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Items: 1 to 50 of 55

1.

Differential responses of Miocene rodent metacommunities to global climatic changes were mediated by environmental context.

Blanco F, Gómez Cano AR, Cantalapiedra JL, Domingo MS, Domingo L, Menéndez I, Flynn LJ, Hernández Fernández M.

Sci Rep. 2018 Feb 6;8(1):2502. doi: 10.1038/s41598-018-20900-5.

2.

Body-size structure of Central Iberian mammal fauna reveals semidesertic conditions during the middle Miocene Global Cooling Event.

Menéndez I, Gómez Cano AR, García Yelo BA, Domingo L, Domingo MS, Cantalapiedra JL, Blanco F, Hernández Fernández M.

PLoS One. 2017 Oct 26;12(10):e0186762. doi: 10.1371/journal.pone.0186762. eCollection 2017.

3.

Ecomorphological characterization of murines and non-arvicoline cricetids (Rodentia) from south-western Europe since the latest Middle Miocene to the Mio-Pliocene boundary (MN 7/8-MN13).

Gomez Cano AR, Kimura Y, Blanco F, Menéndez I, Álvarez-Sierra MA, Hernández Fernández M.

PeerJ. 2017 Sep 25;5:e3646. doi: 10.7717/peerj.3646. eCollection 2017.

4.

Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort.

Cengiz FB, Yilmazer R, Olgun L, Sennaroglu L, Kirazli T, Alper H, Olgun Y, Incesulu A, Atik T, Huesca-Hernandez F, Domínguez-Aburto J, González-Rosado G, Hernandez-Zamora E, Arenas-Sordo ML, Menendez I, Orhan KS, Avci H, Mahdieh N, Bonyadi M, Foster J 2nd, Duman D, Ozkinay F, Blanton SH, Bademci G, Tekin M.

Int J Pediatr Otorhinolaryngol. 2017 Oct;101:167-171. doi: 10.1016/j.ijporl.2017.08.006. Epub 2017 Aug 8.

PMID:
28964290
5.

Novel EYA1 variants causing Branchio-oto-renal syndrome.

Klingbeil KD, Greenland CM, Arslan S, Llamos Paneque A, Gurkan H, Demir Ulusal S, Maroofian R, Carrera-Gonzalez A, Montufar-Armendariz S, Paredes R, Elcioglu N, Menendez I, Behnam M, Foster J 2nd, Guo S, Escarfuller S, Cengiz FB, Duman D, Bademci G, Tekin M.

Int J Pediatr Otorhinolaryngol. 2017 Jul;98:59-63. doi: 10.1016/j.ijporl.2017.04.037. Epub 2017 Apr 26.

PMID:
28583505
6.

Dominant deafness-onychodystrophy syndrome caused by an ATP6V1B2 mutation.

Menendez I, Carranza C, Herrera M, Marroquin N, Foster J 2nd, Cengiz FB, Bademci G, Tekin M.

Clin Case Rep. 2017 Feb 8;5(4):376-379. doi: 10.1002/ccr3.761. eCollection 2017 Apr.

7.

Saharan dust and the impact on adult and elderly allergic patients: the effect of threshold values in the northern sector of Gran Canaria, Spain.

Menéndez I, Derbyshire E, Carrillo T, Caballero E, Engelbrecht JP, Romero LE, Mayer PL, Rodríguez de Castro F, Mangas J.

Int J Environ Health Res. 2017 Apr;27(2):144-160. doi: 10.1080/09603123.2017.1292496.

PMID:
28245676
8.

Ultrastructural and biochemical basis for hepatitis C virus morphogenesis.

Falcón V, Acosta-Rivero N, González S, Dueñas-Carrera S, Martinez-Donato G, Menéndez I, Garateix R, Silva JA, Acosta E, Kourı J.

Virus Genes. 2017 Apr;53(2):151-164. doi: 10.1007/s11262-017-1426-2. Epub 2017 Feb 23. Review.

PMID:
28233195
9.

Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern Brazil.

