Results 51 to 60 of about 412,948 (294)

Human embryonic hemoglobins [PDF]

open access: yes, 1981
There are a lot of contrary opinions concerning the riumber and structure of embryo hemoglobins. The aim of this paper is to gather the recent works on this subjects.
Gondko, Roman, Hryniewicz, Justyna
core   +1 more source

How abnormal is the behaviour of captive, zoo-living, chimpanzees? [PDF]

open access: yes, 2011
Background. Many captive chimpanzees (Pan troglodytes) show a variety of serious behavioural abnormalities, some of which have been considered as possible signs of compromised mental health.
Newton-Fisher, Nicholas E.   +7 more
core   +2 more sources

Diffuse MRI Edema Predicts Relapse in Cerebral Amyloid Angiopathy–Related Inflammation

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To identify MRI predictors of relapse and quantify relapse and mortality risk in cerebral amyloid angiopathy–related inflammation (CAA‐RI). A secondary objective was to assess the association between mycophenolate mofetil use and relapse risk. Methods We performed a retrospective cohort study of 36 patients with CAA‐RI treated at the
G. Abbas Kharal   +10 more
wiley   +1 more source

Comparative Biochemistry of Hemoglobins [PDF]

open access: yes, 1963
The problem of the molecular evolution of hemoglobin has been studied by comparing agar-gel electrophoresis, ultraviolet absorption spectra and resistance to alkalis in fifteen varieties of hemoglobins ranging from human hemoglobin to fish hemoglobin ...
Maita, Tetsuo   +7 more
core   +2 more sources

Prevalence and mutations of β-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey

open access: yesBalkan Journal of Medical Genetics, 2016
The prevalence of β-thalassemia (β-thal) carriers in Turkey varies according to region but in general it is 2.0%. Çanakkale is a city in the Aegean region of Turkey but no study about β-thal frequency in Çanakkale has been published to date.
Uludağ A   +7 more
doaj   +1 more source

Developing and Evaluating a Laboratory‐Based Frailty Index for the Prediction of Long‐Term Health Outcomes in Systemic Lupus Erythematosus

open access: yesArthritis Care &Research, EarlyView.
Objective We aimed to construct and evaluate the first laboratory‐based frailty index (FI‐Lab) for predicting adverse outcomes in systemic lupus erythematosus (SLE) and to compare its predictive ability to that of an existing clinical FI. Methods We used data from a single‐center prospective cohort of adult patients with SLE whose baseline visit ...
Grace Burns   +2 more
wiley   +1 more source

Phylogeny of Echinoderm Hemoglobins [PDF]

open access: yes, 2015
Recent genomic information has revealed that neuroglobin and cytoglobin are the two principal lineages of vertebrate hemoglobins, with the latter encompassing the familiar myoglobin and α-globin/β-globin tetramer hemoglobin, and several minor groups.
Maurice R. Elphick (138400)   +49 more
core   +2 more sources

The Lupus Damage Index Revision Program: Results From the Item Generation and Reduction Phases

open access: yesArthritis Care &Research, EarlyView.
Objective A data‐driven and expert/patient consensus‐based project to develop a revised Systemic Lupus International Collaborating Clinics (SLICC)/American College of Rheumatology (ACR) Damage Index (SDI) is under way supported by SLICC, ACR, and the Lupus Foundation of America. Our objective is to report the item generation and reduction phase results
Burak Kundakci   +25 more
wiley   +1 more source

Structure and Reactivity of Hexacoordinate Hemoglobins [PDF]

open access: yes, 2010
The heme prosthetic group in hemoglobins is most often attached to the globin through coordination of either one or two histidine side chains. Those proteins with one histidine coordinating the heme iron are called “pentacoordinate” hemoglobins, a group ...
Kakar, Smita
core   +3 more sources

α-Thalassemia impairs the cytoadherence of Plasmodium falciparum-infected erythrocytes. [PDF]

open access: yesPLoS ONE, 2012
α-Thalassemia results from decreased production of α-globin chains that make up part of hemoglobin tetramers (Hb; α(2)β(2)) and affects up to 50% of individuals in some regions of sub-Saharan Africa.
Michael A Krause   +10 more
doaj   +1 more source

Home - About - Disclaimer - Privacy