| 1577776 |
Polymorphism of human glycoprotein Ib alpha results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macroglycopeptide region. Structure/function implications. |
| 1586750 |
Genetic and structural characterization of an amino acid dimorphism in glycoprotein Ib alpha involved in platelet transfusion refractoriness. |
| 1730088 |
Mutation of leucine-57 to phenylalanine in a platelet glycoprotein Ib alpha leucine tandem repeat occurring in patients with an autosomal dominant variant of Bernard-Soulier disease. |
| 2052556 |
Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease. |
| 2070794 |
Identification of the disulphide bonds in human platelet glycocalicin. |
| 2845978 |
Structure of the human blood platelet membrane glycoprotein Ib alpha gene. |
| 3303030 |
Cloning of the alpha chain of human platelet glycoprotein Ib: a transmembrane protein with homology to leucine-rich alpha 2-glycoprotein. |
| 3497398 |
Amino acid sequence of the von Willebrand factor-binding domain of platelet membrane glycoprotein Ib. |
| 7632942 |
The largest variant of platelet glycoprotein Ib alpha has four tandem repeats of 13 amino acids in the macroglycopeptide region and a genetic linkage with methionine145. |
| 7690774 |
Point mutation in a leucine-rich repeat of platelet glycoprotein Ib alpha resulting in the Bernard-Soulier syndrome. |
| 7819107 |
Cys209 Ser mutation in the platelet membrane glycoprotein Ib alpha gene is associated with Bernard-Soulier syndrome. |
| 7873390 |
A three-base deletion removing a leucine residue in a leucine-rich repeat of platelet glycoprotein Ib alpha associated with a variant of Bernard-Soulier syndrome (Nancy I). |
| 8384898 |
Pseudo-von Willebrand disease: a mutation in the platelet glycoprotein Ib alpha gene associated with a hyperactive surface receptor. |
| 8486780 |
Expression of the phenotypic abnormality of platelet-type von Willebrand disease in a recombinant glycoprotein Ib alpha fragment. |
| 9088113 |
StyI polymorphism at nucleotide 1610 in the human platelet glycoprotein Ib alpha gene. |
| 9639514 |
Naturally occurring mutations in glycoprotein Ibalpha that result in defective ligand binding and synthesis of a truncated protein. |
| 9651345 |
Human beta-filamin is a new protein that interacts with the cytoplasmic tail of glycoprotein Ibalpha. |
| 10089893 |
Molecular characterization of two mutations in platelet glycoprotein (GP) Ib alpha in two Finnish Bernard-Soulier syndrome families. |
| 10391209 |
Characterization of single-nucleotide polymorphisms in coding regions of human genes. |
| 11222377 |
Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome. |
| 11858495 |
Molecular modeling of the seven tandem leucine-rich repeats within the ligand-binding region of platelet glycoprotein Ib alpha. |
| 12038791 |
A novel polymorphism, 70Leu/Phe, disrupts a consensus Leu residue within the leucine-rich repeat sequence of platelet glycoprotein Ibalpha. |
| 12087105 |
Crystal structure of the platelet glycoprotein Ibalpha N-terminal domain reveals an unmasking mechanism for receptor activation. |
| 12183630 |
Structures of glycoprotein Ibalpha and its complex with von Willebrand factor A1 domain. |
| 12665801 |
Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides. |
| 14521605 |
Identification of a novel point mutation in platelet glycoprotein Ibalpha, Gly to Ser at residue 233, in a Japanese family with platelet-type von Willebrand disease. |
| 14711733 |
Nonarteritic anterior ischemic optic neuropathy is associated with a specific platelet polymorphism located on the glycoprotein Ibalpha gene. |
| 15489334 |
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |
| 16263699 |
Elucidation of N-glycosylation sites on human platelet proteins: a glycoproteomic approach. |
| 16625196 |
DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage. |
| 17008541 |
Glycoprotein Ibalpha forms disulfide bonds with 2 glycoprotein Ibbeta subunits in the resting platelet. |
| 18088087 |
Phosphoproteome of resting human platelets. |
| 19828450 |
Identification and characterization of multiple similar ligand-binding repeats in filamin: implication on filamin-mediated receptor clustering and cross-talk. |
