Nature Search

Dopamine D₂ and Adenosine A_2A Receptors Regulate NMDA-Mediated Excitation in Accumbens Neurons Through A_2A–D₂ Receptor Heteromerization

Karima Azdad
David Gall
Serge N Schiffmann
Research17 Sept 2008
Neuropsychopharmacology

Volume: 34, P: 972-986
Lucerastat, an oral therapy for Fabry disease: results from a pivotal randomized phase 3 study and its open-label extension

Lucerastat was well-tolerated, but did not reduce neuropathic pain, abdominal pain, or diarrhea compared with placebo. Lucerastat reduced biomarkers of Fabry Disease at 6 months, and these reductions were maintained at the 18-month interim analysis.

Peter Nordbeck
Ozlem Goker-Alpan
Derralynn Hughes
ResearchOpen Access10 Jan 2026
Nature Communications

Volume: 17, P: 1-14
Rapid Stimulation of protein carboxymethylation in leukocytes by a chemotactic peptide

R. F. O'DEA
O. H. VIVEROS
B. A. CORCORAN
Research01 Mar 1978
Nature

Volume: 272, P: 462-464
Human foetal palatal corticoid receptors and teratogens for cleft palate

ALLEN S. GOLDMAN
BERNARD H. SHAPIRO
MASUYUKI KATSUMATA
Research01 Mar 1978
Nature

Volume: 272, P: 464-466
Expression of autocrine motility factor receptor correlates with disease progression in human gastric cancer

Y Hirono
S Fushida
A Raz
Research01 Dec 1996
British Journal of Cancer

Volume: 74, P: 2003-2007
Dorsal column input into the reticular formation

N. A. Salibi
N. E. Saadé
S. J. Jabbur
Research04 Dec 1980
Nature

Volume: 288, P: 481-483
Mitochondrial respiration controls neoangiogenesis during wound healing and tumour growth

During angiogenesis the vasculature switches from a quiescent to a proliferative state. Here the authors show that mitochondrial respiration in endothelial cells controls angiogenesis during development, tumour growth and tissue repair.

L. M. Schiffmann
J. P. Werthenbach
H. Kashkar
ResearchOpen Access21 Jul 2020
Nature Communications

Volume: 11, P: 1-13
Leukotrienes are potent constrictors of human bronchi

Sven-Erik Dahlén
Per Hedqvist
Bengt Samuelsson
Research04 Dec 1980
Nature

Volume: 288, P: 484-486
Histone H3 Phosphorylation is Under the Opposite Tonic Control of Dopamine D2 and Adenosine A2A Receptors in Striatopallidal Neurons

Jesus Bertran-Gonzalez
Kerstin Håkansson
Gilberto Fisone
Research21 Jan 2009
Neuropsychopharmacology

Volume: 34, P: 1710-1720
Vitamin E Attenuates the Effects of FMLP on Rabbit Circulating Granulocytes

J E Lafuze
S J Weisman
R L Baehner
Research01 Jun 1984
Pediatric Research

Volume: 18, P: 536-540
Cytosolic Gram-negative bacteria prevent apoptosis by inhibition of effector caspases through lipopolysaccharide

The lipopolysaccharide of the intracellular pathogen Shigella, in particular its O antigen, interacts with caspases and blocks their activation to prevent apoptosis.

Saskia D. Günther
Melanie Fritsch
Hamid Kashkar
Research23 Dec 2019
Nature Microbiology

Volume: 5, P: 354-367
Lamin B1 duplications cause autosomal dominant leukodystrophy

Quasar S Padiath
Kazumasa Saigoh
Ying-Hui Fu
Research03 Sept 2006
Nature Genetics

Volume: 38, P: 1114-1123
Society for Pediatric Research Presidential Address 1995: Marrying Our Medicine to Biology

David H Perlmutter
Research01 Dec 1995
Pediatric Research

Volume: 38, P: 830-834
Inhibition of hepatocyte growth factor-induced motility and in vitro invasion of human colon cancer cells by gamma-linolenic acid

WG Jiang
S Hiscox
MCA Puntis
Research01 Apr 1995
British Journal of Cancer

Volume: 71, P: 744-752
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts

Yanick Crow and colleagues report that biallelic mutations in SNORD118, which encodes the box C/D snoRNA U8, cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts. The mutations affect U8 expression, processing and protein binding and suggest a role for this snoRNA in cerebral vascular homeostasis.

