Nature Search

Conjugal transfer of R plasmids in Neisseria gonorrhoeae

MARILYN ROBERTS
STANLEY FALKOW
Research14 Apr 1977
Nature

Volume: 266, P: 630-631
Initiation of development of diapausing embryo by mammary denervation during lactation in a marsupial

MARILYN B RENFREE
Research01 Apr 1979
Nature

Volume: 278, P: 549-551
Stable restoration of the sarcoglycan complex in dystrophic muscle perfused with histamine and a recombinant adeno-associated viral vector

James P. Greelish
Leonard T. Su
Hansell H. Stedman
Research01 Apr 1999
Nature Medicine

Volume: 5, P: 439-443
1365 HYPOTHERMIA IN TRANSPORTED NEONATES: REWARMING EFFECT OF RADIANT HEAT VERSUS WARMED AIR INCUBATORS

Andrew Macnab
Edward Lau
Margaret Pendray
Research01 Apr 1981
Pediatric Research

Volume: 15, P: 670
Associations of autozygosity with a broad range of human phenotypes

Inbreeding depression has been observed in many different species, but in humans a systematic analysis has been difficult so far. Here, analysing more than 1.3 million individuals, the authors show that a genomic inbreeding coefficient (FROH) is associated with disadvantageous outcomes in 32 out of 100 traits tested.

David W Clark
Yukinori Okada
James F Wilson
ResearchOpen Access31 Oct 2019
Nature Communications

Volume: 10, P: 1-17
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

An analysis of 24,202 critical cases of COVID-19 identifies potentially druggable targets in inflammatory signalling (JAK1), monocyte–macrophage activation and endothelial permeability (PDE4A), immunometabolism (SLC2A5 and AK5), and host factors required for viral entry and replication (TMPRSS2 and RAB2A).

Erola Pairo-Castineira
Konrad Rawlik
J. Kenneth Baillie
ResearchOpen Access17 May 2023
Nature

Volume: 617, P: 764-768
Myosin gene mutation correlates with anatomical changes in the human lineage

Hansell H. Stedman
Benjamin W. Kozyak
Marilyn A. Mitchell
Research25 Mar 2004
Nature

Volume: 428, P: 415-418
1603 URINE N-ACETYL-β-D-GLUCOSAMINIDASE(NAG) AND β₂-MICRO-GLOBULINS (B₂M) IN VERY LOW BIRTHWEIGHT INFANTS FED MINERAL SUPPLEMENTED FORMULA

Laura S Hillman
Sharon J Salmons
Russell W Chesney
Research01 Apr 1985
Pediatric Research

Volume: 19, P: 378
1328 NEONATAL CEREBRAL HEMORRHAGE (CH)/HEMODYNAMICS AND OUTCOME

Henrietta S Bada
Sheldon B Korones
J T Jabbour
Research01 Apr 1985
Pediatric Research

Volume: 19, P: 332
G domain dimerization controls dynamin's assembly-stimulated GTPase activity

Dynamin is a protein that catalyses the fission of clathrin-coated endocytic vesicles from cellular membranes. To carry out fission, it must hydrolyse GTP. The mechanism by which it does so is unknown, although it does require dynamin's GTPase effector domain (GED). Here, the structure of a minimal GTPase–GED fusion protein constructed from human dynamin 1 is presented. The structure reveals the catalytic machinery and provides new insight into the mechanisms underlying dynamin-catalysed membrane fission.

Joshua S. Chappie
Sharmistha Acharya
Fred Dyda
Research28 Apr 2010
Nature

Volume: 465, P: 435-440
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes

An integrated analysis of de novo and inherited coding variants in 42,607 individuals with autism spectrum disorder identifies 60 risk genes of which five have not previously been associated with neurodevelopmental disorders.

Xueya Zhou
Pamela Feliciano
Wendy K. Chung
ResearchOpen Access18 Aug 2022
Nature Genetics

Volume: 54, P: 1305-1319
Site-specific identification and quantitation of endogenous SUMO modifications under native conditions

SUMOylation is post-translational modification implicated in several biological pathways. Here the authors describe an approach for the global profiling of SUMO attachment sites under native conditions that also allows the parallel determination of SUMO and Ub attachments.

