinez ME, Matsuo K, Maurer T, Mavroudis D, Mayes R, McGuffog L, McLean C, Mebirouk N, Meindl A, Miller A, Miller N, Montagna M, Moreno F, Muir K, Mulligan AM, Muñoz-Garzon VM, Muranen TA, Narod SA, Nassir R, Nathanson KL, Neuhausen SL, Nevanlinna H, Neven P, Nielsen FC, Nikitina-Zake L, Norman A, Offit K, Olah E, Olopade OI, Olsson H, Orr N, Osorio A, Pankratz VS, Papp J, Park SK, Park-Simon TW, Parsons MT, Paul J, Pedersen IS, Peissel B, Peshkin B, Peterlongo P, Peto J, Plaseska-Karanfilska D, Prajzendanc K, Prentice R, Presneau N, Prokofyeva D, Pujana MA, Pylkäs K, Radice P, Ramus SJ, Rantala J, Rau-Murthy R, Rennert G, Risch HA, Robson M, Romero A, Rossing M, Saloustros E, Sánchez-Herrero E, Sandler DP, Santamariña M, Saunders C, Sawyer EJ, Scheuner MT, Schmidt DF, Schmutzler RK, Schneeweiss A, Schoemaker MJ, Schöttker B, Schürmann P, Scott C, Scott RJ, Senter L, Seynaeve CM, Shah M, Sharma P, Shen CY, Shu XO, Singer CF, Slavin TP, Smichkoska S, Southey MC, Spinelli JJ, Spurdle AB, Stone J, Stoppa-Lyonnet D, Sutter C, Swerdlow AJ, Tamimi RM, Tan YY, Tapper WJ, Taylor JA, Teixeira MR, Tengström M, Teo SH, Terry MB, Teulé A, Thomassen M, Thull DL, Tischkowitz M, Toland AE, Tollenaar RAEM, Tomlinson I, Torres D, Torres-Mejía G, Troester MA, Truong T, Tung N, Tzardi M, Ulmer HU, Vachon CM, van Asperen CJ, van der Kolk LE, van Rensburg EJ, Vega A, Viel A, Vijai J, Vogel MJ, Wang Q, Wappenschmidt B, Weinberg CR, Weitzel JN, Wendt C, Wildiers H, Winqvist R, Wolk A, Wu AH, Yannoukakos D, Zhang Y, Zheng W, Hunter D, Pharoah PDP, Chang-Claude J, García-Closas M, Schmidt MK, Milne RL, Kristensen VN, French JD, Edwards SL, Antoniou AC, Chenevix-Trench G, Simard J, Easton DF, Kraft P, Dunning AM.

Nat Genet. 2020 Jan;52(1):56-73. doi: 10.1038/s41588-019-0537-1. Epub 2020 Jan 7.

PMID:
31911677
2.

A standardized nomenclature and atlas of the male terminalia of Drosophila melanogaster.

Rice G, David JR, Kamimura Y, Masly JP, Mcgregor AP, Nagy O, Noselli S, Nunes MDS, O'Grady P, Sánchez-Herrero E, Siegal ML, Toda MJ, Rebeiz M, Courtier-Orgogozo V, Yassin A.

Fly (Austin). 2019 Mar - Dec;13(1-4):51-64. doi: 10.1080/19336934.2019.1653733. Epub 2019 Aug 19.

PMID:
31401934
3.

Cooperation of axial and sex specific information controls Drosophila female genitalia growth by regulating the Decapentaplegic pathway.

Romero-Pozuelo J, Foronda D, Martín P, Hudry B, Merabet S, Graba Y, Sánchez-Herrero E.

Dev Biol. 2019 Oct 15;454(2):145-155. doi: 10.1016/j.ydbio.2019.06.014. Epub 2019 Jun 25.

PMID:
31251896
4.

Peritoneal washing is an adequate source for somatic BRCA1/2 mutation testing in ovarian malignancies.

Barquín M, Maximiano C, Pérez-Barrios C, Sanchez-Herrero E, Soriano M, Colmena M, García-Espantaleón M, Tejerina González E, Gutierrez L, Sánchez Ruiz AC, Torrente M, Provencio M, Romero A.

Pathol Res Pract. 2019 Feb;215(2):392-394. doi: 10.1016/j.prp.2018.10.028. Epub 2018 Oct 28.

PMID:
30392916
5.

The Drosophila Hox gene Ultrabithorax controls appendage shape by regulating extracellular matrix dynamics.

De Las Heras JM, García-Cortés C, Foronda D, Pastor-Pareja JC, Shashidhara LS, Sánchez-Herrero E.

