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Showing 1–20 of 20 results

Advanced filters: Author: N Nadarajah Clear advanced filters

A diamond voltage imaging microscope

Nitrogen-vacancy centres in surface-engineered diamond are demonstrated to operate as charge-sensitive fluorescent reporters, enabling an optical scheme for voltage recording in physical and biological systems.

D. J. McCloskey
N. Dontschuk
D. A. Simpson
Research08 Sept 2022
Nature Photonics

Volume: 16, P: 730-736
Manipulating the EphB4-ephrinB2 axis to reduce metastasis in HNSCC

Khalid N. M. Abdelazeem
Diemmy Nguyen
Sana D. Karam
ResearchOpen Access03 Nov 2024
Oncogene

Volume: 44, P: 130-146
Relationships of PGRN with sTREM2 in AD continuum and non-AD pathophysiology and their reciprocal roles in modulating amyloid pathology: two population-based study

Liang-Yu Huang
Chen-Chen Tan
Dariella Fernandez
ResearchOpen Access08 Jul 2025
Translational Psychiatry

Volume: 15, P: 1-11
Spinal injuries admitted to a specialist centre over a 5-year period: a study to evaluate delayed admission

A Amin
J Bernard
S Tucker
Research08 Mar 2005
Spinal Cord

Volume: 43, P: 434-437
Staging tau pathology with tau PET in Alzheimer’s disease: a longitudinal study

Shi-Dong Chen
Jia-Ying Lu
Michelle Zmuda
ResearchOpen Access18 Sept 2021
Translational Psychiatry

Volume: 11, P: 1-12
Evaluation of serum MMP-9 as predictive biomarker for antisense therapy in Duchenne

A. Lourbakos
N. Yau
P. Spitali
ResearchOpen Access20 Dec 2017
Scientific Reports

Volume: 7, P: 1-10
The Polygenic Risk Score Knowledge Base offers a centralized online repository for calculating and contextualizing polygenic risk scores

The Polygenic Risk Score Knowledge Base (PRSKB) is a web-based interface that stores data from >2,300 distinct genome-wide association studies, and can estimate polygenic risk scores for general use.

Madeline L. Page
Elizabeth L. Vance
John S. K. Kauwe
ResearchOpen Access02 Sept 2022
Communications Biology

Volume: 5, P: 1-15
Plasma phosphorylated-tau181 as a predictive biomarker for Alzheimer’s amyloid, tau and FDG PET status

Xue-Ning Shen
Yu-Yuan Huang
Michelle Zmuda
ResearchOpen Access13 Nov 2021
Translational Psychiatry

Volume: 11, P: 1-10
WT1 mutations are secondary events in AML, show varying frequencies and impact on prognosis between genetic subgroups

M-T Krauth
T Alpermann
S Schnittger
Research11 Aug 2014
Leukemia

Volume: 29, P: 660-667
High number of additional genetic lesions in acute myeloid leukemia with t(8;21)/RUNX1-RUNX1T1: frequency and impact on clinical outcome

M-T Krauth
C Eder
S Schnittger
Research09 Jan 2014
Leukemia

Volume: 28, P: 1449-1458
BAALC expression: a suitable marker for prognostic risk stratification and detection of residual disease in cytogenetically normal acute myeloid leukemia

S Weber
T Alpermann
S Schnittger
ResearchOpen Access10 Jan 2014
Blood Cancer Journal

Volume: 4, P: e173
Landscape of TET2 mutations in acute myeloid leukemia

S Weissmann
T Alpermann
A Kohlmann
Research25 Nov 2011
Leukemia

Volume: 26, P: 934-942
Number of RUNX1 mutations, wild-type allele loss and additional mutations impact on prognosis in adult RUNX1-mutated AML

A Stengel
W Kern
C Haferlach
Research28 Jul 2017
Leukemia

Volume: 32, P: 295-302
Landmark analysis of DNMT3A mutations in hematological malignancies

