Zobrazeno 1 - 10
of 212
pro vyhledávání: '"Sung Han Shim"'
Autor:
Hyunjin Kim, Ji Eun Park, Kyung Min Kang, Hee Yeon Jang, Minyeon Go, So Hyun Yang, Jong Chul Kim, Seo Young Lim, Dong Hyun Cha, Jungah Choi, Sung Han Shim
Publikováno v:
BMC Pregnancy and Childbirth, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background To evaluate the clinical significance of noninvasive prenatal testing (NIPT) for detecting fetal sex chromosome aneuploidies (SCAs) in Korean pregnant women. Methods We retrospectively analyzed NIPT data from 9,176 women with sing
Externí odkaz:
https://doaj.org/article/6cbd8b5b2e88430cbbd7a1b4bc7c20fc
Publikováno v:
Investigative and Clinical Urology, Vol 65, Iss 1, Pp 77-83 (2024)
Purpose: Infertility affects 10% to 15% of couples, and male factor accounts for 50% of the cases. The relevant male genetic factors, which account for at least 15% of male infertility, include Y-chromosome microdeletions. We investigated clinical da
Externí odkaz:
https://doaj.org/article/1f5e65f7cdd74d0eac9aed86c98b94bf
Autor:
Kyung Min Kang, Soo Hyun Kim, Ji Eun Park, Hyunjin Kim, Hee Yeon Jang, Minyeon Go, So Hyun Yang, Sang Woo Ryu, Sung Mi Bae, Dong Hyun Cha, Sung Han Shim
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
We aimed to identify the causes of inconsistent results between non-invasive prenatal testing (NIPT) and invasive testing methods for trisomy 21. In the first case, NIPT was performed at 11 weeks of pregnancy, and the result showed a high risk of tri
Externí odkaz:
https://doaj.org/article/d87d809026d1465893a3e1f034baf350
Autor:
Kirim Hong, Hee Jin Park, Hee Yeon Jang, Sung Han Shim, Yoon Jang, Soo Hyun Kim, Dong Hyun Cha
Publikováno v:
Diagnostics, Vol 13, Iss 15, p 2532 (2023)
As the prevalence of pregnancies with advanced maternal age increases, the risk of fetal chromosomal abnormalities is on the rise. Therefore, prenatal genetic screening and diagnosis have become essential elements in contemporary obstetrical care. Tr
Externí odkaz:
https://doaj.org/article/c365177ee2ad43e8b78fc8b427f3aa49
Autor:
Eun-Young Shin, Da-Seul Kim, Min Ji Lee, Ah Reum Lee, Sung Han Shim, Seung Woon Baek, Dong Keun Han, Dong Ryul Lee
Publikováno v:
Stem Cell Research & Therapy, Vol 12, Iss 1, Pp 1-20 (2021)
Abstract Background Premature ovarian insufficiency (POI) is one of the most serious side effects of chemotherapy in young cancer survivors. It may not only reduce fecundity but also affect lifelong health. There is no standard therapy for preserving
Externí odkaz:
https://doaj.org/article/31f3742fd58e4e528fcbaaa63d14deb3
Autor:
Soo Hyun Kim, So Yeon Hong, Min Jin Lee, Kyung Min Kang, Ji Eun Park, Sung Han Shim, Dong Hyun Cha
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 60, Iss 3, Pp 570-573 (2021)
Objective: Dystrophinopathy is an X-linked recessive muscular dystrophy caused by mutations in the DMD gene. Herein we describe the prenatal detection of DMD gene mutations in a patient with no family history, by multiplex ligation-dependent probe am
Externí odkaz:
https://doaj.org/article/7dbcfe0f5381425fa31993681e7f1ba3
Publikováno v:
Annals of Child Neurology, Vol 29, Iss 1, Pp 47-50 (2021)
Externí odkaz:
https://doaj.org/article/01e3ed83ab9d4c879f491c4998d66db4
Autor:
Ok-Hee Lee, Siyoung Lee, Miseon Park, Sohyeon Moon, Semi Hwang, Byeongseok Kim, C-Yoon Kim, Dong Ryul Lee, Sung Han Shim, Keun-Hong Park, Hyung Min Chung, Youngsok Choi
Publikováno v:
Stem Cell Research, Vol 59, Iss , Pp 102643- (2022)
Beta2-microglobulin (B2M) is a subunit of human leukocyte antigen class-I (HLA-I) heterodimer that mediates immune rejection through activation of cytotoxic T cells. B2M binding to HLA-I proteins is essential for functional HLA-I on the cell surface.
Externí odkaz:
https://doaj.org/article/4e9016da851f4729a2aed98e77593fcc
Autor:
Yeojung Nam, Kyung Min Kang, Se Ra Sung, Ji Eun Park, Yun-Jeong Shin, Seung Hun Song, Ju Tae Seo, Tae Ki Yoon, Sung Han Shim
Publikováno v:
Asian Journal of Andrology, Vol 22, Iss 1, Pp 106-111 (2020)
The stromal antigen 3 (STAG3) gene, encoding a meiosis-specific cohesin component, is a strong candidate for causing male infertility, but little is known about this gene so far. We identified STAG3 in patients with nonobstructive azoospermia (NOA) a
Externí odkaz:
https://doaj.org/article/75269b28f52e49b1bf58638b413dfc2d
Autor:
Da Kyung Hong, Ji Eun Park, Kyung Min Kang, Sung Han Shim, So Hyun Shim, You Jung Han, Hee Young Cho, Dong Hyun Cha
Publikováno v:
Diagnostics, Vol 13, Iss 4, p 580 (2023)
Rare autosomal trisomies (RATs) other than common aneuploidies can be detected using noninvasive prenatal testing (NIPT). However, conventional karyotyping is insufficient for evaluating diploid fetuses with uniparental disomy (UPD) due to trisomy re
Externí odkaz:
https://doaj.org/article/fb64abee88b743d68790f5b52c8c7a94