UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 185

Sortiert nach

Mutations of KIF14 cause primary microcephaly by impairing cytokinesis

Annals of neurology, 2017-10, Vol.82 (4), p.562-577

2017

Volltextzugriff (PDF)

Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy

Nature communications, 2020-07, Vol.11 (1), p.3698-3698, Article 3698

2020

Volltextzugriff (PDF)

A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative features

Human genomics, 2018-03, Vol.12 (1), p.11-11, Article 11

2018

Volltextzugriff (PDF)

Diet of the brown bear in Himalaya: Combining classical and molecular genetic techniques

PloS one, 2019-12, Vol.14 (12), p.e0225698-e0225698

2019

Volltextzugriff (PDF)

A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family

BMC medical genetics, 2017-04, Vol.18 (1), p.42-42, Article 42

2017

Volltextzugriff (PDF)

Segment IV hepatic artery in potential donors for living related liver transplantation: Evaluation with multi-detector CT

Journal of the Pakistan Medical Association, 2019-06, Vol.69 (6), p.799-805

2019

Volltextzugriff (PDF)

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

The Journal of clinical investigation, 2020-01, Vol.130 (1), p.108-125

2020

Volltextzugriff (PDF)

Novel SACS mutations associated with intellectual disability, epilepsy and widespread supratentorial abnormalities

Journal of the neurological sciences, 2016-12, Vol.371, p.105-111

2016

Volltextzugriff (PDF)

A missense variant in ITPR1 provides evidence for autosomal recessive SCA29 with asymptomatic cerebellar hypoplasia in carriers

European journal of human genetics : EJHG, 2017-06, Vol.25 (7), p.848-853

2017

Volltextzugriff (PDF)

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

American journal of human genetics, 2017-11, Vol.101 (5), p.789-802

2017

Volltextzugriff (PDF)

A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family

British journal of dermatology (1951), 2018-02, Vol.178 (2), p.556-558

2018

Volltextzugriff (PDF)

Viral load speaks little about toll on liver

Hepatobiliary & pancreatic diseases international, 2007-10, Vol.6 (5), p.483-486

2007

Volltextzugriff (PDF)

Genetics of human Bardet-Biedl syndrome, an updates

Clinical genetics, 2016-07, Vol.90 (1), p.3-15

2016

Volltextzugriff (PDF)

Significant Effects of Oral Phenylbutyrate and Vitamin D3 Adjunctive Therapy in Pulmonary Tuberculosis: A Randomized Controlled Trial

PloS one, 2015-09, Vol.10 (9), p.e0138340-e0138340

2015

Volltextzugriff (PDF)

LPS/TLR4 Pathways in Breast Cancer: Insights into Cell Signalling

Current medicinal chemistry, 2022-01, Vol.29 (13), p.2274

2022

Volltextzugriff (PDF)

Post-discharge quality of life of COVID-19 patients at 1-month follow-up: A cross-sectional study in the largest tertiary care hospital of Bangladesh

PloS one, 2023-01, Vol.18 (1), p.e0280882-e0280882

2023

Volltextzugriff (PDF)

Mycobacterium avium subsp. paratuberculosis and microbiome profile of patients in a referral gastrointestinal diseases centre in the Sudan

PloS one, 2022-04, Vol.17 (4), p.e0266533-e0266533

2022

Volltextzugriff (PDF)

Roosting ecology and morphometric analysis of Pteropus medius (Indian flying fox) in Lower Dir, district, Pakistan

Brazilian journal of biology, 2021, Vol.81 (1), p.77-82

2021

Volltextzugriff (PDF)

Smokeless tobacco ( paan and gutkha ) consumption, prevalence, and contribution to oral cancer

Epidemiology and Health, 2017, 39(0), , pp.1-11

2017

Volltextzugriff (PDF)

Prevention of Intraoperative Awareness in a High-Risk Surgical Population

The New England journal of medicine, 2011-08, Vol.365 (7), p.591-600

2011

Volltextzugriff (PDF)

Bariatric surgery for patients with type 2 diabetes mellitus requiring insulin: Clinical outcome and cost-effectiveness analyses

PLoS medicine, 2020-12, Vol.17 (12), p.e1003228-e1003228

2020

Volltextzugriff (PDF)

Characteristics and Predictors of Missed Opportunities in Lung Cancer Diagnosis: An Electronic Health Record–Based Study

Journal of clinical oncology, 2010-07, Vol.28 (20), p.3307-3315

2010

Volltextzugriff (PDF)

Alarming multidrug resistance in Staphylococcus aureus isolated from raw milk of cows with subclinical mastitis: Antibiotic resistance patterns and occurrence of selected resistance genes

PloS one, 2024-05, Vol.19 (5), p.e0301200-e0301200

2024

Volltextzugriff (PDF)

1 – 25 von 185

Suche als RSS-Feed

Aktive Filter

SpracheEnglisch

ThemaFemale

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(141)
Mit Volltextzugriff
(158)

Publikationsform

Artikel
(185)

Sprache

Japanisch
(12)
Portugiesisch
(4)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mutations of KIF14 cause primary microcephaly by impairing cytokinesis

Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy

A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative features

Diet of the brown bear in Himalaya: Combining classical and molecular genetic techniques

A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family

Segment IV hepatic artery in potential donors for living related liver transplantation: Evaluation with multi-detector CT

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

Novel SACS mutations associated with intellectual disability, epilepsy and widespread supratentorial abnormalities

Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies

A missense variant in ITPR1 provides evidence for autosomal recessive SCA29 with asymptomatic cerebellar hypoplasia in carriers

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia

A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family

Viral load speaks little about toll on liver

Genetics of human Bardet-Biedl syndrome, an updates

Significant Effects of Oral Phenylbutyrate and Vitamin D3 Adjunctive Therapy in Pulmonary Tuberculosis: A Randomized Controlled Trial

LPS/TLR4 Pathways in Breast Cancer: Insights into Cell Signalling

Post-discharge quality of life of COVID-19 patients at 1-month follow-up: A cross-sectional study in the largest tertiary care hospital of Bangladesh

Mycobacterium avium subsp. paratuberculosis and microbiome profile of patients in a referral gastrointestinal diseases centre in the Sudan

Roosting ecology and morphometric analysis of Pteropus medius (Indian flying fox) in Lower Dir, district, Pakistan

Smokeless tobacco ( paan and gutkha ) consumption, prevalence, and contribution to oral cancer

Prevention of Intraoperative Awareness in a High-Risk Surgical Population

Bariatric surgery for patients with type 2 diabetes mellitus requiring insulin: Clinical outcome and cost-effectiveness analyses

Characteristics and Predictors of Missed Opportunities in Lung Cancer Diagnosis: An Electronic Health Record–Based Study

Alarming multidrug resistance in Staphylococcus aureus isolated from raw milk of cows with subclinical mastitis: Antibiotic resistance patterns and occurrence of selected resistance genes

Aktive Filter

Suchergebnisse filtern