Hepatic glycogen storage disorders: what have we learned in recent years? by Burda, Patricie, Hochuli, Michel

Gene therapy for glycogen storage diseases by Koeberl, Dwight D., Koch, Rebecca L., Lim, Jeong‐A., Brooks, Elizabeth D., Arnson, Benjamin D., Sun, Baodong, Kishnani, Priya S.

Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource by Koch, Rebecca L., Soler-Alfonso, Claudia, Kiely, Bridget T., Asai, Akihiro, Smith, Ariana L., Bali, Deeksha S., Kang, Peter B., Landstrom, Andrew P., Akman, H. Orhan, Burrow, T. Andrew, Orthmann-Murphy, Jennifer L., Goldman, Deberah S., Pendyal, Surekha, El-Gharbawy, Areeg H., Austin, Stephanie L., Case, Laura E., Schiffmann, Raphael, Hirano, Michio, Kishnani, Priya S.

Liver transplantation in glycogen storage disease: a single-center experience by Beyzaei, Zahra, Shamsaeefar, Alireza, Kazemi, Kurosh, Nikeghbalian, Saman, Bahador, Ali, Dehghani, Masoud, Malekhosseini, Seyed-Ali, Geramizadeh, Bita

In vitro formation and growth of glycogen: experimental verification of theoretical predictions by Liu, Xin, Wang, Ziyi, Lin, Xin, Xu, Wang, Gilbert, Robert G.

Environmental salinity differentially impacts branchial and hepatic carbohydrate metabolism in tilapia by Chang, Ryan J. A., Celino‐Brady, Fritzie T., Breves, Jason P., Seale, Andre P.

Glycogen metabolism and structure: A review by Neoh, Galex K.S., Tan, Xinle, Chen, Si, Roura, Eugeni, Dong, Xin, Gilbert, Robert G.

A novel CD71 Centyrin:Gys1 siRNA conjugate reduces glycogen synthesis and glycogen levels in a mouse model of Pompe disease by Holt, Bryce D., Elliott, Samuel J., Meyer, Rebecca, Reyes, Daniela, O’Neil, Karyn, Druzina, Zhanna, Kulkarni, Swapnil, Thurberg, Beth L., Nadler, Steven G., Pederson, Bartholomew A.

Molecular architecture and catalytic mechanism of human glycogen debranching enzyme by Guan, Huiyi, Chen, Huan, Geng, He, Ma, Ruifang, Liu, Zhongmin, Wang, Yong, Chen, Yifang, Yan, Kaige

Skeletal Muscle Glycogen Chain Length Correlates with Insolubility in Mouse Models of Polyglucosan-Associated Neurodegenerative Diseases by Sullivan, Mitchell A., Nitschke, Silvia, Skwara, Evan P., Wang, Peixiang, Zhao, Xiaochu, Pan, Xiao S., Chown, Erin E., Wang, Travis, Perri, Ami M., Lee, Jennifer P.Y., Vilaplana, Francisco, Minassian, Berge A., Nitschke, Felix

Glycogen synthase downregulation rescues the amylopectinosis of murine RBCK1 deficiency by Nitschke, Silvia, Sullivan, Mitchell A, Mitra, Sharmistha, Marchioni, Charlotte R, Lee, Jennifer P  Y, Smith, Brandon H, Ahonen, Saija, Wu, Jun, Chown, Erin E, Wang, Peixiang, Petković, Sara, Zhao, Xiaochu, DiGiovanni, Laura F, Perri, Ami M, Israelian, Lori, Grossman, Tamar R, Kordasiewicz, Holly, Vilaplana, Francisco, Iwai, Kazuhiro, Nitschke, Felix, Minassian, Berge A

First‐in‐Human Evaluation of Safety, Pharmacokinetics and Muscle Glycogen Lowering of a Novel Glycogen Synthase 1 Inhibitor for the Treatment of Pompe Disease by Ullman, Julie C., Dick, Ryan A., Linzner, Daniela, Minga, Todd, Tep, Samnang, Satterfield, Terrence F., Xi, Yannan, Beattie, David T., Marmon, Tonya, Neutel, Joel M., Chung, Bernard, Leeds, Janet M., Noonberg, Sarah B., Green, Eric M., Bernstein, Harold S.

