Detalhe da pesquisa
1.
Aneuploidy rate and Stemness in Low-level Mosaic Human Embryonic Stem Cells in the Presence/Absence of Bortezomib, Paclitaxel and Lapatinib.
Cells Tissues Organs
; 2022 Jul 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35901725
2.
HOX cluster and their cofactors showed an altered expression pattern in eutopic and ectopic endometriosis tissues.
Reprod Biol Endocrinol
; 19(1): 132, 2021 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34470627
3.
Lapatinib Decreases the Preimplantation Aneuploidy Rate of in vitro Fertilized Mouse Embryos without Affecting Completion of Preimplantation Development.
Cytogenet Genome Res
; 160(11-12): 680-687, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33176309
4.
Chromosomal instability reducing effect of paclitaxel and lapatinib in mouse embryonic stem cells with chromosomal abnormality.
Mol Biol Rep
; 47(11): 8605-8614, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057993
5.
Taxol Improves Pre-Implantation Development Potential of Mouse Embryos.
Gynecol Obstet Invest
; 85(1): 94-99, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31743930
6.
An improved method for vitrification of in vitro matured ovine oocytes; beneficial effects of Ethylene Glycol Tetraacetic acid, an intracellular calcium chelator.
Cryobiology
; 84: 82-90, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30244698
7.
Developmental competence of in vitro matured ovine oocytes vitrified in solutions with different concentrations of trehalose.
Reprod Domest Anim
; 53(5): 1159-1167, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29938846
8.
Upregulation of Oxidative Phosphorylation Genes in Cumulus Cells of The Polycystic Ovary Syndrome Patients with or without Insulin Resistance.
Cell J
; 26(4): 235-242, 2024 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38736407
9.
Causes for hospitalization and death in Iranian patients with ß-thalassemia major.
Pediatr Hematol Oncol
; 28(2): 134-9, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20795770
10.
Frequency of Sperm Aneuploidy in Oligoasthenoteratozoospermic (OAT) Patients by Comprehensive Chromosome Screening: A Proof of Concept.
J Reprod Infertil
; 22(1): 57-64, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33680886
11.
Noninvasive sexing of human preimplantation embryos using RT-PCR in the spent culture media: A proof-of-concept study.
Eur J Obstet Gynecol Reprod Biol
; 252: 89-93, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32590167
12.
Frequency of cystathionine beta-synthase 844INS68 polymorphism in Southern Iran.
Mol Biol Rep
; 36(2): 353-6, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18046625
13.
Association between The Number of Retrieved Mature Oocytes and Insulin Resistance or Sensitivity in Infertile Women with Polycystic Ovary Syndrome.
Int J Fertil Steril
; 12(4): 310-315, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30291692
14.
Origins of Intraindividual Genetic Variation in Human Fetuses.
Reprod Sci
; 26(8): 1139-1145, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30453833
15.
Downregulation of Extracellular Matrix and Cell Adhesion Molecules in Cumulus Cells of Infertile Polycystic Ovary Syndrome Women with and without Insulin Resistance.
Cell J
; 21(1): 35-42, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30507086
16.
Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases.
Mol Genet Genomic Med
; 7(8): e820, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31210028
17.
Genetic counseling in southern Iran: consanguinity and reason for referral.
J Genet Couns
; 17(5): 472-9, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18551360
18.
Editorial: Genetics of female infertility.
Front Genet
; 14: 1297173, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37842647
19.
Apolipoprotein E gene polymorphism and left ventricular function in Iranian patients with thalassemia major.
Haematologica
; 92(2): 256-7, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17296580
20.
Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis.
Case Rep Genet
; 2017: 2706098, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28133555