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1.
Regulatory myeloid cells paralyze T cells through cell-cell transfer of the metabolite methylglyoxal.
Nat Immunol
; 21(5): 555-566, 2020 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-32327756
2.
Comparison of post-COVID-19 symptoms in patients infected with the SARS-CoV-2 variants delta and omicron-results of the Cross-Sectoral Platform of the German National Pandemic Cohort Network (NAPKON-SUEP).
Infection
; 2024 May 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-38700656
3.
Analysis of acute COVID-19 including chronic morbidity: protocol for the deep phenotyping National Pandemic Cohort Network in Germany (NAPKON-HAP).
Infection
; 52(1): 93-104, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-37434025
4.
Persistent symptoms and risk factors predicting prolonged time to symptom-free after SARSCoV2 infection: an analysis of the baseline examination of the German COVIDOM/NAPKON-POP cohort.
Infection
; 51(6): 1679-1694, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-37231313
5.
Ethical and coordinative challenges in setting up a national cohort study during the COVID-19 pandemic in Germany.
BMC Med Ethics
; 24(1): 84, 2023 10 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-37848886
6.
Systemic Jak1 activation provokes hepatic inflammation and imbalanced FGF23 production and cleavage.
FASEB J
; 35(2): e21302, 2021 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33475190
7.
The German National Pandemic Cohort Network (NAPKON): rationale, study design and baseline characteristics.
Eur J Epidemiol
; 37(8): 849-870, 2022 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-35904671
8.
Diagnostic exome sequencing in non-acquired focal epilepsies highlights a major role of GATOR1 complex genes.
J Med Genet
; 57(9): 624-633, 2020 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-32086284
9.
Mitochondrial DNA mutation analysis from exome sequencing-A more holistic approach in diagnostics of suspected mitochondrial disease.
J Inherit Metab Dis
; 42(5): 909-917, 2019 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-31059585
10.
The elevation of circulating fibroblast growth factor 23 without kidney disease does not increase cardiovascular disease risk.
Kidney Int
; 94(1): 49-59, 2018 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-29735309
11.
Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island.
Am J Hum Genet
; 96(5): 826-31, 2015 May 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-25913036
12.
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.
Mamm Genome
; 27(3-4): 111-21, 2016 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-26803617
13.
Viable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation.
Mamm Genome
; 27(11-12): 587-598, 2016 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-27671791
14.
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis.
Nat Genet
; 38(11): 1248-50, 2006 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-17033625
15.
An ENU mutagenesis-derived mouse model with a dominant Jak1 mutation resembling phenotypes of systemic autoimmune disease.
Am J Pathol
; 183(2): 352-68, 2013 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-23791841
16.
Unusually severe hypophosphatemic rickets caused by a novel and complex re-arrangement of the PHEX gene.
Am J Med Genet A
; 164A(11): 2931-7, 2014 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-25124877
17.
Depression and fatigue six months post-COVID-19 disease are associated with overlapping symptom constellations: A prospective, multi-center, population-based cohort study.
J Affect Disord
; 352: 296-305, 2024 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38360365
18.
Development of a long noncoding RNA-based machine learning model to predict COVID-19 in-hospital mortality.
Nat Commun
; 15(1): 4259, 2024 May 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-38769334
19.
Loss-of-function ENPP1 mutations cause both generalized arterial calcification of infancy and autosomal-recessive hypophosphatemic rickets.
Am J Hum Genet
; 86(2): 267-72, 2010 Feb 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-20137773
20.
The Importance of Being FAIR and FAST - The Clinical Epidemiology and Study Platform of the German Network University Medicine (NUKLEUS).
Stud Health Technol Inform
; 302: 93-97, 2023 May 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-37203616