Results 11 to 20 of about 62,280 (291)

In Silico approach for identification, prediction of AMPD1 gene nsSNPs associated with Myoadenylate Deaminase deficiency [PDF]

Journal of Bioscience and Applied Research, 2023
Background: Myoadenylate deaminase deficiency is an autosomal recessive metabolic myopathy caused by mutations in the Adenosine monophosphate deaminase 1 gene.
Abrar Mohamed, Abdelrahman Hamza, Hiba Fadl, Afra Albkrye, Hadeel Ahmed, Hazem Abubaker, Sahar Elbager   +6 more
doaj   +1 more source

Tubercular Pericardial Effusion Presenting as Cardiac Tamponade

Journal of Nepal Health Research Council, 2021
Pericardial effusion is an uncommon extra-pulmonary manifestation of tuberculosis, tamponade being even rarer. Here, a 14-year female presented with cough, chest pain and fever.
Alok Pradhan, Ranjit Babu Jasaraj, Bhesh Raj Karki, Anish Joshi   +3 more
doaj   +1 more source

EFFECT OF SOME ANTIBIOTICS IN ACTIVITY OF ADENOSINE DEAMINASE IN SERUM [PDF]

مجلة جامعة الانبار للعلوم الصرفة, 2012
The aim of this study is to know the effect of same antibiotics such as tetracycline, benzyl pencillin and ampicillin on activity of adenosine deaminase (ADA) level in patients with brucellosis.
WESAM M. MOHAMMED ATEA
doaj   +1 more source

Expanding a fluorescent RNA alphabet: synthesis, photophysics and utility of isothiazole-derived purine nucleoside surrogates. [PDF]

, 2017
A series of emissive ribonucleoside purine mimics, all comprised of an isothiazolo[4,3-d]pyrimidine core, was prepared using a divergent pathway involving a key Thorpe-Ziegler cyclization.
Fin, Andrea, Rovira, Alexander R, Tor, Yitzhak   +2 more
core   +1 more source

Ability of γδ T cells to modulate the Foxp3 T cell response is dependent on adenosine. [PDF]

, 2018
Whether γδ T cells inhibit or enhance the Foxp3 T cell response depends upon their activation status. The critical enhancing effector in the supernatant is adenosine.
Born, Willi K, Kaplan, Henry J, Liang, Dongchun, O'Brien, Rebecca L, Shao, Hui, Sun, Deming, Woo, Jeong-Im   +6 more
core   +13 more sources

The ADA*2 allele of the adenosine deaminase gene (20q13.11) and recurrent spontaneous abortions: an age-dependent association

Clinics, 2011
OBJECTIVE: Adenosine deaminase acts on adenosine and deoxyadenosine metabolism and modulates the immune response. The adenosine deaminase G22A polymorphism (20q.11.33) influences the level of adenosine deaminase enzyme expression, which seems to play a ...
Daniela Prudente Teixeira Nunes, Lígia Cosentino Junqueira Franco Spegiorin, Cinara Cássia Brandão de Mattos, Antonio Helio Oliani, Denise Cristina Mós Vaz-Oliani, Luiz Carlos de Mattos   +5 more
doaj   +1 more source

Diagnostic value of effusion adenosine deaminase, γ-interferon release assay and effusion lactatedehy drogenase/effusion adenosine deaminase for tuberculous pleural effusion in patients aged 60 years and above. [PDF]

Front Cell Infect Microbiol
Guo F, Huimin C, Xia W, Xu Y, Jin W, Liu F.   +5 more
europepmc   +3 more sources

Biosensor measurement of purine release from cerebellar cultures and slices [PDF]

, 2010
We have previously described an action-potential and Ca2+-dependent form of adenosine release in the molecular layer of cerebellar slices. The most likely source of the adenosine is the parallel fibres, the axons of granule cells. Using microelectrode
Dale, Nicholas, Eason, Robert, Wall, Mark J.   +2 more
core   +3 more sources

Serum adenosine deaminase, catalase and carbonic anhydrase activities in patients with bladder cancer

Clinics, 2012
OBJECTIVES: The relationship between adenosine deaminase and various cancers has been investigated in several studies. However, serum adenosine deaminase activity and carbonic anhydrase and catalase activities in patients with bladder cancer have not ...
Necip Pirinççi, Ilhan Geçit, Mustafa Güneş, Mehmet Bilgehan Yüksel, Mehmet Kaba, Serhat Tanık, Halit Demir, Mehmet Aslan   +7 more
doaj   +1 more source

A novel mutation in the ADA gene causing severe combined immunodeficiency in an Arab patient: a case report

Journal of Medical Case Reports, 2009
Introduction About 20% of the cases of human severe combined immunodeficiency are the result of the child being homozygous for defective genes encoding the enzyme adenosine deaminase.
Hellani Ali, Almassri Nidal, Abu-Amero Khaled K   +2 more
doaj   +1 more source