(Q33347025)

26 July 2017

title

Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-beta (English)

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26 July 2017

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Taichi Kato

1

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26 July 2017

Kazuki Kosaka

2

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26 July 2017

Misa Kimura

3

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26 July 2017

Shin-Ichiro Imamura

4

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26 July 2017

Osamu Yamada

5

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26 July 2017

Kazumasa Iwai

6

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26 July 2017

Masahiko Ando

7

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26 July 2017

Kunitaka Joh-o

8

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26 July 2017

Kenji Kuroe

9

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26 July 2017

Akira Ohtake

10

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26 July 2017

Atsuyoshi Takao

11

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26 July 2017

Kazuo Momma

12

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26 July 2017

Rumiko Matsuoka

13

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26 July 2017

language of work or name

English

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publication date

1 March 2003

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26 July 2017

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26 July 2017

volume

5

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26 July 2017

issue

2

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26 July 2017

page(s)

113-119

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A new concept of the cellular basis of immunity

26 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Velo-cardio-facial syndrome: a review of 120 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Complementary DNA cloning of the alternatively expressed endothelial cell glycoprotein Ib beta (GPIb beta) and localization of the GPIb beta gene to chromosome 22

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

The 5' flanking region and chromosomal localization of the gene encoding human platelet membrane glycoprotein Ib alpha

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

A rapid method for starting a culture for the establishment of Epstein-Barr virus-transformed human lymphoblastoid cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

A monoclonal antibody to human platelet glycoprotein IIIa detects a related protein in cultured human endothelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Identification of a mutation in a GATA binding site of the platelet glycoprotein Ibbeta promoter resulting in the Bernard-Soulier syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Structure and expression of the human septin gene HCDCREL-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Reciprocal expression of infant- and adult-preferring transcripts of CDCrel-1 septin gene in the rat neocortex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

The septin CDCrel-1 binds syntaxin and inhibits exocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Human platelet glycoprotein IX

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Identification of Sequence Variants and Analysis of the Role of the Catechol-O-Methyl-Transferase Gene in Schizophrenia Susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

A deletion in chromosome 22 can cause DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/velo-cardio-facial chromosomal region in 22q11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Velocardiofacial syndrome patients with a heterozygous chromosome 22q11 deletion have giant platelets

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

Duration of psychosis and outcome in first-episode schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F01.GIM.0000056828.03164.30

10.1097/01.GIM.0000056828.03164.30

21 January 2018

Identifiers

DOI

1 reference

26 July 2017

1 reference