Jin Lin
5 Papers
14 Citations
Jin Lin is an academic researcher. The author has contributed to research in topics: Dicentric chromosome & Mutation (genetic algorithm). The author has an hindex of 2, co-authored 5 publications.
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Papers
Non-chimerism and chimerism pseudo dicentric Y chromosome: two case reports about azoospermia and cytogenetic/molecular genetic analysis in the Chinese population
TL;DR: Pseudodicentric Y chromosome affecting the long arm may lead to a male phenotype by duplicating the sex-determining region of Y chromosome (SRY) fragment and chimeric status may further impact patient's hormone levels, which obstruct spermatogenesis.
Patent
New virulence gene for severe asthenospermia, and application thereof
Sha Yanwei,Li Ping,Lin Li,Ling Zhang,Xiaohui Xu,Bing-Bing Deng,Xuemei He,Jin Lin,Yaping Ye,Gao Haijie,Jing Chen,Wang Xiong +11 more
- 15 Sep 2017
TL;DR: In this paper, a new virulence gene SPAG17 for severe asthenospermia was found for the first time, and the mutation was used to detect the severe asthespermia.
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Effects of hepatitis B virus infection in women with different ovarian reserve on outcomes of in vitro fertilization and embryo transfer
Jin Lin,Sha Yanwei,Ping-Ping Qiu,Ling Zhang,Xuemei He,Shi Yingying,Yaping Ye,Zhi-Ying Su,Ping Li +8 more
- 25 Feb 2017
TL;DR: HBV carrier in women of low ovarian reserve and normal ovarian reserve group could affect the outcomes of IVF-ET treatment.
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Predictive value of serum HCG concentrations for outcomes of vitrified-warmed blastocyst transfers in women of different ages.
TL;DR: This study demonstrates that determination of initial serum β-hCG concentrations on day 10 after SBT in frozen transfer cycles can help to predict the pregnancy outcome of IVF in women of different ages.
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A Case of Bilateral Testicular Tumors Subsequently Diagnosed as Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
Yan-Kun Sha,Yanwei Sha,Lu Ding,Wei-Wu Liu,Yue-Qiang Song,Jin Lin,Xuemei He,Ping-Ping Qiu,Ling Zhang,Ping Li +9 more
TL;DR: A case of simple virilizing CAH with TARTs in a 15-year-old boy was described in this paper, where the patient showed physical signs of precocious puberty and the levels of blood adrenocorticotropic hormone (ACTH), urinary 17-ketone steroids (17-KS), dehydroepiandrosterone sulfate (DHEA-S), and serum progesterone (PRGE) were elevated.
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