Dominantly inherited isolated polycystic liver disease (PCLD) consists of liver cysts that are radiologically and pathologically identical to those seen in autosomal dominant polycystic kidney disease, but without clinically relevant kidney cysts. The causative genes are known for fewer than 40% of PCLD index cases. Here, we have used whole exome sequencing in a discovery cohort of 102 unrelated patients who were excluded for mutations in the 2 most common PCLD genes,
Whitney Besse, Ke Dong, Jungmin Choi, Sohan Punia, Sorin V. Fedeles, Murim Choi, Anna-Rachel Gallagher, Emily B. Huang, Ashima Gulati, James Knight, Shrikant Mane, Esa Tahvanainen, Pia Tahvanainen, Simone Sanna-Cherchi, Richard P. Lifton, Terry Watnick, York P. Pei, Vicente E. Torres, Stefan Somlo
Title and authors | Publication | Year |
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The spectrum of diseases, genetic landscape and new mutation sites of hereditary cystic kidney disease
Bi J, Guo W, Ji P, Li S, Wang P, Li Q, Xie Y |
Clinical Kidney Journal | 2025 |
Phenotypic outcomes of PKD1 compared with non-PKD1 genetically confirmed autosomal dominant polycystic kidney disease.
Elhassan EAE, O'Donoghue D, Heneghan S, Teltsh O, Sarihan S, Osman SM, Clince M, Synnott D, Craig S, Hudson A, Doyle B, Lappin D, Sexton DJ, Casserly L, Holian J, Magee C, Denton M, Sweeney C, Awan A, McCann E, Cavalleri GL, Benson KA, Conlon PJ |
Journal of nephrology | 2025 |
Quantifying variant contributions in cystic kidney disease using national-scale whole genome sequencing
Omid Sadeghi-Alavijeh, Melanie Chan, Gabriel Doctor, Catalin Voinescu, Alexander Stuckey, Athanasios Kousathanas, Alexander Ho, Genomics Consortium, Horia Stanescu, Detlef Bockenhauer, Richard Sandford, Adam Levine, Daniel Gale |
Journal of Clinical Investigation | 2024 |
Clinical manifestation, epidemiology, genetic basis, potential molecular targets, and current treatment of polycystic liver disease
Mahboobipour AA, Ala M, Safdari Lord J, Yaghoobi A |
Orphanet Journal of Rare Diseases | 2024 |
Comparative analysis of SEC61A1 mutant R236C in two patient-derived cellular platforms
Weiand M, Sandfort V, Nadzemova O, Schierwagen R, Trebicka J, Schlevogt B, Kabar I, Schmidt H, Zibert A |
Scientific Reports | 2024 |
How Does ADPKD Severity Differ Between Family Members?
Yeung KC, Fryml E, Lanktree MB |
Kidney International Reports | 2024 |
Pathogenic relationship between phenotypes of ARPKD and novel compound heterozygous mutations of PKHD1
Zhang X, Wu J, Zhou J, Liang J, Han Y, Qi Y, Zhu T, Yuan D, Zhu Z, Zhai J |
Frontiers in Genetics | 2024 |
Single-Base Substitution Causing Dual-Exon Skipping Event in PKD2 Gene: Unusual Molecular Finding from Exome Sequencing in a Patient with Autosomal Dominant Polycystic Kidney Disease
De Paolis E, Raspaglio G, Ciferri N, Zangrilli I, Ricciardi Tenore C, Urbani A, Ferraro PM, Minucci A, Concolino P |
Journal of Clinical Medicine | 2024 |
Exquisite sensitivity of Polycystin-1 to H2O2 concentration in the endoplasmic reticulum
Speranza E, Sorrentino I, Boletta A, Sitia R |
Redox Biology | 2024 |
Liver manifestations in autosomal dominant polycystic kidney disease (ADPKD) and their impact on quality of life
Arjune S, Todorova P, Bartram MP, Grundmann F, Müller RU |
Clinical Kidney Journal | 2024 |
Predominant Liver Cystic Disease in a New Heterozygotic PKHD1 Variant: A Case Report
Van Buren JD, Neuman JT, Sidlow R |
2023 | |
The ER Protein Translocation Channel Subunit Sbh1 Controls Virulence of Cryptococcus neoformans
Santiago-Tirado FH, Hurtaux T, Geddes-McAlister J, Nguyen D, Helms V, Doering TL, Römisch K |
mBio | 2023 |
KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease.
Boulogne F, Claus LR, Wiersma H, Oelen R, Schukking F, de Klein N, Li S, Westra HJ, van der Zwaag B, van Reekum F, Sierks D, Schönauer R, Li Z, Bijlsma EK, Bos WJW, Halbritter J, Knoers NVAM, Besse W, Deelen P, Franke L, van Eerde AM |
European journal of human genetics : EJHG | 2023 |
The C-terminal tail of polycystin-1 suppresses cystic disease in a mitochondrial enzyme-dependent fashion.
Onuchic L, Padovano V, Schena G, Rajendran V, Dong K, Shi X, Pandya R, Rai V, Gresko NP, Ahmed O, Lam TT, Wang W, Shen H, Somlo S, Caplan MJ |
Nature Communications | 2023 |
Activation of ACLY by SEC63 deploys metabolic reprogramming to facilitate hepatocellular carcinoma metastasis upon endoplasmic reticulum stress
Hu C, Xin Z, Sun X, Hu Y, Zhang C, Yan R, Wang Y, Lu M, Huang J, Du X, Xing B, Liu X |
Journal of experimental & clinical cancer research : CR | 2023 |
Identified eleven exon variants in PKD1 and PKD2 genes that altered RNA splicing by minigene assay
Liu X, Shi X, Xin Q, Liu Z, Pan F, Qiao D, Chen M, Zhang Y, Guo W, Li C, Zhang Y, Shao L, Zhang R |
BMC Genomics | 2023 |
Hypomorphic PKD1 Alleles Impact Disease Variability in Autosomal Dominant Polycystic Kidney Disease.
Gulati A, Dahl NK, Hartung EA, Clark SL, Moudgil A, Goodwin J, Somlo S |
2023 | |
NOTCH signalling – a core regulator of bile duct disease?
Martinez Lyons A, Boulter L |
Disease models & mechanisms | 2023 |
Novel α-1,3-Glucosyltransferase Variants and Their Broad Clinical Polycystic Liver Disease Spectrum
Boerrigter MM, te Morsche RH, Venselaar H, Pastoors N, Geerts AM, Hoorens A, Drenth JP |
Genes & development | 2023 |
Dnajb11-Kidney Disease Develops from Reduced Polycystin-1 Dosage but not Unfolded Protein Response in Mice
Ghosh Roy S, Li Z, Guo Z, Tran Long K, Rehrl S, Tian X, Dong K, Besse W |
Journal of the American Society of Nephrology : JASN | 2023 |
Heterozygosity of ALG9 in Association with Autosomal Dominant Polycystic Liver Disease
Boerrigter MM, Duijzer R, te Morsche RH, Drenth JP |
Genes & development | 2023 |
Quantitative Mass Spectrometry Characterizes Client Spectra of Components for Targeting of Membrane Proteins to and Their Insertion into the Membrane of the Human ER
Jung M, Zimmermann R |
International journal of molecular sciences | 2023 |
A TGFβ-ECM-Integrin signalling axis drives structural reconfiguration of the bile duct to promote polycystic liver disease
Waddell SH, Yao Y, Olaizola P, Walker A, Jarman EJ, Gournopanos K, Gradinaru A, Christodoulou E, Gautier P, Boerrigter MM, Cadamuro M, Fabris L, Drenth JP, Kendall TJ, Banales JM, Khamseh A, Mill P, Boulter L |
Science Translational Medicine | 2023 |
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease
Claus LR, Chen C, Stallworth J, Turner JL, Slaats GG, Hawks AL, Mabillard H, Senum SR, Srikanth S, Flanagan-Steet H, Louie RJ, Silver J, Lerner-Ellis J, Morel C, Mighton C, Sleutels F, van Slegtenhorst M, van Ham T, Brooks AS, Dorresteijn EM, Barakat TS, Dahan K, Demoulin N, Goffin EJ, Olinger E, Larsen M, Hertz JM, Lilien MR, Obeidová L, Seeman T, Stone HK, Kerecuk L, Gurgu M, Yengej FA, Ammerlaan CM, Rookmaaker MB, Hanna C, Rogers RC, Duran K, Peters E, Sayer JA, van Haaften G, Harris PC, Ling K, Mason JM, van Eerde AM, Steet R |
