Nature Search

Synthesis of Hæm in Normal and Leukæmic Leucocytes

THOMAS R. WALTERS
T. JOHN GRIBBLE
HERBERT C. SCHWARTZ
Research23 Mar 1963
Nature

Volume: 197, P: 1213-1214
Molecular cloning of cDNA for murine interleukin-3

M. C. Fung
A. J. Hapel
I. G. Young
Research19 Jan 1984
Nature

Volume: 307, P: 233-237
Promiscuous coupling between the sulphonylurea receptor and inwardly rectifying potassium channels

Carlna Ämmälä
Andrew Moorhouse
Frances M. Ashcroft
Research08 Feb 1996
Nature

Volume: 379, P: 545-548
Hypohaptoglobinæmia in an American Negro Family

ARLAN J. GOTTLIEB
JOHN ROSS
NATHANIEL WISCH
Research23 Mar 1963
Nature

Volume: 197, P: 1214-1215
Hemoglobin Hasharon in a Premature Infant with Hemolytic Anemia

Rodney L Levine
David R Lincoln
Herbert C Schwartz
Research01 Jan 1975
Pediatric Research

Volume: 9, P: 7-11
Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individuals

Julia Baptista
Elena Prigmore
John A Crolla
Research24 Aug 2005
European Journal of Human Genetics

Volume: 13, P: 1205-1212
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

The authors analyzed the whole-exome sequences of over 16,000 individuals and found that very rare variants predicted to disrupt the SETD1A gene confer substantial risk for schizophrenia. Damaging variants in SETD1A were also associated with diverse, severe developmental disorders, providing an important genetic link between schizophrenia and other neurodevelopmental disorders.

Tarjinder Singh
Mitja I Kurki
Jeffrey C Barrett
Research14 Mar 2016
Nature Neuroscience

Volume: 19, P: 571-577
Origin of corundum-normative intrusive and extrusive magmas

R. GRANT CAWTHORN
D. F. STRONG
P. A. BROWN
Research15 Jan 1976
Nature

Volume: 259, P: 102-104
A cross-platform approach identifies genetic regulators of human metabolism and health

A large-scale genome-wide meta-analysis conducted across different platforms identifies genetic loci regulating levels of circulating metabolites.

Luca A. Lotta
Maik Pietzner
Claudia Langenberg
Research07 Jan 2021
Nature Genetics

Volume: 53, P: 54-64
The DNA sequence of the human X chromosome

Mark T. Ross
Darren V. Grafham
David R. Bentley
Research17 Mar 2005
Nature

Volume: 434, P: 325-337
Publisher Correction: GDF15 mediates the effects of metformin on body weight and energy balance

Anthony P. Coll
Michael Chen
Stephen O’Rahilly
Amendments and Corrections13 Feb 2020
Nature

Volume: 578, P: E24
GDF15 mediates the effects of metformin on body weight and energy balance

In mouse studies, metformin treatment results in increased secretion of growth/differentiation factor 15 (GDF15), which prevents weight gain in response to high-fat diet, and GDF15-independent lowering of circulating blood glucose.

Anthony P. Coll
Michael Chen
Stephen O’Rahilly
Research25 Dec 2019
Nature

Volume: 578, P: 444-448
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Chromodomain Helicase DNA-binding (CHD) proteins have been implicated in neurodevelopmental processes. Here, the authors identify missense variants in CHD3 that disturb its chromatin remodeling activities and cause a neurodevelopmental disorder with macrocephaly and speech and language impairment.

Lot Snijders Blok
Justine Rousseau
Philippe M. Campeau
ResearchOpen Access05 Nov 2018
Nature Communications

Volume: 9, P: 1-12
The synaptic receptor Lrp4 promotes peripheral nerve regeneration

Axons of the peripheral nervous system regenerate along Schwann cells following injury. Here, the authors show that regenerating axons follow pioneer axons and this process is mediated by lipoprotein receptor-related protein 4 (Lrp4), a protein otherwise known for its role in synapse formation.

