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JE Sadler
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Journal Articles

Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor

JC Eikenboom, T Matsushita, PH Reitsma, EA Tuley, G Castaman, E Briet, JE Sadler
Journal: Blood
Blood (1996) 88 (7): 2433–2441.
https://doi.org/10.1182/blood.V88.7.2433.bloodjournal8872433
Published: 1996
Journal Articles

Analysis of Arg834Gln and Val902Glu type 2A von Willebrand disease mutations: studies with recombinant von Willebrand factor and correlation with patient characteristics

T Englender, A Lattuada, PM Mannucci, JE Sadler, A Inbal
Journal: Blood
Blood (1996) 87 (7): 2788–2794.
https://doi.org/10.1182/blood.V87.7.2788.bloodjournal8772788
Published: 1996
Journal Articles

Commentary: a new classification for von Willebrand disease

JE Sadler, HR Gralnick
Journal: Blood
Blood (1994) 84 (3): 676–679.
https://doi.org/10.1182/blood.V84.3.676.676
Published: 1994
Journal Articles

Identification of three candidate mutations causing type IIA von Willebrand disease using a rapid, nonradioactive, allele-specific hybridization method

A Inbal, T Englender, N Kornbrot, AM Randi, G Castaman, PM Mannucci, JE Sadler
Journal: Blood
Blood (1993) 82 (3): 830–836.
https://doi.org/10.1182/blood.V82.3.830.830
Published: 1993
Journal Articles

New variant of von Willebrand disease type II with markedly increased levels of von Willebrand factor antigen and dominant mode of inheritance: von Willebrand disease type IIC Miami

MR Ledford, I Rabinowitz, JE Sadler, JW Kent, F Civantos
Journal: Blood
Blood (1993) 82 (1): 169–175.
https://doi.org/10.1182/blood.V82.1.169.bloodjournal821169
Published: 1993
Journal Articles

Homocysteine inhibits von Willebrand factor processing and secretion by preventing transport from the endoplasmic reticulum

SR Lentz, JE Sadler
Journal: Blood
Blood (1993) 81 (3): 683–689.
https://doi.org/10.1182/blood.V81.3.683.683
Published: 1993
Journal Articles

The mutation Arg (53)----Trp causes von Willebrand disease Normandy by abolishing binding to factor VIII. Studies with recombinant von Willebrand factor

S Jorieux, EA Tuley, C Gaucher, C Mazurier, JE Sadler
Journal: Blood
Blood (1992) 79 (3): 563–567.
https://doi.org/10.1182/blood.V79.3.563.563
Published: 1992
Journal Articles

Regulation of thrombomodulin by tumor necrosis factor-alpha: comparison of transcriptional and posttranscriptional mechanisms

SR Lentz, M Tsiang, JE Sadler
Journal: Blood
Blood (1991) 77 (3): 542–550.
https://doi.org/10.1182/blood.V77.3.542.542
Published: 1991
Journal Articles

Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor gene

IR Peake, D Bowen, P Bignell, MB Liddell, JE Sadler, G Standen, AL Bloom
Journal: Blood
Blood (1990) 76 (3): 555–561.
https://doi.org/10.1182/blood.V76.3.555.555
Published: 1990
Journal Articles

Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: family studies that identify carriers of the condition and a compound heterozygous individual

IR Peake, MB Liddell, P Moodie, G Standen, DJ Mancuso, EA Tuley, LA Westfield, JM Sorace, JE Sadler, CL Verweij
Journal: Blood
Blood (1990) 75 (3): 654–661.
https://doi.org/10.1182/blood.V75.3.654.654
Published: 1990