(Q42605051)

English

Identification of allele-specific p22-phox mutations in a compound heterozygous patient with chronic granulomatous disease by mismatch PCR and restriction enzyme analysis

scientific article published on April 1994

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Identification of allele-specific p22-phox mutations in a compound heterozygous patient with chronic granulomatous disease by mismatch PCR and restriction enzyme analysis (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

chronic granulomatous disease

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

J P Hossle

1

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

M de Boer

2

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

R A Seger

3

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

D Roos

4

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

publication date

1 April 1994

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

93

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

437-442

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single nucleotide primer extension to detect genetic diseases: experimental application to hemophilia B (factor IX) and cystic fibrosis genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A dot-blot screening procedure for mutated ras oncogenes using synthetic oligodeoxynucleotides

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of the autosomal recessive forms of chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of mononuclear cells and granulocytes from human blood. Isolation of monuclear cells by one centrifugation, and of granulocytes by combining centrifugation and sedimentation at 1 g

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of two monoclonal antibodies against cytochrome b558 of human neutrophils

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular abnormalities of a phosphoglycerate kinase variant generated by spontaneous mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification and partial characterization of the b-type cytochrome from human polymorphonuclear leukocytes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Point mutations in the beta-subunit of cytochrome b558 leading to X-linked chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification and cryopreservation of phagocytes from human blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch amplification mutation assay (MAMA): application to the c-H-ras gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective superoxide production by granulocytes from patients with chronic granulomatous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nitroblue‐Tetrazolium Test for the Detection of Chronic Granulomatous Disease—Technical Modification

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Classification of chronic granulomatous disease on the basis of monoclonal antibody-defined surface cytochrome b deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A study of 25 patients with chronic granulomatous disease: a new classification by correlating respiratory burst, cytochrome b, and flavoprotein

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal Diagnosis of Glucose-6-Phosphate-Dehydrogenase Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid, nonradioactive screening for activating ras oncogene mutations using PCR-primer introduced restriction analysis (PCR-PIRA)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8168815

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00201671

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

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