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I R Peake

Showing results (31-40 of 120) with videos related to

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The Biochemical Journal|October 1, 1970
Some studies on the biosynthesis of tocochromanolsI R Peake, B G Audley, J F Pennock
Lancet (London, England)|February 5, 1994
Factor VIII gene rearrangements in patients with severe haemophilia AA C Goodeve, F E Preston, I R Peake
Lancet (London, England)|February 4, 1984
Carrier detection by direct gene analysis in a family with haemophilia B (factor IX deficiency)I R Peake, B L Furlong, A L Bloom
British Medical Journal|October 4, 1975
Vitamin E deficiency and platelet functional defect in a jaundiced infantM Khurshid, T J Lee, I R Peake, et al.
British Journal of Haematology|May 1, 1993
An MseI RFLP in the 5' flanking region of the factor IX gene: its use for haemophilia B carrier detection in Caucasian and Thai populationsP R Winship, C E Nichols, A Chuansumrit, et al.
British Journal of Haematology|September 1, 1988
Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragment length polymorphismsP Moodie, M B Liddell, I R Peake, et al.
Thrombosis and Haemostasis|December 1, 1994
A single base pair deletion in the promoter region of the factor IX gene is associated with haemophilia BA J Hall, A Chuansumrit, I R Peake, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 3, 2016
In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletionA Cartwright, I R Peake, A C Goodeve, et al.
Biochemical and Biophysical Research Communications|February 13, 2001
Endoplasmic reticulum retention and prolonged association of a von Willebrand's disease-causing von Willebrand factor variant with ERp57 and calnexinS Allen, A C Goodeve, I R Peake, et al.
Thrombosis and Haemostasis|July 15, 2000
Relationship between factor VIII mutation type and inhibitor development in a cohort of previously untreated patients treated with recombinant factor VIII (Recombinate). Recombinate PUP Study GroupA C Goodeve, I Williams, G L Bray, et al.
Pageof 12

Showing results (31-40 of 120) with videos related to

Sort By:
Pageof 12
The Biochemical Journal|October 1, 1970
Some studies on the biosynthesis of tocochromanolsI R Peake, B G Audley, J F Pennock
Lancet (London, England)|February 5, 1994
Factor VIII gene rearrangements in patients with severe haemophilia AA C Goodeve, F E Preston, I R Peake
Lancet (London, England)|February 4, 1984
Carrier detection by direct gene analysis in a family with haemophilia B (factor IX deficiency)I R Peake, B L Furlong, A L Bloom
British Medical Journal|October 4, 1975
Vitamin E deficiency and platelet functional defect in a jaundiced infantM Khurshid, T J Lee, I R Peake, et al.
British Journal of Haematology|May 1, 1993
An MseI RFLP in the 5' flanking region of the factor IX gene: its use for haemophilia B carrier detection in Caucasian and Thai populationsP R Winship, C E Nichols, A Chuansumrit, et al.
British Journal of Haematology|September 1, 1988
Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragment length polymorphismsP Moodie, M B Liddell, I R Peake, et al.
Thrombosis and Haemostasis|December 1, 1994
A single base pair deletion in the promoter region of the factor IX gene is associated with haemophilia BA J Hall, A Chuansumrit, I R Peake, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 3, 2016
In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletionA Cartwright, I R Peake, A C Goodeve, et al.
Biochemical and Biophysical Research Communications|February 13, 2001
Endoplasmic reticulum retention and prolonged association of a von Willebrand's disease-causing von Willebrand factor variant with ERp57 and calnexinS Allen, A C Goodeve, I R Peake, et al.
Thrombosis and Haemostasis|July 15, 2000
Relationship between factor VIII mutation type and inhibitor development in a cohort of previously untreated patients treated with recombinant factor VIII (Recombinate). Recombinate PUP Study GroupA C Goodeve, I Williams, G L Bray, et al.
Pageof 12