UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 95

Sortiert nach

Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population

Human genetics, 2021-03, Vol.140 (3), p.505-528

2021

Link zum Volltext

Verfügbarkeit prüfen

The salivary microbiome is altered in the presence of a high salivary glucose concentration

PloS one, 2017-03, Vol.12 (3), p.e0170437-e0170437

2017

Link zum Volltext

Verfügbarkeit prüfen

Unraveling a fine-scale high genetic heterogeneity and recent continental connections of an Arabian Peninsula population

European journal of human genetics : EJHG, 2022-03, Vol.30 (3), p.307-319

2022

Link zum Volltext

Verfügbarkeit prüfen

Linkage analysis using whole exome sequencing data implicates SLC17A1, SLC17A3, TATDN2 and TMEM131L in type 1 diabetes in Kuwaiti families

Scientific reports, 2023-09, Vol.13 (1), p.14978-14978, Article 14978

2023

Link zum Volltext

Verfügbarkeit prüfen

Vitamin D insufficiency in Arabs and South Asians positively associates with polymorphisms in GC and CYP2R1 genes

PloS one, 2014-11, Vol.9 (11), p.e113102-e113102

2014

Link zum Volltext

Verfügbarkeit prüfen

Genetic risk variants for metabolic traits in Arab populations

Scientific reports, 2017-01, Vol.7 (1), p.40988-40988, Article 40988

2017

Link zum Volltext

Verfügbarkeit prüfen

Metabolic disease risk in children by salivary biomarker analysis

PloS one, 2014-06, Vol.9 (6), p.e98799-e98799

2014

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population

Journal of lipid research, 2018-10, Vol.59 (10), p.1951-1966

2018

Link zum Volltext

Verfügbarkeit prüfen

Factors that predict severity of infection and seroconversion in immunocompromised children and adolescents with COVID-19 infection

Frontiers in immunology, 2022-08, Vol.13, p.919762-919762

2022

Link zum Volltext

Verfügbarkeit prüfen

Genetic substructure of Kuwaiti population reveals migration history

PloS one, 2013-09, Vol.8 (9), p.e74913-e74913

2013

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population

Scientific reports, 2020-01, Vol.10 (1), p.152-152, Article 152

2020

Link zum Volltext

Verfügbarkeit prüfen

Impact of the SARS‐CoV‐2 pandemic on the overall respiratory viruses' transmission in a cancer care setting

Immunity, Inflammation and Disease, 2023-11, Vol.11 (11), p.e1073-n/a

2023

Link zum Volltext

Verfügbarkeit prüfen

Genome at juncture of early human migration: a systematic analysis of two whole genomes and thirteen exomes from Kuwaiti population subgroup of inferred Saudi Arabian tribe ancestry

PloS one, 2014-06, Vol.9 (6), p.e99069-e99069

2014

Link zum Volltext

Verfügbarkeit prüfen

Whole genome amplification from a single cell: a new era for preimplantation genetic diagnosis

Prenatal diagnosis, 2007-04, Vol.27 (4), p.297-302

2007

Link zum Volltext

Verfügbarkeit prüfen

A Review of Adult Obesity Prevalence, Trends, Risk Factors, and Epidemiologic Methods in Kuwait

Journal of Obesity, 2013-01, Vol.2013, p.378650-14

2013

Link zum Volltext

Verfügbarkeit prüfen

Continuous Metabolic Syndrome Scores for Children Using Salivary Biomarkers

PloS one, 2015-09, Vol.10 (9), p.e0138979-e0138979

2015

Link zum Volltext

Verfügbarkeit prüfen

Obesity and dental decay: inference on the role of dietary sugar

PloS one, 2013-10, Vol.8 (10), p.e74461-e74461

2013

Link zum Volltext

Verfügbarkeit prüfen

MC4R Variant rs17782313 Associates With Increased Levels of DNAJC27, Ghrelin, and Visfatin and Correlates With Obesity and Hypertension in a Kuwaiti Cohort

Frontiers in endocrinology (Lausanne), 2020-07, Vol.11, p.437-437

2020

Link zum Volltext

Verfügbarkeit prüfen

Investigation of genetic variation and lifestyle determinants in vitamin D levels in Arab individuals

Journal of translational medicine, 2018-01, Vol.16 (1), p.20-20, Article 20

2018

Link zum Volltext

Verfügbarkeit prüfen

Genetic and clinical characteristics of pediatric patients with familial hemophagocytic lymphohistiocytosis