Manzoli GN, Bademci G, Acosta AX, Félix TM, Cengiz FB, Foster J 2nd, Da Silva DS, Menendez I, Sanchez-Pena I, Tekin D, Blanton SH, Abe-Sandes K, Liu XZ, Tekin M.

Ann Hum Genet. 2016 Nov;80(6):327-331. doi: 10.1111/ahg.12177.

10.

Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss.

Bademci G, Cengiz FB, Foster Ii J, Duman D, Sennaroglu L, Diaz-Horta O, Atik T, Kirazli T, Olgun L, Alper H, Menendez I, Loclar I, Sennaroglu G, Tokgoz-Yilmaz S, Guo S, Olgun Y, Mahdieh N, Bonyadi M, Bozan N, Ayral A, Ozkinay F, Yildirim-Baylan M, Blanton SH, Tekin M.

Sci Rep. 2016 Aug 26;6:31622. doi: 10.1038/srep31622.

11.

Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents.

Yan D, Tekin D, Bademci G, Foster J 2nd, Cengiz FB, Kannan-Sundhari A, Guo S, Mittal R, Zou B, Grati M, Kabahuma RI, Kameswaran M, Lasisi TJ, Adedeji WA, Lasisi AO, Menendez I, Herrera M, Carranza C, Maroofian R, Crosby AH, Bensaid M, Masmoudi S, Behnam M, Mojarrad M, Feng Y, Duman D, Mawla AM, Nord AS, Blanton SH, Liu XZ, Tekin M.

Hum Genet. 2016 Aug;135(8):953-61. doi: 10.1007/s00439-016-1697-z. Epub 2016 Jun 25.

12.

Neurosurgery at the University of Miami.

Alberga L, Menendez I, Landy HJ, Morcos JJ, Levi AD.

J Neurosurg. 2017 Apr;126(4):1285-1295. doi: 10.3171/2016.4.JNS152356. Epub 2016 Jun 24.

PMID:
27341044
13.

A Mayan founder mutation is a common cause of deafness in Guatemala.

Carranza C, Menendez I, Herrera M, Castellanos P, Amado C, Maldonado F, Rosales L, Escobar N, Guerra M, Alvarez D, Foster J 2nd, Guo S, Blanton SH, Bademci G, Tekin M.

Clin Genet. 2015 Sep 8. doi: 10.1111/cge.12676. [Epub ahead of print]

14.

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.

Bademci G, Foster J 2nd, Mahdieh N, Bonyadi M, Duman D, Cengiz FB, Menendez I, Diaz-Horta O, Shirkavand A, Zeinali S, Subasioglu A, Tokgoz-Yilmaz S, Huesca-Hernandez F, de la Luz Arenas-Sordo M, Dominguez-Aburto J, Hernandez-Zamora E, Montenegro P, Paredes R, Moreta G, Vinueza R, Villegas F, Mendoza-Benitez S, Guo S, Bozan N, Tos T, Incesulu A, Sennaroglu G, Blanton SH, Ozturkmen-Akay H, Yildirim-Baylan M, Tekin M.

Genet Med. 2016 Apr;18(4):364-71. doi: 10.1038/gim.2015.89. Epub 2015 Jul 30. Erratum in: Genet Med. 2016 Aug;18(8):859.

15.

Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations.

Bademci G, Lasisi A, Yariz KO, Montenegro P, Menendez I, Vinueza R, Paredes R, Moreta G, Subasioglu A, Blanton S, Fitoz S, Incesulu A, Sennaroglu L, Tekin M.

BMC Med Genet. 2015 Feb 25;16:9. doi: 10.1186/s12881-015-0149-2.

16.

Working in direct contact with the public as a predictor of burnout in the banking sector.

Amigo I, Asensio E, Menéndez I, Redondo S, Ledesma JA.

Psicothema. 2014 May;26(2):222-6. doi: 10.7334/psicothema2013.282.

PMID:
24755024
17.

An amino acid deletion inSZT2 in a family with non-syndromic intellectual disability.

Falcone M, Yariz KO, Ross DB, Foster J 2nd, Menendez I, Tekin M.

