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M

Michał Witt

Polish Academy of Sciences

H指数:29

被引数:3,112

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The lack of homozygotes with a large deletion encompassing SPAG1 and POLR2K in primary ciliary dyskinesia patients suggests the lethal effect of the loss of POLR2K protein

缺乏包含SPAG1和POLR2K的大片段缺失的纯合子在原发性纤毛运动障碍患者中，提示了POLR2K蛋白缺失的致死效应

Genes & Diseases

IF9.4

2025-01-200

OAAI

The hero of American and Polish nations: a molecular look at Thaddeus Kosciuszko's cause of death suggests a contribution of endocarditis caused by Cutibacterium acnes infection

MICROBIAL CELL FACTORIES

IF4.9

2022-11-230

OA

Multiomics to investigate the mechanisms contributing to repression of PTPRC and SOCS2 in pediatric T-ALL: Focus on miR-363-3p and promoter methylation

GENES CHROMOSOMES & CANCER

IF2.8

2022-07-180

OAAI

CRISPRi for specific inhibition of miRNA clusters and miRNAs with high sequence homology

SCIENTIFIC REPORTS

IF3.9

2022-04-1514

OAAI

Discrimination between human populations using a small number of differentially methylated CpG sites: a preliminary study using lymphoblastoid cell lines and peripheral blood samples of European and Chinese origin

IF3.7

2020-10-127

OAAI

hsa-miR-20b-5p and hsa-miR-363-3p Affect Expression of PTEN and BIM Tumor Suppressor Genes and Modulate Survival of T-ALL Cells In Vitro

IF5.2

2020-05-0528

OAAI

Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms

JOURNAL OF MEDICAL GENETICS

IF3.7

2019-07-3138

PREAI

Comprehensive Investigation of miRNome Identifies Novel Candidate miRNA-mRNA Interactions Implicated in T-Cell Acute Lymphoblastic Leukemia

IF7.7

2019-03-0126

OAAI

PTEN abnormalities predict poor outcome in children with T-cell acute lymphoblastic leukemia treated according to ALL IC-BFM protocols

AMERICAN JOURNAL OF HEMATOLOGY

IF9.9

2019-01-2422

OAAI

DNAI2 Mutations Cause Primary Ciliary Dyskinesia with Defects in the Outer Dynein Arm

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2008-11-01212

OAAI

Correlation between the level of cytogenetic aberrations in cultured human lymphocytes and the age and gender of donors

JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES

IF3.8

2006-08-0140

OAAI

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene:: a cystic fibrosis mutation of Slavic origin common in Central and East Europe

IF3.6

2000-03-30115

PREAI

Dörk, T; Macek, M; Mekus, F; Tümmler, B; Tzountzouris, J; Casals, T; Krebsová, A; Koudová, M; Sakmaryová, I; Macek, M; Vávrová, V; Zemková, D; Ginter, E; Petrova, NV; Ivaschenko, T; Baranov, V; Witt, M; Pogorzelski, A; Bal, J; Zékanowsky, C; Wagner, K; Stuhrmann, M; Bauer, I; Seydewitz, HH; Neumann, T; Jakubiczka, S; Kraus, C; Thamm, B; Nechiporenko, M; Livshits, L; Mosse, N; Tsukerman, G; Kadási, L; Ravnik-Glavac, M; Glavac, D; Komel, R; Vouk, K; Kucinskas, V; Krumina, A; Teder, M; Kocheva, S; Efremov, GD; Onay, T; Kirdar, B; Malone, G; Schwarz, M; Zhou, ZQ; Friedman, KJ; Carles, S; Claustres, M; Bozon, D; Verlingue, C; Férec, C; Tzetis, M; Kanavakis, E; Cuppens, H; Bombieri, C; Pignatti, PF; Sangiuolo, F; Jordanova, A; Kusic, J; Radojkovic, D; Sertic, J; Richter, D; Rukavina, AS; Bjorck, E; Strandvik, B; Cardoso, H; Montgomery, M; Nakielna, B; Hughes, D; Estivill, X; Aznarez, I; Tullis, E; Tsui, LC; Zielenski, J