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 *

133 related articles for article (PubMed ID: 16194214)

  • 1. An additional Glu30Lys substitution in the Gla domain of the protein Z gene is not a common polymorphism but a rare mutation, which would cause its deficiency.
    Iwata H; Souri M; Kemkes-Matthes B; Ichinose A
    J Thromb Haemost; 2005 Oct; 3(10):2360-1. PubMed ID: 16194214
    [No Abstract]   [Full Text] [Related]  

  • 2. A naturally occurring E30Q mutation in the Gla domain of protein Z causes its impaired secretion and subsequent deficiency.
    Souri M; Koseki-Kuno S; Iwata H; Kemkes-Matthes B; Ichinose A
    Blood; 2005 Apr; 105(8):3149-54. PubMed ID: 15626740
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A proposed structural model of human protein Z.
    Lee CJ; Chandrasekaran V; Duke RE; Perera L; Pedersen LG
    J Thromb Haemost; 2007 Jul; 5(7):1558-61. PubMed ID: 17456189
    [No Abstract]   [Full Text] [Related]  

  • 4. R255h amino acid substitution of protein Z identified in patients with factor V Leiden mutation.
    Kemkes-Matthes B; Matthes KJ; Souri M; Koseki-Kuno S; Ichinose A
    Br J Haematol; 2005 Jan; 128(2):248-52. PubMed ID: 15638861
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of the protein Z-dependent protease inhibitor interactive-sites of protein Z.
    Qureshi SH; Lu Q; Manithody C; Yang L; Rezaie AR
    Biochim Biophys Acta; 2014 Sep; 1844(9):1631-7. PubMed ID: 24960590
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Band 3 Tuscaloosa: Pro327----Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2.
    Jarolim P; Palek J; Rubin HL; Prchal JT; Korsgren C; Cohen CM
    Blood; 1992 Jul; 80(2):523-9. PubMed ID: 1378323
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON).
    Bouhassira EE; Schwartz RS; Yawata Y; Ata K; Kanzaki A; Qiu JJ; Nagel RL; Rybicki AC
    Blood; 1992 Apr; 79(7):1846-54. PubMed ID: 1558976
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gene symbol: PROS1. Disease: Protein S deficiency.
    Steidle M; Pfanner G; Haug B
    Hum Genet; 2008 Oct; 124(3):313. PubMed ID: 18846658
    [No Abstract]   [Full Text] [Related]  

  • 9. Gene symbol: PROS1. Disease: Protein S deficiency.
    Steidle M; Pfanner G; Haug B
    Hum Genet; 2008 Oct; 124(3):316. PubMed ID: 18846666
    [No Abstract]   [Full Text] [Related]  

  • 10. A fever gene comes in from the cold.
    Kastner DL; O'Shea JJ
    Nat Genet; 2001 Nov; 29(3):241-2. PubMed ID: 11687785
    [No Abstract]   [Full Text] [Related]  

  • 11. A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome).
    Orrico A; Galli L; Falciani M; Bracci M; Cavaliere ML; Rinaldi MM; Musacchio A; Sorrentino V
    FEBS Lett; 2000 Aug; 478(3):216-20. PubMed ID: 10930571
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis.
    Kanzaki A; Hayette S; Morlé L; Inoue F; Matsuyama R; Inoue T; Yawata A; Wada H; Vallier A; Alloisio N; Yawata Y; Delaunay J
    Br J Haematol; 1997 Dec; 99(3):522-30. PubMed ID: 9401060
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structural analysis of protein Z gene variants in patients with foetal losses.
    Caliandro R; Nico G; Tiscia G; Favuzzi G; De Stefano V; Rossi E; Margaglione M; Grandone E
    Thromb Haemost; 2013 Sep; 110(3):534-42. PubMed ID: 23846529
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human erythrocyte membrane protein band 4.2 (pallidin).
    Cohen CM; Dotimas E; Korsgren C
    Semin Hematol; 1993 Apr; 30(2):119-37. PubMed ID: 8480187
    [No Abstract]   [Full Text] [Related]  

  • 15. Phosphorylation-induced changes in backbone dynamics of the dematin headpiece C-terminal domain.
    Vugmeyster L; McKnight CJ
    J Biomol NMR; 2009 Jan; 43(1):39-50. PubMed ID: 19030997
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The leucine 10 residue in the pleckstrin homology domain of ceramide kinase is crucial for its catalytic activity.
    Kim TJ; Mitsutake S; Kato M; Igarashi Y
    FEBS Lett; 2005 Aug; 579(20):4383-8. PubMed ID: 16081073
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Erythrocyte dematin is a candidate gene for Marie Unna hereditary hypotrichosis and related hairloss disorders.
    Mohseni M; Chishti AH
    Am J Hematol; 2008 May; 83(5):430-2. PubMed ID: 18273904
    [No Abstract]   [Full Text] [Related]  

  • 18. Protein C Sapporo (protein C Glu 25 --> Lys): a heterozygous missense mutation in the Gla domain provides new insight into the interaction between protein C and endothelial protein C receptor.
    Nakabayashi T; Mizukami K; Naitoh S; Takeda M; Shikamoto Y; Nakagawa T; Kaneko H; Tarumi T; Mizoguchi I; Mizuno H; Ieko M; Koike T
    Thromb Haemost; 2005 Nov; 94(5):942-50. PubMed ID: 16363234
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Protein Z.
    Kemkes-Matthes B; Matthes KJ
    Semin Thromb Hemost; 2001 Oct; 27(5):551-6. PubMed ID: 11668427
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Protein Z G79A polymorphism in patients with severe sepsis.
    Sipahi T; Kuybulu A; Ozturk A; Akar N
    Clin Appl Thromb Hemost; 2010 Jun; 16(3):334-6. PubMed ID: 19124455
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.