Zhi-ying Su

10 Zhenhai Road, P.R. China
Xiamen, 361001, China

Last Updated: 09/26/2026

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Found 11 publications

Overexpression of the PLK4 Gene as a Novel Strategy for the Treatment of Autosomal Recessive Microcephaly by Improving Centrosomal Dysfunction.

Overexpression of the PLK4 Gene as a Novel Strategy for the Treatment of Autosomal Recessive Microcephaly by Improving Centrosomal Dysfunction.

Journal: Journal of molecular neuroscience : MN

Published: March 27, 2021

Biallelic mutations in PMFBP1 cause acephalic spermatozoa.

Biallelic mutations in PMFBP1 cause acephalic spermatozoa.

Journal: Clinical genetics

Published: July 24, 2018

Patients with multiple morphological abnormalities of the sperm flagella harbouring CFAP44 or CFAP43 mutations have a good pregnancy outcome following intracytoplasmic sperm injection.

Patients with multiple morphological abnormalities of the sperm flagella harbouring CFAP44 or CFAP43 mutations have a good pregnancy outcome following intracytoplasmic sperm injection.

Journal: Andrologia

Published: June 24, 2018

Identification of a novel mutation in FGFR1 gene in patients with Kallmann syndrome by high throughput sequencing.

Identification of a novel mutation in FGFR1 gene in patients with Kallmann syndrome by high throughput sequencing.

Journal: Systems biology in reproductive medicine

Published: April 17, 2018

Two cases of complex balanced autosomal translocations associated with severe oligozoospermia.

Two cases of complex balanced autosomal translocations associated with severe oligozoospermia.

Journal: Gene

Published: January 29, 2018

Novel Mutations in CFAP44 and CFAP43 Cause Multiple Morphological Abnormalities of the Sperm Flagella (MMAF).

Novel Mutations in CFAP44 and CFAP43 Cause Multiple Morphological Abnormalities of the Sperm Flagella (MMAF).

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: December 27, 2017

TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family.

TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family.

Journal: Gene

Published: December 04, 2017

Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian China.

Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian China.

Journal: Gene

Published: September 27, 2017

A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.

A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.

Journal: Gene

Published: June 29, 2017

A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF).

A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF).

Journal: Gene

Published: June 18, 2017

Identification of two novel genes SLC15A2 and SLCO1B3 associated with maintenance dose variability of warfarin in a Chinese population.

Identification of two novel genes SLC15A2 and SLCO1B3 associated with maintenance dose variability of warfarin in a Chinese population.

Journal: Scientific reports

Published: November 18, 2016

Showing 1-11 of 11

Last Updated: 09/26/2026