Rongrong Yin
Shanghai, China
Last Updated: 09/26/2026
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Found 12 publications
The precise molecular diagnosis of novel GLDC compound heterozygous variants highlights the benefits for a Chinese family with nonketotic hyperglycinemia.
Journal: Molecular genetics and metabolism reports
Published: January 10, 2025
Plasticity changes in iron homeostasis in hibernating Daurian ground squirrels (Spermophilus dauricus) may counteract chronically inactive skeletal muscle atrophy.
Journal: Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology
Published: July 30, 2023
Segawa syndrome caused by TH gene mutation and its mechanism.
Journal: Frontiers in genetics
Published: July 27, 2022
Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.2800 G>A) in the KCNT1 gene.
Journal: Stem cell research
Published: February 13, 2022
Generation of an induced pluripotent stem cell line from an Ohtahara syndrome patient with the hemizygous mutation p.Q503Afs*28 (c.1507_1508del) in the ARX gene.
Journal: Stem cell research
Published: April 13, 2021
Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene.
Journal: Frontiers in pediatrics
Published: March 22, 2021
Generation and characterization of the induced pluripotent stem cell line SHCDNi004-A from a ten-year-old Chinese boy with X-linked mental retardation in IL1RAPL1 deficiency.
Journal: Stem cell research
Published: February 06, 2021
Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan-Herndon-Dudley syndrome.
Journal: Stem cell research
Published: May 25, 2020
Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndrome.
Journal: Stem cell research
Published: April 12, 2020
Generation of an induced pluripotent stem cell line SHCDNi001-A from a one-year-old Chinese girl with mitochondrial DNA depletion syndrome 13.
Journal: Stem cell research
Published: January 21, 2020
CHRNE compound heterozygous mutations in congenital myasthenic syndrome: A case report.
Journal: Medicine
Published: April 29, 2018
Dopa-Responsive Dystonia in Han Chinese Patients: One Novel Heterozygous Mutation in GTP Cyclohydrolase 1 (GCH1) and Three Known Mutations in TH.
Journal: Medical science monitor : international medical journal of experimental and clinical research
Published: February 07, 2018
Showing 1-12 of 12
Last Updated: 09/26/2026