Found: 49
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Human embryo research in France.
- Published in:
- 2002
- By:
- Publication type:
- journal article
The place of 'social sexing' in medicine and science.
- Published in:
- 2002
- By:
- Publication type:
- commentary
A systematic review and evidence assessment of monogenic gene–disease relationships in human female infertility and differences in sex development.
- Published in:
- Human Reproduction Update, 2023, v. 29, n. 2, p. 218, doi. 10.1093/humupd/dmac044
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- Publication type:
- Article
An ESHG–ESHRE survey on the current practice of expanded carrier screening in medically assisted reproduction.
- Published in:
- Human Reproduction, 2024, v. 39, n. 8, p. 1844, doi. 10.1093/humrep/deae131
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- Publication type:
- Article
Genetics of infertility: a paradigm shift for medically assisted reproduction.
- Published in:
- Human Reproduction, 2023, v. 38, n. 12, p. 2289, doi. 10.1093/humrep/dead199
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- Publication type:
- Article
A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest.
- Published in:
- Human Reproduction, 2023, v. 38, n. 2, p. 306, doi. 10.1093/humrep/deac259
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- Publication type:
- Article
Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy†.
- Published in:
- Human Reproduction, 2014, v. 29, n. 8, p. 1603
- By:
- Publication type:
- Article
The mammalian-specific Tex19.1 gene plays an essential role in spermatogenesis and placenta-supported development.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
The mammalian-specific Tex19.1 gene plays an essential role in spermatogenesis and placenta-supported development.
- Published in:
- Human Reproduction, 2013, v. 28, n. 8, p. 2201, doi. 10.1093/humrep/det129
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- Publication type:
- Article
Identification of a new recurrent Aurora kinase C mutation in both European and African men with macrozoospermia.
- Published in:
- Human Reproduction, 2012, v. 27, n. 11, p. 3337, doi. 10.1093/humrep/des296
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- Publication type:
- Article
The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 7, p. 1301, doi. 10.1093/hmg/ddp029
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- Publication type:
- Article
Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policyEuropean Society of Human Genetics and European Society of Human Reproduction and Embryology.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, p. S1, doi. 10.1038/ejhg.2013.219
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- Publication type:
- Article
Programmed Cell Death 2-Like (Pdcd2l) Is Required for Mouse Embryonic Development.
- Published in:
- G3: Genes | Genomes | Genetics, 2020, v. 10, n. 12, p. 4449, doi. 10.1534/g3.120.401714
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- Publication type:
- Article
Towards unravelling the Igf2/H19 imprinted domain.
- Published in:
- BioEssays, 1995, v. 17, n. 10, p. 835, doi. 10.1002/bies.950171004
- By:
- Publication type:
- Article
Evaluation of a Custom Design Gene Panel as a Diagnostic Tool for Human Non-Syndromic Infertility.
- Published in:
- Genes, 2021, v. 12, n. 3, p. 410, doi. 10.3390/genes12030410
- By:
- Publication type:
- Article
Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect.
- Published in:
- Genes, 2020, v. 11, n. 4, p. 1, doi. 10.3390/genes11040382
- By:
- Publication type:
- Article
Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 9, p. 1010, doi. 10.1038/ejhg.2012.122
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- Publication type:
- Article
Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 4, p. 368, doi. 10.1038/ejhg.2011.202
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- Publication type:
- Article
New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 12, p. 1007, doi. 10.1038/sj.ejhg.5201291
- By:
- Publication type:
- Article
Highly Dynamic and Sex-Specific Expression of microRNAs During Early ES Cell Differentiation.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 8, p. 1, doi. 10.1371/journal.pgen.1000620
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- Publication type:
- Article
High-efficiency derivation of human embryonic stem cell lines following pre-implantation genetic diagnosis.
- Published in:
- In Vitro Cellular & Developmental Biology Animal, 2010, v. 46, n. 3/4, p. 376, doi. 10.1007/s11626-010-9300-8
- By:
- Publication type:
- Article
Genetic evaluation of patients with non-syndromic male infertility.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2018, v. 35, n. 11, p. 1939, doi. 10.1007/s10815-018-1301-7
- By:
- Publication type:
- Article
A new mutation identified in SPATA16 in two globozoospermic patients.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2016, v. 33, n. 6, p. 815, doi. 10.1007/s10815-016-0715-3
- By:
- Publication type:
- Article
Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermia.
- Published in:
- Molecular Human Reproduction, 2016, v. 22, n. 1, p. 35, doi. 10.1093/molehr/gav061
- By:
- Publication type:
- Article
ONSL and OSKM cocktails act synergistically in reprogramming human somatic cells into induced pluripotent stem cells.
- Published in:
- Molecular Human Reproduction, 2014, v. 20, n. 6, p. 538, doi. 10.1093/molehr/gau012
- By:
- Publication type:
- Article
Nuclear proteome analysis of undifferentiated mouse embryonic stem and germ cells.
- Published in:
- Electrophoresis, 2008, v. 29, n. 11, p. 2381, doi. 10.1002/elps.200700738
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- Publication type:
- Article
Proteome analysis of the culture environment supporting undifferentiated mouse embryonic stem and germ cell growth.
