Kenia B El-Jaick
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Explore the profile of Kenia B El-Jaick including associated specialties, affiliations and a list of published articles.
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10
Citations
164
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Recent Articles
1.
Oliveira T, Maues T, Ramundo M, Figueiredo A, de Mello M, El-Jaick K, et al.
J Vet Diagn Invest
. 2017 Jul;
29(6):865-868.
PMID: 28754073
The protein p53 is considered to be one of the most important tumor suppressor factors. Despite this importance, a potential association between TP53 messenger (m)RNA levels and tumor aggressiveness has...
2.
Zaverucha-do-Valle C, Monteiro S, El-Jaick K, Rosadas L, Costa M, Quintana M, et al.
Tuberculosis (Edinb)
. 2014 May;
94(3):299-305.
PMID: 24793319
Tuberculosis (TB) is still a major health concern and side-effects related to the treatment, especially drug-induced hepatotoxicity (DIH), should be better investigated. In the present study, a possible association between...
3.
Jeovanio-Silva A, Monteiro T, El-Jaick K, do Brasil P, Rolla V, De Castro L
Mol Med Rep
. 2011 Oct;
5(1):153-61.
PMID: 21964586
CYP3A4 is involved in tuberculosis (TB) and human immunodeficiency virus (HIV) drug metabolism. Transcriptional activation by rifampicin involves the CYP3A4 gene 5'-upstream region. Consequently, variation may interfere with transcription and...
4.
Costa-Lima M, Meneses H, El-Jaick K, Amorim M, Castilla E, Orioli I
Mol Med Rep
. 2011 Apr;
1(3):443-6.
PMID: 21479430
The ZIC genes comprise a family of transcriptional factors associated with neural tube defects (NTDs) in mice and with holoprosencephaly in humans. An allelic variant of ZIC2, a CAC repeat...
5.
Roessler E, El-Jaick K, Dubourg C, Velez J, Solomon B, Pineda-Alvarez D, et al.
Hum Mutat
. 2009 Jul;
30(10):E921-35.
PMID: 19603532
Mutations within either the SHH gene or its related pathway components are the most common, and best understood, pathogenetic changes observed in holoprosencephaly patients; this fact is consistent with the...
6.
Amorim M, Figueiredo A, Splendore A, Magalhaes I, Pombo-de-Oliveira M, El-Jaick K, et al.
Leuk Lymphoma
. 2009 May;
50(5):834-40.
PMID: 19452320
Denaturing high-performance liquid chromatography (dHPLC) was developed to screen DNA variations by separating heteroduplex and homoduplex DNA fragments by ion-pair reverse-phase liquid chromatography. In this study, we have evaluated the...
7.
Domene S, Roessler E, El-Jaick K, Snir M, Brown J, Velez J, et al.
Hum Mol Genet
. 2008 Sep;
17(24):3919-28.
PMID: 18791198
Holoprosencephaly (HPE) is the most common developmental anomaly of the human forebrain; however, the genetics of this heterogeneous and etiologically complex malformation is incompletely understood. Heterozygous mutations in SIX3, a...
8.
El-Jaick K, Fonseca R, Moreira M, Ribeiro M, Bolognese A, Dias S, et al.
Birth Defects Res A Clin Mol Teratol
. 2007 Jun;
79(8):573-80.
PMID: 17584896
Background: Single median maxillary central incisor (SMMCI) is a rare anomaly that may occur alone or associated with other conditions, frequently as part of the holoprosencephaly (HPE) spectrum. However, it...
9.
Ribeiro L, El-Jaick K, Muenke M, Richieri-Costa A
Am J Med Genet A
. 2006 Sep;
140(23):2577-83.
PMID: 17001667
Here, we report six Brazilian patients with holoprosencephaly caused by SIX3 mutations. Missense mutations were more common than frameshift mutations. Comparison of patients with missense versus frameshift mutations was essentially...
10.
El-Jaick K, Powers S, Bartholin L, Myers K, Hahn J, Orioli I, et al.
Mol Genet Metab
. 2006 Sep;
90(1):97-111.
PMID: 16962354
Holoprosencephaly (HPE) is the most common structural malformation of the forebrain and face in humans. Our current understanding of the pathogenesis of HPE attempts to integrate genetic susceptibility, evidenced by...