Results 51 to 60 of about 1,740,227 (374)

Recent Applications of Mesoporous Silica Nanoparticles in Gene Therapy

open access: yesAdvanced Healthcare Materials, EarlyView.
The review summarizes the synthesis of mesoporous silica nanoparticles (MSNs) with modifiable surface properties, functionalization strategies, mechanism of therapeutic payload release, and current applications in gene therapy, focusing on their capabilities in the targeted delivery of therapeutic nucleic acids, CRISPR‐Cas systems, and other genetic ...
Tamanna Binte Huq   +4 more
wiley   +1 more source

Inherited hemolytic disorders with high occurrence of b-thalassemia in Sindhi community of Jabalpur town in Madhya Pradesh, India [PDF]

open access: yes, 2010
Hereditary hemolytic disorders such as hemoglobin disorders, β-thalassemia syndrome, G6PD deficiency, and ABO and Rhesus blood groups are the most common public health problems in India.
Balgir, RS
core   +1 more source

Spectrum of hemoglobin variants in Eastern Indian population; a study of 14,145 cases [PDF]

open access: yesAl Ameen Journal of Medical Sciences, 2013
Background: Inherited disorders of hemoglobin are extremely common in Indian population ranging from near structurally normal hemoglobins to severe transfusion dependant hemoglobinopathies.
Suprio Ray Chaudhury   +5 more
doaj  

Photonic Nanomaterials for Wearable Health Solutions

open access: yesAdvanced Materials, EarlyView.
This review discusses the fundamentals and applications of photonic nanomaterials in wearable health technologies. It covers light‐matter interactions, synthesis, and functionalization strategies, device assembly, and sensing capabilities. Applications include skin patches and contact lenses for diagnostics and therapy. Future perspectives emphasize AI‐
Taewoong Park   +3 more
wiley   +1 more source

Studies on abnormal hemoglobins. II. Their identification by means of the method of fractional denaturation.

open access: yesBlood, 1951
vanced that these abnormally denaturing fractions may represent a continued production of fetal pigment beyond the physiologic age limit in the former conditions, and a reactivation of such a mechanism in the latter.
Karl Singer, A. Chernoff, L. Singer
semanticscholar   +1 more source

Dificuldades no diagnóstico laboratorial das hemoglobinopatias Dificulties on the laboratorial diagnosis of hemoglobinopathies

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2007
Há vários tipos de hemoglobinopatias que são caracterizados por variantes das hemoglobinas anormais (ex: Hb S, Hb C, Hb Instáveis,etc) e por talassemias (ex: tal. alfa, tal.
Paulo Cesar Naoum   +1 more
doaj   +1 more source

Materials Advances in Devices for Heart Disease Interventions

open access: yesAdvanced Materials, EarlyView.
This review examines the crucial role of materials in heart disease interventions, focusing on strategies for monitoring, managing, and repairing heart conditions. It discusses the material requirements for medical devices, highlighting recent innovations and their impact on cardiovascular health.
Gagan K. Jalandhra   +11 more
wiley   +1 more source

Analysis of thalassemia syndromes and abnormal hemoglobins in patients from the Aegean region of Turkey

open access: yesThe Turkish Journal of Pediatrics, 2002
Turkey is located in a geographic area of the world where thalassemia syndromes and abnormal hemoglobins are common. In this study we aimed to evaluate the thalassemia syndromes and abnormal hemoglobins in patients from the Aegean region of Turkey.
Gülersu Irken   +6 more
doaj  

HB D Los Angeles in a Brazilian family Hb D Los Angeles em família brasileira

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2001
Inherited disorders of hemoglobin, the most common monogenic disease, are now well understood at the molecular level, knowledge, which has led to considerable improvements in their control and management.
Guilherme G. Leoneli   +4 more
doaj   +1 more source

Neonatal Screening for Sickle Cell Disease in Congo

open access: yesAnemia, 2022
Introduction. Sickle cell disease is an autosomal recessive inherited disorder due to the mutation of a gene coding for the globin beta chain. The aim of this study is to update the epidemiological data on hemoglobinoses, in particular sickle cell ...
Alexis Elira Dokekias   +10 more
doaj   +1 more source

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