PLoS One. 2013 Dec 6;8(12):e82810. doi: 10.1371/journal.pone.0082810. eCollection 2013.

18.

Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss.

Diaz-Horta O, Duman D, Foster J 2nd, Sırmacı A, Gonzalez M, Mahdieh N, Fotouhi N, Bonyadi M, Cengiz FB, Menendez I, Ulloa RH, Edwards YJ, Züchner S, Blanton S, Tekin M.

PLoS One. 2012;7(11):e50628. doi: 10.1371/journal.pone.0050628. Epub 2012 Nov 30.

19.

Unique spectrum of GJB2 mutations in Mexico.

de la Luz Arenas-Sordo M, Menendez I, Hernández-Zamora E, Sirmaci A, Gutiérrez-Tinajero D, McGetrick M, Murphy-Ruiz P, Leyva-Juárez X, Huesca-Hernández F, Dominguez-Aburto J, Tekin M.

Int J Pediatr Otorhinolaryngol. 2012 Nov;76(11):1678-80. doi: 10.1016/j.ijporl.2012.08.005. Epub 2012 Aug 24.

PMID:
22925408
20.

Dengue virus identification by transmission electron microscopy and molecular methods in fatal dengue hemorrhagic fever.

Limonta D, Falcón V, Torres G, Capó V, Menéndez I, Rosario D, Castellanos Y, Alvarez M, Rodríguez-Roche R, de la Rosa MC, Pavón A, López L, González K, Guillén G, Diaz J, Guzmán MG.

Infection. 2012 Dec;40(6):689-94. doi: 10.1007/s15010-012-0260-7. Epub 2012 Apr 20.

PMID:
22527878
21.

A novel fusion protein domain III-capsid from dengue-2, in a highly aggregated form, induces a functional immune response and protection in mice.

Valdés I, Bernardo L, Gil L, Pavón A, Lazo L, López C, Romero Y, Menendez I, Falcón V, Betancourt L, Martín J, Chinea G, Silva R, Guzmán MG, Guillén G, Hermida L.

Virology. 2009 Nov 25;394(2):249-58. doi: 10.1016/j.virol.2009.08.029. Epub 2009 Sep 23.

22.

In vitro assembly of nucleocapsid-like particles from purified recombinant capsid protein of dengue-2 virus.

López C, Gil L, Lazo L, Menéndez I, Marcos E, Sánchez J, Valdés I, Falcón V, de la Rosa MC, Márquez G, Guillén G, Hermida L.

Arch Virol. 2009;154(4):695-8. doi: 10.1007/s00705-009-0350-8. Epub 2009 Mar 21.

PMID:
19305942
23.

Ronald Tasker Award: Intrathecal transplantation of a human neuronal cell line for the treatment of neuropathic pain in a spinal cord injury model.

Quintero Wolfe SC, Cumberbatch N, Menendez I, Martinez M, Eaton M.

Clin Neurosurg. 2007;54:220-5. No abstract available.

PMID:
18504923
24.

Pathogenic validation of unique germline intronic variants of RB1 in retinoblastoma patients using minigenes.

Gámez-Pozo A, Palacios I, Kontic M, Menéndez I, Camino I, García-Miguel P, Abelairas J, Pestaña A, Alonso J.

Hum Mutat. 2007 Dec;28(12):1245.

PMID:
18000883
25.

[Molecular diagnosis of retinoblastoma: molecular epidemiology and genetic counseling].

Alonso J, Palacios I, Gámez A, Camino I, Frayle H, Menéndez I, Kontic M, García-Miguel P, Sastre A, Abelairas J, Sarret E, Sabado C, Navajas A, Artigas M, Indiano JM, Carbone A, Rosell J, Pestaña A.

Med Clin (Barc). 2006 Mar 25;126(11):401-5. Spanish.

PMID:
16595082
26.

[Comparison between the 1993 and 2002 Guidelines of the Spanish Society of Pulmonology and Thoracic Surgery (SEPAR) for identifying respiratory events in polysomnography tests].

Aguirregomoscorta JI, Altube L, Menéndez I, Romaní A, Basualdo LV, Vallejo G.