Kidney International | 2023 |
Genetic Spectrum of Polycystic Kidney and Liver Diseases and the Resulting Phenotypes
Yang H, Sieben CJ, Schauer RS, Harris PC |
2023 | |
Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype
S Senum, Y Li, K Benson, G Joli, E Olinger, S Lavu, C Madsen, A Gregory, R Neatu, T Kline, M Audrézet, P Outeda, C Nau, E Meijer, H Ali, T Steinman, M Mrug, P Phelan, T Watnick, D Peters, A Ong, P Conlon, R Perrone, E Gall, M Hogan, V Torres, J Sayer, P Harris |
The American Journal of Human Genetics | 2022 |
Genetics, pathobiology and therapeutic opportunities of polycystic liver disease
P Olaizola, P Rodrigues, F Caballero-Camino, L Izquierdo-Sanchez, P Aspichueta, L Bujanda, N Larusso, J Drenth, M Perugorria, J Banales |
Nature Reviews Gastroenterology & Hepatology | 2022 |
Polycystic Liver Disease: Advances in Understanding and Treatment
T Masyuk, A Masyuk, N LaRusso |
Annual review of pathology | 2022 |
Imaging of fibropolycystic liver disease
K Sharbidre, M Zahid, S Venkatesh, C Bhati, N Lalwani |
Abdominal Radiology | 2022 |
GANAB and N-Glycans Substrates Are Relevant in Human Physiology, Polycystic Pathology and Multiple Sclerosis: A Review
De Masi R, Orlando S |
International journal of molecular sciences | 2022 |
Signal Peptide Features Determining the Substrate Specificities of Targeting and Translocation Components in Human ER Protein Import.
Lang S, Nguyen D, Bhadra P, Jung M, Helms V, Zimmermann R |
Frontiers in physiology | 2022 |
Polycystic Liver Disease: Pathophysiology, Diagnosis and Treatment
Norcia LF, Watanabe EM, Hamamoto Filho PT, Hasimoto CN, Pelafsky L, de Oliveira WK, Sassaki LY |
Hepatic medicine : evidence and research | 2022 |
A single-center analysis of genotype–phenotype characteristics of Chinese patients with autosomal dominant polycystic kidney disease by targeted exome sequencing
Yan Z, Wang Y, Deng W, Zhou Y, Hu Y, Qi K, Liu D, Xia R, Liu R, Zeng W, Zhang W, Xu J, Xiong F, Miao Y |
Frontiers in Genetics | 2022 |
A Practical Guide to Genetic Testing for Kidney Disorders of Unknown Etiology
Aron AW, Dahl NK, Besse W |
2022 | |
Modelling polycystic liver disease progression using age-adjusted liver volumes and targeted mutational analysis
Sierks D, Schönauer R, Friedrich A, Hantmann E, de Fallois J, Linder N, Fischer J, Herber A, Bergmann C, Berg T, Halbritter J |
2022 | |
The GPCR properties of polycystin-1- A new paradigm
Maser RL, Calvet JP, Parnell SC |
Frontiers in Molecular Biosciences | 2022 |
Signal sequences encode information for protein folding in the endoplasmic reticulum.
Sun S, Li X, Mariappan M |
The Journal of Cell Biology | 2022 |
Individuals heterozygous for ALG8 protein-truncating variants are at increased risk of a mild cystic kidney disease.