Structural basis of glycogen branching enzyme deficiency and pharmacologic rescue by rational peptide design by Froese, D. Sean, Michaeli, Amit, McCorvie, Thomas J., Krojer, Tobias, Sasi, Meitav, Melaev, Esther, Goldblum, Amiram, Zatsepin, Maria, Lossos, Alexander, Álvarez, Rafael, Escribá, Pablo V., Minassian, Berge A., von Delft, Frank, Kakhlon, Or, Yue, Wyatt W.

The dynamic life of the glycogen granule by Prats, Clara, Graham, Terry E., Shearer, Jane

Severe neuromuscular forms of glycogen storage disease type IV: Histological, clinical, biochemical, and molecular findings in a large French case series by Centre Hospitalier Universitaire de Bordeaux (CHU Bordeaux), Centre de Biologie et Pathologie Est [Bron] (CBPE), Service Maladies Infectieuses et Tropicales [CHU Clermont-Ferrand], Pôle RHEUNNIRS [CHU Clermont-Ferrand], CHU Gabriel Montpied [Clermont-Ferrand], CHU Clermont-Ferrand-CHU Clermont-Ferrand-CHU Gabriel Montpied [Clermont-Ferrand], CHU Clermont-Ferrand-CHU Clermont-Ferrand, Laffargue, F, Prieur, F, Société Française de Foetopathologie [Paris] (SOFFOET), Streichenberger, N, Hôpital de la Croix-Rousse [CHU - HCL], Hospices Civils de Lyon (HCL), Service de pharmacologie biologique et toxicologie [Rennes], Centre Hospitalier Universitaire de Rennes [CHU Rennes] = Rennes University Hospital [Pontchaillou], Laurichesse, H, Acquaviva-Bourdain, C, Pettazzoni, M, Hospices Civils de Lyon (HCL), Physiopathologie et génétique du neurone et du muscle (PGNM), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Biologie Médicale MultiSites [Bron] (LBMMS), Hospices Civils de Lyon (HCL)-Centre de Biologie et Pathologie Est [Bron] (CBPE), Collardeau-Frachon, S, Lefèvre, C. R, Centre Hospitalier Universitaire de Saint-Etienne [CHU Saint-Etienne] (CHU ST-E), Massardier, J, Service Génétique Médicale [CHU Clermont-Ferrand], CHU Estaing [Clermont-Ferrand], CHU Clermont-Ferrand-CHU Clermont-Ferrand-Pôle Femme et Enfant [CHU Clermont-Ferrand], CHU Estaing [Clermont-Ferrand], CHU Clermont-Ferrand-CHU Clermont-Ferrand, Cardiovasculaire, métabolisme, diabétologie et nutrition (CarMeN), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Hospices Civils de Lyon (HCL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Berenguer-Martin, S, Froissart, R, Clémenson, A

The structure of brain glycogen phosphorylase—from allosteric regulation mechanisms to clinical perspectives by Mathieu, Cécile, Dupret, Jean‐Marie, Rodrigues Lima, Fernando

Glycogen synthase kinase 3: A key regulator of cellular fate by Forde, J. E, Dale, T. C

Large variation in effects during 10 years of enzyme therapy in adults with Pompe disease by Harlaar, Laurike, Hogrel, Jean-Yves, Perniconi, Barbara, Kruijshaar, Michelle E., Rizopoulos, Dimitris, Taouagh, Nadjib, Canal, Aurélie, Brusse, Esther, van Doorn, Pieter A., van der Ploeg, Ans T., Laforêt, Pascal, van der Beek, Nadine A. M. E.

Glycogen synthase kinases: Moonlighting proteins with theranostic potential in cancer by Nagini, Siddavaram, Sophia, Josephraj, Mishra, Rajakishore

Glucose Utilization via Glycogen Phosphorylase Sustains Proliferation and Prevents Premature Senescence in Cancer Cells by Favaro, Elena, Bensaad, Karim, Chong, Mei G., Tennant, Daniel A., Ferguson, David J.P., Snell, Cameron, Steers, Graham, Turley, Helen, Li, Ji-Liang, Günther, Ulrich L., Buffa, Francesca M., McIntyre, Alan, Harris, Adrian L.