X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
pfcp (4) 4
hematology (3) 3
epor (2) 2
erythrocytosis (2) 2
erythropoietin (2) 2
erythropoietin receptor (2) 2
gene (2) 2
genetic aspects (2) 2
genetic disorders (2) 2
glycoproteins (2) 2
humans (2) 2
increased sensitivity (2) 2
index medicus (2) 2
male (2) 2
pedigree (2) 2
polycythaemia (2) 2
polycythemia - genetics (2) 2
primary familial congenital polycythemia (2) 2
receptors, erythropoietin - genetics (2) 2
acquired vhl mutations (1) 1
analysis (1) 1
artificial neural network (1) 1
base sequence (1) 1
bleeding (1) 1
blood (1) 1
blood volume (1) 1
clinical disorders of erythropoietin (1) 1
cloning (1) 1
complicated malaria (1) 1
congenital polycythemia (1) 1
cytoplasmic region (1) 1
defects (1) 1
deficiency states (1) 1
distribution management system (1) 1
erythroid precursor cells - pathology (1) 1
female (1) 1
frameshift mutation (1) 1
genes (1) 1
genetic algorithm (1) 1
genetic analysis (1) 1
genetic research (1) 1
genetics (1) 1
hematopoietic-cell phosphatase (1) 1
hemoglobin (1) 1
jak2 (1) 1
k ma hematology (1) 1
medical research (1) 1
medicine & public health (1) 1
medicine, experimental (1) 1
menarche (1) 1
menstruation (1) 1
microarray (1) 1
molecular sequence data (1) 1
mutation (1) 1
oncology (1) 1
outage management system (1) 1
paraneoplastic syndrome (1) 1
parasitic diseases (1) 1
pfcp, conserved hypothetical protein (1) 1
pfemp1 (1) 1
pfeno, enolase (1) 1
pfgk, glycerol kinase (1) 1
pfrom3, rhomboid protease 3 (1) 1
pfsec14, sec 14 domain containing protein (1) 1
phlebotomy (1) 1
plasmodium falciparum (1) 1
point mutation (1) 1
polycythemia (1) 1
polymerase chain reaction (1) 1
power flow calculation program (1) 1
priority foreign country practice (1) 1
production of erythropoietin in tumors (1) 1
receptor mutation (1) 1
regular (1) 1
regular article (1) 1
remission (1) 1
rifin (1) 1
secondary hypoxic stimuli (1) 1
shp-1 (1) 1
shp‐1 (1) 1
signal transmission (1) 1
stimulation (1) 1
taiwan power company (1) 1
the section 301 of the u.s. trade law (1) 1
uncomplicated malaria (1) 1
ustr (1) 1
von hippel‐lindau disease (1) 1
wto (1) 1
young adult (1) 1
停限電管理系統 (1) 1
基因演算法 (1) 1
電力潮流計算軟體 (1) 1
類神經網路 (1) 1
미무역대표부 (1) 1
스페셜 301조 (1) 1
우선협상 대상국관행 (1) 1
통상법 301조 (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


International Journal of Hematology, ISSN 0925-5710, 09/2018, Volume 108, Issue 3, pp. 339 - 343
A 10-year-old girl with persistent erythrocytosis and ruddy complexion was diagnosed with primary familial congenital polycythemia (PFCP) involving a novel... 
Menarche | Menstruation | PFCP | EPOR | Phlebotomy | GENE | ERYTHROPOIETIN RECEPTOR | HEMATOLOGY | ERYTHROCYTOSIS | Medical research | Genetic disorders | Polycythemia | Analysis | Genetic research | Medicine, Experimental | Genetic aspects | Glycoproteins | Blood volume | Erythropoietin | Genetic analysis | Signal transmission | Remission | Mutation | Bleeding | Blood | Primary familial congenital polycythemia
Journal Article
Genomics Data, ISSN 2213-5960, 09/2016, Volume 9, Issue C, pp. 118 - 125
Malarial parasite , an apicomplexan protozoan has a 23.3 MB nuclear genome and encodes ~ 5600 transcripts. The genetic diversity of the parasite within and... 
Uncomplicated malaria | Plasmodium falciparum | RIFIN | Complicated malaria | Microarray | PfEMP1
Journal Article
International Journal of Hematology, ISSN 0925-5710, 4/2011, Volume 93, Issue 4, pp. 542 - 544
Primary familial and congenital polycythaemia (PFCP) is a rare form of inherited erythrocytosis caused by heterozygous mutations in the erythropoietin receptor... 
Medicine & Public Health | Hematology | Erythropoietin | PFCP | Oncology | Polycythaemia | EPOR | INCREASED SENSITIVITY | HEMATOLOGY | ERYTHROCYTOSIS | Polycythemia - genetics | Young Adult | Frameshift Mutation | Pedigree | Humans | Male | Receptors, Erythropoietin - genetics | Hemoglobin | Genetic aspects | Glycoproteins | Genetic disorders | Genes
Journal Article
British Journal of Haematology, ISSN 0007-1048, 10/1997, Volume 99, Issue 1, pp. 222 - 227
Journal Article
電力系統無效電力與電壓之運轉是電力公司營運的重要課題之一,為使電力系統之各節點電壓維持在系統電壓控制之目標容許範圍內,並確保配電線路之損失成本最小化。... 
基因演算法 | Distribution Management System (DMS) | 類神經網路 | Power Flow Calculation Program (PFCP) | Genetic Algorithm (GA) | 電力潮流計算軟體 | 停限電管理系統 | Outage Management System (OMS) | Taiwan Power Company (TPC) | Artificial Neural Network (ANN)
Dissertation
01/2005, ISBN 9783527304950, 15
Erythropoietin Production by Tumors: Paraneoplastic Syndromes von Hippel‐Lindau (VHL) Disease and Acquired VHL Mutations Other Tumors Producing Erythropoietin... 
clinical disorders of erythropoietin | secondary hypoxic stimuli | primary familial congenital polycythemia (PFCP) | defects | acquired VHL mutations | production of erythropoietin in tumors | von Hippel‐Lindau (VHL) disease | deficiency states | paraneoplastic syndrome | receptor mutation
Book Chapter
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.