Transient surfactant protein B deficiency in a term infant with severe respiratory failure (Q56960293)

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10 November 2019

title

Transient surfactant protein B deficiency in a term infant with severe respiratory failure (English)

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10 November 2019

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1

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10 November 2019

Edward F Bell

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10 November 2019

Paul B McCray

7

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10 November 2019

author name string

M W Thompson

2

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10 November 2019

J M Snyder

3

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10 November 2019

T N George

4

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10 November 2019

J A Whitsett

5

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10 November 2019

L M Nogee

8

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10 November 2019

language of work or name

English

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publication date

1 February 1998

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The Journal of Pediatrics

10 November 2019

published in

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10 November 2019

volume

132

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10 November 2019

issue

2

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10 November 2019

page(s)

244-248

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Function and regulation of expression of pulmonary surfactant-associated proteins

10 November 2019

cites work

1 reference

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Human surfactant protein B: structure, function, regulation, and genetic disease

7 January 2021

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Molecular and phenotypic variability in the congenital alveolar proteinosis syndrome associated with inherited surfactant protein B deficiency

7 January 2021

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Brief report: deficiency of pulmonary surfactant protein B in congenital alveolar proteinosis

7 January 2021

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Surfactant protein B deficiency: antenatal diagnosis and prospective treatment with surfactant replacement

7 January 2021

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A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindreds

7 January 2021

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Targeted disruption of the surfactant protein B gene disrupts surfactant homeostasis, causing respiratory failure in newborn mice

7 January 2021

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Localization of epidermal growth factor receptor in alveolar epithelium during human fetal lung development in vitro

7 January 2021

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Inhibition of tyrosine kinase activity decreases expression of surfactant protein A in a human lung adenocarcinoma cell line independent of epidermal growth factor receptor

7 January 2021

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Isolation and partial characterization of human low molecular weight protein associated with pulmonary surfactant

7 January 2021

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A simple salting out procedure for extracting DNA from human nucleated cells

7 January 2021

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Molecular basis of cystathionine beta-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuria

7 January 2021

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Cytochrome c oxidase mutations in Leber hereditary optic neuropathy

7 January 2021

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Characterization of three osteogenesis imperfecta collagen alpha 1(I) glycine to serine mutations demonstrating a position-dependent gradient of phenotypic severity

7 January 2021

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Substitution of aspartic acid for glycine at position 310 in type II collagen produces achondrogenesis II, and substitution of serine at position 805 produces hypochondrogenesis: analysis of genotype-phenotype relationships

7 January 2021

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Dinucleotide repeats in the human surfactant protein-B gene and respiratory-distress syndrome

7 January 2021

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Surfactant chemical composition and biophysical activity in acute respiratory distress syndrome

7 January 2021

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10.1016/S0022-3476(98)70439-1

7 January 2021

Identifiers

DOI

1 reference

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10 November 2019

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