Apple B, Sartori G, Moore B, Chintam K, Singh G, Anand PM, Strande NT, Mirshahi T, Triffo W, Chang AR |
Kidney International | 2022 |
Molecular Pathophysiology of Autosomal Recessive Polycystic Kidney Disease
A Cordido, M Vizoso-Gonzalez, MA Garcia-Gonzalez |
International journal of molecular sciences | 2021 |
Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings
MP Wilson, A Garanto, FP e Vairo, BG Ng, WK Ranatunga, M Ventouratou, M Baerenfaenger, K Huijben, C Thiel, A Ashikov, L Keldermans, E Souche, S Vuillaumier-Barrot, T Dupré, H Michelakakis, A Fiumara, J Pitt, SM White, SC Lim, L Gallacher, H Peters, D Rymen, P Witters, A Ribes, B Morales-Romero, A Rodríguez-Palmero, D Ballhausen, P de Lonlay, R Barone, MC Janssen, J Jaeken, HH Freeze, G Matthijs, E Morava, DJ Lefeber |
The American Journal of Human Genetics | 2021 |
Inhibition of NAE‐dependent protein hyper‐NEDDylation in cystic cholangiocytes halts cystogenesis in experimental models of polycystic liver disease
PY LeeLaw, P Olaizola, FJ CaballeroCamino, L IzquierdoSanchez, PM Rodrigues, MJ Perugorria, M Azkargorta, F Elortza, ML MartinezChantar, P Aspichueta, M Marzioni, L Bujanda, JP Drenth, JM Banales |
United European gastroenterology journal | 2021 |
Complexity and Specificity of Sec61-Channelopathies: Human Diseases Affecting Gating of the Sec61 Complex
M Sicking, S Lang, F Bochen, A Roos, JP Drenth, M Zakaria, R Zimmermann, M Linxweiler |
Cells | 2021 |
Polycystic liver disease with lethal abdominal wall rupture: a case report
D Akuzawa, Y Uchida, T Ishimura, H Kakita, T Endo, N Matsuzaki, H Terajima, T Tsukamoto |
Journal of medical case reports | 2021 |
Challenging Disease Ontology by Instances of Atypical PKHD1 and PKD1 Genetics
J de Fallois, R Schönauer, J Münch, M Nagel, B Popp, J Halbritter |
Frontiers in Genetics | 2021 |
Association of a novel PKHD1 mutation in a family with autosomal dominant polycystic liver disease
J Wang, H Yang, R Guo, X Sang, Y Mao |
Annals of translational medicine | 2021 |
A Novel Glycosyltransferase-Related Gene Signature for Overall Survival Prediction in Patients with Ovarian Cancer
L Wang |
International journal of general medicine | 2021 |
The Molecular Biodiversity of Protein Targeting and Protein Transport Related to the Endoplasmic Reticulum
A Tirincsi, M Sicking, D Hadzibeganovic, S Haßdenteufel, S Lang |
International journal of molecular sciences | 2021 |
Adhesion GPCRs as a paradigm for understanding polycystin-1 G protein regulation
RL Maser, JP Calvet |
Cellular Signalling | 2020 |
Regulation of polycystin expression, maturation and trafficking
J Hu, PC Harris |
Cellular Signalling | 2020 |
Novel GANAB variants associated with polycystic liver disease
LF van de Laarschot, RH te Morsche, A Hoischen, H Venselaar, HM Roelofs, WR Cnossen, JM Banales, R Roepman, JP Drenth |
Orphanet Journal of Rare Diseases | 2020 |
Gene Panel Analysis in a Large Cohort of Patients With Autosomal Dominant Polycystic Kidney Disease Allows the Identification of 80 Potentially Causative Novel Variants and the Characterization of a Complex Genetic Architecture in a Subset of Families
V Mantovani, S Bin, C Graziano, I Capelli, R Minardi, V Aiello, E Ambrosini, CP Cristalli, A Mattiaccio, M Pariali, SD Fanti, F Faletra, E Grosso, R Cantone, E Mancini, F Mencarelli, A Pasini, A Wischmeijer, N Sciascia, M Seri, GL Manna |
Frontiers in Genetics | 2020 |
Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genes