A Roller
V Grossmann
A Kohlmann
Correspondence01 Mar 2013
Leukemia

Volume: 27, P: 1573-1578
Monitoring of residual disease by next-generation deep-sequencing of RUNX1 mutations can identify acute myeloid leukemia patients with resistant disease

A Kohlmann
N Nadarajah
T Haferlach
Research20 Aug 2013
Leukemia

Volume: 28, P: 129-137
Landscape of genetic lesions in 944 patients with myelodysplastic syndromes

T Haferlach
Y Nagata
S Ogawa
ResearchOpen Access13 Nov 2013
Leukemia

Volume: 28, P: 241-247
Molecular analysis of RAS-RAF tyrosine-kinase signaling pathway alterations in patients with plasma cell myeloma

V Grossmann
U Bacher
C Haferlach
CorrespondenceOpen Access31 Aug 2012
Blood Cancer Journal

Volume: 2, P: e85
Next-generation deep-sequencing detects multiple clones of CALR mutations in patients with BCR-ABL1 negative MPN

S Jeromin
A Kohlmann
S Schnittger
Correspondence29 Jul 2015
Leukemia

Volume: 30, P: 973-976
Aberrations identified by genomic arrays in normal karyotype CMML can be detected in 40% of patients, but do not add prognostic information to molecular mutations

C Vetro
C Haferlach
M Meggendorfer
Correspondence25 May 2016
Leukemia

Volume: 30, P: 2235-2238
Robustness of comprehensive DNA- and RNA-based assays at diagnosis of acute myeloid leukemia using blood and bone marrow stored on filter cards

T Haferlach
S Weber
M Meggendorfer
Correspondence25 May 2016
Leukemia

Volume: 30, P: 2123-2125

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A diamond voltage imaging microscope

Manipulating the EphB4-ephrinB2 axis to reduce metastasis in HNSCC

Relationships of PGRN with sTREM2 in AD continuum and non-AD pathophysiology and their reciprocal roles in modulating amyloid pathology: two population-based study

Spinal injuries admitted to a specialist centre over a 5-year period: a study to evaluate delayed admission

Staging tau pathology with tau PET in Alzheimer’s disease: a longitudinal study

Evaluation of serum MMP-9 as predictive biomarker for antisense therapy in Duchenne

The Polygenic Risk Score Knowledge Base offers a centralized online repository for calculating and contextualizing polygenic risk scores

Plasma phosphorylated-tau181 as a predictive biomarker for Alzheimer’s amyloid, tau and FDG PET status

WT1 mutations are secondary events in AML, show varying frequencies and impact on prognosis between genetic subgroups

High number of additional genetic lesions in acute myeloid leukemia with t(8;21)/RUNX1-RUNX1T1: frequency and impact on clinical outcome

BAALC expression: a suitable marker for prognostic risk stratification and detection of residual disease in cytogenetically normal acute myeloid leukemia

Landscape of TET2 mutations in acute myeloid leukemia

Number of RUNX1 mutations, wild-type allele loss and additional mutations impact on prognosis in adult RUNX1-mutated AML

Landmark analysis of DNMT3A mutations in hematological malignancies

Monitoring of residual disease by next-generation deep-sequencing of RUNX1 mutations can identify acute myeloid leukemia patients with resistant disease

Landscape of genetic lesions in 944 patients with myelodysplastic syndromes

Molecular analysis of RAS-RAF tyrosine-kinase signaling pathway alterations in patients with plasma cell myeloma

Next-generation deep-sequencing detects multiple clones of CALR mutations in patients with BCR-ABL1 negative MPN

Aberrations identified by genomic arrays in normal karyotype CMML can be detected in 40% of patients, but do not add prognostic information to molecular mutations

Robustness of comprehensive DNA- and RNA-based assays at diagnosis of acute myeloid leukemia using blood and bone marrow stored on filter cards

Search

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