The plasma membrane of the erythrocyte accounts for all of its antigenic, transport, and mechanical characteristics, particularly its ability to undergo large passive deformations during repeated passage through the narrow capillaries of the microvasculature, throughout its 120-day life span. The determinant of normal membrane cohesion is the system of vertical linkages between phospholipid bilayer and membrane skeleton, formed by the interactions of the cytoplasmic domains of various membrane proteins with the spectrin-based skeletal network. Band 3 and RhAG provide such links by interacting with ankyrin, which in turn binds to b-spectrin. Protein 4.2 binds to both band 3 and ankyrin and can regulate the avidity of the interaction between ...
Hereditary spherocytosis (HS) is a very heterogenous condition both at clinical and biochemical leve...
Band 3 which is the one of the most abundant membrane protein in red blood cell membrane. It is boun...
Establishing the diagnosis in a patient with hereditary hemolytic anemia is a complex and laborious ...
Hemolytic anemia due to abnormalities of the erythrocyte membrane comprises an important group of in...
Hereditary spherocytosis (HS) originates from defective anchoring of the cytoskeletal network to the...
Hereditary Spherocytosis (HS) is a haemolytic anaemia caused by erythrocyte protein membrane defects...
PubMedID: 22889517Hereditary spherocytosis (HS) is a congenital hemolytic anemia which is characteri...
Hereditary spherocytosis is a common inherited disorder that is characterised by anaemia, jaundice, ...
Hereditary Spherocytosis (HS), or congenital hemolytic jaundice, is an important hemolytic anemia wi...
Hereditary spherocytosis is a common hemolytic anemia associated with deficiencies in spectrin, the ...
Hereditary spherocytosis (HS) is due to different membrane protein defects (i.e., deficiency of spec...
AbstractThe red cell membrane is comprised of a lipid bilayer studded with transmembrane proteins, a...
Fresh human blood samples were collected from healthy controls and splenectomized and unsplenectomiz...
Hereditary spherocytosis (HS) is a very heterogenous condition both at clinical and biochemical leve...
Band 3 which is the one of the most abundant membrane protein in red blood cell membrane. It is boun...
Establishing the diagnosis in a patient with hereditary hemolytic anemia is a complex and laborious ...
Hemolytic anemia due to abnormalities of the erythrocyte membrane comprises an important group of in...
Hereditary spherocytosis (HS) originates from defective anchoring of the cytoskeletal network to the...
Hereditary Spherocytosis (HS) is a haemolytic anaemia caused by erythrocyte protein membrane defects...
PubMedID: 22889517Hereditary spherocytosis (HS) is a congenital hemolytic anemia which is characteri...
Hereditary spherocytosis is a common inherited disorder that is characterised by anaemia, jaundice, ...
Hereditary Spherocytosis (HS), or congenital hemolytic jaundice, is an important hemolytic anemia wi...
Hereditary spherocytosis is a common hemolytic anemia associated with deficiencies in spectrin, the ...
Hereditary spherocytosis (HS) is due to different membrane protein defects (i.e., deficiency of spec...
AbstractThe red cell membrane is comprised of a lipid bilayer studded with transmembrane proteins, a...
Fresh human blood samples were collected from healthy controls and splenectomized and unsplenectomiz...
Hereditary spherocytosis (HS) is a very heterogenous condition both at clinical and biochemical leve...
Band 3 which is the one of the most abundant membrane protein in red blood cell membrane. It is boun...
Establishing the diagnosis in a patient with hereditary hemolytic anemia is a complex and laborious ...