Emma M Jenkinson
Mathieu P Rodero
Yanick J Crow
Research29 Aug 2016
Nature Genetics

Volume: 48, P: 1185-1192
Protein methylation in behavioural control mechanisms and in signal transduction

Martin S. Springer
Michael F. Goy
Julius Adler
Reviews26 Jul 1979
Nature

Volume: 280, P: 279-284
Quantitative dysmorphology assessment in Fabry disease

Markus Ries
David F Moore
Donna Krasnewich
Research01 Feb 2006
Genetics in Medicine

Volume: 8, P: 96-101
Tumor characteristics, treatments, and oncological outcomes of prostate cancer in men aged ≤50 years: a population-based study

Raisa S. Pompe
Ariane Smith
Pierre I. Karakiewicz
Research16 Jan 2018
Prostate Cancer and Prostatic Diseases

Volume: 21, P: 71-77
Smoking, diet, pregnancy and oral contraceptive use as risk factors for cervical intra-epithelial neoplasia in relation to human papillomavirus infection

L Kjellberg
G Hallmans
J Dillner
ResearchOpen Access07 Mar 2000
British Journal of Cancer

Volume: 82, P: 1332-1338
DNA copy number loss and allelic imbalance at 2p16 in lung cancer associated with asbestos exposure

E Kettunen
M Aavikko
S Anttila
ResearchOpen Access31 Mar 2009
British Journal of Cancer

Volume: 100, P: 1336-1342
INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse

Stephane Schurmans and colleagues show that mice lacking the enzyme inositol polyphosphate-5-phosphatase E (Inpp5e) develop a multiorgan disorder with defects in primary cilia. They also report a mutation in human INPP5E in a family with MORM syndrome, a condition similar to Bardet-Biedl syndrome.

Monique Jacoby
James J Cox
Stéphane Schurmans
Research09 Aug 2009
Nature Genetics

Volume: 41, P: 1027-1031
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus

Yanick Crow and colleagues show that mutations in CTC1, which encodes a homolog of a yeast telomere maintenance protein, cause Coats plus, a highly pleiotropic disorder sharing phenotypic overlap with dyskeratosis congenita and other disorders of telomere maintenance.

Beverley H Anderson
Paul R Kasher
Yanick J Crow
Research22 Jan 2012
Nature Genetics

Volume: 44, P: 338-342
Structural trends in atomic nuclei from laser spectroscopy of tin

Measurements of the hyperfine structure of chemical elements isotopes provide unique insight into the atomic nucleus in a nuclear model-independent way. The authors present collinear laser spectroscopy data obtained at the CERN ISOLDE and measure hyperfine splitting along a long chain of odd-mass tin isotopes.

Deyan T. Yordanov
Liss V. Rodríguez
Xiaofei Yang
ResearchOpen Access08 Jun 2020
Communications Physics

Volume: 3, P: 1-9
Niemann–Pick disease type C (a cellular cholesterol lipidosis) treated by bone marrow transplantation

Y-S Hsu
W-L Hwu
K-H Lin
Research23 Jul 1999
Bone Marrow Transplantation

Volume: 24, P: 103-107
Age-related shift in LTD is dependent on neuronal adenosine A_2A receptors interplay with mGluR5 and NMDA receptors

Mariana Temido-Ferreira
Diana G. Ferreira
Luísa V. Lopes
ResearchOpen Access27 Jun 2018
Molecular Psychiatry

Volume: 25, P: 1876-1900
Identification of human renal cell carcinoma associated genes by suppression subtractive hybridization

M J J G Stassar
G Devitt
M Zöller
ResearchOpen Access30 Oct 2001
British Journal of Cancer

Volume: 85, P: 1372-1382
Altered cell-matrix contact: a prerequisite for breast cancer metastasis?

