Results 171 to 180 of about 176,600 (181)

X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome

European Journal of Human Genetics, 2003
Francisco Martinez, Roger Stevenson, Charles Schwartz   +2 more
exaly  

Diagnostic screening for spermine synthase deficiency by liquid chromatography tandem mass spectrometry

Clinica Chimica Acta, 2011
Charles Schwartz
exaly  

Spermine Synthase Deficiency Resulting in X-Linked Intellectual Disability (Snyder–Robinson Syndrome)

Methods in Molecular Biology, 2011
Roger Stevenson, Charles Schwartz
exaly  

Spermine Deficiency Resulting from Targeted Disruption of the Spermine Synthase Gene in Embryonic Stem Cells Leads to Enhanced Sensitivity to Antiproliferative Drugs

Molecular Pharmacology, 2001
Leena Alhonen, Juhani Janne, Carl W Porter   +2 more
exaly  

Spermine dependent activation of the N-methyl-d-aspartate receptor and the effect of nitric oxide synthase inhibition during hypoxia in the cerebral cortex of newborn piglets

Brain Research, 2000
Maria Delivoria-Papadopoulos, Karen I Fritz, Alan B Zubrow   +2 more
exaly  

Snyder-Robinson syndrome : Synonym: Spermine Synthase Deficiency

2020
Charles E Schwartz, Angela Peron, Mary Jo Kutler   +2 more
openaire   +1 more source

[42] Rapid assays for putrescine aminopropyltransferase (spermidine synthase) and spermidine aminopropyltransferase (spermine synthase)

1983
Aarne Raina, Terho Eloranta, Raija-Leena Pajula   +2 more
openaire   +1 more source

Rapid assays for putrescine aminopropyltransferase (spermidine synthase) and spermidine aminopropyltransferase (spermine synthase).

Methods in enzymology, 1983
A, Raina, T, Eloranta, R L, Pajula
openaire   +1 more source

The function of spermine

IUBMB Life, 2014
exaly  

Purification of spermidine aminopropyltransferase (spermine synthase) from bovine brain.

Methods in enzymology, 1983
A, Raina, R L, Pajula, T, Eloranta
openaire   +1 more source