201 related articles for article (PubMed ID: 21327094)
1. An in vitro model for Pelger-Huët anomaly: stable knockdown of lamin B receptor in HL-60 cells.
Olins AL; Ernst A; Zwerger M; Herrmann H; Olins DE
Nucleus; 2010; 1(6):506-12. PubMed ID: 21327094
[TBL] [Abstract][Full Text] [Related]
2. Granulocytic nuclear differentiation of lamin B receptor-deficient mouse EPRO cells.
Zwerger M; Herrmann H; Gaines P; Olins AL; Olins DE
Exp Hematol; 2008 Aug; 36(8):977-87. PubMed ID: 18495328
[TBL] [Abstract][Full Text] [Related]
3. The granulocyte nucleus and lamin B receptor: avoiding the ovoid.
Hoffmann K; Sperling K; Olins AL; Olins DE
Chromosoma; 2007 Jun; 116(3):227-35. PubMed ID: 17245605
[TBL] [Abstract][Full Text] [Related]
4. Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly).
Hoffmann K; Dreger CK; Olins AL; Olins DE; Shultz LD; Lucke B; Karl H; Kaps R; Müller D; Vayá A; Aznar J; Ware RE; Sotelo Cruz N; Lindner TH; Herrmann H; Reis A; Sperling K
Nat Genet; 2002 Aug; 31(4):410-4. PubMed ID: 12118250
[TBL] [Abstract][Full Text] [Related]
5. [Nuclear abnormalities in Pelger-Huet anomaly; progress in blood cell morphology].
Tomonaga M
Rinsho Byori; 2005 Jan; 53(1):54-60. PubMed ID: 15724491
[TBL] [Abstract][Full Text] [Related]
6. The lamin B receptor under transcriptional control of C/EBPepsilon is required for morphological but not functional maturation of neutrophils.
Cohen TV; Klarmann KD; Sakchaisri K; Cooper JP; Kuhns D; Anver M; Johnson PF; Williams SC; Keller JR; Stewart CL
Hum Mol Genet; 2008 Oct; 17(19):2921-33. PubMed ID: 18621876
[TBL] [Abstract][Full Text] [Related]
7. Lamin B-receptor mutations in Pelger-Huët anomaly.
Best S; Salvati F; Kallo J; Garner C; Height S; Thein SL; Rees DC
Br J Haematol; 2003 Nov; 123(3):542-4. PubMed ID: 14617022
[TBL] [Abstract][Full Text] [Related]
8. Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein.
Clayton P; Fischer B; Mann A; Mansour S; Rossier E; Veen M; Lang C; Baasanjav S; Kieslich M; Brossuleit K; Gravemann S; Schnipper N; Karbasyian M; Demuth I; Zwerger M; Vaya A; Utermann G; Mundlos S; Stricker S; Sperling K; Hoffmann K
Nucleus; 2010; 1(4):354-66. PubMed ID: 21327084
[TBL] [Abstract][Full Text] [Related]
9. Nuclear envelope composition determines the ability of neutrophil-type cells to passage through micron-scale constrictions.
Rowat AC; Jaalouk DE; Zwerger M; Ung WL; Eydelnant IA; Olins DE; Olins AL; Herrmann H; Weitz DA; Lammerding J
J Biol Chem; 2013 Mar; 288(12):8610-8618. PubMed ID: 23355469
[TBL] [Abstract][Full Text] [Related]
10. Dosage effect of zero to three functional LBR-genes in vivo and in vitro.
Gravemann S; Schnipper N; Meyer H; Vaya A; Nowaczyk MJ; Rajab A; Hofmann WK; Salewsky B; Tönnies H; Neitzel H; Stassen HH; Sperling K; Hoffmann K
Nucleus; 2010; 1(2):179-89. PubMed ID: 21326950
[TBL] [Abstract][Full Text] [Related]
