Detalhe da pesquisa
1.
A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest.
Hum Reprod
; 38(2): 306-314, 2023 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36524333
2.
Genetics of infertility: a paradigm shift for medically assisted reproduction.
Hum Reprod
; 38(12): 2289-2295, 2023 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37801292
3.
Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopy.
Reprod Biomed Online
; 47(5): 103328, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37742467
4.
Toxoplasma gondii ROP16 kinase silences the cyclin B1 gene promoter by hijacking host cell UHRF1-dependent epigenetic pathways.
Cell Mol Life Sci
; 77(11): 2141-2156, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31492965
5.
A dual role of linker histone H1.4 Lys 34 acetylation in transcriptional activation.
Genes Dev
; 26(8): 797-802, 2012 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22465951
6.
Tex19 paralogs are new members of the piRNA pathway controlling retrotransposon suppression.
J Cell Sci
; 130(8): 1463-1474, 2017 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28254886
7.
Comparison of sperm morphology and nuclear sperm quality in SPATA16- and DPY19L2-mutated globozoospermic patients.
Andrologia
; 51(6): e13277, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30912172
8.
Genetic evaluation of patients with non-syndromic male infertility.
J Assist Reprod Genet
; 35(11): 1939-1951, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30259277
9.
Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia.
Hum Mutat
; 38(11): 1592-1605, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28801929
10.
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.
Hum Mol Genet
; 24(19): 5581-8, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26199321
11.
Adjuncts in the IVF laboratory: where is the evidence for 'add-on' interventions?
Hum Reprod
; 32(3): 485-491, 2017 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28158511
12.
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
J Assist Reprod Genet
; 34(5): 683-694, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28401488
13.
TRIM28 repression of retrotransposon-based enhancers is necessary to preserve transcriptional dynamics in embryonic stem cells.
Genome Res
; 23(3): 452-61, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23233547
14.
Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermia.
Mol Hum Reprod
; 22(1): 35-45, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26516168
15.
A new mutation identified in SPATA16 in two globozoospermic patients.
J Assist Reprod Genet
; 33(6): 815-20, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27086357
16.
Tex19 and Sectm1 concordant molecular phylogenies support co-evolution of both eutherian-specific genes.
BMC Evol Biol
; 15: 222, 2015 Oct 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26459560
17.
Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots.
Hum Mol Genet
; 21(16): 3695-702, 2012 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22653751
18.
DPY19L2 deletion as a major cause of globozoospermia.
Am J Hum Genet
; 88(3): 344-50, 2011 Mar 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-21397063
19.
A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.
Am J Hum Genet
; 88(3): 351-61, 2011 Mar 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-21397064
20.
ONSL and OSKM cocktails act synergistically in reprogramming human somatic cells into induced pluripotent stem cells.
Mol Hum Reprod
; 20(6): 538-49, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24501429