- Published in:
- Electrophoresis, 2007, v. 28, n. 10, p. 1615, doi. 10.1002/elps.200600497
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- Publication type:
- Article
Birth after pre-implantation genetic diagnosis (PGD) of spinocerebellar ataxia 2 (Sca2).
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 2, p. 126, doi. 10.1002/pd.1909
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- Publication type:
- Article
Case report: birth after preimplantation genetic diagnosis of a subtle mutation in SMN1 gene.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 11, p. 1037, doi. 10.1002/pd.1551
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- Publication type:
- Article
Duplex, triplex and quadruplex PCR for the preimplantation genetic diagnosis (PGD) of cystic fibrosis (CF), an exhaustive approach.
- Published in:
- Prenatal Diagnosis, 2004, v. 24, n. 7, p. 562, doi. 10.1002/pd.924
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- Publication type:
- Article
Preimplantation genetic diagnosis (PGD), a collaborative activity of clinical genetic departments and IVF centres.
- Published in:
- Prenatal Diagnosis, 2001, v. 21, n. 12, p. 1086, doi. 10.1002/pd.249
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- Publication type:
- Article
Allele-specific amplification for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy.
- Published in:
- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 498, doi. 10.1002/pd.110
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- Publication type:
- Article
Improvement of preimplantation genetic diagnosis (PGD) for the cystic fibrosis mutation Δ F508 by fluorescent polymerase chain reaction.
- Published in:
- Prenatal Diagnosis, 1999, v. 19, n. 13, p. 1248, doi. 10.1002/(SICI)1097-0223(199912)19:13<1248::AID-PD737>3.0.CO;2-G
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- Publication type:
- Article
Results of a survey of the legal status and attitudes towards preimplantation genetic diagnosis conducted in 13 different countries.
- Published in:
- Prenatal Diagnosis, 1998, v. 18, n. 13, p. 1374, doi. 10.1002/(SICI)1097-0223(199812)18:13<1374::AID-PD492>3.0.CO;2-W
- By:
- Publication type:
- Article
Tex19, a Mammalian-Specific Protein with a Restricted Expression in Pluripotent Stem Cells and Germ Line.
- Published in:
- Stem Cells, 2008, v. 26, n. 3, p. 734, doi. 10.1634/stemcells.2007-0772
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- Publication type:
- Article
Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest.
- Published in:
- Nature Genetics, 1998, v. 20, n. 2, p. 163, doi. 10.1038/2464
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- Publication type:
- Article
Preimplantation genetic diagnosis for achondroplasia: genetics and gynaecological limits and difficulties.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Is preimplantation genetic diagnosis for 'social sexing' desirable in today's and tomorrow's society?
- Published in:
- Human Reproduction, 2003, v. 18, n. 2, p. 463, doi. 10.1093/humrep/deg063
- By:
- Publication type:
- Article
Do morphological anomalies reflect chromosomal aneuploidies?
- Published in:
- Human Reproduction, 2000, v. 15, n. 12, p. 2563, doi. 10.1093/humrep/15.12.2563
- By:
- Publication type:
- Article
Histological and genetic analysis and risk assessment for chromosomal aberration after ICSI for patients presenting with CBAVD.
- Published in:
- 2000
- By:
- Publication type:
- journal article
Toxoplasma gondii ROP16 kinase silences the cyclin B1 gene promoter by hijacking host cell UHRF1-dependent epigenetic pathways.
- Published in:
- Cellular & Molecular Life Sciences, 2020, v. 77, n. 11, p. 2141, doi. 10.1007/s00018-019-03267-2
- By:
- Publication type:
- Article
Comparison of sperm morphology and nuclear sperm quality in SPATA16‐ and DPY19L2‐mutated globozoospermic patients.
- Published in:
- Andrologia, 2019, v. 51, n. 6, p. N.PAG, doi. 10.1111/and.13277
- By:
- Publication type:
- Article
Genetic diagnosis of embryos: clear explanation, not rhetoric, is needed.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Genetic diagnosis of embryos: Clear explanation, not rhetoric, is needed.
- Published in:
- Canadian Medical Association Journal (CMAJ), 2009, v. 181, n. 6/7, p. 387, doi. 10.1503/cmaj.080658
- By:
- Publication type:
- Article
The influence of invariant chain on the positive selection of single T cell receptor specificities.
- Published in:
- European Journal of Immunology, 1995, v. 25, n. 7, p. 1851, doi. 10.1002/eji.1830250709
- By:
- Publication type:
- Article
Retinoids and spermatogenesis: Lessons from mutant mice lacking the plasma retinol binding protein.
- Published in:
- Developmental Dynamics, 2006, v. 235, n. 6, p. 1608
- By:
- Publication type:
- Article
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 19, p. 5581, doi. 10.1093/hmg/ddv290
- By:
- Publication type:
- Article
Genomic Structure and Parent-of-Origin-Specific Methylation of Peg1.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 11, p. 1907, doi. 10.1093/hmg/6.11.1907
- By:
- Publication type:
- Article
Tex19 and Sectm1 concordant molecular phylogenies support co-evolution of both eutherian-specific genes.
- Published in:
- BMC Evolutionary Biology, 2015, v. 15, p. 1, doi. 10.1186/s12862-015-0506-y
- By:
- Publication type:
- Article