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The Cube Surface Light Field for Interactive Free-Viewpoint Rendering

Applied sciences, 2022-07, Vol.12 (14), p.7212

2022

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Multiplex ligation-dependent probe amplification identifies copy number changes in normal and undetectable karyotype MDS patients

Annals of hematology, 2021-09, Vol.100 (9), p.2207-2214

2021

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Calreticulin mutations in Chinese with primary myelofibrosis

Haematologica (Roma), 2014-11, Vol.99 (11), p.1697-1700

2014

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An analysis on the current situation of energy development and its environmental problems in Yulin City

Energy reports, 2020-02, Vol.6 (1), p.15-20

2020

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WebLFR: An interactive light field renderer in web browsers

Multimedia tools and applications, 2024-02, Vol.83 (32), p.77377-77392

2024

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A new HLA‐DQB1 allele, HLA‐DQB104:62, identified in a Chinese family

HLA, 2021-09, Vol.98 (3), p.248-249

2021

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A new HLA‐DQB1 allele, HLA‐DQB1 04:62 , identified in a Chinese family

HLA : immune response genetics, 2021-09, Vol.98 (3), p.248-249

2021

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Omnidirectional stereo video using a hybrid representation

Multimedia tools and applications, 2023, Vol.82 (3), p.3995-4010

2023

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A new HLA‐C allele, HLA‐C15:144, identified in a Chinese family

HLA, 2019-07, Vol.94 (1), p.82-83

2019

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Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization for detecting chromosome abnormalities in myelodysplastic syndromes: A retrospective study

Medicine (Baltimore), 2021-05, Vol.100 (18), p.e25768-e25768

2021

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An Intelligent Identification Approach of Assembly Interface for CAD Models

Computer modeling in engineering & sciences, 2023, Vol.137 (1), p.859-878

2023

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Predicting survival in patients with myelodysplastic/myeloproliferative neoplasms with SF3B1 mutation and thrombocytosis

Leukemia, 2024-06, Vol.38 (6), p.1334-1341

2024

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STAT3 and STAT5B mutations have unique distribution in T-cell large granular lymphocyte proliferations and advanced myeloid neoplasms

Leukemia & lymphoma, 2021-05, Vol.62 (6), p.1506-1509

2021

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The Prevalence of JAK2, MPL, and CALR Mutations in Chinese Patients With BCR-ABL1–Negative Myeloproliferative Neoplasms

American journal of clinical pathology, 2015-07, Vol.144 (1), p.165-171

2015

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The different prognostic impact of type‐1 or type‐1 like and type‐2 or type‐2 like CALR mutations in patients with primary myelofibrosis

American journal of hematology, 2016-07, Vol.91 (7), p.E320-E321

2016

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TET2, ASXL1 and EZH2 mutations in Chinese with myelodysplastic syndromes

Leukemia research, 2013-03, Vol.37 (3), p.305-311

2013

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Polymorphisms of tumor necrosis factor gene in primary myelofibrosis

European journal of haematology, 2012-10, Vol.89 (4), p.367-368

2012

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Personalized Quality Centric Service Recommendation

Service-Oriented Computing, p.528-544

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Detection of recurrent cytogenetic aberrations in multiple myeloma: a comparison between MLPA and iFISH

Oncotarget, 2015-10, Vol.6 (33), p.34276-34287

2015

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Multiplex ligation-dependent probe amplification assay identifies additional copy number changes compared with R-band karyotype and provide more accuracy prognostic information in myelodysplastic syndromes

Oncotarget, 2017-01, Vol.8 (1), p.1603-1612

2017

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252A/G polymorphism in lymphotoxin-α gene influences long-term survival in patients with myelodysplastic syndrome with excess blasts

Leukemia & lymphoma, 2014-06, Vol.55 (6), p.1406-1407

2014

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Application of BIOMED- 2 standardized Ig gene rearrangement system in multiple myeloma

Zhōnghuá xuèyèxué zázhì, 2015-11, Vol.36 (11), p.918-921

2015

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Uncovering Self-Supervised Learning: From Current Applications to Future Trends

Proceedings of the 2023 International Conference on Power, Communication, Computing and Networking Technologies, 2023, p.1-8

2023

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Significance of BIOMED-2 standardized IG/TCR gene rearrangement detection in paraffin-embedded section in lymphoma diagnosis

Zhōnghuá xuèyèxué zázhì, 2014-06, Vol.35 (6), p.495-498

2014

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NPM1 and CEBPA mutations in pediatric cytogenetically normal acute myeloid leukemia

Zhonghua er ke za zhi, 2014-04, Vol.52 (4), p.303

2014

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The Cube Surface Light Field for Interactive Free-Viewpoint Rendering

Multiplex ligation-dependent probe amplification identifies copy number changes in normal and undetectable karyotype MDS patients

Calreticulin mutations in Chinese with primary myelofibrosis

An analysis on the current situation of energy development and its environmental problems in Yulin City

WebLFR: An interactive light field renderer in web browsers

A new HLA‐DQB1 allele, HLA‐DQB104:62, identified in a Chinese family

A new HLA‐DQB1 allele, HLA‐DQB1 04:62 , identified in a Chinese family

Omnidirectional stereo video using a hybrid representation

A new HLA‐C allele, HLA‐C15:144, identified in a Chinese family

Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization for detecting chromosome abnormalities in myelodysplastic syndromes: A retrospective study

An Intelligent Identification Approach of Assembly Interface for CAD Models

Predicting survival in patients with myelodysplastic/myeloproliferative neoplasms with SF3B1 mutation and thrombocytosis

STAT3 and STAT5B mutations have unique distribution in T-cell large granular lymphocyte proliferations and advanced myeloid neoplasms

The Prevalence of JAK2, MPL, and CALR Mutations in Chinese Patients With BCR-ABL1–Negative Myeloproliferative Neoplasms

The different prognostic impact of type‐1 or type‐1 like and type‐2 or type‐2 like CALR mutations in patients with primary myelofibrosis

TET2, ASXL1 and EZH2 mutations in Chinese with myelodysplastic syndromes

Polymorphisms of tumor necrosis factor gene in primary myelofibrosis

Personalized Quality Centric Service Recommendation

Detection of recurrent cytogenetic aberrations in multiple myeloma: a comparison between MLPA and iFISH

Multiplex ligation-dependent probe amplification assay identifies additional copy number changes compared with R-band karyotype and provide more accuracy prognostic information in myelodysplastic syndromes

252A/G polymorphism in lymphotoxin-α gene influences long-term survival in patients with myelodysplastic syndrome with excess blasts

Application of BIOMED- 2 standardized Ig gene rearrangement system in multiple myeloma

Uncovering Self-Supervised Learning: From Current Applications to Future Trends

Significance of BIOMED-2 standardized IG/TCR gene rearrangement detection in paraffin-embedded section in lymphoma diagnosis

NPM1 and CEBPA mutations in pediatric cytogenetically normal acute myeloid leukemia

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