Results 201 to 210 of about 33,034 (254)

Radiogenomics and the DNA damage response: opportunities for biomarker-guided radiosensitization in pancreatic cancer. [PDF]

open access: yesFront Oncol
Karam MN   +10 more
europepmc   +1 more source

The return of metabolism: biochemistry and physiology of glycolysis. [PDF]

open access: yesBiol Rev Camb Philos Soc
Grüning NM   +19 more
europepmc   +1 more source

The GATA1 N terminus coordinates metabolic reprogramming in erythropoiesis.

open access: yesBlood
Ling T   +20 more
europepmc   +1 more source

Liver pyruvate kinase (PK) isozymes in a PK‐deficient patient*

Annals of Human Genetics, 1968
SUMMARYLiver from a patient with hereditary haemolytic anaemia due to pyruvate kinase deficiency is a deficient in the ‘erythrocyte’ PK isozyme as are her erythrocytes. The chromatographic, electrophoretic, antigenic, heat stability and kinetic properties of the patient's enzyme were not different from normal.
R H, Bigley, R D, Koler
openaire   +2 more sources

Four New Pyruvate Kinase (PK) Variants and a Classical PK Deficiency

British Journal of Haematology, 1975
Summary. Four new red‐cell pyruvate kinase (PK) variants are presented along with one case of so‐called classical type PK deficiency. PK ‘Tokyo II’ had a low activity, Km (PEP) and Vmax, but a normal urea stability and only slight deviation from normal in neutralization tests by antiserum.
S. Miwa   +5 more
openaire   +2 more sources

Change of pyruvate kinase (PK) isozymes in classical type pk deficiency and other PK deficiency cases during red cell maturation

American Journal of Hematology, 1984
AbstractConversion of pyruvate kinase (PK) isozymes during the maturation of erythroblasts in five cases of PK deficiency was compared with that in normal subjects using immunofluorescent antibody techniques. In normal erythroblasts, M2‐type PK was clearly seen at the proerythroblast stage, then markedly declined with cell maturation whereas L‐type PK ...
S, Takegawa, S, Miwa
openaire   +2 more sources

Two homozygous cases of erythrocyte pyruvate kinase (PK) deficiency in Japan: PK sendai and PK shinshu

American Journal of Hematology, 1988
AbstractTwo new erythrocyte pyruvate kinase (PK) variants with severe nonspherocytic hemolytic anemia are presented. These cases are both considered to be homozygous because of the consanguineous marriages in their parents. Their erythrocyte PK's were characterized by the recommended methods of the International Committee for Standardization in ...
Kenzaburo Tani   +11 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy