Shaobin Lin

Xiamen Key Laboratory Of Reproduction And Genetics
Xiamen, 361003, China

Last Updated: 09/26/2026

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Found 13 publications

Sensitive and quick electrochemiluminescence biosensor for the detection of reactive oxygen species in seminal plasma based on the valence regulation of gold nanoclusters.

Sensitive and quick electrochemiluminescence biosensor for the detection of reactive oxygen species in seminal plasma based on the valence regulation of gold nanoclusters.

Journal: Analytica chimica acta

Published: July 21, 2024

Simple and rapid multicolor sensor for seminal plasma ROS detection based on synergistic catalytic etching of gold nanobipyramids dopped agarose composite gel.

Simple and rapid multicolor sensor for seminal plasma ROS detection based on synergistic catalytic etching of gold nanobipyramids dopped agarose composite gel.

Journal: Talanta

Published: June 20, 2024

Clinical and genetic analysis of a patient with 17-hydroxylase/17,20-lyase deficiency

Clinical and genetic analysis of a patient with 17-hydroxylase/17,20-lyase deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: August 21, 2020

CCDC9 is identified as a novel candidate gene of severe asthenozoospermia.

CCDC9 is identified as a novel candidate gene of severe asthenozoospermia.

Journal: Systems biology in reproductive medicine

Published: September 11, 2019

DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella.

DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella.

Journal: Annals of human genetics

Published: May 06, 2019

Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype.

Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype.

Journal: Journal of human genetics

Published: April 09, 2019

Analysis of a pedigree with partial trisomy 9 and partial monosomy 13 derived from a maternal balanced t(9;13) translocation

Analysis of a pedigree with partial trisomy 9 and partial monosomy 13 derived from a maternal balanced t(9;13) translocation

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 06, 2019

EIF4G1 is a novel candidate gene associated with severe asthenozoospermia.

EIF4G1 is a novel candidate gene associated with severe asthenozoospermia.

Journal: Molecular genetics & genomic medicine

Published: January 16, 2019

Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF).

Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF).

Journal: Journal of medical genetics

Published: December 18, 2018

Exome sequencing identifies compound heterozygous KCTD7 mutations in a girl with progressivemyoclonus epilepsy.

Exome sequencing identifies compound heterozygous KCTD7 mutations in a girl with progressivemyoclonus epilepsy.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: December 13, 2018

DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella.

DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella.

Journal: Clinical genetics

Published: December 02, 2018

Comprehensive Genome Profiling of Single Sperm Cells by Multiple Annealing and Looping-Based Amplification Cycles and Next-Generation Sequencing from Carriers of Robertsonian Translocation.

Comprehensive Genome Profiling of Single Sperm Cells by Multiple Annealing and Looping-Based Amplification Cycles and Next-Generation Sequencing from Carriers of Robertsonian Translocation.

Journal: Annals of human genetics

Published: November 13, 2016

Showing 1-12 of 13

Last Updated: 09/26/2026