159 related articles for article (PubMed ID: 33053321)
1. Structural and Functional Impact of SRP54 Mutations Causing Severe Congenital Neutropenia.
Juaire KD; Lapouge K; Becker MMM; Kotova I; Michelhans M; Carapito R; Wild K; Bahram S; Sinning I
Structure; 2021 Jan; 29(1):15-28.e7. PubMed ID: 33053321
[TBL] [Abstract][Full Text] [Related]
2. Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features.
Carapito R; Konantz M; Paillard C; Miao Z; Pichot A; Leduc MS; Yang Y; Bergstrom KL; Mahoney DH; Shardy DL; Alsaleh G; Naegely L; Kolmer A; Paul N; Hanauer A; Rolli V; Müller JS; Alghisi E; Sauteur L; Macquin C; Morlon A; Sancho CS; Amati-Bonneau P; Procaccio V; Mosca-Boidron AL; Marle N; Osmani N; Lefebvre O; Goetz JG; Unal S; Akarsu NA; Radosavljevic M; Chenard MP; Rialland F; Grain A; Béné MC; Eveillard M; Vincent M; Guy J; Faivre L; Thauvin-Robinet C; Thevenon J; Myers K; Fleming MD; Shimamura A; Bottollier-Lemallaz E; Westhof E; Lengerke C; Isidor B; Bahram S
J Clin Invest; 2017 Nov; 127(11):4090-4103. PubMed ID: 28972538
[TBL] [Abstract][Full Text] [Related]
3. Mutations in the
Bellanné-Chantelot C; Schmaltz-Panneau B; Marty C; Fenneteau O; Callebaut I; Clauin S; Docet A; Damaj GL; Leblanc T; Pellier I; Stoven C; Souquere S; Antony-Debré I; Beaupain B; Aladjidi N; Barlogis V; Bauduer F; Bensaid P; Boespflug-Tanguy O; Berger C; Bertrand Y; Carausu L; Fieschi C; Galambrun C; Schmidt A; Journel H; Mazingue F; Nelken B; Quah TC; Oksenhendler E; Ouachée M; Pasquet M; Saada V; Suarez F; Pierron G; Vainchenker W; Plo I; Donadieu J
Blood; 2018 Sep; 132(12):1318-1331. PubMed ID: 29914977
[TBL] [Abstract][Full Text] [Related]
4. SRP54 mutations induce congenital neutropenia via dominant-negative effects on XBP1 splicing.
Schürch C; Schaefer T; Müller JS; Hanns P; Arnone M; Dumlin A; Schärer J; Sinning I; Wild K; Skokowa J; Welte K; Carapito R; Bahram S; Konantz M; Lengerke C
Blood; 2021 Mar; 137(10):1340-1352. PubMed ID: 33227812
[TBL] [Abstract][Full Text] [Related]
5. Cellular Traffic Jam and Disease Due to Mutations in SRP54.
Weichenrieder O
Structure; 2021 Jan; 29(1):3-5. PubMed ID: 33417891
[TBL] [Abstract][Full Text] [Related]
6. Severe congenital neutropenia, SRP54 pathogenicity, and a framework for surveillance.
Fan EM; Vagher J; Meznarich JA; Ubico EM; Goteti S; Peterson D; Rayes A; Maese LD
Am J Med Genet A; 2023 May; 191(5):1434-1441. PubMed ID: 36815775
[TBL] [Abstract][Full Text] [Related]
7. Case Report: Association between cyclic neutropenia and SRP54 deficiency.
Erdős M; Boyarchuk O; Maródi L
Front Immunol; 2022; 13():975017. PubMed ID: 36159802
[TBL] [Abstract][Full Text] [Related]
8. Congenital neutropenia with variable clinical presentation in novel mutation of the SRP54 gene.
Goldberg L; Simon AJ; Rechavi G; Lev A; Barel O; Kunik V; Toren A; Schiby G; Tamary H; Steinberg-Shemer O; Somech R
Pediatr Blood Cancer; 2020 Jun; 67(6):e28237. PubMed ID: 32277798
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. SRP54 and a need for a new neutropenia nosology.
Oyarbide U; Corey SJ
Blood; 2018 Sep; 132(12):1220-1222. PubMed ID: 30237254
[TBL] [Abstract][Full Text] [Related]
11. A complex of the signal sequence binding protein and the SRP RNA promotes translocation of nascent proteins.
Hauser S; Bacher G; Dobberstein B; Lütcke H
EMBO J; 1995 Nov; 14(22):5485-93. PubMed ID: 8521805
[TBL] [Abstract][Full Text] [Related]
12. A pediatric case of congenital neutropenia with SRP54 gene mutation in which monocytosis and gingival swelling were useful in differentiating from autoimmune neutropenia.
Manabe T; Taku K; Hoshina T; Higuchi N; Karakawa S; Kusuhara K
Pediatr Blood Cancer; 2022 Sep; 69(9):e29648. PubMed ID: 35253356
[No Abstract] [Full Text] [Related]
13. Crystal structure of the complete core of archaeal signal recognition particle and implications for interdomain communication.
Rosendal KR; Wild K; Montoya G; Sinning I
Proc Natl Acad Sci U S A; 2003 Dec; 100(25):14701-6. PubMed ID: 14657338
[TBL] [Abstract][Full Text] [Related]
14. Signal sequence recognition and targeting of ribosomes to the endoplasmic reticulum by the signal recognition particle do not require GTP.
Rapiejko PJ; Gilmore R
Mol Biol Cell; 1994 Aug; 5(8):887-97. PubMed ID: 7803856
[TBL] [Abstract][Full Text] [Related]
15. Systematic site-directed mutagenesis of human protein SRP54: interactions with signal recognition particle RNA and modes of signal peptide recognition.
Huang Q; Abdulrahman S; Yin J; Zwieb C
Biochemistry; 2002 Sep; 41(38):11362-71. PubMed ID: 12234178
[TBL] [Abstract][Full Text] [Related]
16. Regulation by the ribosome of the GTPase of the signal-recognition particle during protein targeting.
Bacher G; Lütcke H; Jungnickel B; Rapoport TA; Dobberstein B
Nature; 1996 May; 381(6579):248-51. PubMed ID: 8622769
[TBL] [Abstract][Full Text] [Related]
17. Recognition of a signal peptide by the signal recognition particle.
Janda CY; Li J; Oubridge C; Hernández H; Robinson CV; Nagai K
Nature; 2010 May; 465(7297):507-10. PubMed ID: 20364120
[TBL] [Abstract][Full Text] [Related]
18. A structural step into the SRP cycle.
Wild K; Rosendal KR; Sinning I
Mol Microbiol; 2004 Jul; 53(2):357-63. PubMed ID: 15228518
[TBL] [Abstract][Full Text] [Related]
19. Evidence for a novel GTPase priming step in the SRP protein targeting pathway.
Lu Y; Qi HY; Hyndman JB; Ulbrandt ND; Teplyakov A; Tomasevic N; Bernstein HD
EMBO J; 2001 Dec; 20(23):6724-34. PubMed ID: 11726508
[TBL] [Abstract][Full Text] [Related]
20. Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman-Diamond-like syndrome.
Saettini F; Cattoni A; D'Angio' M; Corti P; Maitz S; Pagni F; Seminati D; Pezzoli L; Iascone M; Biondi A; Bonanomi S
Br J Haematol; 2020 May; 189(4):e171-e174. PubMed ID: 32196641
[No Abstract] [Full Text] [Related]
[Next] [New Search]