نتایج جستجو برای: preimplantation embryo

تعداد نتایج: 70221  

Journal: :Human reproduction 2011
G L Harton M C Magli K Lundin M Montag J Lemmen J C Harper

In 2005, the European Society for Human Reproduction and Embryology (ESHRE) Preimplantation Genetic Diagnosis (PGD) Consortium published a set of Guidelines for Best Practice to give information, support and guidance to potential, existing and fledgling PGD programmes (Thornhill AR, De Die-Smulders CE, Geraedts JP, Harper JC, Harton GL, Lavery SA, Moutou C, Robinson MD, Schmutzler AG, Scriven P...

Journal: :Prenatal diagnosis 2002
Harvey J Stern Gary L Harton Michael E Sisson Shirley L Jones Lee A Fallon Lilli P Thorsell Michael E Getlinger Susan H Black Joseph D Schulman

OBJECTIVES Individuals at risk for Huntington disease face difficult decisions regarding their reproductive options. Most do not wish to pass on the gene for Huntington disease to their children, but may not be prepared themselves to undergo presymptomatic testing and learn their genetic status. For these reasons, many at-risk individuals with a family history of HD would choose a method of gen...

Journal: :The Journal of clinical endocrinology and metabolism 1998
J S Krüssel H Y Huang C Simón B Behr A R Pape Y Wen P Bielfeld M L Polan

Gaining knowledge about the physiological timetable of gene expression during preimplantation embryo development is crucial, and a better understanding of cytokine and growth factor expression in early embryonic development could lead to improved in vitro culture conditions and enhance in vitro fertilization implantation rates. Our aim was to detect the patterns and levels of two messenger ribo...

2016
Lin Zhou Pei Wang Juanjuan Zhang Boon Chin Heng Guo Qing Tong

ING2 (inhibitor of growth protein-2) is a member of the ING-gene family and participates in diverse cellular processes involving tumor suppression, DNA repair, cell cycle regulation, and cellular senescence. As a subunit of the Sin3 histone deacetylase complex co-repressor complex, ING2 binds to H3K4me3 to regulate chromatin modification and gene expression. Additionally, ING2 recruits histone ...

2012
Patricia Grasa Heidy Kaune Suzannah A Williams

Female mice generating oocytes lacking complex N- and O-glycans (double mutants (DM)) produce only one small litter before undergoing premature ovarian failure (POF) by 3 months. Here we investigate the basis of the small litter by evaluating ovulation rate and embryo development in DM (Mgat1(F/F)C1galt1(F/F):ZP3Cre) and Control (Mgat1(F/F)C1galt1(F/F)) females. Surprisingly, DM ovulation rate ...

2015
Tiffini Charieace Gibson Randall Armant Michael Diamond James Rillema Derek Wildman

THE IMPACT OF MITOCHONDRIA ON PREIMPLANTATION DEVELOPMENT INTHE RHESUS MACAQUEby TIFFINI C. GIBSONAUGUST 2010Advisor: Carol Brenner, Ph.D.Major: PhysiologyDegree: Doctor of PhilosophyAssisted Reproduction Technologies (ART) have been used to treat infertility since 1790.In the centuries following, dramatic advances have been made in the field of infertility r...

Journal: :European journal of obstetrics, gynecology, and reproductive biology 2003
Jan-S Krüssel Peter Bielfeld Mary Lake Polan Carlos Simón

The preimplantation embryo produces several factors during its development to signal its presence to the maternal organism. This paper will focus on the role of two distinctive cytokine and growth factor systems (interleukin-1 (IL-1) system and the vascular endothelial growth factor (VEGF) system) during early embryonic development and implantation. IL-1 receptor is expressed in the endometrium...

Journal: :Development 2008
Mami Ohsugi Ping Zheng Boris Baibakov Lei Li Jurrien Dean

Initial cell lineages that presage the inner cell mass and extra-embryonic trophectoderm are established when eight blastomeres compact to form polarized morulae in preimplantation mouse development. FILIA has been identified as a binding partner to MATER (maternal antigen that embryos require; also known as NLRP5), which is encoded by a maternal effect gene. Products of each gene are detected ...

2010
S. Turner H.P. Wong J. Rai G.M. Hartshorne

Telomeres are repeated sequences that protect the ends of chromosomes and harbour DNA repair proteins. Telomeres shorten during each cell division in the absence of telomerase. When telomere length becomes critically short, cell senescence occurs. Telomere length therefore reflects both cellular ageing and capacity for division. We have measured telomere length in human germinal vesicle (GV) oo...

2017
Bianca Bianco Denise Maria Christofolini Gabriel Seixas Conceição Caio Parente Barbosa

Duchenne muscular dystrophy is the most common muscle disease found in male children. Currently, there is no effective therapy available for Duchenne muscular dystrophy patients. Therefore, it is essential to make a prenatal diagnosis and provide genetic counseling to reduce the birth of such boys. We report a case of preimplantation genetic diagnosis associated with Duchenne muscular dystrophy...

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