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Human umbilical cord‐derived mesenchymal stem cell transplantation improves the long COVID.
- Published in:
- Journal of Medical Virology, 2024, v. 96, n. 6, p. 1, doi. 10.1002/jmv.29757
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- Publication type:
- Article
SARS-CoV-2 infection is detrimental to pregnancy outcomes after embryo transfer in IVF/ICSI: a prospective cohort study.
- Published in:
- BMC Medicine, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12916-024-03336-9
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- Publication type:
- Article
Extended application of PGT-M strategies for small pathogenic CNVs.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 3, p. 739, doi. 10.1007/s10815-024-03028-6
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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
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- Publication type:
- Article
Navigation of Knowledge: the Impact of COVID-19 on Pregnancy-a Bibliometric Analysis.
- Published in:
- Reproductive Sciences, 2023, v. 30, n. 12, p. 3548, doi. 10.1007/s43032-023-01312-x
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- Publication type:
- Article
Transcriptomic profiles reveal the characteristics of oocytes and cumulus cells at GV, MI, and MII in follicles before ovulation.
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- Journal of Ovarian Research, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13048-023-01291-2
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- Publication type:
- Article
Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression.
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- Cell Discovery, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41421-023-00580-w
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- Publication type:
- Article
The effect of carrier characteristics and female age on preimplantation genetic testing results of blastocysts from Robertsonian translocation carriers.
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- Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 8, p. 1995, doi. 10.1007/s10815-023-02853-5
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- Publication type:
- 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
Single-cell transcriptome analysis of NEUROG3+ cells during pancreatic endocrine differentiation with small molecules.
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- Stem Cell Research & Therapy, 2023, v. 14, n. 1, p. 1, doi. 10.1186/s13287-023-03338-z
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- Publication type:
- Article
Selective Translation of Maternal mRNA by eIF4E1B Controls Oocyte to Embryo Transition.
- Published in:
- Advanced Science, 2023, v. 10, n. 11, p. 1, doi. 10.1002/advs.202205500
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- 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
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- 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
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- Publication type:
- Letter
Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility.
- Published in:
- 2023
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- Publication type:
- Case Study
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
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- Publication type:
- Article
Novel mutation in TTC21A triggers partial nonsense‐mediated mRNA decay and causes male infertility with MMAF.
- Published in:
- Clinical Genetics, 2022, v. 102, n. 5, p. 459, doi. 10.1111/cge.14197
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- Publication type:
- Article
A novel multifunctional haplotyping-based preimplantation genetic testing for different genetic conditions.
- Published in:
- 2022
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- Publication type:
- journal 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
Clinical Utility of Medical Exome Sequencing: Expanded Carrier Screening for Patients Seeking Assisted Reproductive Technology in China.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.943058
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- Publication type:
- Article
Non-invasive preimplantation genetic testing for conventional IVF blastocysts.
- Published in:
- 2022
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- Publication type:
- journal article
Clinical Utility of Medical Exome Sequencing: Expanded Carrier Screening for Patients Seeking Assisted Reproductive Technology in China.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.943058
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- Publication type:
- Article
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
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- 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
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- Publication type:
- Article
Metformin abrogates pathological TNF-α-producing B cells through mTOR-dependent metabolic reprogramming in polycystic ovary syndrome.
- Published in:
- eLife, 2022, p. 1, doi. 10.7554/eLife.74713
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- Publication type:
- 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
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- Publication type:
- journal article
The de novo aberration rate of prenatal karyotype was comparable between 1496 fetuses conceived via IVF/ICSI and 1396 fetuses from natural conception.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2022, v. 39, n. 7, p. 1683, doi. 10.1007/s10815-022-02500-5
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- Publication type:
- Article
Identification of Novel Variants of Thyroid Hormone Receptor Interaction Protein 13 That Cause Female Infertility Characterized by Zygotic Cleavage Failure.
- Published in:
- Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.899149
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- Publication type:
- Article
Risk Factors Affecting Alternate Segregation in Blastocysts From Preimplantation Genetic Testing Cycles of Autosomal Reciprocal Translocations.
- Published in:
- Frontiers in Genetics, 2022, p. 1, doi. 10.3389/fgene.2022.880208
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- 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
Experience of Low-Pass Whole-Genome Sequencing-Based Copy Number Variant Analysis: A Survey of Chinese Tertiary Hospitals.
- Published in:
- Diagnostics (2075-4418), 2022, v. 12, n. 5, p. N.PAG, doi. 10.3390/diagnostics12051098
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- Publication type:
- Article
Identification of a heterozygous variant of ZP2 as a novel cause of empty follicle syndrome in humans and mice.
- Published in:
- 2022
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- Publication type:
- journal article
Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella development.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 2, p. 219, doi. 10.1093/hmg/ddab234
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- Publication type:
- Article
CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 24, p. 2240, doi. 10.1093/hmg/ddab185
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- Publication type:
- Article
CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 23, p. 2240, doi. 10.1093/hmg/ddab185
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- Publication type:
- Article
Non-invasive Metabolomic Profiling of Embryo Culture Medium Using Raman Spectroscopy With Deep Learning Model Predicts the Blastocyst Development Potential of Embryos.
- Published in:
- Frontiers in Physiology, 2021, v. 12, p. 1, doi. 10.3389/fphys.2021.777259
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- Publication type:
- Article
An increase of phosphatidylcholines in follicular fluid implies attenuation of embryo quality on day 3 post-fertilization.
- Published in:
- BMC Biology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12915-021-01118-w
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- Publication type:
- Article
Publisher Correction to: An increase of phosphatidylcholines in follicular fluid implies attenuation of embryo quality on day 3 post-fertilization.
- Published in:
- 2021
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- Publication type:
- Correction Notice
An increase of phosphatidylcholines in follicular fluid implies attenuation of embryo quality on day 3 post-fertilization.
- Published in:
- BMC Biology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12915-021-01118-w
- By:
- Publication type:
- Article
Patients with acephalic spermatozoa syndrome linked to novel TSGA10/PMFBP1 variants have favorable pregnancy outcomes from intracytoplasmic sperm injection.
- Published in:
- Clinical Genetics, 2021, v. 100, n. 3, p. 334, doi. 10.1111/cge.14007
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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
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- 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
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- 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
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- 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
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- Publication type:
- Article
Expanding the genetic and phenotypic spectrum of the subcortical maternal complex genes in recurrent preimplantation embryonic arrest.
- Published in:
- Clinical Genetics, 2021, v. 99, n. 2, p. 286, doi. 10.1111/cge.13858
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- 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
Clinical value of histologic endometrial dating for personalized frozen-thawed embryo transfer in patients with repeated implantation failure in natural cycles.
- Published in:
- 2020
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- Publication type:
- journal article
Identification of paternal germline mosaicism by MicroSeq and targeted next‐generation sequencing.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1394
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- Publication type:
- Article
Front Cover.
- Published in:
- Clinical Genetics, 2020, v. 97, n. 5, p. i, doi. 10.1111/cge.13758
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- Publication type:
- Article
An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family.
- Published in:
- Clinical Genetics, 2020, v. 97, n. 5, p. 741, doi. 10.1111/cge.13712
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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