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List of works by Ying Liu

A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family ⬇️

scientific article published on 06 August 2011

CERKL gene knockout disturbs photoreceptor outer segment phagocytosis and causes rod-cone dystrophy in zebrafish

scientific article published on 7 April 2017

CERKL interacts with mitochondrial TRX2 and protects retinal cells from oxidative stress-induced apoptosis.

scientific article published on 13 April 2014

Cloning and functional characterization of novel variants and tissue-specific expression of alternative amino and carboxyl termini of products of slc4a10

scientific article

Effect of simultaneously replacing putative TM6 and TM12 of human NBCe1-A with those from NBCn1 on surface abundance in Xenopus oocytes

scientific article

Effects of Nt-truncation and coexpression of isolated Nt domains on the membrane trafficking of electroneutral Na+/HCO3- cotransporters

scientific article published on 20 July 2015

Effects of optional structural elements, including two alternative amino termini and a new splicing cassette IV, on the function of the sodium-bicarbonate cotransporter NBCn1 (SLC4A7).

scientific article

Expression and distribution of NBCn2 (Slc4a10) splice variants in mouse brain: cloning of novel variant NBCn2-D.

scientific article

IRBIT activates NBCe1-B by releasing the auto-inhibition module from the transmembrane domain

scientific article published on 25 November 2020

Identification of three mutations in the MVK gene in six patients associated with disseminated superficial actinic porokeratosis

scientific article

Loss-of-function Mutation in PMVK Causes Autosomal Dominant Disseminated Superficial Porokeratosis

scientific article published on 7 April 2016

Mucolipidosis in a Chinese family with compound heterozygous mutations at the GNPTAB gene ⬇️

scientific article published on April 28, 2011

Multiple acid-base and electrolyte disturbances upregulate NBCn1, NBCn2, IRBIT and L-IRBIT in the mTAL

scientific article published on 02 May 2020

Mutation p.Leu354Pro in EDA causes severe hypohidrotic ectodermal dysplasia in a Chinese family ⬇️

scientific article published on October 10, 2011

Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1

scientific article published on 21 March 2013

Physiology and pathophysiology of Na⁺/HCO₃⁻ cotransporter NBCe1

scientific article

Role of an extracellular loop in determining the stoichiometry of Na+-HCO₃⁻ cotransporters

scientific article

Structure and Function of SLC4 Family [Formula: see text] Transporters.

scientific article

The Balance of [Formula: see text] Secretion vs. Reabsorption in the Endometrial Epithelium Regulates Uterine Fluid pH.

scientific article published on 25 January 2018

Towards bridging the gap between acid-base transporters and neuronal excitability modulation

scientific article published on 15 December 2014

Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa

scientific article published on 18 March 2016

[Bicarbonate reabsorption in proximal renal tubule: molecular mechanisms and metabolic acidosis].

scientific article published in August 2014

[Electrophysiology principles of Na(+)/HCO3(-) cotransporters]

scientific article published in June 2016

pVHL interacts with Ceramide kinase like (CERKL) protein and ubiquitinates it for oxygen dependent proteasomal degradation.

scientific article published on 18 August 2015

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