Results 181 to 190 of about 388,321 (340)

THE MICROESTIMATION OF THREONINE

Journal of Biological Chemistry, 1939
Diana Bolling, Richard J. Block
openaire   +2 more sources

Regulation of insulin sensitivity by serine/threonine phosphorylation of insulin receptor substrate proteins IRS1 and IRS2

Diabetologia, 2012
Kyle D. Copps, M. White
semanticscholar   +1 more source

LncRNA Foxo6os as a Novel “ Scaffold” Mediates MYBPC3 in Combating Pathological Cardiac Hypertrophy and Heart Failure

Advanced Science, EarlyView.
Schematic overview showing that forkhead box O6, opposite strand (Foxo6os) acts as a “scaffold”, directly binding myosin‐binding protein‐C (MYBPC3) and recruiting protein kinase C (PKC‐α) to mediate site‐specific phosphorylation of MYBPC3. This post‐translational modification supports cardiac contraction by regulating L‐type Ca2+ channels, especially ...
Jie Sheng, Qin Lin, Yizhuo Sun, Yilei Meng, Sangyu Hu, Huaming Cao, Fang Lin, Yuping Zhu, Luying Peng, Li Li   +9 more
wiley   +1 more source

Examining the Role of Threonine Phosphorylation in Ubiquitin's Function Using Chemical Protein Synthesis. [PDF]

JACS Au
Wang B, Li C, Zhao F, Shi L, Li X, Liu Y, Sun S, Yuan L, Sun M, Zhang Y, Shi J, Liang LJ.   +11 more
europepmc   +1 more source

Fatty acid composition of portal fatty liver in lysine- and threonine-deficient rats

, 1964
Roberto Viviani, Anna Maria Sechi, Giorgio Lenaz   +2 more
openalex   +1 more source

Endogenous formation of phosphatidylhomoserine in Escherichia coli through phosphatidylserine synthase. [PDF]

J Biol Chem
Ng EZQ, Lee E, Chng SS, Kim J, Guan XL.
europepmc   +1 more source

The pH Dependence of the Kinetic Parameters of Threonine Dehydrase

, 1962
Leodis Davis, David E. Metzler
openalex   +1 more source

The Expanding Clinical and Genetic Spectrum of Muscle Glycogen Storage Disease 0, (GSD0B)

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Glycogen storage disorders are a group of genetic disorders affecting glucose homeostasis in the body. Muscular glycogen stores are essential for liberating glucose for energy supply during bursts of activity and sustained muscle work. Muscle glycogen storage disease 0 (GSD0B) is associated with biallelic variants in GYS1 causing muscular ...
Sarah Donoghue, Smitha Kumble, Pontus Wasling, Lars Alberg, Pia Linton‐Dahlöf, Yilmaz Yildiz, İlker Ertuğrul, Terry Derks, Dwight Koeberl, Emmeline Lagrange, Sabrina Vergnaud, Lidia Pezzani, Maria Iascone, Zornitza Stark, Adam M. Bournazos, Sandra T. Cooper, Gittan Kollberg   +16 more
wiley   +1 more source

Multiple routes for non-physiological l-threonine uptake in <i>Escherichia coli</i> K-12. [PDF]

Front Microbiol
Bubnov DM, Khozov AA, Vybornaya TV, Stepanova AA, Molev SV, Melkina OE, Badun GA, Chernysheva MG, Skob IA, Netrusov AI, Sineoky SP.   +10 more
europepmc   +1 more source

A Novel Pathogenic Variant in CRB1 as the Cause of Non‐Syndromic Retinitis Pigmentosa in a Geographical Isolate in Northern Italy

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Non‐syndromic Retinitis Pigmentosa (NsRP) was well known as one of the causes of visual impairment already in the 19th century. Giuseppe Albertotti, Professor of Ophthalmology at the University of Modena (Italy) in 1893, described a high prevalence of NsRP in a geographic isolate, the small village of Colloro, in northwestern Italy.
Andrea Guala, Fabio Sirchia, Claudia Scotti, Elena Rossi, Roberta Falcioni, Silvano Ragozza, Antonella Casella, Enza Maria Valente, Cesare Danesino   +8 more
wiley   +1 more source