R Schönauer, S Baatz, M Nemitz-Kliemchen, V Frank, F Petzold, S Sewerin, B Popp, J Münch, S Neuber, C Bergmann, J Halbritter |
Genetics in Medicine | 2020 |
Proteostasis disturbances and endoplasmic reticulum stress contribute to polycystic liver disease: New therapeutic targets
A SantosLaso, L IzquierdoSanchez, PM Rodrigues, BQ Huang, M Azkargorta, A Lapitz, P MunozGarrido, A Arbelaiz, FJ Caballero-Camino, MG FernándezBarrena, R JimenezAgüero, J Argemi, T Aragon, F Elortza, M Marzioni, JP Drenth, NF LaRusso, L Bujanda, MJ Perugorria, JM Banales, E Andersson |
Liver International | 2020 |
Polycystic liver disease: Classification, diagnosis, treatment process, and clinical management
ZY Zhang, ZM Wang, Y Huang |
World journal of hepatology | 2020 |
Epidemiology of autosomal-dominant polycystic liver disease in Olmsted county
T Suwabe, AM Chamberlain, JM Killian, BF King, AV Gregory, CD Madsen, X Wang, TL Kline, FT Chebib, MC Hogan, PS Kamath, PC Harris, VE Torres |
2020 | |
Long-acting somatostatin analogue treatments in autosomal dominant polycystic kidney disease and polycystic liver disease: a systematic review and meta-analysis
J Griffiths, MT Mills, AC Ong |
BMJ Open | 2020 |
Type IV choledochal cyst with polycystic kidney disease: a case report
Y He, Z Yu, W Chen |
BMC Gastroenterology | 2020 |
Use of patient derived urine renal epithelial cells to confirm pathogenicity of PKHD1 alleles
E Molinari, S Srivastava, RM Dewhurst, JA Sayer |
BMC Nephrology | 2020 |
Exploring the Spectrum of Kidney Ciliopathies
M Santoni, F Piva, A Cimadamore, M Giulietti, N Battelli, R Montironi, L Cosmai, C Porta |
Diagnostics | 2020 |
Pansomatostatin Agonist Pasireotide Long-Acting Release for Patients with Autosomal Dominant Polycystic Kidney or Liver Disease with Severe Liver Involvement: A Randomized Clinical Trial
MC Hogan, JA Chamberlin, LE Vaughan, AL Waits, C Banks, K Leistikow, T Oftsie, C Madsen, M Edwards, J Glockner, WK Kremers, PC Harris, NF LaRusso, VE Torres, TV Masyuk |
Clinical journal of the American Society of Nephrology : CJASN | 2020 |
Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease
Huynh VT, Audrézet MP, Sayer JA, Ong AC, Lefevre S, Le Brun V, Després A, Senum SR, Chebib FT, Barroso-Gil M, Patel C, Mallett AJ, Goel H, Mallawaarachchi AC, Van Eerde AM, Ponlot E, Kribs M, Le Meur Y, Harris PC, Gall EC |
Kidney International | 2020 |
Pathobiology of inherited biliary diseases: a roadmap to understand acquired liver diseases
L Fabris, R Fiorotto, C Spirli, M Cadamuro, V Mariotti, MJ Perugorria, JM Banales, M Strazzabosco |
Nature Reviews Gastroenterology & Hepatology | 2019 |
Synergistic Genetic Interactions between Pkhd1 and Pkd1 Result in an ARPKD-Like Phenotype in Murine Models
RJ Olson, K Hopp, H Wells, JM Smith, J Furtado, MM Constans, DL Escobar, AM Geurts, VE Torres, PC Harris |
Journal of the American Society of Nephrology : JASN | 2019 |
Heterozygous Pkhd1C642* mice develop cystic liver disease and proximal tubule ectasia that mimics radiographic signs of medullary sponge kidney
D Shan, G Rezonzew, S Mullen, R Roye, J Zhou, P Chumley, DZ Revell, A Challa, H Kim, ME Lockhart, TR Schoeb, MJ Croyle, RA Kesterson, BK Yoder, LM Guay-Woodford, M Mrug |
American journal of physiology. Renal physiology | 2019 |
Contributions of Rare Gene Variants to Familial and Sporadic FSGS
M Wang, J Chun, G Genovese, AU Knob, A Benjamin, MS Wilkins, DJ Friedman, GB Appel, RP Lifton, S Mane, MR Pollak |
Journal of the American Society of Nephrology : JASN | 2019 |
Epidemiology of Autosomal Dominant Polycystic Kidney Disease in Olmsted County
