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Showing 1–50 of 53 results

Advanced filters: Author: J Sturge Clear advanced filters

Photodynamic Therapy of Choroidal Haemangioma Associated with Sturge–Weber Syndrome

A D Singh
P A Rundle
I G Rennie
Correspondence30 Jul 2004
Eye

Volume: 19, P: 365-367
Robust compression and detection of epileptiform patterns in ECoG using a real-time spiking neural network hardware framework

Costa et al. designed a modular spiking neural network in a neuromorphic device with heterogeneous silicon neurons that remotely detects epileptiform discharges and High Frequency Oscillations in intra-operative EEG during epilepsy surgery in real-time.

Filippo Costa
Eline V. Schaft
Johannes Sarnthein
ResearchOpen Access16 Apr 2024
Nature Communications

Volume: 15, P: 1-12
Endo180 modulation by bisphosphonates and diagnostic accuracy in metastatic breast cancer

C Palmieri
M P Caley
J Sturge
ResearchOpen Access20 Dec 2012
British Journal of Cancer

Volume: 108, P: 163-169
Dr. J. F. Cameron

J. CHADWICK
Comments & Opinion10 May 1952
Nature

Volume: 169, P: 777
Spiral Development of Mycelium in Aspergillus niger Colonies

J. L. YUILL
E. YUILL
Research03 Apr 1954
Nature

Volume: 173, P: 643
Histological Demonstration of Alkaline Phosphatase and Non-specific Esterase by Azo-dye Methods

J. F. BURTON
Research03 Apr 1954
Nature

Volume: 173, P: 642-643
The Einstein Relation between Relative Viscosity and Volume Concentration of Suspensions of Spheres

A. J. HUGHES
Research05 Jun 1954
Nature

Volume: 173, P: 1089-1090
MEK inhibition reduced vascular tumor growth and coagulopathy in a mouse model with hyperactive GNAQ

Life-threatening vascular tumors can be associated with uncontrolled activity of the guanine nucleotide-binding protein subunit alpha (Gαq). Here, the authors develop a murine model for these tumors and show that MEK inhibition prevents formation of vascular lesions and improves survival.

Sandra Schrenk
Lindsay J. Bischoff
Elisa Boscolo
ResearchOpen Access06 Apr 2023
Nature Communications

Volume: 14, P: 1-20
Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause

Sequence analysis identifies gain-of-function somatic mutations in GNA11 or GNAQ in CTNNB1-mutant aldosterone-producing adenomas. Most patients with these mutations presented during puberty, pregnancy or menopause, with elevated LHCGR expression.

Junhua Zhou
Elena A. B. Azizan
Morris J. Brown
Research12 Aug 2021
Nature Genetics

Volume: 53, P: 1360-1372
Mantle-derived fluids in diamond micro-inclusions

O. Navon
I. D. Hutcheon
G. J. Wasserburg
Research27 Oct 1988
Nature

Volume: 335, P: 784-789
Machine learning reveals bilateral distribution of somatic L1 insertions in human neurons and glia

Zhu et al. discover that in human brain there is widespread anatomic distribution of low-frequency somatic, mosaic L1 insertions, using deep whole-genome sequencing of neuronal and glial fractions and machine-learning analysis.

Xiaowei Zhu
Bo Zhou
Alexander E. Urban
Research11 Jan 2021
Nature Neuroscience

Volume: 24, P: 186-196
East–West pairing

R. J. Elliott
Books & Arts09 Feb 1984
Nature

Volume: 307, P: 572
Identification of a new type of electronic state in the magnetoresistive orthomanganites

J.-S. Zhou
W. Archibald
J. B. Goodenough
Research27 Jun 1996
Nature

Volume: 381, P: 770-772
Gingival overgrowth: Part 1: aetiology and clinical diagnosis

J. Beaumont
J. Chesterman
K. Durey
Research27 Jan 2017
British Dental Journal

Volume: 222, P: 85-91
New transformations between crystalline and amorphous ice

R. J. Hemley
L. C. Chen
H. K. Mao
Research20 Apr 1989
Nature

Volume: 338, P: 638-640
L1-associated genomic regions are deleted in somatic cells of the healthy human brain

The healthy human brain is a mosaic of varied genomes. Using a single cell sequencing approach targeting L1 elements, the authors show that the contribution of L1 to somatic mosaicism goes beyond retrotransposition and includes deletion of genomic regions associated with L1.

Jennifer A Erwin
Apuã C M Paquola
Fred H Gage
Research12 Sept 2016
Nature Neuroscience

Volume: 19, P: 1583-1591
Brain arteriovenous malformations

Arteriovenous malformations are characterized by a direct link between arteries and veins without intervening capillaries. This Primer highlights high rupture and haemorrhage risk when these occur in the brain, as well as the diagnosis and management options available to patients.

