Janczar相关文献与解析，生知库 | 链接生命科学的每一步

GFI1B mutations define an emerging form of inherited thrombocytopenia: insights from a case report and literature review

GFI1B 基因突变定义了一种新出现的遗传性血小板减少症：病例报告和文献综述的启示

Urbański, Bartosz; Bąbol-Pokora, Katarzyna; Braun, Marcin; Janczar, Szymon; Michalak, Marta; Sałacińska-Łoś, Elżbieta; Młynarski, Wojciech; Treliński, Jacek

血小板

发表日期：2026

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The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign

波兰先天性中性粒细胞减少症的遗传图谱：全国筛查活动概述

期刊:Frontiers in Immunology

影响因子:5.9

doi:10.3389/fimmu.2025.1688208

Bąbol-Pokora, Katarzyna; Dobrewa, Weronika; Bielska, Marta; Janczar, Szymon; Madzio, Joanna; Jaworowska, Aleksandra; Kołtan, Sylwia; Hennig, Marcin; Renke, Joanna; Dachowska-Kałwak, Iwona; Cienkusz, Magdalena; Młynarski, Wojciech

IGH::IL3-Rearranged B-Cell Precursor Acute Lymphoblastic Leukemia With Hypereosinophilia in a Child With a Novel PAX5 Germline Variant

携带新型PAX5种系变异的儿童发生IGH::IL3重排B细胞前体急性淋巴细胞白血病伴嗜酸性粒细胞增多症

期刊:Genes Chromosomes & Cancer

影响因子:2.8

doi:10.1002/gcc.70080

Urbański, Bartosz; Miarka-Walczyk, Karolina; Urbańska, Zuzanna; Wąsikowska, Marta; Sałacińska-Łoś, Elżbieta; Bukowska-Strakova, Karolina; Lejman, Monika; Jaroszek, Ewelina; Piątosa, Barbara; Młynarski, Wojciech; Pastorczak, Agata; Janczar, Szymon

Landscape assessment to characterize baseline access and multilevel barriers to IMProve Access to CAR-T CD19 therapy (IMPACT study) across Europe

开展一项旨在描述欧洲各地 CAR-T CD19 疗法可及性现状及多层次障碍的概况研究（IMPACT 研究）。

期刊:

影响因子:

doi:10.1101/2025.11.04.25339516

Oszer, Aleksandra; Galimard, Jacques-Emmanuel; Wardell, Joseph R; Devidas, Meenakshi; Dalissier, Arnaud; Perez-Martinez, Antonio; Bolous, Nancy S; Janczar, Szymon; Styczyński, Jan; Yakimkova, Taisiya; Rodriguez-Galindo, Carlos; Młynarski, Wojciech; Agulnik, Asya; Duffy, Caitlyn; Kałwak, Krzysztof; Schmiegelow, Kjeld

CD19

发表日期：2025

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D-Loop Mutations as Prognostic Markers in Glioblastoma-A Pilot Study

D-Loop 突变作为胶质母细胞瘤预后标志物——一项初步研究

期刊:International Journal of Molecular Sciences

影响因子:0.7

doi:10.3390/ijms25084334

Bartosz Szmyd, Patrycja Stanisławska, Małgorzata Podstawka, Karol Zaczkowski, Patryk M Izbiński, Dominika Kulczycka-Wojdala, Robert Stawski, Karol Wiśniewski, Karolina Janczar, Marcin Braun, Piotr Białasiewicz, Dariusz J Jaskólski, Ernest J Bobeff

The paradox of autoimmunity and autoinflammation in inherited neutrophil disorders - in search of common patterns

遗传性中性粒细胞疾病中自身免疫和自身炎症的悖论——探寻共同模式

期刊:Frontiers in Immunology

影响因子:5.9

doi:10.3389/fimmu.2023.1128581

Krzyzanowski, Damian; Oszer, Aleksandra; Madzio, Joanna; Zdunek, Maciej; Kolodrubiec, Julia; Urbanski, Bartosz; Mlynarski, Wojciech; Janczar, Szymon

