Absorption of Co58 Labeled Cyanocobalamin in Protein Deficiency

1964 ◽  
Vol 46 (2) ◽  
pp. 167-174 ◽  
Author(s):  
M.G. Deo ◽  
V. Ramalingaswami
Keyword(s):  
Protein Deficiency

Alterations in Serum Diastase and Albumin Values in Protein Deficiency

1955 ◽  
Vol 28 (4) ◽  
pp. 550-562 ◽  
Author(s):  
James F. Sullivan ◽  
Robert J. Healey ◽  
William A. Knight
Keyword(s):  
Protein Deficiency

Prevention of disorders of protein deficiency in growing bulls of dairy breeds

2020 ◽  
Vol 23 (9) ◽  
pp. 50-55
Author(s):  
E.L. Kharitonov ◽  
◽  
K.S. Ostrenko ◽  
V.O. Lemiasheuski ◽  
◽  
...  
Keyword(s):  
Protein Deficiency

Vesicular stomatitis virus growth in Drosophila melanogaster cells: G protein deficiency.

1980 ◽  
Vol 33 (1) ◽  
pp. 411-422 ◽  
Author(s):  
F Wyers ◽  
C Richard-Molard ◽  
D Blondel ◽  
S Dezelee
Keyword(s):  
Drosophila Melanogaster ◽  
G Protein ◽  
Vesicular Stomatitis Virus ◽  
Protein Deficiency ◽  
Virus Growth ◽  
Vesicular Stomatitis

scholarly journals Some Effects of Protein Deficiency in Young Growing Pigs. III. Ferrokinetic Investigations

1970 ◽  
Vol 11 (1) ◽  
pp. 16-30
Author(s):  
V. Hristic ◽  
J. A. Nikolié ◽  
D. Stoëic
Keyword(s):  
Growing Pigs ◽  
Protein Deficiency

scholarly journals ATF4 Protein Deficiency Protects against High Fructose-induced Hypertriglyceridemia in Mice

2013 ◽  
Vol 288 (35) ◽  
pp. 25350-25361 ◽  
Author(s):  
Guozhi Xiao ◽  
Ting Zhang ◽  
Shibing Yu ◽  
Sojin Lee ◽  
Virtu Calabuig-Navarro ◽  
...  
Keyword(s):  
Protein Deficiency ◽  
High Fructose

Two patients from Turkey with a novel variant in the GM2A gene and review of the literature

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Aslı İnci ◽  
Filiz Başak Cengiz Ergin ◽  
Gürsel Biberoğlu ◽  
İlyas Okur ◽  
Fatih Süheyl Ezgü ◽  
...  
Keyword(s):  
Sandhoff Disease ◽  
Pathogenic Variant ◽  
Protein Deficiency ◽  
Gm2 Gangliosidosis ◽  
Infantile Form ◽  
Rare Form ◽  
Inborn Errors ◽  
Activator Protein ◽  
Gm2 Activator ◽  
Gm2 Activator Protein

Abstract Objectives GM2 gangliosidosis is a rare form of inborn errors of metabolism including Tay-Sachs disease, Sandhoff disease, and GM2 activator deficiency. GM2 activator protein deficiency is an ultra-rare form of GM2 gangliosidosis. To date, 16 cases of GM2 activator protein deficiency have been reported in the literature, and among them, 11 cases were the infantile form of the disease. Here we report the first two patients from Turkey with the infantile form of the disease with a novel likely pathogenic variant. Case presentation A boy of eight months old presented to the metabolic department with very mild neurological deterioration, although he had achieved early developmental milestones at the appropriate time. The parents also had a daughter who had lost skills progressively before one year of age. The boy was evaluated and bilateral cherry-red spots were found with no abnormality in either metabolic screening including β-hexosaminidase or cranial magnetic resonance imaging. A novel homozygous likely pathogenic variant in GM2A was detected in a next-generation sequence panel revealing GM2 activator protein deficiency. His sister was investigated after he was diagnosed with GM2 activator deficiency and it was found that she had the same variant as her brother. Conclusions This case report emphasizes that in the event of normal β-hexosaminidase activity, GM2 activator protein deficiency could be underdiagnosed, and further molecular analysis should be performed. To the best of our knowledge, this boy is one of the youngest patient diagnosed with very mild symptoms. With this novel pathogenic variant, these patients have expanded the mutation spectrum of GM2 activator protein deficiency.

The Magnitude of the Acute Phase Protein Response is Attenuated by Protein Deficiency in Rats

1992 ◽  
Vol 122 (6) ◽  
pp. 1325-1331 ◽  
Author(s):  
Graham Jennings ◽  
Christelle Bourgeois ◽  
Marinos Elia
Keyword(s):  
Acute Phase ◽  
Acute Phase Protein ◽  
Protein Deficiency ◽  
Acute Phase Protein Response ◽  
Phase Protein ◽  
Protein Response
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