BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 36223592)

  • 1. Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.
    Linder MI; Mizoguchi Y; Hesse S; Csaba G; Tatematsu M; Łyszkiewicz M; Ziȩtara N; Jeske T; Hastreiter M; Rohlfs M; Liu Y; Grabowski P; Ahomaa K; Maier-Begandt D; Schwestka M; Pazhakh V; Isiaku AI; Briones Miranda B; Blombery P; Saito MK; Rusha E; Alizadeh Z; Pourpak Z; Kobayashi M; Rezaei N; Unal E; Hauck F; Drukker M; Walzog B; Rappsilber J; Zimmer R; Lieschke GJ; Klein C
    Blood; 2023 Feb; 141(6):645-658. PubMed ID: 36223592
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic correction of HAX1 in induced pluripotent stem cells from a patient with severe congenital neutropenia improves defective granulopoiesis.
    Morishima T; Watanabe K; Niwa A; Hirai H; Saida S; Tanaka T; Kato I; Umeda K; Hiramatsu H; Saito MK; Matsubara K; Adachi S; Kobayashi M; Nakahata T; Heike T
    Haematologica; 2014 Jan; 99(1):19-27. PubMed ID: 23975175
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A zebrafish model for HAX1-associated congenital neutropenia.
    Doll L; Aghaallaei N; Dick AM; Welte K; Skokowa J; Bajoghli B
    Haematologica; 2021 May; 106(5):1311-1320. PubMed ID: 32327498
    [TBL] [Abstract][Full Text] [Related]  

  • 4. HAX1-dependent control of mitochondrial proteostasis governs neutrophil granulocyte differentiation.
    Fan Y; Murgia M; Linder MI; Mizoguchi Y; Wang C; Łyszkiewicz M; Ziȩtara N; Liu Y; Frenz S; Sciuccati G; Partida-Gaytan A; Alizadeh Z; Rezaei N; Rehling P; Dennerlein S; Mann M; Klein C
    J Clin Invest; 2022 May; 132(9):. PubMed ID: 35499078
    [TBL] [Abstract][Full Text] [Related]  

