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1.
Molecular Analysis by Gene Expression of Mitochondrial ATPase Subunits in Papillary Thyroid Cancer: Is ATP5E Transcript a Possible Early Tumor Marker?
Med Sci Monit
; 21: 1745-51, 2015 Jun 16.
Article
in English
| MEDLINE | ID: mdl-26079849
2.
Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event.
Mol Genet Genomic Med
; 9(9): e1762, 2021 09.
Article
in English
| MEDLINE | ID: mdl-34288579
3.
Trypanocidal and toxicological assessment in vitro and in silico of three sesquiterpene lactones from Asteraceae plant species.
Food Chem Toxicol
; 125: 55-61, 2019 Mar.
Article
in English
| MEDLINE | ID: mdl-30572063
4.
Identification of genomic copy number variations in lung benign metastasizing leiomyomatosis.
Clin Respir J
; 13(2): 105-113, 2019 Feb.
Article
in English
| MEDLINE | ID: mdl-30597752
5.
BRAF 1799T>A Mutation Frequency in Mexican Mestizo Patients with Papillary Thyroid Cancer.
Biomed Res Int
; 2018: 2582179, 2018.
Article
in English
| MEDLINE | ID: mdl-29808165
6.
Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.
Ophthalmic Genet
; 39(1): 56-62, 2018.
Article
in English
| MEDLINE | ID: mdl-28922055
7.
Copy Number Alterations Associated with Acute Lymphoblastic Leukemia in Mexican Children. A report from The Mexican Inter-Institutional Group for the identification of the causes of childhood leukemia.
Arch Med Res
; 47(8): 706-711, 2016 11.
Article
in English
| MEDLINE | ID: mdl-28476198
8.
Conserved domains in polynucleotide phosphorylase among eubacteria.
Biochimie
; 87(8): 737-45, 2005 Aug.
Article
in English
| MEDLINE | ID: mdl-16054527
9.
PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome.
Eur J Hum Genet
; 23(12): 1615-26, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-25853300
10.
19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype.
Mol Cytogenet
; 7(1): 61, 2014.
Article
in English
| MEDLINE | ID: mdl-25516771
11.
Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.
BMC Med Genomics
; 7: 55, 2014 Sep 15.
Article
in English
| MEDLINE | ID: mdl-25223409
12.
Diagnosis of familial Wolf-Hirschhorn syndrome due to a paternal cryptic chromosomal rearrangement by conventional and molecular cytogenetic techniques.
Biomed Res Int
; 2013: 209204, 2013.
Article
in English
| MEDLINE | ID: mdl-23484094
13.
Overexpression of Ipe protein from the coliphage mEp021 induces pleiotropic effects involving haemolysis by HlyE-containing vesicles and cell death.
Biochimie
; 94(6): 1262-73, 2012 Jun.
Article
in English
| MEDLINE | ID: mdl-22365985
14.
α-Enolase binds to RNA.
Biochimie
; 93(9): 1520-8, 2011 Sep.
Article
in English
| MEDLINE | ID: mdl-21621582
15.
Congenital hypertrichosis universalis in Mexican female twins.
Int J Dermatol
; 55(1): e29-31, 2016 Jan.
Article
in English
| MEDLINE | ID: mdl-26518157
16.
Nucleic acid and protein factors involved in Escherichia coli polynucleotide phosphorylase function on RNA.
Biochimie
; 92(5): 445-54, 2010 May.
Article
in English
| MEDLINE | ID: mdl-20114069
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