HB Mississippi [β44(CD3)SeråG]: A New Variant with Anomalous Properties

about

HB Mississippi [β44(CD3)SeråG]: A New Variant with Anomalous Properties

Item

http://www.wikidata.org/entity/Q57625328

description

im Jahr 1987 veröffentlichter wissenschaftlicher Artikel

@de

scientific article published on 01 January 1987

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована в січні 1987

@uk

name

HB Mississippi [β44

@nl

HB Mississippi [β44(CD3)SeråG]: A New Variant with Anomalous Properties

@en

type

Item

label

HB Mississippi [β44

@nl

HB Mississippi [β44(CD3)SeråG]: A New Variant with Anomalous Properties

@en

prefLabel

HB Mississippi [β44

@nl

HB Mississippi [β44(CD3)SeråG]: A New Variant with Anomalous Properties

@en

P1476

Hb Mississippi [beta 44(CD3)Ser----Arg]: a new variant with anomalous properties

@en

P2093

J G Adams

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

R L Barlow

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

W T Morrison

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

P2860

Mutations in collagen genes. Consequences for rare and common diseases

Human insulin B24 (Phe----Ser). Secretion and metabolic clearance of the abnormal insulin in man and in a dog model.

Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).

alpha-Thalassemia caused by an unstable alpha-globin mutant.

Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in a patient with the Lesch-Nyhan syndrome

A single amino Acid substitution (asparagine to aspartic Acid) between normal (b+) and the common negro variant (a+) of human glucose-6-phosphate dehydrogenase

Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia.

Identification of the molecular defect in factor IX Chapel Hill: substitution of histidine for arginine at position 145.

Hb Long Island: a hemoglobin variant with a methionyl extension at the NH2 terminus and a prolyl substitution for the normal histidyl residue 2 of the beta chain

Amino-terminal processing of proteins: hemoglobin South Florida, a variant with retention of initiator methionine and N alpha-acetylation.

P304

435-452

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

P31

scholarly article

P356

10.3109/03630268708998004

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

P433

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

P478

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

P50

Martin H Steinberg

P577

1987-01-01T00:00:00Z

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

P698

3429243

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