Development. 2018 Jul 9;145(13). pii: dev161844. doi: 10.1242/dev.161844.

6.

Critical role for Fat/Hippo and IIS/Akt pathways downstream of Ultrabithorax during haltere specification in Drosophila.

Singh S, Sánchez-Herrero E, Shashidhara LS.

Mech Dev. 2015 Nov;138 Pt 2:198-209. doi: 10.1016/j.mod.2015.07.017. Epub 2015 Aug 20.

7.

The study of the Bithorax-complex genes in patterning CCAP neurons reveals a temporal control of neuronal differentiation by Abd-B.

Moris-Sanz M, Estacio-Gómez A, Sánchez-Herrero E, Díaz-Benjumea FJ.

Biol Open. 2015 Aug 14;4(9):1132-42. doi: 10.1242/bio.012872.

8.

The elimination of an adult segment by the Hox gene Abdominal-B.

Foronda D, Curt JR, Prieto N, Martín P, Sánchez-Herrero E.

Mech Dev. 2015 Nov;138 Pt 2:210-217. doi: 10.1016/j.mod.2015.08.002. Epub 2015 Aug 7.

9.

A genetic strategy to obtain P-Gal4 elements in the Drosophila Hox genes.

de Navas L, Foronda D, Del Saz D, Sánchez-Herrero E.

Methods Mol Biol. 2014;1196:49-57. doi: 10.1007/978-1-4939-1242-1_4.

PMID:
25151157
10.

Homeotic function of Drosophila Bithorax-complex miRNAs mediates fertility by restricting multiple Hox genes and TALE cofactors in the CNS.

Garaulet DL, Castellanos MC, Bejarano F, Sanfilippo P, Tyler DM, Allan DW, Sánchez-Herrero E, Lai EC.

Dev Cell. 2014 Jun 23;29(6):635-48. doi: 10.1016/j.devcel.2014.04.023. Epub 2014 Jun 5.

11.

Hox targets and cellular functions.

Sánchez-Herrero E.

Scientifica (Cairo). 2013;2013:738257. doi: 10.1155/2013/738257. Epub 2013 Dec 30. Erratum in: Scientifica (Cairo). 2014;2014:529298.

12.

The zinc finger homeodomain-2 gene of Drosophila controls Notch targets and regulates apoptosis in the tarsal segments.

Guarner A, Manjón C, Edwards K, Steller H, Suzanne M, Sánchez-Herrero E.

Dev Biol. 2014 Jan 15;385(2):350-65. doi: 10.1016/j.ydbio.2013.10.011. Epub 2013 Oct 19.

13.

Differential activity of Drosophila Hox genes induces myosin expression and can maintain compartment boundaries.

Curt JR, de Navas LF, Sánchez-Herrero E.

PLoS One. 2013;8(2):e57159. doi: 10.1371/journal.pone.0057159. Epub 2013 Feb 25.

14.

Drosophila Hox and sex-determination genes control segment elimination through EGFR and extramacrochetae activity.

Foronda D, Martín P, Sánchez-Herrero E.

PLoS Genet. 2012;8(8):e1002874. doi: 10.1371/journal.pgen.1002874. Epub 2012 Aug 9.

15.

Integration of RNA processing and expression level control modulates the function of the Drosophila Hox gene Ultrabithorax during adult development.

de Navas LF, Reed H, Akam M, Barrio R, Alonso CR, Sánchez-Herrero E.

Development. 2011 Jan;138(1):107-16. doi: 10.1242/dev.051409. Epub 2010 Nov 29.

16.

Function and specificity of Hox genes.

Foronda D, de Navas LF, Garaulet DL, Sánchez-Herrero E.

Int J Dev Biol. 2009;53(8-10):1404-19. doi: 10.1387/ijdb.072462df. Review.

17.

Polycomb-dependent Ultrabithorax Hox gene silencing induced by high Ultrabithorax levels in Drosophila.

Garaulet DL, Foronda D, Calleja M, Sánchez-Herrero E.

Development. 2008 Oct;135(19):3219-28. doi: 10.1242/dev.025809. Epub 2008 Aug 20.

18.

Sharp boundaries of Dpp signalling trigger local cell death required for Drosophila leg morphogenesis.

Manjón C, Sánchez-Herrero E, Suzanne M.

Nat Cell Biol. 2007 Jan;9(1):57-63. Epub 2006 Dec 3.

19.

The ultrabithorax Hox gene of Drosophila controls haltere size by regulating the Dpp pathway.

de Navas LF, Garaulet DL, Sánchez-Herrero E.

Development. 2006 Nov;133(22):4495-506. Epub 2006 Oct 18.

20.

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