(Q39352391)

English

Molecular basis of a new type of C1q-deficiency associated with a non-functional low molecular weight (LMW) C1q: parallels and differences to other known genetic C1q-defects

scientific article published on December 1997

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Molecular basis of a new type of C1q-deficiency associated with a non-functional low molecular weight (LMW) C1q: parallels and differences to other known genetic C1q-defects (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

author name string

Petry F

1

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Hauptmann G

2

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Goetz J

3

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Grosshans E

4

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Loos M

5

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

publication date

1 December 1997

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Immunopharmacology

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

38

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

1-2

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

189-201

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Enzyme-linked immunosorbent assay for C1q in human serum by use of monoclonal antibodies

1 reference

https://api.crossref.org/works/10.1016%2FS0162-3109%2897%2900065-9

7 January 2021

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Complete functional C1q deficiency associated with systemic lupus erythematosus (SLE)

1 reference

https://api.crossref.org/works/10.1016%2FS0162-3109%2897%2900065-9

7 January 2021

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Thalidomide as an anti-TNF-alpha inhibitor: implications for clinical use.

1 reference

https://api.crossref.org/works/10.1016%2FS0162-3109%2897%2900065-9

7 January 2021

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A homozygous point mutation results in a stop codon in the C1q B-chain of a C1q-deficient individual

1 reference

https://api.crossref.org/works/10.1016%2FS0162-3109%2897%2900065-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and functional analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0162-3109%2897%2900065-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization of a non-functional form of Clq found in patients with a genetically linked deficiency of Clq activity

1 reference

https://api.crossref.org/works/10.1016%2FS0162-3109%2897%2900065-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family

1 reference

https://api.crossref.org/works/10.1016%2FS0162-3109%2897%2900065-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0162-3109(97)00065-9

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

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