Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific (Q28295563)

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English	Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific	scientific article

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title

Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific (English)

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author name string

Isao Yuasa

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1

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Mayumi Nakagawa

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2

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Kazuo Umetsu

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3

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Shinji Harihara

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4

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Aya Matsusue

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5

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Hiroaki Nishimukai

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6

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Yasuo Fukumori

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7

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Naruya Saitou

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8

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Kyung Sook Park

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9

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Feng Jin

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10

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Gérard Lucotte

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11

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Prasanta K Chattopadhyay

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12

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Lotte Henke

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13

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Jürgen Henke

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14

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language of work or name

English

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publication date

2008

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published in

Journal of Human Genetics

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volume

53

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issue

11-12

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page(s)

1016-21

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cites work

Characterization of primary amino acid sequence of human complement control protein factor I from an analysis of cDNA clones

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Crossref

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https://api.crossref.org/works/10.1007%2FS10038-008-0337-4

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21 January 2018

Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic origins of the Japanese: a partial support for the dual structure hypothesis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of action of the C3b inactivator: Requiremen for a high molecular weight cofactor (C3b-C4bINA cofactor) and production of a new C3b derivative (C3b′)

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of hereditary complement factor I deficiency

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Male demography in East Asia: a north-south contrast in human population expansion times

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor I (C3b inactivator) polymorphism among five populations in Eurasia

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Arlequin (version 3.0): an integrated software package for population genetics data analysis

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biosynthesis and postsynthetic processing of human C3b/C4b inactivator (factor I) in three hepatoma cell lines

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of the human complement factor I gene to 4q25

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The organization of the human complement factor I gene (IF): a member of the serine protease gene family

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human complement C3b inactivator: isolation, characterization, and demonstration of an absolute requirement for the serum protein beta1H for cleavage of C3b and C4b in solution

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial genome variation in eastern Asia and the peopling of Japan

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of homozygous hereditary factor I deficiency

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fusion gene at the ABO-secretor locus (FUT2): absence in Chinese populations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphism of human factor I (C3b inactivator)

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amplified product length polymorphism (APLP): a novel strategy for genotyping the ABO blood group

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

OCA2 481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations.

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human complement factor I: analysis of cDNA-derived primary structure and assignment of its gene to chromosome 4

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor I reference typing report

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of alpha 2HS-glycoprotein phenotypes by isoelectric focusing and immunoblotting: polymorphic occurrence of HSGA*5 in Okinawa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphism of human complement factor I (C3b inactivator) in the Chinese Han population

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18825487

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S10038-008-0337-4

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PubMed publication ID

18825487

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ResearchGate publication ID

23287592

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