  • 5. CRISPR/Cas9-mediated
    Nasri M; Ritter M; Mir P; Dannenmann B; Aghaallaei N; Amend D; Makaryan V; Xu Y; Fletcher B; Bernhard R; Steiert I; Hahnel K; Berger J; Koch I; Sailer B; Hipp K; Zeidler C; Klimiankou M; Bajoghli B; Dale DC; Welte K; Skokowa J
    Haematologica; 2020 Mar; 105(3):598-609. PubMed ID: 31248972
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PML-controlled responses in severe congenital neutropenia with ELANE-misfolding mutations.
    Olofsen PA; Bosch DA; Roovers O; van Strien PMH; de Looper HWJ; Hoogenboezem RM; Barnhoorn S; Mastroberardino PG; Ghazvini M; van der Velden VHJ; Bindels EMJ; de Pater EM; Touw IP
    Blood Adv; 2021 Feb; 5(3):775-786. PubMed ID: 33560392
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cooperative assembly of signal recognition particle RNA with protein SRP19.
    Walker KP; Black SD; Zwieb C
    Biochemistry; 1995 Sep; 34(37):11989-97. PubMed ID: 7547936
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic defects in severe congenital neutropenia: emerging insights into life and death of human neutrophil granulocytes.
    Klein C
    Annu Rev Immunol; 2011; 29():399-413. PubMed ID: 21219176
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interaction of rice and human SRP19 polypeptides with signal recognition particle RNA.
    Chittenden K; Gowda K; Black SD; Zwieb C
    Plant Mol Biol; 1997 Jun; 34(3):507-15. PubMed ID: 9225861
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Proteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent Acquisition.
    Grabowski P; Hesse S; Hollizeck S; Rohlfs M; Behrends U; Sherkat R; Tamary H; Ünal E; Somech R; Patıroğlu T; Canzar S; van der Werff Ten Bosch J; Klein C; Rappsilber J
    Mol Cell Proteomics; 2019 Apr; 18(4):760-772. PubMed ID: 30630937
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pathogenic mechanisms and clinical implications of congenital neutropenia syndromes.
    Hauck F; Klein C
    Curr Opin Allergy Clin Immunol; 2013 Dec; 13(6):596-606. PubMed ID: 24145314
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Structural insights into the assembly of the human and archaeal signal recognition particles.
    Wild K; Bange G; Bozkurt G; Segnitz B; Hendricks A; Sinning I
    Acta Crystallogr D Biol Crystallogr; 2010 Mar; 66(Pt 3):295-303. PubMed ID: 20179341
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Use of Induced Pluripotent Stem Cells to Study the Effects of Adenosine Deaminase Deficiency on Human Neutrophil Development.
    Tsui M; Min W; Ng S; Dobbs K; Notarangelo LD; Dror Y; Grunebaum E
    Front Immunol; 2021; 12():748519. PubMed ID: 34777360
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Two strategically placed base pairs in helix 8 of mammalian signal recognition particle RNA are crucial for the SPR19-dependent binding of protein SRP54.
    Yin J; Yang CH; Zwieb C
    RNA; 2004 Apr; 10(4):574-80. PubMed ID: 15037766
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Clinical and Molecular Assessment of Iranian Families with Severe Congenital Neutropenia, Identification of HYOU1 and SHOC2 as Potential Novel Gene Defects.
    Arab F; Rezaei N; Taheri F; Kouhpeikar H; Rayzan E; Mirbeyk M; Zare-Abdollahi D; Ghadami M
    Iran J Allergy Asthma Immunol; 2022 Jun; 21(3):344-354. PubMed ID: 35822684
    [TBL] [Abstract][Full Text] [Related]  

  • 16. In vitro study of HAX1 gene therapy by retro viral transduction as a therapeutic target in severe congenital neutropenia.
    Farajifard H; Zavvar M; Rajaei T; Noorbakhsh F; Nikougoftar-Zarif M; Azadmanesh K; Kompani F; Rezaei N
    Eur Cytokine Netw; 2018 Nov; 29(4):146-152. PubMed ID: 30698159
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Site-directed mutagenesis of signal-recognition particle RNA. Identification of the nucleotides in helix 8 required for interaction with protein SRP19.
    Zwieb C
    Eur J Biochem; 1994 Jun; 222(3):885-90. PubMed ID: 7517868
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Structures of SRP54 and SRP19, the two proteins that organize the ribonucleic core of the signal recognition particle from Pyrococcus furiosus.
    Egea PF; Napetschnig J; Walter P; Stroud RM
    PLoS One; 2008; 3(10):e3528. PubMed ID: 18953414
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.
    Yılmaz Karapınar D; Patıroğlu T; Metin A; Çalışkan Ü; Celkan T; Yılmaz B; Karakaş Z; Karapınar TH; Akıncı B; Özkınay F; Onay H; Yeşilipek MA; Akar HH; Tüysüz G; Tokgöz H; Özdemir GN; Aslan Kıykım A; Karaman S; Kılınç Y; Oymak Y; Küpesiz A; Olcay L; Keskin Yıldırım Z; Aydoğan G; Gökçe M; İleri T; Aral YZ; Bay A; Atabay B; Kaya Z; Söker M; Özdemir Karadaş N; Özbek U; Özsait Selçuk B; Özdemir HH; Uygun V; Tezcan Karasu G; Yılmaz Ş
    Pediatr Blood Cancer; 2019 Oct; 66(10):e27923. PubMed ID: 31321910
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cyclic manner of neutropenia in a patient with
    Cipe FE; Celiksoy MH; Erturk B; Aydogmus Ç
    Pediatr Hematol Oncol; 2018 Apr; 35(3):181-185. PubMed ID: 30346863
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.