(Q41135275)

27 September 2017

A novel transcription factor regulates expression of the vacuolar H+-ATPase B2 subunit through AP-2 sites during monocytic differentiation (English)

1 reference

27 September 2017

Lee BS

1

1 reference

27 September 2017

Krits I

series ordinal

2

1 reference

27 September 2017

Crane-Zelkovic MK

series ordinal

3

1 reference

27 September 2017

Gluck SL

series ordinal

4

1 reference

27 September 2017

language of work or name

English

0 references

publication date

1 January 1997

1 reference

Journal of Biological Chemistry

27 September 2017

1 reference

27 September 2017

272

1 reference

27 September 2017

1

1 reference

27 September 2017

174-181

1 reference

Implications of the three-dimensional structure of alpha 1-antitrypsin for structure and function of serpins

27 September 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

The alpha 1-antitrypsin gene and its deficiency states

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Antielastases of the human alveolar structures. Implications for the protease-antiprotease theory of emphysema

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

What do dysfunctional serpins tell us about molecular mobility and disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

The mechanism of Z alpha 1-antitrypsin accumulation in the liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

alpha 1-Antitrypsin Mmalton (Phe52-deleted) forms loop-sheet polymers in vivo. Evidence for the C sheet mechanism of polymerization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Mutations which impede loop/sheet polymerization enhance the secretion of human alpha 1-antitrypsin deficiency variants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

The biostructural pathology of the serpins: critical function of sheet opening mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Rapid and efficient site-specific mutagenesis without phenotypic selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Intracellular precursors and secretion of alkaline extracellular protease of Yarrowia lipolytica

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Quality control in the secretory pathway: retention of a misfolded viral membrane glycoprotein involves cycling between the ER, intermediate compartment, and Golgi apparatus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

The Z type variation of human alpha 1-antitrypsin causes a protein folding defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

A lag in intracellular degradation of mutant alpha 1-antitrypsin correlates with the liver disease phenotype in homozygous PiZZ alpha 1-antitrypsin deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

The endoplasmic reticulum degradation pathway for mutant secretory proteins alpha1-antitrypsin Z and S is distinct from that for an unassembled membrane protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Selective protein degradation in the yeast exocytic pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Quality control in the endoplasmic reticulum: folding and misfolding of vesicular stomatitis virus G protein in cells and in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Role of N-linked oligosaccharide recognition, glucose trimming, and calnexin in glycoprotein folding and quality control

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Association of folding intermediates of glycoproteins with calnexin during protein maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Defective protein folding as a basis of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Probing the native strain iin alpha1-antitrypsin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

High-level secretion of human alpha 1-antitrypsin from Saccharomyces cerevisiae using inulinase signal sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

A thermostable mutation located at the hydrophobic core of alpha 1-antitrypsin suppresses the folding defect of the Z-type variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Defective protein folding as a cause of disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Effect of the Z mutation on the physical and inhibitory properties of alpha 1-antitrypsin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

Specificity of abnormal assembly in immunoglobulin light chain deposition disease and amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.1.510

21 January 2018

Identifiers

DOI

10.1074/JBC.272.1.510

1 reference

27 September 2017

1 reference