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Pflugers Archiv : European Journal of Physiology
|
March 23, 1999
IP3-induced Ca2+ release in A7r5 vascular smooth-muscle cells represents a partial emptying of the stores and not an all-or-none Ca2+ release of separate quanta
L Missiaen, H Sipma, J B Parys, et al.
Biochemical Society Transactions
|
May 1, 1995
Haplotype analysis of the BYR1 gene in malignant hyperthermia and central core disease
K A Quane, K E Keating, J M Healy, et al.
Human Molecular Genetics
|
July 11, 2000
A novel ryanodine receptor mutation and genotype-phenotype correlation in a large malignant hyperthermia New Zealand Maori pedigree
R L Brown, A N Pollock, K G Couchman, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 31, 1999
A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease
P J Lynch, J Tong, M Lehane, et al.
Genomics
|
September 1, 1994
Mutation screening of the RYR1 gene in malignant hyperthermia: detection of a novel Tyr to Ser mutation in a pedigree with associated central cores
K A Quane, K E Keating, J M Healy, et al.
British Journal of Anaesthesia
|
December 9, 1997
Detection of a novel mutation at amino acid position 614 in the ryanodine receptor in malignant hyperthermia
K A Quane, H Ording, K E Keating, et al.
Human Mutation
|
February 5, 1998
Novel mutations at a CpG dinucleotide in the ryanodine receptor in malignant hyperthermia
B M Manning, K A Quane, P J Lynch, et al.
American Journal of Human Genetics
|
April 29, 1998
Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlation
B M Manning, K A Quane, H Ording, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 48) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 48 results.
Pflugers Archiv : European Journal of Physiology
|
March 23, 1999
IP3-induced Ca2+ release in A7r5 vascular smooth-muscle cells represents a partial emptying of the stores and not an all-or-none Ca2+ release of separate quanta
L Missiaen, H Sipma, J B Parys, et al.
Biochemical Society Transactions
|
May 1, 1995
Haplotype analysis of the BYR1 gene in malignant hyperthermia and central core disease
K A Quane, K E Keating, J M Healy, et al.
Human Molecular Genetics
|
July 11, 2000
A novel ryanodine receptor mutation and genotype-phenotype correlation in a large malignant hyperthermia New Zealand Maori pedigree
R L Brown, A N Pollock, K G Couchman, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 31, 1999
A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease
P J Lynch, J Tong, M Lehane, et al.
Genomics
|
September 1, 1994
Mutation screening of the RYR1 gene in malignant hyperthermia: detection of a novel Tyr to Ser mutation in a pedigree with associated central cores
K A Quane, K E Keating, J M Healy, et al.
British Journal of Anaesthesia
|
December 9, 1997
Detection of a novel mutation at amino acid position 614 in the ryanodine receptor in malignant hyperthermia
K A Quane, H Ording, K E Keating, et al.
Human Mutation
|
February 5, 1998
Novel mutations at a CpG dinucleotide in the ryanodine receptor in malignant hyperthermia
B M Manning, K A Quane, P J Lynch, et al.
American Journal of Human Genetics
|
April 29, 1998
Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlation
B M Manning, K A Quane, H Ording, et al.
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of 5