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Literature DB >> 2793170

Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation.

P Patracchini¹, E Calzolari, V Aiello, P Palazzi, P Banin, G Marchetti, F Bernardi.

Abstract

The von Willebrand factor pseudogene, previously mapped to chromosome 22, was sublocalized by in situ hybridization using as probe a von Willebrand factor cDNA fragment completely contained in the pseudogenic region. Chromosome spreads were from a patient carrying a unique balanced de novo translocation 46,X,t(X;22)(pter;q11.21). Silver grain analysis indicated that the human von Willebrand factor pseudogene is located on 22q,11,22-q11,23, a region relevant for several somatic and constitutional chromosomal alterations.

Entities: Gene Species

Mesh：

Substances：
von Willebrand Factor
DNA

Year: 1989 PMID： 2793170 DOI： 10.1007/bf00285168

Source DB: PubMed Journal: Hum Genet ISSN： 0340-6717 Impact factor: 4.132

30 in total

1. Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma.

Authors: B R Seizinger; R L Martuza; J F Gusella
Journal: Nature Date: 1986 Aug 14-20 Impact factor: 49.962

2. A high resolution in situ hybridization technique for the direct visualization of labeled G-banded early metaphase and prophase chromosomes.

Authors: M E Chandler; J J Yunis
Journal: Cytogenet Cell Genet Date: 1978

Review 3. Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.

Authors: T Ogata; N Matsuo
Journal: Hum Genet Date: 1995-06 Impact factor: 4.132

4. Genetic heterogeneity in a large cohort of Indian type 3 von Willebrand disease patients.

Authors: Priyanka Kasatkar; Shrimati Shetty; Kanjaksha Ghosh
Journal: PLoS One Date: 2014-03-27 Impact factor: 3.240

4 in total

Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation.

1. Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma.

2. A high resolution in situ hybridization technique for the direct visualization of labeled G-banded early metaphase and prophase chromosomes.

3. Report of the committee on the genetic constitution of chromosome 22.

4. Gene deletions correlate with the development of alloantibodies in von Willebrand disease.

5. X-autosome translocations: cytogenetic characteristics and their consequences.

6. Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization.

7. Molecular analysis of both translocation products of a Philadelphia-positive CML patient.

8. De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma.

9. Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22.

10. Von Willebrand factor in the vessel wall mediates platelet adherence.

1. Characterization and mapping of the 5' portion of von Willebrand factor pseudogene.

Review 2. Role of von Willebrand factor in the haemostasis.

Review 3. Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.

4. Genetic heterogeneity in a large cohort of Indian type 3 von Willebrand disease patients.