Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 39

1.

Aging-related tau astrogliopathy (ARTAG): not only tau phosphorylation in astrocytes.

Ferrer I, García MA, González IL, Lucena DD, Villalonga AR, Tech MC, Llorens F, Garcia-Esparcia P, Martinez-Maldonado A, Mendez MF, Escribano BT, Bech-Serra JJ, Sabido E, de la Torre Gómez C, Del Rio JA.

Brain Pathol. 2018 Nov;28(6):965-985. doi: 10.1111/bpa.12593. Epub 2018 Feb 25.

2.

A Semi-automated Approach to Preparing Antibody Cocktails for Immunophenotypic Analysis of Human Peripheral Blood.

Koguchi Y, Gonzalez IL, Meeuwsen TL, Miller WL, Haley DP, Tanibata-Branham AN, Bahjat KS.

J Vis Exp. 2016 Feb 8;(108):e53485. doi: 10.3791/53485.

3.

A homozygous double mutation in SMN1: a complicated genetic diagnosis of SMA.

Kirwin SM, Vinette KM, Gonzalez IL, Abdulwahed HA, Al-Sannaa N, Funanage VL.

Mol Genet Genomic Med. 2013 Jul;1(2):113-7. doi: 10.1002/mgg3.10. Epub 2013 May 30.

4.

Tafazzin splice variants and mutations in Barth syndrome.

Kirwin SM, Manolakos A, Barnett SS, Gonzalez IL.

Mol Genet Metab. 2014 Jan;111(1):26-32. doi: 10.1016/j.ymgme.2013.11.006. Epub 2013 Nov 19.

PMID:
24342716
5.

A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome.

Fan Y, Steller J, Gonzalez IL, Kulik W, Fox M, Chang R, Westerfield BA, Batra AS, Wang RY, Gallant NM, Pena LS, Wang H, Huang T, Bhuta S, Penny DJ, McCabe ER, Kimonis VE.

JIMD Rep. 2013;11:99-106. doi: 10.1007/8904_2013_228. Epub 2013 Apr 19.

6.

Barth syndrome.

Clarke SL, Bowron A, Gonzalez IL, Groves SJ, Newbury-Ecob R, Clayton N, Martin RP, Tsai-Goodman B, Garratt V, Ashworth M, Bowen VM, McCurdy KR, Damin MK, Spencer CT, Toth MJ, Kelley RI, Steward CG.

Orphanet J Rare Dis. 2013 Feb 12;8:23. doi: 10.1186/1750-1172-8-23. Review.

7.

Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth.

Steward CG, Newbury-Ecob RA, Hastings R, Smithson SF, Tsai-Goodman B, Quarrell OW, Kulik W, Wanders R, Pennock M, Williams M, Cresswell JL, Gonzalez IL, Brennan P.

Prenat Diagn. 2010 Oct;30(10):970-6. doi: 10.1002/pd.2599.

8.

[Arthroscopic treatment for anterolateral ankle impingement of athletes].

Villarreal JM, Cerecedo RB, Cal y Mayor FF, González IL.

Acta Ortop Mex. 2008 Mar-Apr;22(2):103-6. Spanish.

9.

Vasoactive intestinal peptide receptor expression in chronic periapical lesions.

Caviedes-Bucheli J, Azuero-Holguín MM, Moreno GC, González IL, Mateu E, Salazar JF, Munoz HR.

Int Endod J. 2007 Jul;40(7):521-5. Epub 2007 May 18.

PMID:
17511789
10.

Multiple transmissions of Barth syndrome through an oocyte donor with a de novo TAZ mutation.

Kirwin SM, Vinette KM, Schwartz SB, Funanage VL, Gonzalez IL.

Fertil Steril. 2007 Apr;87(4):976.e5-7. Epub 2007 Jan 22.

PMID:
17241629
11.

Cardiac and clinical phenotype in Barth syndrome.

Spencer CT, Bryant RM, Day J, Gonzalez IL, Colan SD, Thompson WR, Berthy J, Redfearn SP, Byrne BJ.

Pediatrics. 2006 Aug;118(2):e337-46. Epub 2006 Jul 17.

PMID:
16847078
12.

Paternal bias in parental origin of HRAS mutations in Costello syndrome.

Sol-Church K, Stabley DL, Nicholson L, Gonzalez IL, Gripp KW.

Hum Mutat. 2006 Aug;27(8):736-41.

PMID:
16835863
13.

HRAS mutation analysis in Costello syndrome: genotype and phenotype correlation.

Gripp KW, Lin AE, Stabley DL, Nicholson L, Scott CI Jr, Doyle D, Aoki Y, Matsubara Y, Zackai EH, Lapunzina P, Gonzalez-Meneses A, Holbrook J, Agresta CA, Gonzalez IL, Sol-Church K.

Am J Med Genet A. 2006 Jan 1;140(1):1-7.

PMID:
16329078
14.

Barth syndrome: TAZ gene mutations, mRNAs, and evolution.

Gonzalez IL.

Am J Med Genet A. 2005 May 1;134(4):409-14.

PMID:
15793838
15.

Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy.

Frisch R, Singleton KR, Moses PA, Gonzalez IL, Carango P, Marks HG, Funanage VL.

Mol Genet Metab. 2001 Sep-Oct;74(1-2):281-91.

PMID:
11592825
16.
17.

Control of ticks resistant to immunization with Bm86 in cattle vaccinated with the recombinant antigen Bm95 isolated from the cattle tick, Boophilus microplus.

