Increased PiZ gene frequency for alpha 1 antitrypsin in patients with genetic haemochromatosis - Wikidata - awgldk - TriplyDB

Increased PiZ gene frequency for alpha 1 antitrypsin in patients with genetic haemochromatosis

Increased PiZ gene frequency for alpha 1 antitrypsin in patients with genetic haemochromatosis

http://www.wikidata.org/entity/Q34408182

about

Expression of hereditary hemochromatosis C282Y HFE protein in HEK293 cells activates specific endoplasmic reticulum stress responses.Impaired hepcidin expression in alpha-1-antitrypsin deficiency associated with iron overload and progressive liver disease.American Thoracic Society/European Respiratory Society statement: standards for the diagnosis and management of individuals with alpha-1 antitrypsin deficiency.

P2860

Q33291582-41FAA7D4-6481-4895-9160-D379E69E4CE6 Q36142416-631DCD2F-AD80-4E89-A798-4851614148B4 Q51651054-EE4F6C2A-774E-4CB8-BB7D-A6D788BEA48F

P2860

Increased PiZ gene frequency for alpha 1 antitrypsin in patients with genetic haemochromatosis

http://www.wikidata.org/entity/Q34408182

description

1995 nî lūn-bûn

@nan

1995 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

1995 թվականի հունիսին հրատարակված գիտական հոդված

@hy

1995年の論文

@ja

1995年論文

@yue

1995年論文

@zh-hant

1995年論文

@zh-hk

1995年論文

@zh-mo

1995年論文

@zh-tw

1995年论文

@wuu

name

Increased PiZ gene frequency f ...... with genetic haemochromatosis

@ast

Increased PiZ gene frequency f ...... with genetic haemochromatosis

@en

Increased PiZ gene frequency f ...... with genetic haemochromatosis

@nl

type

label

Increased PiZ gene frequency f ...... with genetic haemochromatosis

@ast

Increased PiZ gene frequency f ...... with genetic haemochromatosis

@en

Increased PiZ gene frequency f ...... with genetic haemochromatosis

@nl

prefLabel

Increased PiZ gene frequency f ...... with genetic haemochromatosis

@ast

Increased PiZ gene frequency f ...... with genetic haemochromatosis

@en

Increased PiZ gene frequency f ...... with genetic haemochromatosis

@nl

P1433

Q34408182-CD1A81AE-65E1-4AD7-BB99-642927265AD6

P1476

Q34408182-FB9F837F-C7A1-42CB-9B65-2792235E653F

P2093

Q34408182-0405617B-B3CC-445F-93E4-09C251273644

Q34408182-41CD9572-C241-48FE-8923-464306390EF6

Q34408182-79C76E90-BDA4-4892-AF0B-CD1B2A242888

Q34408182-A4C3437E-2914-4ED2-8E2D-B704D50BBCBA

Q34408182-B0638730-DB70-4CC9-96A8-7A2600352057

P2860

Q34408182-0AEB82E0-4856-4BDE-A954-8557C1010875

Q34408182-0F8D0FE1-2609-464A-BFBE-434202ED579F

Q34408182-2ABBAE37-21E8-4D44-9445-45EC37B71710

Q34408182-3FEB924B-C6DB-4E26-9348-D173C7B205F2

Q34408182-5FE2C765-B6E7-42EB-96AE-2AAE50A8B0F6

Q34408182-650CD61B-13E9-4E81-9321-920386441957

Q34408182-654C46D9-95E4-4A02-82CB-74638B251688

Q34408182-70295458-6EF7-40D2-8039-EE9FE7C58E2D

Q34408182-790C9302-055A-4933-88CF-25A02E460BFC

Q34408182-8927CEAA-6F3B-4E03-A70E-5E8C7F31DD9A

P304

Q34408182-7B7F19CE-B4CD-49D2-B8F1-AA3586DE7E3B

P31

Q34408182-BB9F2F5A-4607-4CDA-9A44-F390C077DE12

P356

Q34408182-9EC74757-C142-41D9-A0F0-74F270D2C8AC

P407

Q34408182-2D5210F0-10D9-441E-933E-669CFBE23F0A

P433

Q34408182-45D4DFEB-9934-4274-9D92-226032B3774F

P478

Q34408182-D51CB8A0-BE94-45EC-98F2-407BEF2EA962

P577

Q34408182-C73A786D-3F71-4BEC-879C-DE37E4EDB253

P5875

Q34408182-34254C0F-7308-4844-9CE0-4A6E3EE768F9

P698

Q34408182-CB480016-12B6-4C97-A798-F65A37A4A2BD

P932

Q34408182-311272D6-45C7-4338-8742-8DD2C854A0D8

P356

P1433

P1476

Increased PiZ gene frequency f ...... with genetic haemochromatosis

@en

P2093

Befrits R

http://www.w3.org/2001/XMLSchema#string

Elzouki AN

http://www.w3.org/2001/XMLSchema#string

Eriksson S

http://www.w3.org/2001/XMLSchema#string

Hultcrantz R

http://www.w3.org/2001/XMLSchema#string

Stål P

http://www.w3.org/2001/XMLSchema#string

P2860

Human alpha 1-proteinase inhibitor. Crystal structure analysis of two crystal modifications, molecular model and preliminary analysis of the implications for function.

Idiopathic hemochromotosis and alpha-1-antitrypsin deficiency: coexistence in a family with progressive liver disease in the proband

Accumulation of PiZ alpha 1-antitrypsin causes liver damage in transgenic mice.

Molecular basis for defective secretion of the Z variant of human alpha-1-proteinase inhibitor: secretion of variants having altered potential for salt bridge formation between amino acids 290 and 342.

Monoclonal antibody specific for the mutant PiZ alpha 1-antitrypsin and its application in an ELISA procedure for identification of PiZ gene carriers.

The cellular basis for liver injury in alpha 1-antitrypsin deficiency.

Simultaneous spectrophotometry of Fe2+ and Cu2+ in serum denatured with guanidine hydrochloride.

Prevalence of hereditary haemochromatosis in two Swedish urban areas.

Microdroplet testing for HLA-A, -B, -C, and -D antigens. The Phillip Levine Award Lecture.

Molecular basis of alpha-1-antitrypsin deficiency.

P304

922-926

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1136/GUT.36.6.922

http://www.w3.org/2001/XMLSchema#string

P407

P433

6

http://www.w3.org/2001/XMLSchema#string

P478

36

http://www.w3.org/2001/XMLSchema#string

P577

1995-06-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

15584431

http://www.w3.org/2001/XMLSchema#string

P698

7615285

http://www.w3.org/2001/XMLSchema#string

P932

1382634

http://www.w3.org/2001/XMLSchema#string