H. Christensen

发表

Discrepant platelet and plasma von Willebrand factor in von Willebrand disease patients with p.Pro2808Leufs*24

P. James, D. Lillicrap, A. Tuttle, 2017, Journal of thrombosis and haemostasis : JTH.

The VPS33B-binding protein VPS16B is required in megakaryocyte and platelet α-granule biogenesis.

J. Parkinson, J. Wasmuth, W. Kahr, 2012, Blood.

Abnormal megakaryocyte development and platelet function in Nbeal2(-/-) mice.

C. Hawkins, A. Weyrich, J. Di Paola, 2013, Blood.

Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome

J. Parkinson, A. Weyrich, Jesse Hinckley, 2011, Nature Genetics.

Transient myeloproliferative disorder (transient leukemia) and hematologic manifestations of Down syndrome.

A. Zipursky, H. Christensen, J. Doyle, 1999, Clinics in laboratory medicine.

Dynamin 2‐Dependent Endocytosis is Required For Normal Megakaryocyte Development

W. Kahr, M. Bender, F. Pluthero, 2015, Blood.

PLATELETS AND THROMBOPOIESIS Dynamin 2 – dependent endocytosis is required for normal megakaryocyte development in mice

W. Kahr, M. Bender, F. Pluthero, 2015 .

Requirement of VPS33B, a member of the Sec1/Munc18 protein family, in megakaryocyte and platelet -granule biogenesis Running title: VPS33B required for platelet -granule biogenesis

D. Chitayat, P. Gissen, W. Kahr, 2013 .

Requirement of VPS 33 B , a member of the Sec 1 / Munc 18 protein family , in megakaryocyte and platelet-granule biogenesis

D. Chitayat, P. Gissen, W. Kahr, 2005 .

FlnA binding to PACSIN2 F-BAR domain regulates membrane tubulation in megakaryocytes and platelets.

J. Hartwig, F. Nakamura, M. Plomann, 2015, Blood.

Requirement of VPS33B, a member of the Sec1/Munc18 protein family, in megakaryocyte and platelet alpha-granule biogenesis.

D. Chitayat, P. Gissen, W. Kahr, 2005, Blood.

Leukemia and/or myeloproliferative syndrome in neonates with Down syndrome.

A. Zipursky, R. Sutherland, H. Christensen, 1997, Seminars in perinatology.

Platelet-associated complement factor H in healthy persons and patients with atypical HUS.

D. Geary, P. Zipfel, B. Hoppe, 2009, Blood.

Myelodysplasia and acute megakaryoblastic leukemia in Down's syndrome.

A. Zipursky, P. Thorner, H. Christensen, 1994, Leukemia research.

Analysis of procoagulant phosphatidylserine‐exposing platelets by imaging flow cytometry

S. Israels, E. McMillan-Ward, M. Rand, 2018, Research and practice in thrombosis and haemostasis.

Transient leukemia with extreme basophilia in a phenotypically normal infant with blast cells containing a pseudodiploid clone, 46,XY i(21)(q10).

A. Zipursky, L. Worth, H. Christensen, 1999, Journal of pediatric hematology/oncology.

Double labelling of cell surface antigens with colloidal gold markers

D. Soligo, H. Christensen, E. Harven, 2005, The Histochemical Journal.

Diagnosis of Platelet Disorders by Electron Microscopy

W. Kahr, H. Christensen, 2012 .

A novel approach for scanning electron microscopy of colloidal gold- labeled cell surfaces

H. Christensen, É. de Harven, R. Leung, 1984, The Journal of cell biology.

Loss of the F-BAR protein CIP4 reduces platelet production by impairing membrane-cytoskeleton remodeling.

D. R. Myers, G. Voth, S. Corey, 2013, Blood.

Long-term docosahexaenoic acid therapy in a congenic murine model of cystic fibrosis.

M. Corey, C. Ackerley, R. Yantiss, 2007, American journal of physiology. Gastrointestinal and liver physiology.

Ultrastructural studies of the megakaryoblastic leukemias of Down syndrome.

A. Zipursky, H. Christensen, É. de Harven, 1995, Leukemia & lymphoma.

Immunogold labeling for the diagnosis of leukemia by transmission and scanning electron microscopy.

D. Soligo, H. Christensen, É. de Harven, 1995, Scanning microscopy.

Immunogold labelling of leukemic hairy cells with the B‐ly7 monoclonal antibody: An SEM and TEM study

S. Poppema, H. Christensen, É. de Harven, 1994, Microscopy research and technique.

Hairy Cell Leukemia, an Ultrastructural Study with Double Immunogold Labeling

A. Polliack, D. Soligo, D. Bailey, 1992 .

Should we be counting immunogold marker particles on cell surfaces with the SEM?

D. Soligo, H. Christensen, E. Harven, 1987, Journal of microscopy.

Decreased numbers of dense granules in fetal and neonatal platelets

D. Chitayat, V. Blanchette, P. Shah, 2017, Haematologica.

Proteasome function is required for platelet production.

Robert A. Campbell, Dean Y. Li, R. Miles, 2014, The Journal of clinical investigation.

Interstitial deletion of 11q‐implicating the KIRREL3 gene in the neurocognitive delay associated with Jacobsen syndrome

D. Chitayat, S. Chénier, D. Stavropoulos, 2012, American journal of medical genetics. Part A.

Lymphomatoid papulosis: a follow-up study of 41 patients.

K. Thomsen, G. Vejlsgaard, H. Christensen, 1994, Seminars in dermatology.

Megakaryocyte and platelet abnormalities in a patient with a W33C mutation in the conserved SH3-like domain of myosin heavy chain IIA

J. Forman-Kay, A. Savoia, V. Blanchette, 2009, Thrombosis and Haemostasis.

Abnormal megakaryocyte development and platelet function in Nbeal2(-/-) mice.

C. Hawkins, A. Weyrich, J. Di Paola, 2013, Blood.

Platelet-associated complement factor H in healthy persons and patients with atypical HUS.

D. Geary, P. Zipfel, B. Hoppe, 2009, Blood.

Abnormal Megakaryocyte Development and Platelet Function in Nbeal2 2/2 Mice

W. Kahr, Richard W. Lo, F. Pluthero, 2022 .