GPH Gui
JR Puddefoot
R Carpenter
Research01 Mar 1997
British Journal of Cancer

Volume: 75, P: 623-633
Perinatal Nitric Oxide Synthase Inhibition Retards Neonatal Growth by Inducing Hypertrophic Pyloric Stenosis in Rats

Cynthia A Voelker
Mark J S Miller
Maria R Pierce
Research01 Nov 1995
Pediatric Research

Volume: 38, P: 768-774
Combined analysis of HLA class I, HLA-E and HLA-G predicts prognosis in colon cancer patients

E C M Zeestraten
M S Reimers
P J K Kuppen
ResearchOpen Access05 Nov 2013
British Journal of Cancer

Volume: 110, P: 459-468
Establishment of two new scirrhous gastric cancer cell lines: analysis of factors associated with disseminated metastasis

M Yashiro
YS Chung
M Sowa
Research01 Nov 1995
British Journal of Cancer

Volume: 72, P: 1200-1210
p53 mutations in human cutaneous melanoma correlate with sun exposure but are not always involved in melanomagenesis

S F Zerp
A van Elsas
P I Schrier
ResearchOpen Access29 Jan 1999
British Journal of Cancer

Volume: 79, P: 921-926
Changes in plasma and urine globotriaosylceramide levels do not predict Fabry disease progression over 1 year of agalsidase alfa

Raphael Schiffmann
Markus Ries
Pedro Huertas
ResearchOpen Access16 May 2013
Genetics in Medicine

Volume: 15, P: 983-989
Expanded phenotype of AARS1-related white matter disease

Guy Helman
Marisa I. Mendes
Ralf A. Husain
Research27 Aug 2021
Genetics in Medicine

Volume: 23, P: 2352-2359
Experience with Mucolipidosis Type IV in Newfoundland

C Prasad
D J Buckley
R Schiffinann
Research Highlights01 Jan 1999
Genetics in Medicine

Volume: 1, P: 51
Hypomyelinating leukodystrophies — unravelling myelin biology

In this Review, Wolf et al. provide an overview of the hypomyelinating leukodystrophies and discuss how identification of the genes involved in these disorders have provided insight into the clinical presentations of these disorders and into myelin biology.

Nicole I. Wolf
Charles ffrench-Constant
Marjo S. van der Knaap
Reviews15 Dec 2020
Nature Reviews Neurology

Volume: 17, P: 88-103
Cell-mediated reduction of human β-defensin 1: a major role for mucosal thioredoxin

S U Jaeger
B O Schroeder
J Wehkamp
ResearchOpen Access10 Apr 2013
Mucosal Immunology

Volume: 6, P: 1179-1190
Misassembly of full-length Disrupted-in-Schizophrenia 1 protein is linked to altered dopamine homeostasis and behavioral deficits

S V Trossbach
V Bader
C Korth
ResearchOpen Access12 Jan 2016
Molecular Psychiatry

Volume: 21, P: 1561-1572
Lack of parvalbumin in mice leads to behavioral deficits relevant to all human autism core symptoms and related neural morphofunctional abnormalities

M Wöhr
D Orduz
B Schwaller
ResearchOpen Access10 Mar 2015
Translational Psychiatry

Volume: 5, P: e525
The validation of pharmacogenetics for the identification of Fabry patients to be treated with migalastat

Elfrida R. Benjamin
Maria Cecilia Della Valle
David J. Lockhart
ResearchOpen Access22 Sept 2016
Genetics in Medicine

Volume: 19, P: 430-438
A combination of low-dose bevacizumab and imatinib enhances vascular normalisation without inducing extracellular matrix deposition

L M Schiffmann
M Brunold
O Coutelle
ResearchOpen Access31 Jan 2017
British Journal of Cancer

Volume: 116, P: 600-608

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