Ryan J. Lumpkin
Hongbo Gu
Elizabeth A. Komives
ResearchOpen Access27 Oct 2017
Nature Communications

Volume: 8, P: 1-11
Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference

Progressive diseases tend to be heterogeneous in their underlying aetiology mechanism, disease manifestation, and disease time course. Here, Young and colleagues devise a computational method to account for both phenotypic heterogeneity and temporal heterogeneity, and demonstrate it using two neurodegenerative disease cohorts.

Alexandra L Young
Razvan V Marinescu
Ansgar J Furst
ResearchOpen Access15 Oct 2018
Nature Communications

Volume: 9, P: 1-16
PREDICTORS OF DEVELOPMENTAL OUTCOME AT 12 MONTHS OF <1250 GRAM INBORN NEONATES

Cheryl Cipriani
Marilyn Escobedo
Jill Schlansker
Research01 Apr 1984
Pediatric Research

Volume: 18, P: 102
835 PURIFICATION, BIOCHEMICAL CHARACTERIZATION AND FUNCTION OF FETAL AT-III

Marilyn M Mcdonald
E Basil Reeve
Wm E Hathaway
Research01 Apr 1981
Pediatric Research

Volume: 15, P: 581
Non-immunogenic utrophin gene therapy for the treatment of muscular dystrophy animal models

A gene therapy vector expressing micro-utrophin provides functional replacement of lost dystrophin, and lacks the adverse immunogenicity associated with direct dystrophin therapy, in rodent and canine models of Duchenne muscular dystrophy.

Yafeng Song
Leon Morales
Hansell H. Stedman
Research07 Oct 2019
Nature Medicine

Volume: 25, P: 1505-1511
Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Erola Pairo-Castineira
Konrad Rawlik
J. Kenneth Baillie
Amendments and CorrectionsOpen Access11 Jul 2023
Nature

Volume: 619, P: E61
Monitoring of carbon-water fluxes at Eurasian meteorological stations using random forest and remote sensing

Mingjuan Xie
Xiaofei Ma
Geping Luo
ResearchOpen Access07 Sept 2023
Scientific Data

Volume: 10, P: 1-18
HELPing older people with very severe chronic obstructive pulmonary disease (HELP-COPD): mixed-method feasibility pilot randomised controlled trial of a novel intervention

Susan Buckingham
Marilyn Kendall
Hilary Pinnock
ResearchOpen Access16 Apr 2015
npj Primary Care Respiratory Medicine

Volume: 25, P: 1-9

Search

Conjugal transfer of R plasmids in Neisseria gonorrhoeae

Initiation of development of diapausing embryo by mammary denervation during lactation in a marsupial

Stable restoration of the sarcoglycan complex in dystrophic muscle perfused with histamine and a recombinant adeno-associated viral vector

1365 HYPOTHERMIA IN TRANSPORTED NEONATES: REWARMING EFFECT OF RADIANT HEAT VERSUS WARMED AIR INCUBATORS

Associations of autozygosity with a broad range of human phenotypes

GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Myosin gene mutation correlates with anatomical changes in the human lineage

1603 URINE N-ACETYL-β-D-GLUCOSAMINIDASE(NAG) AND β₂-MICRO-GLOBULINS (B₂M) IN VERY LOW BIRTHWEIGHT INFANTS FED MINERAL SUPPLEMENTED FORMULA

1328 NEONATAL CEREBRAL HEMORRHAGE (CH)/HEMODYNAMICS AND OUTCOME

G domain dimerization controls dynamin's assembly-stimulated GTPase activity

Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes

Site-specific identification and quantitation of endogenous SUMO modifications under native conditions

Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference

PREDICTORS OF DEVELOPMENTAL OUTCOME AT 12 MONTHS OF <1250 GRAM INBORN NEONATES

835 PURIFICATION, BIOCHEMICAL CHARACTERIZATION AND FUNCTION OF FETAL AT-III

Non-immunogenic utrophin gene therapy for the treatment of muscular dystrophy animal models

Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Monitoring of carbon-water fluxes at Eurasian meteorological stations using random forest and remote sensing

HELPing older people with very severe chronic obstructive pulmonary disease (HELP-COPD): mixed-method feasibility pilot randomised controlled trial of a novel intervention

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