Michael T. Lawton
W. Caleb Rutledge
Robert F. Spetzler
Reviews28 May 2015
Nature Reviews Disease Primers

Volume: 1, P: 1-20
Alternative diagnoses with ectopia lentis

A Chandra
J A Aragon Martin
D G Charteris
Correspondence02 Dec 2011
Eye

Volume: 26, P: 481
Alcohol and Eugenics ¹

E. H. J. S.
News09 Feb 1911
Nature

Volume: 85, P: 479-480
Proceedings of the Yorkshire Geological Society

G. A. J. C.
Books & Arts17 Feb 1916
Nature

Volume: 96, P: 675
Genome-wide screening of mouse knockouts reveals novel genes required for normal integumentary and oculocutaneous structure and function

Bret A. Moore
Ann M. Flenniken
Ala Moshiri
ResearchOpen Access01 Aug 2019
Scientific Reports

Volume: 9, P: 1-9
Use of propranolol for treatment of hemangiomas in PHACE syndrome

T Solomon
J Ninnis
A Hopper
Research31 Oct 2011
Journal of Perinatology

Volume: 31, P: 739-741
Knowledge-based prediction of protein structures and the design of novel molecules

T. L. Blundell
B. L. Sibanda
J. M. Thornton
Reviews26 Mar 1987
Nature

Volume: 326, P: 347-352
Dissipation and noise immunity in computation and communication

Rolf Landauer
Reviews27 Oct 1988
Nature

Volume: 335, P: 779-784
Human and ecological determinants of the spatial structure of local breed diversity

Victor J. Colino-Rabanal
Roberto Rodríguez-Díaz
Miguel Lizana
ResearchOpen Access24 Apr 2018
Scientific Reports

Volume: 8, P: 1-10
Parasite-induced T_H1 cells and intestinal dysbiosis cooperate in IFN-γ-dependent elimination of Paneth cells

Immune responses can cause immunopathology. Yarovinsky and colleagues show that IFN-γ induced by T cell–intrinsic TLR signaling in CD4⁺ T_H1 cells during Toxoplasma gondii infection causes dysbiosis and loss of Paneth cells.

Megan Raetz
Sun-hee Hwang
Felix Yarovinsky
Research23 Dec 2012
Nature Immunology

Volume: 14, P: 136-142
Primary aldosteronism: molecular medicine meets public health

Primary aldosteronism is the most common cause of endocrine arterial hypertension and is characterized by the autonomous production of aldosterone from one or both adrenal glands. This Review describes the molecular discoveries and developments that have the potential to transform the clinical management of patients with this disease.

Elena A. B. Azizan
William M. Drake
Morris J. Brown
Reviews23 Aug 2023
Nature Reviews Nephrology

Volume: 19, P: 788-806
Zoology at the British Association

J. H. ASHWORTH
News09 Dec 1920
Nature

Volume: 106, P: 485-487
Physiology at the British Association

J. BARCROFT
News19 Sept 1907
Nature

Volume: 76, P: 533-535
Systems modeling of oncogenic G-protein and GPCR signaling reveals unexpected differences in downstream pathway activation

Michael Trogdon
Kodye Abbott
Edward C. Stites
ResearchOpen Access16 Jul 2024
npj Systems Biology and Applications

Volume: 10, P: 1-17
Epilepsy

Epilepsy is characterized by an enduring predisposition to epileptic seizures and is associated with high morbidity. This Primer by Devinsky and colleagues describes the mechanisms underlying epilepsy and seizure development, and discusses how this disorder is diagnosed and managed.

Orrin Devinsky
Annamaria Vezzani
Piero Perucca
Reviews03 May 2018
Nature Reviews Disease Primers

Volume: 4, P: 1-24
Gingival overgrowth: Part 2: management strategies

J. Chesterman
J. Beaumont
K. Durey
Research10 Feb 2017
British Dental Journal

Volume: 222, P: 159-165
General medicine and surgery for dental practitioners Part 4: Neurological disorders

M Greenwood
J G Meechan
Research12 Jul 2003
British Dental Journal

Volume: 195, P: 19-25
Rare antibody phage isolation and discrimination (RAPID) biopanning enables identification of high-affinity antibodies against challenging targets

A FACS aided selection process combined with characterization of the selected clones facilitates phage display screening to obtain antibodies against a given target from libraries.

