Cargando…

Karyomapping—a comprehensive means of simultaneous monogenic and cytogenetic PGD: comparison with standard approaches in real time for Marfan syndrome

Detalles Bibliográficos
Autores principales:	Thornhill, Alan R., Handyside, Alan H., Ottolini, Christian, Natesan, Senthil A, Taylor, Jon, Sage, Karen, Harton, Gary, Cliffe, Kerry, Affara, Nabeel, Konstantinidis, Michalis, Wells, Dagan, Griffin, Darren K.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer US 2015
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4363232/ https://www.ncbi.nlm.nih.gov/pubmed/25561157 http://dx.doi.org/10.1007/s10815-014-0405-y

Ejemplares similares

Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro
por: Natesan, Senthilkumar A., et al.
Publicado: (2014)

Importance of embryo aneuploidy screening in preimplantation genetic diagnosis for monogenic diseases using the karyomap gene chip
por: Li, Gang, et al.
Publicado: (2018)

Karyomaps of cultured and cryobanked Litoria infrafrenata frog and tadpole cells
por: Mollard, Richard
Publicado: (2018)

“Genome-wide recombination and chromosome segregation in human oocytes and embryos reveal selection for maternal recombination rates”
por: Ottolini, Christian S., et al.
Publicado: (2015)

PGD Synthase and PGD(2) in Immune Resposne
por: Joo, Myungsoo, et al.
Publicado: (2012)

Rapid prenatal diagnosis of Facioscapulohumeral Muscular Dystrophy 1 by combined Bionano optical mapping and karyomapping
por: Zheng, Yuting, et al.
Publicado: (2019)

Network analysis of PGD, PTSD and insomnia symptoms in Chinese shidu parents with PGD
por: Xu, Xin, et al.
Publicado: (2022)

Prostaglandin D(2) (PGD(2)); PGD(2) receptor subtype DP1
Publicado: (2011)

PGD: Pineapple Genomics Database
por: Xu, Huimin, et al.
Publicado: (2018)

A healthy HLA-matched baby born by using a combination of aCGH and Karyomapping: the first latin american case
por: Delgado, Andrea, et al.
Publicado: (2017)

Tripolar mitosis and partitioning of the genome arrests human preimplantation development in vitro
por: Ottolini, Christian S., et al.
Publicado: (2017)

PGD-based modeling of materials, structures and processes
por: Chinesta, Francisco, et al.
Publicado: (2014)

ART with PGD: Risky heredity and stratified reproduction
por: Löwy, Ilana
Publicado: (2020)

The politics of human embryo research and the motivation to achieve PGD
por: Theodosiou, Anastasia A., et al.
Publicado: (2011)

PGD: a pangolin genome hub for the research community
por: Tan, Tze King, et al.
Publicado: (2016)

Contested change: how Germany came to allow PGD()
por: Bock von Wülfingen, Bettina
Publicado: (2016)

Transferring embryos with indeterminate PGD results: the ethical implications
por: Insogna, Iris G., et al.
Publicado: (2016)

Subsidizing PGD: The Moral Case for Funding Genetic Selection
por: Kemper, James M., et al.
Publicado: (2019)

Meiotic and mitotic aneuploidies drive arrest of in vitro fertilized human preimplantation embryos
por: McCoy, Rajiv C., et al.
Publicado: (2023)

Unprovoked Pulmonary Embolism in a Young Patient with Marfan Syndrome
por: Pak, Stella, et al.
Publicado: (2017)

Developmental, cytogenetic and epigenetic consequences of removing complex proteins and adding melatonin during in vitro maturation of bovine oocytes
por: Tutt, Desmond A. R., et al.
Publicado: (2023)

Separated representations and PGD-based model reduction: fundamentals and applications
por: Chinesta, Francisco, et al.
Publicado: (2014)

Discovery of Ebselen as an Inhibitor of 6PGD for Suppressing Tumor Growth
por: Feng, Qi, et al.
Publicado: (2020)

Monogenic hypertension
por: Precone, Vincenza, et al.
Publicado: (2019)

Monogenic hyperlipidemias
por: Krasi, Geraldo, et al.
Publicado: (2019)

Choosing embryos: ethical complexity and relational autonomy in staff accounts of PGD
por: Ehrich, Kathryn, et al.
Publicado: (2007)

The embryo as moral work object: PGD/IVF staff views and experiences
por: Ehrich, Kathryn, et al.
Publicado: (2008)

Valid ICD-11 PGD Scales and Structured Clinical Interviews Needed
por: O'Connor, Maja, et al.
Publicado: (2020)

Ventricular‐Vascular Coupling in Marfan and Non‐Marfan Aortopathies
por: Loeper, Farina, et al.
Publicado: (2016)

Novel homozygous leptin receptor mutation in an infant with monogenic obesity
por: Boro, Hiya, et al.
Publicado: (2023)

Marfan's Syndrome
por: Bhatia, Tanuj, et al.
Publicado: (2012)

Marfan on the Move
por: de Waard, Vivian
Publicado: (2017)

Marfan Syndrome
por: Sivasankari, T, et al.
Publicado: (2017)

Monogenic Causes of Strokes
por: Chojdak-Łukasiewicz, Justyna, et al.
Publicado: (2021)

Can Characteristics of Reciprocal Translocations Predict the Chance of Transferable Embryos in PGD Cycles?
por: Dul, Elsbeth, et al.
Publicado: (2014)

Outcomes of 13 ICSI-PGD cycles with ejaculated spermatozoa in patients with Klinefelter syndrome
por: Ni, Tian-Xiang, et al.
Publicado: (2016)

Preimplantation genetic diagnosis and screening (PGD/S) using a semiconductor sequencing platform
por: Wang, Li-Ya, et al.
Publicado: (2019)

PGD: a machine learning-based photosynthetic-related gene detection approach
por: Wang, Yunchuan, et al.
Publicado: (2022)

CXXC5 Mediates DHT-Induced Androgenetic Alopecia via PGD(2)
por: Ryu, Yeong Chan, et al.
Publicado: (2023)

Ferroptosis-related genes LPCAT3 and PGD are potential diagnostic biomarkers for osteoarthritis
por: Wang, Lufei, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_8oa60sn2la0e8qm6qru0jnfmr8