Arch Bronconeumol. 2005 Dec;41(12):649-53. Spanish.

27.

Regional conformational change involving phosphorylation of tau protein at the Thr231, precedes the structural change detected by Alz-50 antibody in Alzheimer's disease.

Luna-Muñoz J, García-Sierra F, Falcón V, Menéndez I, Chávez-Macías L, Mena R.

J Alzheimers Dis. 2005 Sep;8(1):29-41.

PMID:
16155347
28.

A C-terminal truncated hepatitis C virus core protein variant assembles in vitro into virus-like particles in the absence of structured nucleic acids.

Acosta-Rivero N, Rodriguez A, Mussachio A, Poutou J, Falcon V, Torres D, Aguilar JC, Linares M, Alonso M, Perez A, Menendez I, Morales-Grillo J, Marquez G, Dueñas-Carrera S.

Biochem Biophys Res Commun. 2005 Sep 2;334(3):901-6. Erratum in: Biochem Biophys Res Commun. 2005 Nov 11;337(1):410. Poutu, Johana [corrected to Poutou, Joanna].

PMID:
16053919
29.

HCV core protein localizes in the nuclei of nonparenchymal liver cells from chronically HCV-infected patients.

Falcón V, Acosta-Rivero N, Shibayama M, Chinea G, Gavilondo JV, de la Rosa MC, Menéndez I, Gra B, Dueñas-Carrera S, Viña A, García W, González-Bravo M, Luna-Munoz J, Miranda-Sanchez M, Morales-Grillo J, Kouri J, Tsutsumi V.

Biochem Biophys Res Commun. 2005 Apr 22;329(4):1320-8.

PMID:
15766571
30.

Identification of 26 new constitutional RB1 gene mutations in Spanish, Colombian, and Cuban retinoblastoma patients.

Alonso J, Frayle H, Menéndez I, López A, García-Miguel P, Abelairas J, Sarret E, Vendrell MT, Navajas A, Artigas M, Indiano JM, Carbone A, Torrenteras C, Palacios I, Pestaña A.

Hum Mutat. 2005 Jan;25(1):99.

PMID:
15605413
31.

Two independent RB1-inactivating mutations in peripheral blood DNA of a hereditary retinoblastoma patient.

Alonso J, Menéndez I, López A, Frayle H, Ruisánchez N, Pestaña A.

Genes Chromosomes Cancer. 2004 Jul;40(3):271-5.

PMID:
15139006
32.

Nuclear localization of nucleocapsid-like particles and HCV core protein in hepatocytes of a chronically HCV-infected patient.

Falcón V, Acosta-Rivero N, Chinea G, de la Rosa MC, Menéndez I, Dueñas-Carrera S, Gra B, Rodriguez A, Tsutsumi V, Shibayama M, Luna-Munoz J, Miranda-Sanchez MM, Morales-Grillo J, Kouri J.

Biochem Biophys Res Commun. 2003 Oct 10;310(1):54-8.

PMID:
14511647
33.

Structured HCV nucleocapsids composed of P21 core protein assemble primary in the nucleus of Pichia pastoris yeast.

Acosta-Rivero N, Falcón V, Alvarez C, Musacchio A, Chinea G, Cristina de la Rosa M, Rodriguez A, Dueñas-Carrera S, Tsutsumi V, Shibayama M, Menéndez I, Luna-Munoz J, Miranda-Sanchez MM, Kouri J, Morales-Grillo J.

Biochem Biophys Res Commun. 2003 Oct 10;310(1):48-53.

PMID:
14511646
34.

Ultrastructural evidences of HCV infection in hepatocytes of chronically HCV-infected patients.

Falcón V, Acosta-Rivero N, Chinea G, Gavilondo J, de la Rosa MC, Menéndez I, Dueñas-Carrera S, Viña A, García W, Gra B, Noa M, Reytor E, Barceló MT, Alvarez F, Morales-Grillo J.

Biochem Biophys Res Commun. 2003 Jun 13;305(4):1085-90.

PMID:
12767942
35.

Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss.

Migliosi V, Modamio-Høybjør S, Moreno-Pelayo MA, Rodríguez-Ballesteros M, Villamar M, Tellería D, Menéndez I, Moreno F, Del Castillo I.

J Med Genet. 2002 Jul;39(7):502-6. No abstract available.

36.

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.

del Castillo I, Villamar M, Moreno-Pelayo MA, del Castillo FJ, Alvarez A, Tellería D, Menéndez I, Moreno F.

N Engl J Med. 2002 Jan 24;346(4):243-9.

37.

In vitro self-assembled HCV core virus-like particles induce a strong antibody immune response in sheep.

Acosta-Rivero N, Alvarez-Obregón JC, Musacchio A, Falcón V, Dueñas-Carrera S, Marante J, Menéndez I, Morales J.

Biochem Biophys Res Commun. 2002 Jan 11;290(1):300-4.

PMID:
11779169
38.

Assembly of truncated HCV core antigen into virus-like particles in Escherichia coli.

Lorenzo LJ, Dueñas-Carrera S, Falcón V, Acosta-Rivero N, González E, de la Rosa MC, Menéndez I, Morales J.

Biochem Biophys Res Commun. 2001 Mar 9;281(4):962-5.

PMID:
11237755
39.

Lung cancer risk in iron and steel foundry workers: a nested case control study in Asturias, Spain.

Rodríguez V, Tardón A, Kogevinas M, Prieto CS, Cueto A, García M, Menéndez IA, Zaplana J.

Am J Ind Med. 2000 Dec;38(6):644-50.

PMID:
11071687
40.

Sesquiterpene lactones are potent inhibitors of interleukin 8 gene expression in cultured human respiratory epithelium.

Mazor RL, Menendez IY, Ryan MA, Fiedler MA, Wong HR.

Cytokine. 2000 Mar;12(3):239-45.

PMID:
10704251
41.

Hyperoxia synergistically increases TNF-alpha-induced interleukin-8 gene expression in A549 cells.

Allen GL, Menendez IY, Ryan MA, Mazor RL, Wispé JR, Fiedler MA, Wong HR.

Am J Physiol Lung Cell Mol Physiol. 2000 Feb;278(2):L253-60.

42.

Heat shock activates the I-kappaBalpha promoter and increases I-kappaBalpha mRNA expression.

Wong HR, Ryan MA, Menendez IY, Wispé JR.

Cell Stress Chaperones. 1999 Mar;4(1):1-7.

43.
44.
45.

Increased expression of heat shock protein-70 protects A549 cells against hyperoxia.

Wong HR, Menendez IY, Ryan MA, Denenberg AG, Wispé JR.

Am J Physiol. 1998 Oct;275(4 Pt 1):L836-41.

PMID:
9755117
46.

The heat shock response inhibits RANTES gene expression in cultured human lung epithelium.

Ayad O, Stark JM, Fiedler MM, Menendez IY, Ryan MA, Wong HR.

J Immunol. 1998 Sep 1;161(5):2594-9.

47.

Heat shock protein induction protects human respiratory epithelium against nitric oxide-mediated cytotoxicity.

Wong HR, Ryan M, Menendez IY, Denenberg A, Wispé JR.

Shock. 1997 Sep;8(3):213-8.

PMID:
9377169
48.

[Trisomy 5p due to paternal translocation (4;5) (q35;p12)].

Menéndez I, Casaña H.

Bol Med Hosp Infant Mex. 1993 Mar;50(3):194-6. Spanish.

PMID:
8442884
49.

[11q distal trisomy due to a familial 11;18 translocation].

Menéndez I, Rivera H, Morales E, Juan J, Jiménez M.

Bol Med Hosp Infant Mex. 1990 Nov;47(11):792-4. Spanish.

PMID:
2285470
50.

The syndrome of inappropriate secretion of the antidiuretic hormone and self-induced water intoxication in schizophrenic patients.

Pérez-Cruet J, Menéndez I.

Bol Asoc Med P R. 1986 May;78(5):185-90. No abstract available.

PMID:
3460600

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