Four Decades of Carrier Detection and Prenatal Diagnosis in Hemophilia A: Historical Overview, State of the Art and Future Directions

A型血友病携带者检测和产前诊断四十年：历史回顾、现状及未来方向

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms241411846

Dardik, Rima; Janczar, Szymon; Lalezari, Shadan; Avishai, Einat; Levy-Mendelovich, Sarina; Barg, Assaf Arie; Martinowitz, Uri; Babol-Pokora, Katarzyna; Mlynarski, Wojciech; Kenet, Gili

发表日期：2023

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Optimization of Medium Constituents for the Production of Citric Acid from Waste Glycerol Using the Central Composite Rotatable Design of Experiments

利用中心复合旋转设计实验方法优化废甘油生产柠檬酸的培养基成分

期刊:Molecules

影响因子:4.6

doi:10.3390/molecules28073268

Książek, Ewelina Ewa; Janczar-Smuga, Małgorzata; Pietkiewicz, Jerzy Jan; Walaszczyk, Ewa

发表日期：2023

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Venetoclax Use in Paediatric Haemato-Oncology Centres in Poland: A 2022 Survey

2022 年波兰儿科血液肿瘤中心维奈托克使用情况调查

期刊:Children-Basel

影响因子:2.1

doi:10.3390/children10040745

Bobeff, Katarzyna; Pastorczak, Agata; Urbanska, Zuzanna; Balwierz, Walentyna; Juraszewska, Edyta; Wachowiak, Jacek; Derwich, Katarzyna; Samborska, Magdalena; Kalwak, Krzysztof; Dachowska-Kalwak, Iwona; Laguna, Paweł; Malinowska, Iwona; Smalisz, Katarzyna; Gozdzik, Jolanta; Oszer, Aleksandra; Urbanski, Bartosz; Zdunek, Maciej; Szczepanski, Tomasz; Mlynarski, Wojciech; Janczar, Szymon

Established and emerging non-cellular therapies in inherited bone marrow failure syndromes

已建立和新兴的非细胞疗法在遗传性骨髓衰竭综合征中的应用

GFI1B mutations define an emerging form of inherited thrombocytopenia: insights from a case report and literature review

GFI1B 基因突变定义了一种新出现的遗传性血小板减少症：病例报告和文献综述的启示

The genetic landscape of congenital neutropenia in Poland: summary of the nationwide screening campaign

波兰先天性中性粒细胞减少症的遗传图谱：全国筛查活动概述

IGH::IL3-Rearranged B-Cell Precursor Acute Lymphoblastic Leukemia With Hypereosinophilia in a Child With a Novel PAX5 Germline Variant

携带新型PAX5种系变异的儿童发生IGH::IL3重排B细胞前体急性淋巴细胞白血病伴嗜酸性粒细胞增多症

Landscape assessment to characterize baseline access and multilevel barriers to IMProve Access to CAR-T CD19 therapy (IMPACT study) across Europe

开展一项旨在描述欧洲各地 CAR-T CD19 疗法可及性现状及多层次障碍的概况研究（IMPACT 研究）。

D-Loop Mutations as Prognostic Markers in Glioblastoma-A Pilot Study

D-Loop 突变作为胶质母细胞瘤预后标志物——一项初步研究

The paradox of autoimmunity and autoinflammation in inherited neutrophil disorders - in search of common patterns

遗传性中性粒细胞疾病中自身免疫和自身炎症的悖论——探寻共同模式

Four Decades of Carrier Detection and Prenatal Diagnosis in Hemophilia A: Historical Overview, State of the Art and Future Directions

A型血友病携带者检测和产前诊断四十年：历史回顾、现状及未来方向

Optimization of Medium Constituents for the Production of Citric Acid from Waste Glycerol Using the Central Composite Rotatable Design of Experiments

利用中心复合旋转设计实验方法优化废甘油生产柠檬酸的培养基成分

Venetoclax Use in Paediatric Haemato-Oncology Centres in Poland: A 2022 Survey

2022 年波兰儿科血液肿瘤中心维奈托克使用情况调查