These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 15625388)

  • 1. Benign anomaly to malign dysplasia: variable expression of lamin B receptor mutations in humans.
    Kasbekar DP
    J Biosci; 2004 Dec; 29(4):367-8. PubMed ID: 15625388
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes.
    Oosterwijk JC; Mansour S; van Noort G; Waterham HR; Hall CM; Hennekam RC
    J Med Genet; 2003 Dec; 40(12):937-41. PubMed ID: 14684694
    [No Abstract]   [Full Text] [Related]  

  • 7. [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]  

  • 8. Pelger-Huët anomaly in a child with 1q42.3-44 deletion.
    Kalfa TA; Zimmerman SA; Goodman BK; McDonald MT; Ware RE
    Pediatr Blood Cancer; 2006 May; 46(5):645-8. PubMed ID: 16007606
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deletion of LBR N-terminal domains recapitulates Pelger-Huet anomaly phenotypes in mouse without disrupting X chromosome inactivation.
    Young AN; Perlas E; Ruiz-Blanes N; Hierholzer A; Pomella N; Martin-Martin B; Liverziani A; Jachowicz JW; Giannakouros T; Cerase A
    Commun Biol; 2021 Apr; 4(1):478. PubMed ID: 33846535
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Pelger-Huët anomaly: a critical review of the literature.
    Speeckaert MM; Verhelst C; Koch A; Speeckaert R; Lacquet F
    Acta Haematol; 2009; 121(4):202-6. PubMed ID: 19468205
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel case of Greenberg dysplasia and genotype-phenotype correlation analysis for LBR pathogenic variants: An instructive example of one gene-multiple phenotypes.
    Giorgio E; Sirchia F; Bosco M; Sobreira NLM; ; Grosso E; Brussino A; Brusco A
    Am J Med Genet A; 2019 Feb; 179(2):306-311. PubMed ID: 30561119
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Historical perspective and clinical implications of the Pelger-Hüet cell.
    Cunningham JM; Patnaik MM; Hammerschmidt DE; Vercellotti GM
    Am J Hematol; 2009 Feb; 84(2):116-9. PubMed ID: 19021122
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Constitutional familial leucocytopenia with partial Pelger anomaly and delayed development of bone (author's transl)].
    Heyne K
    Eur J Pediatr; 1976 Feb; 121(3):191-201. PubMed ID: 1248491
    [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. 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]  

  • 19. A chance diagnosis of Pelger-Huët anomaly in a 49-year-old woman hospitalized for an acute episode of Crohn disease.
    Schavgoulidze A; Vergez F; Corre J; Rieu JB
    Ann Biol Clin (Paris); 2020 Oct; 78(5):581-582. PubMed ID: 32644046
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.