Katherine D. Gribble
Lauren J. Walker
Michael Granato
ResearchOpen Access19 Jun 2018
Nature Communications

Volume: 9, P: 1-12
An SCN9A channelopathy causes congenital inability to experience pain

James J. Cox
Frank Reimann
C. Geoffrey Woods
Research14 Dec 2006
Nature

Volume: 444, P: 894-898
Prevalence and architecture of de novo mutations in developmental disorders

Whole-exome analysis of individuals with developmental disorders shows that de novo mutations can equally cause loss or altered protein function, but that most mutations causing altered protein function have not yet been described.

Jeremy F. McRae
Stephen Clayton
Matthew E. Hurles
Research25 Jan 2017
Nature

Volume: 542, P: 433-438
Synthesis of conolidine, a potent non-opioid analgesic for tonic and persistent pain

The first total synthesis of conolidine — representing the first asymmetric synthesis of a C5-nor-stemmadenine — is described. The chemical synthesis proceeds in just nine steps and gives an 18% overall yield from a commercially available pyridine — an achievement that led to the discovery that (+)-, (–)- and (±)-conolidine are potent non-opioid analgesics.

Michael A. Tarselli
Kirsten M. Raehal
Glenn C. Micalizio
Research23 May 2011
Nature Chemistry

Volume: 3, P: 449-453
Therapeutic targeting of the NRF2 and KEAP1 partnership in chronic diseases

The transcription factor NRF2 and its repressor KEAP1 have been implicated in the development and progression of chronic diseases. Here, Dinkova-Kostova and colleagues provide an overview of the physiological and pathological roles of NRF2, present emerging pharmacological modulators of the NRF2–KEAP1 axis and highlight associated drug development challenges.

Antonio Cuadrado
Ana I. Rojo
Albena T. Dinkova-Kostova
Reviews04 Jan 2019
Nature Reviews Drug Discovery

Volume: 18, P: 295-317
Isolation and Structures of Novel Fungal Metabolites as Chemokine Receptor (CCR2) Antagonists

Kithsiri B Herath
Hiranthi Jayasuriya
Sheo B Singh
Research01 Nov 2005
The Journal of Antibiotics

Volume: 58, P: 686-694
Infections in the spinal cord-injured population: a systematic review

L Y Garcia-Arguello
J C O'Horo
N Safdar
Research06 Dec 2016
Spinal Cord

Volume: 55, P: 526-534
Accelerating cryoprotectant diffusion kinetics improves cryopreservation of pancreatic islets

Nikola Dolezalova
Anja Gruszczyk
Kourosh Saeb-Parsy
ResearchOpen Access17 May 2021
Scientific Reports

Volume: 11, P: 1-18
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok
Justine Rousseau
Philippe M. Campeau
Amendments and CorrectionsOpen Access15 Feb 2019
Nature Communications

Volume: 10, P: 1-4
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok
Justine Rousseau
Philippe M. Campeau
Amendments and CorrectionsOpen Access02 May 2019
Nature Communications

Volume: 10, P: 1-4
High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression

J Boultwood
J Perry
J S Wainscoat
Research22 Apr 2010
Leukemia

Volume: 24, P: 1139-1145

Search

Synthesis of Hæm in Normal and Leukæmic Leucocytes

Molecular cloning of cDNA for murine interleukin-3

Promiscuous coupling between the sulphonylurea receptor and inwardly rectifying potassium channels

Hypohaptoglobinæmia in an American Negro Family

Hemoglobin Hasharon in a Premature Infant with Hemolytic Anemia

Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individuals

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

Origin of corundum-normative intrusive and extrusive magmas

A cross-platform approach identifies genetic regulators of human metabolism and health

The DNA sequence of the human X chromosome

Publisher Correction: GDF15 mediates the effects of metformin on body weight and energy balance

GDF15 mediates the effects of metformin on body weight and energy balance

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

The synaptic receptor Lrp4 promotes peripheral nerve regeneration

An SCN9A channelopathy causes congenital inability to experience pain

Prevalence and architecture of de novo mutations in developmental disorders

Synthesis of conolidine, a potent non-opioid analgesic for tonic and persistent pain

Therapeutic targeting of the NRF2 and KEAP1 partnership in chronic diseases

Isolation and Structures of Novel Fungal Metabolites as Chemokine Receptor (CCR2) Antagonists

Infections in the spinal cord-injured population: a systematic review

Accelerating cryoprotectant diffusion kinetics improves cryopreservation of pancreatic islets

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression

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