11. The human granulocyte nucleus: Unusual nuclear envelope and heterochromatin composition.
Olins AL; Zwerger M; Herrmann H; Zentgraf H; Simon AJ; Monestier M; Olins DE
Eur J Cell Biol; 2008 May; 87(5):279-90. PubMed ID: 18396345
[TBL] [Abstract][Full Text] [Related]
12. Understanding and recognizing the Pelger-Huët anomaly.
Colella R; Hollensead SC
Am J Clin Pathol; 2012 Mar; 137(3):358-66. PubMed ID: 22338047
[TBL] [Abstract][Full Text] [Related]
13. Cytoskeletal influences on nuclear shape in granulocytic HL-60 cells.
Olins AL; Olins DE
BMC Cell Biol; 2004 Aug; 5():30. PubMed ID: 15317658
[TBL] [Abstract][Full Text] [Related]
14. Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly.
Shultz LD; Lyons BL; Burzenski LM; Gott B; Samuels R; Schweitzer PA; Dreger C; Herrmann H; Kalscheuer V; Olins AL; Olins DE; Sperling K; Hoffmann K
Hum Mol Genet; 2003 Jan; 12(1):61-9. PubMed ID: 12490533
[TBL] [Abstract][Full Text] [Related]
15. Genetic architecture of band neutrophil fraction in Iceland.
Oskarsson GR; Magnusson MK; Oddsson A; Jensson BO; Fridriksdottir R; Arnadottir GA; Katrinardottir H; Rognvaldsson S; Halldorsson GH; Sveinbjornsson G; Ivarsdottir EV; Stefansdottir L; Ferkingstad E; Norland K; Tragante V; Saemundsdottir J; Jonasdottir A; Jonasdottir A; Sigurjonsdottir S; Petursdottir KO; Davidsson OB; Rafnar T; Holm H; Olafsson I; Onundarson PT; Vidarsson B; Sigurdardottir O; Masson G; Gudbjartsson DF; Jonsdottir I; Norddahl GL; Thorsteinsdottir U; Sulem P; Stefansson K
Commun Biol; 2022 Jun; 5(1):525. PubMed ID: 35650273
[TBL] [Abstract][Full Text] [Related]
16. Image analysis of neutrophil nuclear morphology: Learning about phenotypic range and its reliable analysis from patients with pelger-Huët-anomaly and treated with colchicine.
Schnipper N; Stassen HH; Kallinich T; Sperling K; Hoffmann K
Cytometry B Clin Cytom; 2017 Nov; 92(6):541-549. PubMed ID: 27684937
[TBL] [Abstract][Full Text] [Related]
17. Pelger-huet anomaly and a mild skeletal phenotype secondary to mutations in LBR.
Borovik L; Modaff P; Waterham HR; Krentz AD; Pauli RM
Am J Med Genet A; 2013 Aug; 161A(8):2066-73. PubMed ID: 23824842
[TBL] [Abstract][Full Text] [Related]
18. A homozygous variant in the Lamin B receptor gene LBR results in a non-lethal skeletal dysplasia without Pelger-Huët anomaly.
Collins M; Miranda V; Rousseau J; Kratz LE; Campeau PM
Bone; 2020 Dec; 141():115601. PubMed ID: 32827848
[TBL] [Abstract][Full Text] [Related]
19. Mouse neutrophils lacking lamin B-receptor expression exhibit aberrant development and lack critical functional responses.
Gaines P; Tien CW; Olins AL; Olins DE; Shultz LD; Carney L; Berliner N
Exp Hematol; 2008 Aug; 36(8):965-76. PubMed ID: 18550262
[TBL] [Abstract][Full Text] [Related]
20. Lamin B receptor recognizes specific modifications of histone H4 in heterochromatin formation.
Hirano Y; Hizume K; Kimura H; Takeyasu K; Haraguchi T; Hiraoka Y
J Biol Chem; 2012 Dec; 287(51):42654-63. PubMed ID: 23100253
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
