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Vestibular defects in head-tilt mice result from mutations in Nox3, encoding an NADPH oxidase

Genes & development, 2004-03, Vol.18 (5), p.486-491

2004

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Deletion Mapping of the Head Tilt (het) Gene in Mice: A Vestibular Mutation Causing Specific Absence of Otoliths

Genetics (Austin), 1998-10, Vol.150 (2), p.815-822

1998

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Mouse models for the Wolf-Hirschhorn deletion syndrome

Human molecular genetics, 2001-01, Vol.10 (2), p.91-98

2001

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Overlapping deletions spanning the proximal two-thirds of the mouse t complex

Mammalian genome, 2003-12, Vol.14 (12), p.817-829

2003

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Vestibular responses to linear acceleration are absent in otoconia-deficient C57BL/6JEi-het mice

Hearing research, 1999-09, Vol.135 (1-2), p.56-60

1999

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Identification of a cryptic lethal mutation in the mouse t(w73) haplotype

Genetical research, 2004-12, Vol.84 (3), p.153

2004

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Interdigitated deletion complexes on mouse chromosome 5 induced by irradiation of embryonic stem cells

Genome research, 2000-07, Vol.10 (7), p.1043

2000

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DelBank: a mouse ES-cell resource for generating deletions

Nature genetics, 2001-08, Vol.28 (4), p.310-311

2001

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Dynamics of sputum conversion during effective tuberculosis treatment: A systematic review and meta-analysis

PLoS medicine, 2021-04, Vol.18 (4), p.e1003566-e1003566

2021

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The Analgesic Effect of Oxygen in Suspected Acute Myocardial Infarction: A Substudy of the DETO2X-AMI Trial

JACC. Cardiovascular interventions, 2018-08, Vol.11 (16), p.1590-1597

2018

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Expanded HILUS Trial: A Pooled Analysis of Risk Factors for Toxicity From Stereotactic Body Radiation Therapy of Central and Ultracentral Lung Tumors

International journal of radiation oncology, biology, physics, 2023-12, Vol.117 (5), p.1222-1231

2023

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A randomized controlled trial in schools aimed at exploring mechanisms of change of a multifaceted implementation strategy for promoting mental health at the workplace

Implementation science : IS, 2022-09, Vol.17 (1), p.1-59, Article 59

2022

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Abstract B119: Relationship of NaPi2b expression and efficacy of XMT-1536, a NaPi2b targeting antibody-drug conjugate (ADC), in an unselected panel of human primary ovarian mouse xenograft models

Molecular cancer therapeutics, 2018-01, Vol.17 (1_Supplement), p.B119-B119

2018

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Detection of opium alkaloids in a Cypriot base-ring juglet

Analyst (London), 2018-10, Vol.143 (21), p.5127-5136

2018

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Gene Mutations Related to Pathogenesis and Development of Cerebral Arteriovenous Malformations in Pediatric Populations

Neurosurgery, 2019-09, Vol.66 (Supplement 1), p.310-345

2019

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Burden of illness associated with painful diabetic peripheral neuropathy among adults seeking treatment in the US: results from a retrospective chart review and cross-sectional survey

Diabetes, metabolic syndrome and obesity, 2013-01, Vol.6 (default), p.79-92

2013

Volltextzugriff (PDF)

Targeted DNA-seq and RNA-seq of Reference Samples with Short-read and Long-read Sequencing

Scientific data, 2024-08, Vol.11 (1), p.892-13

2024

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Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an “HHT‐like” syndrome in children

Molecular genetics & genomic medicine, 2021-12, Vol.9 (12), p.e1685-n/a

2021

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Npm1ca Overcomes the Differentiation Block of DNMT3A-Mutant LT-HSCs to Transition MDS to Myeloproliferative Disorder

Experimental hematology, 2018-08, Vol.64, p.S108

2018

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3182 - Npm1ca Overcomes the Differentiation Block of DNMT3A-Mutant LT-HSCs to Transition MDS to Myeloproliferative Disorder

Experimental hematology, 2018-08, Vol.64, p.S108-S108

2018

Volltextzugriff (PDF)

Synthetic Heparan Sulfate Mimetic Pixatimod (PG545) Potently Inhibits SARS-CoV‑2 by Disrupting the Spike–ACE2 Interaction

ACS central science, 2022-05, Vol.8 (5), p.527-545

2022

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Economic value of carbon storage in U.S. National Wildlife Refuge wetland ecosystems

Ecosystem services, 2015-12, Vol.16, p.94-104

2015

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Discovery by Virtual Screening of an Inhibitor of CDK5-Mediated PPARγ Phosphorylation

ACS medicinal chemistry letters, 2022-04, Vol.13 (4), p.681-686

2022

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Vestibular defects in head-tilt mice result from mutations in Nox3, encoding an NADPH oxidase

Deletion Mapping of the Head Tilt (het) Gene in Mice: A Vestibular Mutation Causing Specific Absence of Otoliths

Mouse models for the Wolf-Hirschhorn deletion syndrome

Overlapping deletions spanning the proximal two-thirds of the mouse t complex

Vestibular responses to linear acceleration are absent in otoconia-deficient C57BL/6JEi-het mice

Identification of a cryptic lethal mutation in the mouse t(w73) haplotype

Interdigitated deletion complexes on mouse chromosome 5 induced by irradiation of embryonic stem cells

DelBank: a mouse ES-cell resource for generating deletions

Dynamics of sputum conversion during effective tuberculosis treatment: A systematic review and meta-analysis

The Analgesic Effect of Oxygen in Suspected Acute Myocardial Infarction: A Substudy of the DETO2X-AMI Trial

Dormant SOX9-Positive Cells Facilitate MYC-Driven Recurrence of Medulloblastoma

Expanded HILUS Trial: A Pooled Analysis of Risk Factors for Toxicity From Stereotactic Body Radiation Therapy of Central and Ultracentral Lung Tumors

A randomized controlled trial in schools aimed at exploring mechanisms of change of a multifaceted implementation strategy for promoting mental health at the workplace

Abstract B119: Relationship of NaPi2b expression and efficacy of XMT-1536, a NaPi2b targeting antibody-drug conjugate (ADC), in an unselected panel of human primary ovarian mouse xenograft models

Detection of opium alkaloids in a Cypriot base-ring juglet

Gene Mutations Related to Pathogenesis and Development of Cerebral Arteriovenous Malformations in Pediatric Populations

Burden of illness associated with painful diabetic peripheral neuropathy among adults seeking treatment in the US: results from a retrospective chart review and cross-sectional survey

Targeted DNA-seq and RNA-seq of Reference Samples with Short-read and Long-read Sequencing

Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an “HHT‐like” syndrome in children

Npm1ca Overcomes the Differentiation Block of DNMT3A-Mutant LT-HSCs to Transition MDS to Myeloproliferative Disorder

3182 - Npm1ca Overcomes the Differentiation Block of DNMT3A-Mutant LT-HSCs to Transition MDS to Myeloproliferative Disorder

Synthetic Heparan Sulfate Mimetic Pixatimod (PG545) Potently Inhibits SARS-CoV‑2 by Disrupting the Spike–ACE2 Interaction

Mutation discovery in mice by whole exome sequencing

Economic value of carbon storage in U.S. National Wildlife Refuge wetland ecosystems

Discovery by Virtual Screening of an Inhibitor of CDK5-Mediated PPARγ Phosphorylation

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