Found: 30
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Impact of the COVID-19 Pandemic on Partner Relationships and Sexual and Reproductive Health: Cross-Sectional, Online Survey Study.
- Published in:
- 2020
- By:
- Publication type:
- journal article
CALR3 defects disrupt sperm-zona pellucida binding in humans: new insights into male factor fertilization failure and relevant clinical therapeutic approaches.
- Published in:
- Human Reproduction, 2024, v. 39, n. 11, p. 2608, doi. 10.1093/humrep/deae205
- By:
- Publication type:
- Article
Case Report: Novel Biallelic Mutations in ARMC4 Cause Primary Ciliary Dyskinesia and Male Infertility in a Chinese Family.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.715339
- By:
- Publication type:
- Article
Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans.
- Published in:
- Human Genetics, 2022, v. 141, n. 11, p. 1795, doi. 10.1007/s00439-022-02459-4
- By:
- Publication type:
- Article
Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse.
- Published in:
- Human Genetics, 2021, v. 140, n. 9, p. 1367, doi. 10.1007/s00439-021-02313-z
- By:
- Publication type:
- Article
Machine learning in a real-world PFO study: analysis of data from multi-centers in China.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Gone with wind: a novel biodegradable occluder for percutaneous closure of patent foramen ovale.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Association between SLCO1B3 gene polymorphism and prostate cancer risk: A meta-analytic study.
- Published in:
- Bangladesh Journal of Pharmacology, 2018, v. 13, n. 1, p. 98, doi. 10.3329/bjp.v13i1.34544
- By:
- Publication type:
- Article
ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida.
- Published in:
- Human Reproduction, 2023, v. 38, n. 6, p. 1213, doi. 10.1093/humrep/dead059
- By:
- Publication type:
- Article
Differences in the Gut Microbiome of Women With and Without Hypoactive Sexual Desire Disorder: Case Control Study.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Novel MEIOB pathogenic variants including a homozygous non‐canonical splicing variant, cause meiotic arrest and human non‐obstructive azoospermia.
- Published in:
- Clinical Genetics, 2024, v. 105, n. 1, p. 99, doi. 10.1111/cge.14426
- By:
- Publication type:
- Article
Loss of function mutation in DNAH7 induces male infertility associated with abnormalities of the sperm flagella and mitochondria in human.
- Published in:
- Clinical Genetics, 2022, v. 102, n. 2, p. 130, doi. 10.1111/cge.14146
- By:
- Publication type:
- Article
A homozygous loss‐of‐function mutation in FBXO43 causes human non‐obstructive azoospermia.
- Published in:
- Clinical Genetics, 2022, v. 101, n. 1, p. 55, doi. 10.1111/cge.14069
- By:
- Publication type:
- Article
Bi‐allelic mutations in MCIDAS and CCNO cause human infertility associated with abnormal gamete transport.
- Published in:
- Clinical Genetics, 2021, v. 100, n. 6, p. 731, doi. 10.1111/cge.14067
- By:
- Publication type:
- Article
Novel mutations in DNAH17 cause sperm flagellum defects and their influence on ICSI outcome.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 10, p. 2485, doi. 10.1007/s10815-023-02897-7
- By:
- Publication type:
- Article
Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2022, v. 39, n. 1, p. 251, doi. 10.1007/s10815-021-02306-x
- By:
- Publication type:
- Article
A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 6, p. 1421, doi. 10.1007/s10815-020-01779-6
- By:
- Publication type:
- Article
Activation of MT1/MT2 to Protect Testes and Leydig Cells against Cisplatin-Induced Oxidative Stress through the SIRT1/Nrf2 Signaling Pathway.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 10, p. 1690, doi. 10.3390/cells11101690
- By:
- Publication type:
- Article
Novel Mutations in X-Linked, USP26 -Induced Asthenoteratozoospermia and Male Infertility.
- Published in:
- Cells (2073-4409), 2021, v. 10, n. 7, p. 1594, doi. 10.3390/cells10071594
- By:
- Publication type:
- Article
Performance evaluation of differential splicing analysis methods and splicing analytics platform construction.
- Published in:
- Nucleic Acids Research, 2022, v. 50, n. 16, p. 9115, doi. 10.1093/nar/gkac686
- By:
- Publication type:
- Article
Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.
- Published in:
- SCIENCE CHINA Life Sciences, 2024, v. 67, n. 8, p. 1697, doi. 10.1007/s11427-023-2539-1
- By:
- Publication type:
- Article
Safety and Efficacy of Biodegradable Patent Foramen Ovale Occluder in Patients with Migraine: A Clinical Trial.
- Published in:
- Congenital Heart Disease, 2023, v. 18, n. 3, p. 373, doi. 10.32604/chd.2023.028979
- By:
- Publication type:
- Article
Correction: Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.
- Published in:
- Reproductive Biology & Endocrinology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12958-022-00936-z
- By:
- Publication type:
- Article
Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.
- Published in:
- Reproductive Biology & Endocrinology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12958-022-00936-z
- By:
- Publication type:
- Article
Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia.
- Published in:
- Reproductive Biology & Endocrinology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12958-021-00815-z
- By:
- Publication type:
- Article
Biallelic loss‐of‐function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans.
- Published in:
- Human Mutation, 2022, v. 43, n. 12, p. 2079, doi. 10.1002/humu.24475
- By:
- Publication type:
- Article
Cover, Volume 43, Issue 3.
- Published in:
- Human Mutation, 2022, v. 43, n. 3, p. i, doi. 10.1002/humu.24361
- By:
- Publication type:
- Article
Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease.
- Published in:
- Human Mutation, 2022, v. 43, n. 3, p. 434, doi. 10.1002/humu.24322
- By:
- Publication type:
- Article
Atlas and source of the microplastics of male reproductive system in human and mice.
- Published in:
- Environmental Science & Pollution Research, 2024, v. 31, n. 17, p. 25046, doi. 10.1007/s11356-024-32832-x
- By:
- Publication type:
- Article