Biochemical characterization of a disease-causing human osteoprotegerin variant
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2045-2322
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Biochemical characterization of a disease-causing human osteoprotegerin variant ; volume:12 ; number:1 ; day:10 ; month:9 ; year:2022 ; pages:1-12 ; date:12.2022
Scientific reports ; 12, Heft 1 (10.9.2022), 1-12, 12.2022
- Urheber
-
Luo, Yin
Li, Miaomiao
Xu, Ding
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1038/s41598-022-19522-9
- URN
-
urn:nbn:de:101:1-2022112821253921177984
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:22 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Luo, Yin
- Li, Miaomiao
- Xu, Ding
- SpringerLink (Online service)
Ähnliche Objekte (12)
AIP variant causing familial prolactinoma
E148Q variant: a familial Mediterranean fever-causing mutation or a sequence variant?
MDVarP: modifier ~ disease-causing variant pairs predictor
Clinical and functional characterization of p.Lys322stop variant in the SERPINC1 gene causing severe thrombophilia
Therapeutic implications of osteoprotegerin
A genetic variant in osteoprotegerin is associated with progression of joint destruction in rheumatoid arthritis
Micro- and macroadenomas causing primary aldosteronism: molecular and biochemical studies
Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy
Homozygous EPRS1 missense variant causing hypomyelinating leukodystrophy-15 alters variant-distal mRNA m6A site accessibility
Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variant
Heterozygous missense variant in the TTN gene causing Tibial muscular dystrophy
Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variant
AIP variant causing familial prolactinoma
E148Q variant: a familial Mediterranean fever-causing mutation or a sequence variant?
MDVarP: modifier ~ disease-causing variant pairs predictor
Clinical and functional characterization of p.Lys322stop variant in the SERPINC1 gene causing severe thrombophilia
Therapeutic implications of osteoprotegerin
A genetic variant in osteoprotegerin is associated with progression of joint destruction in rheumatoid arthritis
Micro- and macroadenomas causing primary aldosteronism: molecular and biochemical studies
Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy
Homozygous EPRS1 missense variant causing hypomyelinating leukodystrophy-15 alters variant-distal mRNA m6A site accessibility
Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variant
Heterozygous missense variant in the TTN gene causing Tibial muscular dystrophy
Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variant
AIP variant causing familial prolactinoma
E148Q variant: a familial Mediterranean fever-causing mutation or a sequence variant?
MDVarP: modifier ~ disease-causing variant pairs predictor
Clinical and functional characterization of p.Lys322stop variant in the SERPINC1 gene causing severe thrombophilia
Therapeutic implications of osteoprotegerin
A genetic variant in osteoprotegerin is associated with progression of joint destruction in rheumatoid arthritis
Micro- and macroadenomas causing primary aldosteronism: molecular and biochemical studies
Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy
Homozygous EPRS1 missense variant causing hypomyelinating leukodystrophy-15 alters variant-distal mRNA m6A site accessibility
Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variant
Heterozygous missense variant in the TTN gene causing Tibial muscular dystrophy