Results 261 to 270 of about 3,327,333 (431)

Magnetic Resonance Studies on Inactivated Forms of Creatine Kinase

, 1968
W.J. O’Sullivan, Mélanie Cohn
openalex   +1 more source

Automated Method for the Determination of Serum Creatine Kinase Activity [PDF]

, 1967
Gerard A. Fleisher
openalex   +1 more source

Calcium modulating ligand confers risk for Parkinson's disease and impacts lysosomes

Annals of Clinical and Translational Neurology, EarlyView.
Abstract Objective Several genetic loci known to confer risk for Parkinson's disease (PD) function in lysosomal pathways. We systematically screened common variants linked to PD risk by genome‐wide association studies (GWAS) for impact on cerebrospinal fluid (CSF) proteins reflecting lysosomal function.
Hanwen Zhang, Daniel Kargilis, Thomas Tropea, John Robinson, Junchao Shen, Eliza M. Brody, Ann Brinkmalm, Simon Sjödin, Adama J. Berndt, Marc Carceles‐Cordon, EunRan Suh, Vivianna M. Van Deerlin, Kaj Blennow, Daniel Weintraub, Edward B. Lee, Henrik Zetterberg, Alice S. Chen‐Plotkin   +16 more
wiley   +1 more source

Structural pathway for PI3-kinase regulation by VPS15 in autophagy. [PDF]

Science
Cook ASI, Chen M, Nguyen TN, Cabezudo AC, Khuu G, Rao S, Garcia SN, Yang M, Iavarone AT, Ren X, Lazarou M, Hummer G, Hurley JH.   +12 more
europepmc   +1 more source

Shikimate Kinase Isoenzymes in Salmonella typhimurium

, 1968
H. Morell, David B. Sprinson
openalex   +1 more source

Observations on the Fluorometric Measurement of Creatine Kinase Activity [PDF]

, 1968
Sylvan M Sax, John J. Moore
openalex   +1 more source

Skin calcium deposits in primary familial brain calcification: A novel potential biomarker

Annals of Clinical and Translational Neurology, EarlyView.
Abstract Objective Primary Familial Brain Calcification (PFBC) is a rare neurodegenerative disorder characterized by small vessel calcifications in the basal ganglia. PFBC is caused by pathogenic variants in different genes and its physiopathology is still largely unknown. Skin vascular calcifications have been detected in single PFBC cases, suggesting
Aron Emmi, Giulia Bonato, Aleksandar Tushevski, Cinzia Bertolin, Francesco Cavallieri, Andrea Porzionato, Angelo Antonini, Leonardo Salviati, Miryam Carecchio   +8 more
wiley   +1 more source

Asymmetric activation of dimeric ATM/Tel1 kinase. [PDF]

Cell Discov
Wang P, Zheng Z, Wang G, Zhao Z, Qian D, Cai G, Wang X.   +6 more
europepmc   +1 more source

Dietary Starch, Dietary Sucrose and Hepatic Pyruvate Kinase in Rat

, 1967
John Yudkin, Ronald M. Krauss
openalex   +1 more source

UDP‐glucose dehydrogenase variants cause dystroglycanopathy

Annals of Clinical and Translational Neurology, EarlyView.
Abstract UDP‐glucose dehydrogenase (UGDH) variants have been associated with hypotonia, developmental delay, and epilepsy. We report the first pathologic evidence of dystroglycanopathy in siblings with UGDH variants. Both presented around 6 months with developmental delay and elevated creatinine kinase.
Anna M. Reelfs, Carrie M. Stephan, Theresa M. Czech, Mary O. Cox, Soumya Joseph, Benjamin W. Darbro, Steven A. Moore, Kevin P. Campbell, Katherine D. Mathews   +8 more
wiley   +1 more source