Liu Mingxi

[Expression of annexin A7 in spermatogonial stem cells].

HORMAD2/CT46.2, a novel cancer/testis gene, is ectopically expressed in lung cancer tissues.

Transient scrotal hyperthermia induces lipid droplet accumulation and reveals a different ADFP expression pattern between the testes and liver in mice.

In-depth proteomic analysis of the human sperm reveals complex protein compositions.

Scanning of novel cancer/testis proteins by human testis proteomic analysis.

The expression and localization of a novel protein phosphatase inhibitor 2810408A11Rik in mouse testis and sperm.

SHCBP1L, a conserved protein in mammals, is predominantly expressed in male germ cells and maintains spindle stability during meiosis in testis.

A susceptibility locus rs7099208 is associated with non-obstructive azoospermia via reduction in the expression of FAM160B1.

Systematic identification of genes with a cancer-testis expression pattern in 19 cancer types.

Complete Meiosis from Embryonic Stem Cell-Derived Germ Cells In Vitro.

Major spliceosome defects cause male infertility and are associated with nonobstructive azoospermia in humans.

Comparative transcriptome analysis reveals a regulatory network of microRNA-29b during mouse early embryonic development.

The human sperm proteome 2.0: An integrated resource for studying sperm functions at the level of posttranslational modification.

TCTE1 is a conserved component of the dynein regulatory complex and is required for motility and metabolism in mouse spermatozoa.

Ythdc2 is an N-methyladenosine binding protein that regulates mammalian spermatogenesis.

An essential role for PNLDC1 in piRNA 3' end trimming and male fertility in mice.

Cancer-testis gene PIWIL1 promotes cell proliferation, migration, and invasion in lung adenocarcinoma.

MORC2B is essential for meiotic progression and fertility.

Single-cell RNA-seq uncovers dynamic processes and critical regulators in mouse spermatogenesis.

Effects of chemotherapeutic agent bendamustine for non-hodgkin lymphoma on spermatogenesis in mice.

A cancer-testis non-coding RNA LIN28B-AS1 activates driver gene LIN28B by interacting with IGF2BP1 in lung adenocarcinoma.

ATP synthase is required for male fertility and germ cell maturation in Drosophila testes.

Dual functions for the ssDNA-binding protein RPA in meiotic recombination.

Normal spermatogenesis in (fibronectin type 3 and ankyrin repeat domains 1) mutant mice.

RSBP15 interacts with and stabilizes dRSPH3 during sperm axoneme assembly in Drosophila.

Precursor RNA processing 3 is required for male fertility, and germline stem cell self-renewal and differentiation via regulating spliceosome function in Drosophila testes.

Biallelic mutations in cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice.

UHRF1 suppresses retrotransposons and cooperates with PRMT5 and PIWI proteins in male germ cells.

FBXO47 regulates telomere-inner nuclear envelope integration by stabilizing TRF2 during meiosis.

The heat shock protein family gene in male mice is dispensable for fertility.

Human X chromosome exome sequencing identifies as contributor to spermatogenesis.

The 18S rRNA m A methyltransferase METTL5 promotes mouse embryonic stem cell differentiation.

Spermatogenesis is normal in knockout mice.

Retinoic Acid Induced Protein 14 () is dispensable for mouse spermatogenesis.

Sexual Dimorphism in Mouse Meiosis.

is not required for fertility in male mice.

Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse.

Single-cell RNA-Seq reveals a highly coordinated transcriptional program in mouse germ cells during primordial follicle formation.

Knockout Gene-Based Evidence for PIWI-Interacting RNA Pathway in Mammals.

LRRC23 is a conserved component of the radial spoke that is necessary for sperm motility and male fertility in mice.

A homozygous loss-of-function mutation in FBXO43 causes human non-obstructive azoospermia.

Novel bi-allelic variants in ACTL7A are associated with male infertility and total fertilization failure.

Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly.

CFAP61 is required for sperm flagellum formation and male fertility in human and mouse.

ZDHHC19 localizes to the cell membrane of spermatids and is involved in spermatogenesis†.

Testis-enriched is not required for spermatogenesis and fertility in mice.

Bi-allelic variants in human TCTE1/DRC5 cause asthenospermia and male infertility.

Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans.

A hypoxia-dissociable siRNA nanoplatform for synergistically enhanced chemo-radiotherapy of glioblastoma.

Testis-enriched is not required for spermatogenesis and male fertility in mice.

Differential requirements of IQUB for the assembly of radial spoke 1 and the motility of mouse cilia and flagella.

Functional screening of congenital heart disease risk loci identifies 5 genes essential for heart development in zebrafish.

DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice.

Clinical outcomes of subtypes of mosaic single aneuploid embryos after preimplantation genetic testing for aneuploidy.

Recent progress of hydrogel-based local drug delivery systems for postoperative radiotherapy.

Mutation of S461, in the GOLGA3 phosphorylation site, does not affect mouse spermatogenesis.

Fat mass and obesity-associated factor (FTO)-mediated N6-methyladenosine regulates spermatogenesis in an age-dependent manner.

Structures of sperm flagellar doublet microtubules expand the genetic spectrum of male infertility.

Prolyl endopeptidase remodels macrophage function as a novel transcriptional coregulator and inhibits fibrosis.

is not essential for spermatogenesis and male fertility in mice.

Centriolar appendages evolve into the inner sheath of mammalian flagella.

Disruption in leads to acrosome detachment, sperm head deformity, and male in/subfertility in humans and mice.

Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.

Expression of concern: A hypoxia-dissociable siRNA nanoplatform for synergistically enhanced chemo-radiotherapy of glioblastoma.