Blood Research, 2021, 56(2), , pp.86-101

2021

Link zum Volltext

Verfügbarkeit prüfen

Exome sequencing for the differential diagnosis of ciliary chondrodysplasias: Example of a WDR35 mutation case and review of the literature

European journal of medical genetics, 2017-12, Vol.60 (12), p.658-666

2017

Link zum Volltext

Verfügbarkeit prüfen

Major Histocompatibility Complex Class II Deficiency in Kuwait: Clinical Manifestations, Immunological Findings and Molecular Profile

Journal of clinical immunology, 2013-04, Vol.33 (3), p.513-519

2013

Link zum Volltext

Verfügbarkeit prüfen

Caveolin-1 Variant Is Associated With the Metabolic Syndrome in Kuwaiti Children

Frontiers in genetics, 2018-12, Vol.9, p.689-689

2018

Link zum Volltext

Verfügbarkeit prüfen

Kuwaiti population subgroup of nomadic Bedouin ancestry—Whole genome sequence and analysis

Genomics data, 2015-03, Vol.3 (C), p.116-127

2015

Link zum Volltext

Verfügbarkeit prüfen

Corrigendum: Caveolin-1 Variant Is Associated With the Metabolic Syndrome in Kuwaiti Children

Frontiers in genetics, 2019-03, Vol.10, p.221-221

2019

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 95

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(88)
Mit Volltextzugriff
(89)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(59)
Life Sciences & Biomedicine
(46)
Humans
(43)
Male
(30)
Female
(27)
Obesity
(16)
Diabetes
(15)
Genetics & Heredity
(15)
Kuwait
(15)
Genomes
(13)
Middle Aged
(13)
Child
(12)
Genotype
(12)
Genetics
(11)
Multidisciplinary Sciences
(11)
Mutation
(11)
Science & Technology - Other Topics
(11)
Adolescent
(10)
Adult
(10)
Genetic Aspects
(10)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population

The salivary microbiome is altered in the presence of a high salivary glucose concentration

Unraveling a fine-scale high genetic heterogeneity and recent continental connections of an Arabian Peninsula population

Linkage analysis using whole exome sequencing data implicates SLC17A1, SLC17A3, TATDN2 and TMEM131L in type 1 diabetes in Kuwaiti families

Vitamin D insufficiency in Arabs and South Asians positively associates with polymorphisms in GC and CYP2R1 genes

Genetic risk variants for metabolic traits in Arab populations

Metabolic disease risk in children by salivary biomarker analysis

Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population

Factors that predict severity of infection and seroconversion in immunocompromised children and adolescents with COVID-19 infection

Genetic substructure of Kuwaiti population reveals migration history

Genome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population

Impact of the SARS‐CoV‐2 pandemic on the overall respiratory viruses' transmission in a cancer care setting

Genome at juncture of early human migration: a systematic analysis of two whole genomes and thirteen exomes from Kuwaiti population subgroup of inferred Saudi Arabian tribe ancestry

Whole genome amplification from a single cell: a new era for preimplantation genetic diagnosis

A Review of Adult Obesity Prevalence, Trends, Risk Factors, and Epidemiologic Methods in Kuwait

Continuous Metabolic Syndrome Scores for Children Using Salivary Biomarkers

Obesity and dental decay: inference on the role of dietary sugar

MC4R Variant rs17782313 Associates With Increased Levels of DNAJC27, Ghrelin, and Visfatin and Correlates With Obesity and Hypertension in a Kuwaiti Cohort

Investigation of genetic variation and lifestyle determinants in vitamin D levels in Arab individuals

Genetic and clinical characteristics of pediatric patients with familial hemophagocytic lymphohistiocytosis

Exome sequencing for the differential diagnosis of ciliary chondrodysplasias: Example of a WDR35 mutation case and review of the literature

Major Histocompatibility Complex Class II Deficiency in Kuwait: Clinical Manifestations, Immunological Findings and Molecular Profile

Caveolin-1 Variant Is Associated With the Metabolic Syndrome in Kuwaiti Children

Kuwaiti population subgroup of nomadic Bedouin ancestry—Whole genome sequence and analysis

Corrigendum: Caveolin-1 Variant Is Associated With the Metabolic Syndrome in Kuwaiti Children

Suchergebnisse filtern