Mingrong Lv

Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes

Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variants

Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and mice

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility

ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida

Novel variants in DNAH6 cause male infertility associated with multiple morphological abnormalities of the sperm flagella (MMAF) and ICSI outcomes

Biallelic mutations in <i>CFAP54</i> cause male infertility with severe MMAF and NOA

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models

Bi-allelic human<i>TEKT3</i>mutations cause male infertility with oligoasthenoteratozoospermia owing to acrosomal hypoplasia and reduced progressive motility

Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryos

Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders

Novel <scp> <i>MEIOB</i> </scp> pathogenic variants including a homozygous non‐canonical splicing variant, cause meiotic arrest and human non‐obstructive azoospermia

Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia

Loss of function mutation in <i>DNAH7</i> induces male infertility associated with abnormalities of the sperm flagella and mitochondria in human

Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

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

Performance evaluation of differential splicing analysis methods and splicing analytics platform construction

Novel <i>FSIP2</i> Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans

Biallelic loss‐of‐function mutations in <i>SEPTIN4</i> ( <i>C17ORF47</i> ), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans

Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility

Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice

Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella

Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice

Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility

Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse

Melatonin alleviates deoxynivalenol-induced apoptosis of human granulosa cells by reducing mutually accentuated FOXO1 and ER stress

Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia

Identification of Novel Biallelic TLE6 Variants in Female Infertility With Preimplantation Embryonic Lethality

A homozygous loss‐of‐function mutation in <scp> <i>FBXO43</i> </scp> causes human non‐obstructive azoospermia

Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice