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A case report: Pathological complete response to neoadjuvant lorlatinib for Epithelioid inflammatory myofibroblastic sarcoma with EML4-ALK rearrangement

Frontiers in pharmacology, 2024-07, Vol.15, p.1401428

2024

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Successful re-challenge of dabrafenib-trametinib combination therapy in advanced BRAFV600E-mutant non-small cell lung cancer after previous cytotoxic chemotherapy, targeted therapy, and immunotherapy: a case report

Annals of translational medicine, 2022-09, Vol.10 (18), p.1029-1029

2022

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Successful re-challenge of dabrafenib-trametinib combination therapy in advanced BRAF V600E-mutant non-small cell lung cancer after previous cytotoxic chemotherapy, targeted therapy, and immunotherapy: a case report

Annals of translational medicine, 2022, Vol.10 (18), p.1029-1029

2022

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γ-Secretase Gene Mutations in Familial Acne Inversa

Science (American Association for the Advancement of Science), 2010-11, Vol.330 (6007), p.1065-1065

2010

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Protein oxidation‐induced changes in the physicochemical properties and quality of plant food

International journal of food science & technology, 2024-06, Vol.59 (6), p.3537-3544

2024

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Effect of microbial fermentation on the quality of soybean meal

International journal of food science & technology, 2024-01, Vol.59 (1), p.72-83

2024

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Finite-time economic model predictive control for optimal load dispatch and frequency regulation in interconnected power systems

Global Energy Interconnection, 2023-06, Vol.6 (3), p.355-362

2023

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Steam oxidation resistance of plasma sprayed chromium‐containing coatings at 1200 °C

Materials and corrosion, 2019-01, Vol.70 (1), p.37-47

2019

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长波红外制冷杜瓦组件杂散光分析

Zhōngguó jīguāng, 2024, Vol.51 (8), p.810005

2024

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用于冷光学长波红外杜瓦组件杂散光分析与抑制

Infrared and Laser Engineering, 2023, Vol.52 (7), p.20220823

2023

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Copy-Number Mutations on Chromosome 17q24.2-q24.3 in Congenital Generalized Hypertrichosis Terminalis with or without Gingival Hyperplasia

American journal of human genetics, 2009-06, Vol.84 (6), p.807-813

2009

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Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report

Journal of the American Academy of Dermatology, 2011-04, Vol.64 (4), p.e45-e50

2011

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Microstructure and Ablation Property of TaC-SiC Composite Coatings

Key engineering materials, 2016-07, Vol.697, p.535-538

2016

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Strong association of the SNP rs17822931 with wet earwax and bromhidrosis in a Chinese family

Journal of genetics, 2013-08, Vol.92 (2), p.289-291

2013

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Ablation Behavior of Low Pressure Plasma Sprayed TiB2-MoSi2 Composite Coatings

Key engineering materials, 2016-07, Vol.697, p.685-688

2016

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A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family

Journal of human genetics, 2009-07, Vol.54 (7), p.422-425

2009

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Fabrication and Ablation Behavior of Plasma Sprayed ZrC-W Composite Coatings

Key engineering materials, 2014-03, Vol.602-603, p.552-555

2014

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[gamma]-Secretase Gene Mutations in Familial Acne Inversa

Science (American Association for the Advancement of Science), 2010-11, Vol.330 (6007), p.1065

2010

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g-Secretase Gene Mutations in Familial Acne Inversa

Science (American Association for the Advancement of Science), 2010-11, Vol.330 (6007), p.1065-1065

2010

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Light-Emitting Characterization of Vacuum Plasma Sprayed Silicon Coatings

Key engineering materials, 2014-03, Vol.602-603, p.989-992

2014

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In-Flight Behaviors and Properties of Plasma-Sprayed Tungsten Coatings

Materials science forum, 2010-01, Vol.658, p.13-16

2010

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Loss-of-function mutations of an inhibitory upstream orf in the human hairless transcript cause marie unna hereditary hypotrichosis

Nature genetics, 2009-06, Vol.41 (6), p.762

2009

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等离子喷涂TiC-Graphite复合涂层摩擦磨损性能

无机材料学报, 2022, Vol.37 (6), p.643-650

2022

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A case report: Pathological complete response to neoadjuvant lorlatinib for Epithelioid inflammatory myofibroblastic sarcoma with EML4-ALK rearrangement

Successful re-challenge of dabrafenib-trametinib combination therapy in advanced BRAFV600E-mutant non-small cell lung cancer after previous cytotoxic chemotherapy, targeted therapy, and immunotherapy: a case report

Successful re-challenge of dabrafenib-trametinib combination therapy in advanced BRAF V600E-mutant non-small cell lung cancer after previous cytotoxic chemotherapy, targeted therapy, and immunotherapy: a case report

γ-Secretase Gene Mutations in Familial Acne Inversa

Protein oxidation‐induced changes in the physicochemical properties and quality of plant food

Effect of microbial fermentation on the quality of soybean meal

Finite-time economic model predictive control for optimal load dispatch and frequency regulation in interconnected power systems

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

Steam oxidation resistance of plasma sprayed chromium‐containing coatings at 1200 °C

长波红外制冷杜瓦组件杂散光分析

用于冷光学长波红外杜瓦组件杂散光分析与抑制

Copy-Number Mutations on Chromosome 17q24.2-q24.3 in Congenital Generalized Hypertrichosis Terminalis with or without Gingival Hyperplasia

Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report

Microstructure and Ablation Property of TaC-SiC Composite Coatings

Strong association of the SNP rs17822931 with wet earwax and bromhidrosis in a Chinese family

Ablation Behavior of Low Pressure Plasma Sprayed TiB2-MoSi2 Composite Coatings

A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family

Fabrication and Ablation Behavior of Plasma Sprayed ZrC-W Composite Coatings

[gamma]-Secretase Gene Mutations in Familial Acne Inversa

g-Secretase Gene Mutations in Familial Acne Inversa

Light-Emitting Characterization of Vacuum Plasma Sprayed Silicon Coatings

In-Flight Behaviors and Properties of Plasma-Sprayed Tungsten Coatings

Loss-of-function mutations of an inhibitory upstream orf in the human hairless transcript cause marie unna hereditary hypotrichosis

等离子喷涂TiC-Graphite复合涂层摩擦磨损性能

Corrigendum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

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