Detalhe da pesquisa
1.
m.4216 T > C polymorphism in JT cluster determines a lower pregnancy rate in response to controlled ovarian stimulation treatment.
J Assist Reprod Genet
; 40(3): 671-682, 2023 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-36701026
2.
Variants Ala307Ala and Ser680Ser of 307 and 680 FSHr polymorphisms negatively influence on assisted reproductive techniques outcome and determine high probability of non-pregnancy in Caucasian patients.
J Assist Reprod Genet
; 38(10): 2769-2779, 2021 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-34346002
3.
Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy.
Biochim Biophys Acta
; 1822(8): 1216-22, 2012 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-22561905
4.
'Progress' renders detrimental an ancient mitochondrial DNA genetic variant.
Hum Mol Genet
; 20(21): 4224-31, 2011 Nov 01.
Artigo
Inglês
| MEDLINE | ID: mdl-21828074
5.
Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.
Hum Mol Genet
; 19(17): 3343-53, 2010 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-20566709
6.
20 years of human mtDNA pathologic point mutations: carefully reading the pathogenicity criteria.
Biochim Biophys Acta
; 1787(5): 476-83, 2009 May.
Artigo
Inglês
| MEDLINE | ID: mdl-18840399
7.
Human mitochondrial variants influence on oxygen consumption.
Mitochondrion
; 9(1): 27-30, 2009 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-18952007
8.
Association of mitochondrial haplogroup J and mtDNA oxidative damage in two different North Spain elderly populations.
Biogerontology
; 10(4): 435-42, 2009 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-18931934
9.
Diseases of the human mitochondrial oxidative phosphorylation system.
Adv Exp Med Biol
; 652: 47-67, 2009.
Artigo
Inglês
| MEDLINE | ID: mdl-20225019
10.
A new pathologic mitochondrial DNA mutation in the cytochrome oxidase subunit I (MT-CO1).
Hum Mutat
; 29(8): E112-22, 2008 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-18484665
11.
Association of human mitochondrial DNA variants with plasma LDL levels.
Mitochondrion
; 8(3): 247-53, 2008 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-18538642
12.
Mitochondrial DNA transcription and diseases: past, present and future.
Biochim Biophys Acta
; 1757(9-10): 1179-89, 2006.
Artigo
Inglês
| MEDLINE | ID: mdl-16697348
13.
Mitochondria from ejaculated human spermatozoa do not synthesize proteins.
FEBS Lett
; 553(1-2): 205-8, 2003 Oct 09.
Artigo
Inglês
| MEDLINE | ID: mdl-14550574
14.
An MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutations.
Front Genet
; 5: 469, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-25642242
15.
Mitochondrial pharma-Q-genomics: targeting the OXPHOS cytochrome b.
Drug Discov Today
; 16(5-6): 176-80, 2011 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-21112412
16.
Mitochondrial pharmacogenomics: barcode for antibiotic therapy.
Drug Discov Today
; 15(1-2): 33-9, 2010 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-19883791
17.
Human mitochondrial haplogroup H: the highest VO2max consumer--is it a paradox?
Mitochondrion
; 10(2): 102-7, 2010 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-19900587
18.
CPEO and KSS differ in the percentage and location of the mtDNA deletion.
Mitochondrion
; 9(5): 314-7, 2009 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-19410662
19.
Steady exercise removes VO(2max) difference between mitochondrial genomic variants.
Mitochondrion
; 9(5): 326-30, 2009 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-19427920
20.
Isolation of biogenetically competent mitochondria from mammalian tissues and cultured cells.
Methods
; 26(4): 292-7, 2002 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-12054919