García-García JC, Montero C, Redondo M, Vargas M, Canales M, Boue O, Rodríguez M, Joglar M, Machado H, González IL, Valdés M, Méndez L, de la Fuente J.

Vaccine. 2000 Apr 28;18(21):2275-87.

PMID:
10717348
18.

Sequence variations in the Boophilus microplus Bm86 locus and implications for immunoprotection in cattle vaccinated with this antigen.

García-García JC, Gonzalez IL, González DM, Valdés M, Méndez L, Lamberti J, D'Agostino B, Citroni D, Fragoso H, Ortiz M, Rodríguez M, de la Fuente J.

Exp Appl Acarol. 1999 Nov;23(11):883-95.

PMID:
10668863
19.

Beyond ribosomal DNA: on towards the telomere.

Gonzalez IL, Sylvester JE.

Chromosoma. 1997 Jun;105(7-8):431-7.

PMID:
9211970
20.

Incognito rRNA and rDNA in databases and libraries.

Gonzalez IL, Sylvester JE.

Genome Res. 1997 Jan;7(1):65-70.

21.

Human ribosomal RNA variants from a single individual and their expression in different tissues.

Kuo BA, Gonzalez IL, Gillespie DA, Sylvester JE.

Nucleic Acids Res. 1996 Dec 1;24(23):4817-24.

22.

Studies of the inheritance of human ribosomal DNA variants detected in two-dimensional separations of genomic restriction fragments.

Kuick R, Asakawa J, Neel JV, Kodaira M, Satoh C, Thoraval D, Gonzalez IL, Hanash SM.

Genetics. 1996 Sep;144(1):307-16.

23.

Complete sequence of the 43-kb human ribosomal DNA repeat: analysis of the intergenic spacer.

Gonzalez IL, Sylvester JE.

Genomics. 1995 May 20;27(2):320-8.

PMID:
7557999
24.

Fixation times of retroposons in the ribosomal DNA spacer of human and other primates.

Gonzalez IL, Tugendreich S, Hieter P, Sylvester JE.

Genomics. 1993 Oct;18(1):29-36.

PMID:
8276415
25.

The topographic organization of repetitive DNA in the human nucleolus.

Kaplan FS, Murray J, Sylvester JE, Gonzalez IL, O'Connor JP, Doering JL, Muenke M, Emanuel BS, Zasloff MA.

Genomics. 1993 Jan;15(1):123-32.

PMID:
8432523
26.

Human ribosomal RNA intergenic spacer sequence.

Gonzalez IL, Wu S, Li WM, Kuo BA, Sylvester JE.

Nucleic Acids Res. 1992 Nov 11;20(21):5846. No abstract available.

27.

Ribosomal RNA gene sequences and hominoid phylogeny.

Gonzalez IL, Sylvester JE, Smith TF, Stambolian D, Schmickel RD.

Mol Biol Evol. 1990 May;7(3):203-19.

PMID:
2359361
28.

Sequence and structure correlation of human ribosomal transcribed spacers.

Gonzalez IL, Chambers C, Gorski JL, Stambolian D, Schmickel RD, Sylvester JE.

J Mol Biol. 1990 Mar 5;212(1):27-35.

PMID:
2319598
29.

Independent insertion of Alu elements in the human ribosomal spacer and their concerted evolution.

Gonzalez IL, Petersen R, Sylvester JE.

Mol Biol Evol. 1989 Jul;6(4):413-23.

PMID:
2559294
30.

Definition of a second dimeric subfamily of human alpha satellite DNA.

Thompson JD, Sylvester JE, Gonzalez IL, Costanzi CC, Gillespie D.

Nucleic Acids Res. 1989 Apr 11;17(7):2769-82.

31.

Human 28S ribosomal RNA sequence heterogeneity.

Gonzalez IL, Sylvester JE, Schmickel RD.

Nucleic Acids Res. 1988 Nov 11;16(21):10213-24.

32.

Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy.

Bodrug SE, Ray PN, Gonzalez IL, Schmickel RD, Sylvester JE, Worton RG.

Science. 1987 Sep 25;237(4822):1620-4.

PMID:
3629260
33.

The secondary structure of human 28S rRNA: the structure and evolution of a mosaic rRNA gene.

Gorski JL, Gonzalez IL, Schmickel RD.

J Mol Evol. 1987;24(3):236-51.

34.

A simple repetitive sequence common to herpes simplex virus type 1 and human ribosomal DNAs.

Parks CL, Jones TR, Gonzalez IL, Schmickel RD, Hyman RW, Spector DJ.

Virology. 1986 Oct 30;154(2):381-8.

PMID:
3020785
35.

The human 18S ribosomal RNA gene: evolution and stability.

Gonzalez IL, Schmickel RD.

Am J Hum Genet. 1986 Apr;38(4):419-27.

36.

Variation among human 28S ribosomal RNA genes.

Gonzalez IL, Gorski JL, Campen TJ, Dorney DJ, Erickson JM, Sylvester JE, Schmickel RD.

Proc Natl Acad Sci U S A. 1985 Nov;82(22):7666-70.

37.

Complementarity between ferritin H mRNA and 28 S ribosomal RNA.

Jain SK, Crampton J, Gonzalez IL, Schmickel RD, Drysdale JW.

Biochem Biophys Res Commun. 1985 Sep 16;131(2):863-7.

PMID:
3840373
38.

Nucleolus organizing genes on chromosome 21: recombination and nondisjunction.

Schmickel RD, Gonzalez IL, Erickson JM.

Ann N Y Acad Sci. 1985;450:121-31. No abstract available.

PMID:
3160285
39.

Supplemental Content

Loading ...
Support Center