(Q47631846)

4 February 2018

title

Nonspecific interstitial pneumonia and usual interstitial pneumonia with mutation in surfactant protein C in familial pulmonary fibrosis (English)

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4 February 2018

nonspecific interstitial pneumonia

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usual interstitial pneumonia

inferred from title

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Rajni Chibbar

1

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4 February 2018

Francis Shih

2

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4 February 2018

Monica Baga

3

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4 February 2018

Emina Torlakovic

4

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4 February 2018

Kumar Ramlall

5

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4 February 2018

Robert Skomro

6

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4 February 2018

Donald W Cockcroft

7

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4 February 2018

Edmond G Lemire

8

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4 February 2018

publication date

1 August 2004

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4 February 2018

published in

Modern Pathology

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4 February 2018

volume

17

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4 February 2018

issue

8

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4 February 2018

page(s)

973-980

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4 February 2018

https://scigraph.springernature.com/pub.10.1038/modpathol.3800149

exact match

0 references

cites work

Fibrosing alveolitis in infancy and childhood

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

Adult familial cryptogenic fibrosing alveolitis in the United Kingdom

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

A mutation in the surfactant protein C gene associated with familial interstitial lung disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

Synthetic processing of surfactant protein C by alevolar epithelial cells. The COOH terminus of proSP-C is required for post-translational targeting and proteolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

Secretion of surfactant protein C, an integral membrane protein, requires the N-terminal propeptide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

Deletion of exon 4 from human surfactant protein C results in aggresome formation and generation of a dominant negative

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

Alpha1-antitrypsin deficiency--a model for conformational diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

A cellular mechanism governing the severity of Pelizaeus-Merzbacher disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

PMP22 accumulation in aggresomes: implications for CMT1A pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

Idiopathic pulmonary fibrosis: clinical relevance of pathologic classification

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

Nonspecific interstitial pneumonia. Individualization of a clinicopathologic entity in a series of 12 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

Familial idiopathic pulmonary fibrosis. Evidence of lung inflammation in unaffected family members

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

7 January 2021

Usual interstitial pneumonitis in infancy. Clinical and pathologic evaluation

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

7 January 2021

Mutations in the surfactant protein C gene associated with interstitial lung disease

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

7 January 2021

The C-terminal domain of the pulmonary surfactant protein C precursor contains signals for intracellular targeting

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

7 January 2021

The natural history of liver disease in alpha 1-antitrypsin deficient children

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

7 January 2021

A histologic pattern of nonspecific interstitial pneumonia is associated with a better prognosis than usual interstitial pneumonia in patients with cryptogenic fibrosing alveolitis

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

7 January 2021

Histopathologic variability in usual and nonspecific interstitial pneumonias

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

7 January 2021

Usual interstitial pneumonia: histologic study of biopsy and explant specimens

1 reference

https://api.crossref.org/works/10.1038%2FMODPATHOL.3800149

7 January 2021

10.1038/MODPATHOL.3800149

Identifiers

DOI

1 reference

4 February 2018

1 reference

4 February 2018