Qing Tan

Study on aluminium oxide doping modification of indium oxide and thermoelectric properties

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility

Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

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

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

Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility

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

Homozygous mutations in <i>DZIP1</i> can induce asthenoteratospermia with severe MMAF

A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia

Patients with severe asthenoteratospermia carrying SPAG6 or RSPH3 mutations have a positive pregnancy outcome following intracytoplasmic sperm injection

A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens

Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice

Biallelic mutations in <i>CFAP65</i> cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice

Homozygous mutations in <i>SPEF2</i> induce multiple morphological abnormalities of the sperm flagella and male infertility

Mono-2-ethylhexyl phthalate induces the expression of genes involved in fatty acid synthesis in HepG2 cells