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Correlation between chromosomal distribution and embryonic findings on ultrasound in early pregnancy loss after IVF-embryo transfer.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Homozygous ACTL9 mutations cause irregular mitochondrial sheath arrangement and abnormal flagellum assembly in spermatozoa and male infertility.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 9, p. 2271, doi. 10.1007/s10815-024-03171-0
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- Publication type:
- Article
Immunological Indicators of Recurrent Pregnancy Loss: A Mendelian Randomization Study.
- Published in:
- Reproductive Sciences, 2024, v. 31, n. 9, p. 2783, doi. 10.1007/s43032-024-01555-2
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- Publication type:
- Article
Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia.
- Published in:
- 2022
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- Publication type:
- journal article
FLI1 and PKC co-activation promote highly efficient differentiation of human embryonic stem cells into endothelial-like cells.
- Published in:
- Cell Death & Disease, 2018, v. 9, n. 2, p. 1, doi. 10.1038/s41419-017-0162-9
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- Publication type:
- Article
Role of telomeric repeat-containing RNA in telomeric chromatin remodeling during the early expansion of human embryonic stem cells.
- Published in:
- FASEB Journal, 2017, v. 31, n. 11, p. 4783, doi. 10.1096/fj.201600939RR
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- Publication type:
- Article
A logistic model to predict early pregnancy loss following in vitro fertilization based on 2601 infertility patients.
- Published in:
- Reproductive Biology & Endocrinology, 2016, v. 14, p. 1, doi. 10.1186/s12958-016-0147-z
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- Publication type:
- Article
First-trimester diagnosis and management of Cesarean scar pregnancies after in vitro fertilization-embryo transfer: a retrospective clinical analysis of 12 cases.
- Published in:
- Reproductive Biology & Endocrinology, 2015, v. 13, p. 1, doi. 10.1186/s12958-015-0120-2
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- Publication type:
- Article
The risk of placenta previa and cesarean section associated with a thin endometrial thickness: a retrospective study of 5251 singleton births during frozen embryo transfer in China.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia.
- Published in:
- Human Reproduction, 2023, v. 38, n. 7, p. 1399, doi. 10.1093/humrep/dead095
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- Publication type:
- Article
A novel multifunctional haplotyping-based preimplantation genetic testing for different genetic conditions.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Estrogen valerate pretreatment with the antagonist protocol does not increase oocyte retrieval in patients with low ovarian response: a randomized controlled trial.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Identification of a heterozygous variant of ZP2 as a novel cause of empty follicle syndrome in humans and mice.
- Published in:
- 2022
- By:
- Publication type:
- journal article
ZP1 mutations are associated with empty follicle syndrome: evidence for the existence of an intact oocyte and a zona pellucida in follicles up to the early antral stage. A case report.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Single embryo transfer by Day 3 time-lapse selection versus Day 5 conventional morphological selection: a randomized, open-label, non-inferiority trial.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Differentiation of primordial germ cells from induced pluripotent stem cells of primary ovarian insufficiency.
- Published in:
- Human Reproduction, 2015, v. 30, n. 3, p. 737, doi. 10.1093/humrep/deu358
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- Publication type:
- Article
Dynamic distribution of NuMA and microtubules in human fetal fibroblasts, developing oocytes and somatic cell nuclear transferred embryos.
- Published in:
- Human Reproduction, 2011, v. 26, n. 5, p. 1052
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- Publication type:
- Article
Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia.
- Published in:
- Molecular Human Reproduction, 2024, v. 30, n. 2, p. 1, doi. 10.1093/molehr/gaae002
- By:
- Publication type:
- Article
Pathogenic variant in ACTL7A causes severe teratozoospermia characterized by bubble-shaped acrosomes and male infertility.
- Published in:
- Molecular Human Reproduction, 2022, v. 28, n. 8, p. 1, doi. 10.1093/molehr/gaac028
- By:
- Publication type:
- Article
Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.
- Published in:
- Molecular Human Reproduction, 2022, v. 28, n. 6, p. 1, doi. 10.1093/molehr/gaac015
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- Publication type:
- Article
Noninvasive prenatal testing (NIPT) in twin pregnancies with treatment of assisted reproductive techniques (ART) in a single center.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Rapid detection of aneuploidies on a benchtop sequencing platform.
- Published in:
- Prenatal Diagnosis, 2013, v. 33, n. 3, p. 232, doi. 10.1002/pd.4049
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- Publication type:
- Article
Cumulative Live Birth Rates in Low Prognosis Patients According to the POSEIDON Criteria: An Analysis of 26,697 Cycles of in vitro Fertilization/Intracytoplasmic Sperm Injection.
- Published in:
- Frontiers in Endocrinology, 2019, p. 1, doi. 10.3389/fendo.2019.00642
- By:
- Publication type:
- Article
IQCN disruption causes fertilization failure and male infertility due to manchette assembly defect.
- Published in:
- EMBO Molecular Medicine, 2022, v. 14, n. 12, p. 1, doi. 10.15252/emmm.202216501
- By:
- Publication type:
- Article
Clinical value of histologic endometrial dating for personalized frozen-thawed embryo transfer in patients with repeated implantation failure in natural cycles.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Developmental incompatibility of human parthenogenetic embryonic stem cells in mouse blastocysts.
- Published in:
- In Vitro Cellular & Developmental Biology Animal, 2012, v. 48, n. 3, p. 156, doi. 10.1007/s11626-012-9483-2
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- Publication type:
- Article
The comprehensive variant and phenotypic spectrum of TUBB8 in female infertility.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 9, p. 2261, doi. 10.1007/s10815-021-02219-9
- By:
- Publication type:
- Article
Reproductive outcomes after preimplantation genetic testing in mosaic Turner syndrome: a retrospective cohort study of 100 cycles.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 5, p. 1247, doi. 10.1007/s10815-021-02127-y
- By:
- Publication type:
- Article
Clinical outcomes following preimplantation genetic testing and microdissecting junction region in couples with balanced chromosome rearrangement.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 3, p. 735, doi. 10.1007/s10815-020-02052-6
- By:
- Publication type:
- Article
The genetic cause of intellectual deficiency and/or congenital malformations in two parental reciprocal translocation carriers and implications for assisted reproduction.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 1, p. 243, doi. 10.1007/s10815-020-01986-1
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- Publication type:
- Article
Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 4, p. 811, doi. 10.1007/s10815-020-01735-4
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- Publication type:
- Article
New biallelic mutations in PADI6 cause recurrent preimplantation embryonic arrest characterized by direct cleavage.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 1, p. 205, doi. 10.1007/s10815-019-01606-7
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- Publication type:
- Article
Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 12, p. 2533, doi. 10.1007/s10815-019-01611-w
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- Publication type:
- Article
Increased pregnancy complications following frozen-thawed embryo transfer during an artificial cycle.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 5, p. 925, doi. 10.1007/s10815-019-01420-1
- By:
- Publication type:
- Article
Correlation analysis between ultrasound findings and abnormal karyotypes in the embryos fromearly pregnancy loss after in vitro fertilization-embryo transfer.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2017, v. 34, n. 1, p. 43, doi. 10.1007/s10815-016-0821-2
- By:
- Publication type:
- Article
Effect of body mass index on the outcomes of controlled ovarian hyperstimulation in Chinese women with polycystic ovary syndrome: a multicenter, prospective, observational study.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2017, v. 34, n. 1, p. 61, doi. 10.1007/s10815-016-0830-1
- By:
- Publication type:
- Article
Progesterone levels on the hCG day and outcomes in vitro fertilization in women with polycystic ovary syndrome.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2012, v. 29, n. 7, p. 603, doi. 10.1007/s10815-012-9762-6
- By:
- Publication type:
- Article
Correlation of serum Anti-Müllerian hormone concentrations on day 3 of the in vitro fertilization stimulation cycle with assisted reproduction outcome in polycystic ovary syndrome patients.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2012, v. 29, n. 5, p. 397, doi. 10.1007/s10815-012-9726-x
- By:
- Publication type:
- Article
A case report: successful pregnancy after controlled ovarian hyperstimulation by using short-acting gonadotropin releasing hormone agonist only.
- Published in:
- 2012
- By:
- Publication type:
- Report
Long Y chromosome is not a fetal loss risk.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2011, v. 28, n. 2, p. 151, doi. 10.1007/s10815-010-9497-1
- By:
- Publication type:
- Article
The number of blastomeres in post-thawing embryos affects the rates of pregnancy and delivery in freeze-embryo-transfer cycles.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2009, v. 26, n. 11/12, p. 569, doi. 10.1007/s10815-009-9360-4
- By:
- Publication type:
- Article
Cytogenetic analysis of human embryos and embryonic stem cells derived from monopronuclear zygotes.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2009, v. 26, n. 11/12, p. 583, doi. 10.1007/s10815-009-9355-1
- By:
- Publication type:
- Article
Comparing the pregnancy rates of one versus two intrauterine inseminations (IUIs) in male factor and idiopathic infertility.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2006, v. 23, n. 2, p. 75, doi. 10.1007/s10815-005-9017-x
- By:
- Publication type:
- Article
DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice.
- Published in:
- 2023
- By:
- Publication type:
- Letter
Human umbilical cord mesenchymal stem cells for psoriasis: a phase 1/2a, single-arm study.
- Published in:
- Signal Transduction & Targeted Therapy, 2022, v. 7, n. 1, p. 1, doi. 10.1038/s41392-022-01059-y
- By:
- Publication type:
- Article
Cytoplast containing reprogramming-related factors from human embryonic stem cells arrested at metaphase.
- Published in:
- Development, Growth & Differentiation, 2011, v. 53, n. 1, p. 18, doi. 10.1111/j.1440-169X.2010.01217.x
- By:
- Publication type:
- Article
Case Report: A Novel Heterozygous ZP3 Deletion Associated With Empty Follicle Syndrome and Abnormal Follicular Development.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.690070
- By:
- Publication type:
- Article
DPY19L2 gene mutations are a major cause of globozoospermia: identification of three novel point mutations.
- Published in:
- Molecular Human Reproduction, 2013, v. 19, n. 6, p. 395, doi. 10.1093/molehr/gat018
- By:
- Publication type:
- Article
An integrated chromatin accessibility and transcriptome landscape of human pre-implantation embryos.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-018-08244-0
- By:
- Publication type:
- Article
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype.
- Published in:
- Clinical Genetics, 2023, v. 103, n. 4, p. 495, doi. 10.1111/cge.14281
- By:
- Publication type:
- Article