Guang-Xiu Lu
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Explore the profile of Guang-Xiu Lu including associated specialties, affiliations and a list of published articles.
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Articles
173
Citations
863
Followers
0
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Recent Articles
1.
Zhao Z, Zhou J, Wang Q, Peng S, Peng Y, Wang Y, et al.
Clin Genet
. 2025 Feb;
PMID: 39924787
Inherited glycosylphosphatidylinositol deficiency disorders (IGDs) are a group of rare recessive genetic conditions characterised by developmental delays and an early onset epilepsy caused by disruptions in the glycosylphosphatidylinositol-anchored biosynthetic pathway....
2.
Liu J, Zeng S, Wang A, Cheng H, Zhang Q, Lu G
World J Gastrointest Oncol
. 2024 Apr;
16(4):1532-1546.
PMID: 38660671
Background: Peutz-Jeghers syndrome (PJS) is a rare hereditary neoplastic disorder mainly associated with serine/threonine kinase 11 (/) gene mutations. Preimplantation genetic testing can protect a patient's offspring from mutated genes;...
3.
Cheng D, Lu C, Gong F, Du J, Yuan S, Luo K, et al.
Hum Reprod
. 2024 Feb;
39(4):849-855.
PMID: 38420683
Individuals with 46,XX/XY chimerism can display a wide range of characteristics, varying from hermaphroditism to complete male or female, and can display sex chromosome chimerism in multiple tissues, including the...
4.
Luo C, Chen Z, Meng L, Tan C, He W, Tu C, et al.
Clin Genet
. 2024 Feb;
106(1):27-36.
PMID: 38342987
Oligoasthenoteratozoospermia (OAT) is a common type of male infertility; however, its genetic causes remain largely unknown. Some of the genetic determinants of OAT are gene defects affecting spermatogenesis. BCORL1 (BCL6...
5.
Meng G, Wang Y, Luo C, Tan Y, Li Y, Tan C, et al.
Hum Reprod Open
. 2024 Feb;
2024(1):hoae003.
PMID: 38312775
Study Question: Are there other pathogenic genes for asthenoteratozoospermia (AT)? Summary Answer: is a novel candidate gene for AT in humans and mice. What Is Known Already: AT is a...
6.
Che J, Wu H, Zeng S, Wu Y, Dai J, Cheng D, et al.
Asian J Androl
. 2023 Dec;
26(2):175-182.
PMID: 38048167
Phospholipase C zeta (PLCζ) is a key sperm-borne oocyte-activating factor that triggers Ca 2+ oscillations and the subsequent block to polyspermy following gamete fusion. Mutations in PLCZ1 , the gene...
7.
Guo J, He W, Dai L, Tian F, Luo Z, Shen F, et al.
HGG Adv
. 2023 Nov;
5(1):100256.
PMID: 37981762
In this study, we report on mosaic variegated aneuploidy (MVA) syndrome with tetraploidy and predisposition to infertility in a family. Sequencing analysis identified that the CEP192 biallelic variants (c.1912C>T, p.His638Tyr...
8.
Immune profiling and RNA-seq uncover the cause of partial unexplained recurrent implantation failure
Fan X, Zhao Q, Li Y, Chen Z, Liao J, Chen H, et al.
Int Immunopharmacol
. 2023 Jun;
121:110513.
PMID: 37336073
Background: Detailed knowledge of the changes in endometrial immune cells during the window of implantation in unexplained recurrent implantation failure (RIF) patients, the functions performed by immune cells, and the...
9.
Li Q, Wang Y, Zheng W, Guo J, Zhang S, Gong F, et al.
Hum Reprod
. 2023 May;
38(7):1390-1398.
PMID: 37140151
Study Question: What is the effect of defects in the manchette protein IQ motif-containing N (IQCN) on sperm flagellar assembly? Summary Answer: Deficiency in IQCN causes sperm flagellar assembly defects...
10.
Li Y, Wen Q, Hu J, Liao J, Fan X, Chen H, et al.
BMC Pregnancy Childbirth
. 2023 Mar;
23(1):199.
PMID: 36949405
Objective: To evaluate the clinical availability and stability of histological endometrial dating as a tool for personalized frozen-thawed embryo transfer (pFET) in patients with repeated implantation failure (RIF) in natural...