Dong hee Chung
Sophie Kong
Charles S. Craik
ResearchOpen Access12 Oct 2023
Communications Biology

Volume: 6, P: 1-13
Tuberous sclerosis complex

Tuberous sclerosis complex (TSC) is a rare inherited disease caused by mutations in the tumour-suppressor genes TSC1 or TSC2. As a chronic disease that manifests as benign tumours in the brain, kidneys, lungs and skin, TSC requires lifelong treatment.

Elizabeth P. Henske
Sergiusz Jóźwiak
Elizabeth A. Thiele
Reviews26 May 2016
Nature Reviews Disease Primers

Volume: 2, P: 1-18
The challenges and innovations for therapy in children with epilepsy

Wilmshurst et al. discuss how appropriate terminology can aid in the diagnosis and treatment of paediatric epilepsies. Furthermore, they give an update on key changes to the organization and terminology of epilepsies by the International League Against Epilepsy and an overview of the challenges in implementing new guidelines to treat paediatric patients particularly in low-income countries.

Jo M. Wilmshurst
Anne T. Berg
J. Helen Cross
Reviews08 Apr 2014
Nature Reviews Neurology

Volume: 10, P: 249-260
Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia

Alison M. Muir
Jennifer F. Gardner
Heather C. Mefford
Research20 Jan 2021
Genetics in Medicine

Volume: 23, P: 881-887
Expanding the clinical and molecular findings in RASA1 capillary malformation-arteriovenous malformation

Whitney L. Wooderchak-Donahue
Peter Johnson
Pinar Bayrak-Toydemir
Research11 Jun 2018
European Journal of Human Genetics

Volume: 26, P: 1521-1536
Congenital enormous high flow capillary hemangioma of forearm

T E Herman
M J Siegel
Research29 Feb 2008
Journal of Perinatology

Volume: 28, P: 235-237
Treatment of fresh human leukaemia cells with actinomycin D enhances their lysability by natural killer cells

H W Ziegler-Heitbrock
J Erhardt
G Riethmüller
Research01 Oct 1983
British Journal of Cancer

Volume: 48, P: 507-514
Hypoxic–ischemic injury causes functional and structural neurovascular degeneration in the juvenile mouse retina

Ismail S. Zaitoun
Pawan K. Shahi
Nader Sheibani
ResearchOpen Access16 Jun 2021
Scientific Reports

Volume: 11, P: 1-13
Should an iridectomy be routinely performed as a part of trabeculectomy? two surgeons' clinical experience

D S M de Barros
R S Da Silva
G L Spaeth
Research09 Nov 2007
Eye

Volume: 23, P: 362-367
Specialist management of routine dental procedures in adults with refractory epilepsy

N. Ransford
I. Soryal
N. Huggins
Research11 Apr 2014
British Dental Journal

Volume: 216, P: 403-407
Activation of the focal adhesion kinase signal transduction pathway in cervical carcinoma cell lines and human genital epithelial cells immortalized with human papillomavirus type 18

Stephen J McCormack
Scott E Brazinski
David J Goldstein
Research17 Jul 1997
Oncogene

Volume: 15, P: 265-274
Synthesis of super bright indium phosphide colloidal quantum dots through thermal diffusion

The low toxicity of indium phosphide quantum dots makes them attractive candidates for biomedical applications but they typically exhibit low low photoluminescent quantum yield in aqueous media. Here the authors report a controlled-cooling based synthetic method which produces super bright quantum dots.

Mitchell T. Clarke
Francesco Narda Viscomi
Graeme J. Stasiuk
ResearchOpen Access22 Mar 2019
Communications Chemistry

Volume: 2, P: 1-7
A case of a 360 degree exuberant trabeculectomy bleb

Jonathan D Rossiter
Stephen J Godfrey
Kate G Claridge
Correspondence01 May 1999
Eye

Volume: 13, P: 369-370
Human fucosyltransferase 6 enables prostate cancer metastasis to bone

J Li
A D Guillebon
M R King
ResearchOpen Access31 Oct 2013
British Journal of Cancer

Volume: 109, P: 3014-3022
Phenotypic divergence of the common toad (Bufo bufo) along an altitudinal gradient: evidence for local adaptation

E Luquet
J-P Léna
S Plénet
Research30 Jul 2014
Heredity

Volume: 114, P: 69-79
Analysis of LINE-1 Elements in DNA from Postmortem Brains of Individuals with Schizophrenia

Glenn A Doyle
Richard C Crist
Wade H Berrettini
Research06 Jun 2017
Neuropsychopharmacology

Volume: 42, P: 2602-2611
The Ahmed Glaucoma Valve in Refractory Glaucoma: experiences in Indian Eyes

J C Das
Z Chaudhuri
S Bhomaj
Research16 Jul 2004
Eye

Volume: 19, P: 183-190

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