Zobrazeno 1 - 10
of 195
pro vyhledávání: '"amniocyte"'
Autor:
Karen Coste, Shaam Bruet, Caroline Chollat-Namy, Odile Filhol, Claude Cochet, Denis Gallot, Geoffroy Marceau, Loïc Blanchon, Vincent Sapin, Corinne Belville
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 4, p 4074 (2023)
At the feto-maternal interface, fetal membranes (FM) play a crucial role throughout pregnancy. FM rupture at term implicates different sterile inflammation mechanisms including pathways activated by the transmembrane glycoprotein receptor for advance
Externí odkaz:
https://doaj.org/article/715625d1d9b949689ed83aff57b87080
Akademický článek
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Autor:
Yu-Hsun Chang, Pui-Yi Chen, Tzu-Ying Li, Chung-Nan Yeh, Yi-Shian Li, Shao-Yin Chu, Ming-Liang Lee
Publikováno v:
Pediatrics and Neonatology, Vol 54, Iss 3, Pp 161-165 (2013)
This study aimed at investigating the results of second-trimester amniocyte karyotyping in western and eastern Taiwan, and identifying any regional differences in the prevalence of fetal chromosomal anomalies. Methods: From 2004 to 2009, pregnant wom
Externí odkaz:
https://doaj.org/article/1e1e0845a057490d8e2066881254ec7f
Autor:
Apoorva Joshi, David E. Condon, Paul Zhipang Wang, Cetewayo S. Rashid, So Won Min, Sara E. Pinney, Victoria Yin
Publikováno v:
J Clin Endocrinol Metab
Context Gestational diabetes (GDM) has profound effects on the intrauterine metabolic milieu and is linked to obesity and diabetes in offspring, but the mechanisms driving these effects remain largely unknown. Alterations in DNA methylation and gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8045394ddee523159570f6905725e2d5
https://doi.org/10.1210/clinem/dgaa466
https://doi.org/10.1210/clinem/dgaa466
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Reza Raoofian, Reza Pazhoomand, Abdorrasoul Malekpour, Raheleh Taheri, Sadegh Shirian, Fatemeh Shahriyari, Reza Mohammadi, Zahra Mohammadi, Farnaz Feiz
Publikováno v:
International Journal of Reproductive Biomedicine
International Journal of Reproductive BioMedicine, Vol 19, Iss 5, Pp 477-482 (2021)
International Journal of Reproductive BioMedicine, Vol 19, Iss 5, Pp 477-482 (2021)
Background: Small supernumerary marker chromosomes (sSMCs) are chromosomal fragments with abnormal structures found in patients with fertility problems and developmental delay. They may be detected in amniotic cell karyotypes. sSMCs are categorized a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ace094eb007d1b46e13b6904746ea61
https://doi.org/10.18502/ijrm.v19i5.9258
https://doi.org/10.18502/ijrm.v19i5.9258
Autor:
Dan Mihailescu, Dorin Alexandru, Florin Bogdan Epureanu, Lorand Savu, Bogdan Amuzescu, Florin Iordache, Razvan Airini, Horia Maniu
Publikováno v:
Journal of Cellular and Molecular Medicine
The aim of the study was to evidence replicative senescence‐induced changes in human amniocytes via flow cytometry, quantitative reverse‐transcription‐polymerase chain reaction (qRT‐PCR) and automated/manual patch‐clamp. Both cryopreserved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39457d9b9d31423042a80a165dd0ca82
https://doi.org/10.1111/jcmm.14495
https://doi.org/10.1111/jcmm.14495
Autor:
Jean R. Lowe, Marina S Oren, Jenny E. Camacho, Tom Cushing, Carol L. Clericuzio, Hongyan Xie, Jessie R. Maxwell
Publikováno v:
Clinical Case Reports
Key Clinical Message Recombinant chromosome 8 syndrome is caused by duplication of 8q and deletion of 8p. A fetus with anomalies was misdiagnosed with this syndrome based on an amniocyte karyotype. Postnatal chromosomal microarray and other studies i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48a1f0dc0db37bf6f7a1355eece24df6
https://doi.org/10.1002/ccr3.2109
https://doi.org/10.1002/ccr3.2109
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 2612, p 2612 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
The amniotic fluid (AF) is a complex biofluid that reflects fetal well-being during development. AF con be divided into two fractions, the supernatant and amniocytes. The supernatant contains cell-free components, including placenta-derived micropart
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8d5f6492a8e345d351917c8bd61a482
https://pubmed.ncbi.nlm.nih.gov/33807645
https://pubmed.ncbi.nlm.nih.gov/33807645
Autor:
Na Hao, David S Cram, Yulin Jiang, Mengnan Xu, Chengkun Liu, Xiya Zhou, Xiangbin Chen, Juntao Liu, Qingwei Qi
Publikováno v:
Life
Life, Vol 11, Iss 98, p 98 (2021)
Volume 11
Issue 2
Life, Vol 11, Iss 98, p 98 (2021)
Volume 11
Issue 2
Next-generation sequencing (NGS) is emerging as a new method for the detection of clinically significant copy number variants (CNVs). In this study, we developed and validated rapid CNV-sequencing (rCNV-seq) for clinical application in prenatal diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b489bceb3ea07f5755f4173ab9ef24d6
https://pubmed.ncbi.nlm.nih.gov/33525582
https://pubmed.ncbi.nlm.nih.gov/33525582