T Suwabe, S Shukoor, AM Chamberlain, JM Killian, BF King, M Edwards, SR Senum, CD Madsen, FT Chebib, MC Hogan, EC Gall, PC Harris, VE Torres |
Clinical journal of the American Society of Nephrology : CJASN | 2019 |
Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney Disease
EC Gall, RJ Olson, W Besse, CM Heyer, VG Gainullin, JM Smith, MP Audrézet, K Hopp, B Porath, B Shi, S Baheti, SR Senum, J Arroyo, CD Madsen, C Férec, D Joly, F Jouret, O Fikri-Benbrahim, C Charasse, JM Coulibaly, AS Yu, K Khalili, Y Pei, S Somlo, YL Meur, VE Torres, PC Harris |
The American Journal of Human Genetics | 2018 |
Polycystin-1, the product of the polycystic kidney disease gene PKD1, is post-translationally modified by palmitoylation
K Roy, EP Marin |
Molecular Biology Reports | 2018 |
Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing
MB Lanktree, A Haghighi, E Guiard, IA Iliuta, X Song, PC Harris, AD Paterson, Y Pei |
Journal of the American Society of Nephrology : JASN | 2018 |
The Value of Genetic Testing in Polycystic Kidney Diseases Illustrated by a Family With PKD2 and COL4A1 Mutations
EC Gall, FT Chebib, CD Madsen, SR Senum, CM Heyer, BC Lanpher, MC Patterson, RC Albright, AS Yu, VE Torres, PC Harris, KZ Abebe, KT Bae, RW Schrier, AB Chapman, RD Perrone, WE Braun, TI Steinman |
American journal of kidney diseases : the official journal of the National Kidney Foundation | 2018 |
PUF60-activated exons uncover altered 3′ splice-site selection by germline missense mutations in a single RRM
J Královičová, I Ševčíková, E Stejskalová, M Obuća, M Hiller, D Staněk, I Vořechovský |
Nucleic Acids Research | 2018 |
A noncoding variant in GANAB explains isolated polycystic liver disease (PCLD) in a large family
W Besse, J Choi, D Ahram, S Mane, S Sanna-Cherchi, V Torres, S Somlo |
Human Mutation | 2018 |
Polycystic liver disease: The interplay of genes causative for hepatic and renal cystogenesis: Hepatology Elsewhere
TV Masyuk, AI Masyuk, NF LaRusso |
Hepatology | 2018 |
A Practical Guide for Treatment of Rapidly Progressive ADPKD with Tolvaptan
FT Chebib, RD Perrone, AB Chapman, NK Dahl, PC Harris, M Mrug, RA Mustafa, A Rastogi, T Watnick, AS Yu, VE Torres |
Journal of the American Society of Nephrology : JASN | 2018 |
Mutations in chromatin modifier and Ephrin signaling genes in Vein of Galen malformation
Duran D, Zeng X, Jin SC, Choi J, Nelson-Williams C, Yatsula B, Gaillard J, Furey CG, Lu Q, Timberlake AT, Dong W, Sorscher MA, Loring E, Klein J, Allocco A, Hunt A, Conine S, Karimy JK, Youngblood MW, Zhang J, DiLuna ML, Matouk CC, Mane S, Tikhonova IR, Castaldi C, López-Giráldez F, Knight J, Haider S, Soban M, Alper SL, Komiyama M, Ducruet AF, Zabramski JM, Dardik A, Walcott BP, Stapleton CJ, Aagaard-Kienitz B, Rodesch G, Jackson E, Smith ER, Orbach DB, Berenstein A, Bilguvar K, Vikkula M, Gunel M, Lifton RP, Kahle KT |
Neuron | 2018 |
New treatment paradigms for ADPKD: moving towards precision medicine
MB Lanktree, AB Chapman |
Nature Reviews Nephrology | 2017 |
Genetic Complexity of Autosomal Dominant Polycystic Kidney and Liver Diseases
EC Gall, VE Torres, PC Harris |
Journal of the American Society of Nephrology : JASN | 2017 |
Genetics: Novel causative genes for polycystic liver disease
MJ Perugorria, JM Banales |
Nature Reviews Gastroenterology & Hepatology | 2017 |
An Update on Sec61 Channel Functions, Mechanisms, and Related Diseases
S Lang, S Pfeffer, PH Lee, A Cavalié, V Helms, F Förster, R Zimmermann |
Frontiers in physiology | 2017 |