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Transcriptomics
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Homo sapiens
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biostudies-arrayexpress
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Lab affiliation
Collège de France, Oncologie Cellulaire et Moléculaire, PSL University, INSERM UMR 1050, CNRS UMR 7241, INSERM UMR 944, CNRS UMR 7212, Université de Paris, IRSL, Hôpital St. Louis Paris France
(1)
St. Giles Laboratory of Human Genetics of Infectious Diseases, The Rockefeller University, New York, New York, USA.
(1)
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A A386G biallelic GPIbα gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesis.
Not available
S-EPMC3232274
|
biostudies-literature
Cite
Generation and rescue of a murine model of platelet dysfunction: the Bernard-Soulier syndrome.
Not available
S-EPMC16010
|
biostudies-literature
Cite
Lentiviral gene therapy reverts GPIX expression and phenotype in Bernard-Soulier syndrome type C.
Not available
S-EPMC10320622
|
biostudies-literature
Cite
Characterization of zebrafish gp1ba mutant and modelling Bernard Soulier syndrome.
Not available
S-EPMC9273021
|
biostudies-literature
Cite
Novel Mutation in Bernard-Soulier Syndrome.
Not available
S-EPMC2980512
|
biostudies-literature
Cite
A Brazilian case of Bernard-Soulier syndrome with two distinct founder mutations.
Not available
S-EPMC5529668
|
biostudies-literature
Cite
Novel Compound Heterozygous Mutations in Two Families With Bernard-Soulier Syndrome.
Not available
S-EPMC7864212
|
biostudies-literature
Cite
A
GP1BA
Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome.
Not available
S-EPMC8777725
|
biostudies-literature
Cite
Increased RhoA pathway activation downstream of αIIbβ3/SRC contributes to heterozygous Bernard Soulier syndrome.
Not available
S-EPMC12208166
|
biostudies-literature
Cite
Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations.
Not available
S-EPMC3046273
|
biostudies-literature
Cite
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