Genetic deficiencies of complement. - Wikidata - awgldk - TriplyDB

Genetic deficiencies of complement.

Genetic deficiencies of complement.

http://www.wikidata.org/entity/Q40921504

about

Genetic deficiencies of complement.

http://www.wikidata.org/entity/Q40921504

description

1995 nî lūn-bûn

@nan

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

1995年论文

@zh

1995年论文

@zh-cn

name

Genetic deficiencies of complement.

@en

type

label

Genetic deficiencies of complement.

@en

prefLabel

Genetic deficiencies of complement.

@en

P1433

Q40921504-30DA14B3-B19A-4A67-92FC-4E8885F0CCCE

P1476

Q40921504-1744D38C-2A3A-41E3-A55F-C8F8B57E3A44

P2093

Q40921504-3A4AA649-64A2-4540-9115-3E1E5BA61DBF

Q40921504-C58700C9-BE5B-4954-A608-BA49AF824776

P2860

Q40921504-0B52B5CD-E6DC-4776-A39E-D8D52352363E

Q40921504-171A6CC7-8470-49E7-90B5-BF3836F4AA7E

Q40921504-1920B714-0910-4EE2-B01C-1FE3A01AEB8D

Q40921504-1ADD7495-C181-43BD-9D97-96DF744EB675

Q40921504-1F863888-367D-448F-B039-CB9E5D737E4F

Q40921504-2154695C-747E-416D-A6DD-17955887197F

Q40921504-37E82080-F60F-4A8B-8AAB-28F9D051DF7C

Q40921504-385BFB1D-9727-49F9-96C7-A3CA267DEF30

Q40921504-425AC6FF-4372-4157-A8E4-50504D370ADA

Q40921504-450D5FBE-0EAF-4BAF-AB43-10F8A5839A72

P304

Q40921504-E425B9D0-0CA0-42DE-BE42-C81BC115D07D

P31

Q40921504-830E7ED5-5661-42EE-986F-F214922429D2

P356

Q40921504-C5E56D6A-23CA-4F8B-A90E-B60F8AD2BC89

P407

Q40921504-7D00C886-FFD9-4F07-959F-FAF7F24B04D5

P433

Q40921504-5DC3F1EB-ED2D-49DE-9F91-327C7A30D3CA

P478

Q40921504-7465C38C-2017-4DA5-A310-1687DE97EF2B

P577

Q40921504-F62C6201-CA36-4169-9284-3C97F3FF8ADA

P698

Q40921504-85C8D812-2076-4CAD-A978-47D18EAB7975

P356

07853899709002453

P1433

Annals of Medicine

P1476

Genetic deficiencies of complement.

@en

P2093

Colten HR

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

Lokki ML

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

P2860

Substitution of a single amino acid (aspartic acid for histidine) converts the functional activity of human complement C4B to C4A

Assignment of the complement serine protease genes C1r and C1s to chromosome 12 region 12p13

A variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirus

Complement factor H and related proteins: an expanding family of complement-regulatory proteins?

A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B

Cell-free synthesis of the fourth component of guinea pig complement (C4): identification of a precursor of serum C4 (pro-C4)

Molecular organization and function of the complement system

A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes)

Homozygous hereditary C3 deficiency due to a partial gene deletion.

P304

451-459

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

P31

scholarly article

P356

10.3109/07853899709002453

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

P407

P433

4

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

P478

27

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

P577

1995-08-01T00:00:00Z

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

P698

8519506

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