scholarly article | Q13442814 |
case report | Q2782326 |
P50 | author | Uzma Zaidi | Q90273539 |
Saba Shahid | Q91913323 | ||
Tahir Shamsi | Q47101301 | ||
P2093 | author name string | Shariq Ahmed | |
Qurratulain Rizvi | |||
P2860 | cites work | Genetics: CALR mutations and a new diagnostic algorithm for MPN. | Q51113576 |
A CALR mutation preceding BCR-ABL1 in an atypical myeloproliferative neoplasm. | Q54291314 | ||
The Prevalence of JAK2, MPL, and CALR Mutations in Chinese Patients With BCR-ABL1-Negative Myeloproliferative Neoplasms. | Q55056597 | ||
Calreticulin is the dominant pro-phagocytic signal on multiple human cancers and is counterbalanced by CD47 | Q24561405 | ||
Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2 | Q24568313 | ||
Calreticulin (CALR) mutation in myeloproliferative neoplasms (MPNs) | Q28084727 | ||
CALR vs JAK2 vs MPL-mutated or triple-negative myelofibrosis: clinical, cytogenetic and molecular comparisons | Q29998841 | ||
Clinical effect of driver mutations of JAK2, CALR, or MPL in primary myelofibrosis | Q33416223 | ||
Somatic mutations of calreticulin in myeloproliferative neoplasms | Q34039270 | ||
Calreticulin mutations in myeloproliferative neoplasms and new methodology for their detection and monitoring | Q38263140 | ||
A multiplex snapback primer system for the enrichment and detection of JAK2 V617F and MPL W515L/K mutations in Philadelphia-negative myeloproliferative neoplasms. | Q38366759 | ||
Primary myelofibrosis: 2017 update on diagnosis, risk-stratification, and management | Q39015300 | ||
Homozygous calreticulin mutations in patients with myelofibrosis lead to acquired myeloperoxidase deficiency. | Q40741460 | ||
From Janus kinase 2 to calreticulin: the clinically relevant genomic landscape of myeloproliferative neoplasms | Q45778614 | ||
CALR mutations in myeloproliferative neoplasms: hidden behind the reticulum. | Q45961187 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P407 | language of work or name | English | Q1860 |
P921 | main subject | phenotype | Q104053 |
myelofibrosis | Q1752571 | ||
chronic idiopathic myelofibrosis | Q3857106 | ||
homozygosity | Q114049690 | ||
P304 | page(s) | 1430170 | |
P577 | publication date | 2019-01-20 | |
P1433 | published in | Case reports in hematology | Q27724373 |
P1476 | title | Homozygous CALR Mutation in Primary Myelofibrosis and Its Effect on Disease Phenotype: A Case Report and Review of the Literature | |
P478 | volume | 2019 |
Q90273548 | A distinct molecular mutational profile and its clinical impact in essential thrombocythemia and primary myelofibrosis patients | cites work | P2860 |
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