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Showing 401–429 of 429 results

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Nanowire-assisted freestanding liquid metal thin-film patterns for highly stretchable electrodes on 3D surfaces

Minwoo Kim
Chulmin Cho
Seung Hwan Ko
ResearchOpen Access26 Dec 2022
npj Flexible Electronics

Volume: 6, P: 1-8
Interrupting peptidoglycan deacetylation during Bdellovibrio predator-prey interaction prevents ultimate destruction of prey wall, liberating bacterial-ghosts

Carey Lambert
Thomas R. Lerner
R. Elizabeth Sockett
ResearchOpen Access23 May 2016
Scientific Reports

Volume: 6, P: 1-19
Diversity and carbon storage across the tropical forest biome

Martin J. P. Sullivan
Joey Talbot
Lise Zemagho
ResearchOpen Access17 Jan 2017
Scientific Reports

Volume: 7, P: 1-12
Host factors are associated with vaginal microbiome structure in pregnancy in the ECHO Cohort Consortium

Kimberly McKee
Christine M. Bassis
Lynne M. Smith
ResearchOpen Access23 May 2024
Scientific Reports

Volume: 14, P: 1-19
A proteogenomic view of Parkinson’s disease causality and heterogeneity

Sergio Kaiser
Luqing Zhang
Pablo Serrano-Fernandez
ResearchOpen Access11 Feb 2023
npj Parkinson's Disease

Volume: 9, P: 1-13
On the survival of the quantum depletion of a condensate after release from a magnetic trap

J. A. Ross
P. Deuar
A. G. Truscott
ResearchOpen Access01 Aug 2022
Scientific Reports

Volume: 12, P: 1-15
An era of single-cell genomics consortia

Yoshinari Ando
Andrew Tae-Jun Kwon
Jay W. Shin
ReviewsOpen Access15 Sept 2020
Experimental & Molecular Medicine

Volume: 52, P: 1409-1418
Single-cell transcriptome analyses reveal distinct gene expression signatures of severe COVID-19 in the presence of clonal hematopoiesis

Baekgyu Choi
Chang Kyung Kang
Inkyung Jung
ResearchOpen Access13 Oct 2022
Experimental & Molecular Medicine

Volume: 54, P: 1756-1765
CohortFinder: an open-source tool for data-driven partitioning of digital pathology and imaging cohorts to yield robust machine-learning models

Fan Fan
Georgia Martinez
Andrew Janowczyk
ResearchOpen Access01 Jul 2024
npj Imaging

Volume: 2, P: 1-7
Recombinant human B cell repertoires enable screening for rare, specific, and natively paired antibodies

Saravanan Rajan et al. describe a high-throughput method for isolating unique human monoclonal antibodies using picoliter sized droplets containing primary B cells. They show this approach can rapidly drive selection towards novel antibodies against clinically-relevant influenza hemagglutinin subtypes.

Saravanan Rajan
Michael R. Kierny
Partha S. Chowdhury
ResearchOpen Access22 Jan 2018
Communications Biology

Volume: 1, P: 1-8
Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment

Marie Morimoto
Vikas Bhambhani
May Christine V. Malicdan
ResearchOpen Access10 Feb 2023
npj Genomic Medicine

Volume: 8, P: 1-16
The United States COVID-19 Forecast Hub dataset

Estee Y. Cramer
Yuxin Huang
Nicholas G. Reich
ResearchOpen Access01 Aug 2022
Scientific Data

Volume: 9, P: 1-15
The bacterium Wolbachia exploits host innate immunity to establish a symbiotic relationship with the dengue vector mosquito Aedes aegypti

Xiaoling Pan
Andrew Pike
Zhiyong Xi
ResearchOpen Access03 Nov 2017
The ISME Journal

Volume: 12, P: 277-288
Investigating the neuroimmunogenic architecture of schizophrenia

R Birnbaum
A E Jaffe
D R Weinberger
Research09 May 2017
Molecular Psychiatry

Volume: 23, P: 1251-1260
Mixed versus pure variants of desmoplastic melanoma: a genetic and immunohistochemical appraisal

Daniel D Miller
Andrew Emley
Meera Mahalingam
Research09 Dec 2011
Modern Pathology

Volume: 25, P: 505-515
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Lance H. Rodan
Rebecca C. Spillmann
Vandana Shashi
Research23 Jun 2021
Genetics in Medicine

Volume: 23, P: 1922-1932
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Sacha Ferdinandusse
Kirsty McWalter
Frédéric M. Vaz
ResearchOpen Access26 Nov 2020
Genetics in Medicine

Volume: 23, P: 740-750
Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

Felix Marbach
Georgi Stoyanov
Christian P. Schaaf
ResearchOpen Access08 Apr 2021
Genetics in Medicine

Volume: 23, P: 1465-1473
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

Thomas A. Ravenscroft
Jennifer B. Phillips
Hugo J. Bellen
Research10 Jun 2021
Genetics in Medicine

Volume: 23, P: 1889-1900
Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

Kelly Schoch
Cecilia Esteves
Vandana Shashi
Research23 Oct 2020
Genetics in Medicine

Volume: 23, P: 259-271
Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

Shilpa Nadimpalli Kobren
Dustin Baldridge
Isaac S. Kohane
ResearchOpen Access12 Feb 2021
Genetics in Medicine

Volume: 23, P: 1075-1085
Engineering and characterisation of chimeric monoclonal antibody 806 (ch806) for targeted immunotherapy of tumours expressing de2-7 EGFR or amplified EGFR

C Panousis
V M Rayzman
A M Scott
ResearchOpen Access15 Mar 2005
British Journal of Cancer

Volume: 92, P: 1069-1077
Author Correction: Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis

Joana Carlevaro-Fita
Andrés Lanzós
Christian von Mering
Amendments and CorrectionsOpen Access08 Dec 2022
Communications Biology

Volume: 5, P: 1
Differential expression of MicroRNAs in Alzheimer’s disease: a systematic review and meta-analysis

Sojung Yoon
Sung Eun Kim
Paolo Fusar-Poli
Reviews09 Mar 2022
Molecular Psychiatry

Volume: 27, P: 2405-2413
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

Ida E. Sønderby
Ómar Gústafsson
Ole A. Andreassen
Amendments and Corrections31 Jan 2019
Molecular Psychiatry

Volume: 25, P: 692-695
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

A Hinney
M Kesselmeier
J Hebebrand
Research17 May 2016
Molecular Psychiatry

Volume: 22, P: 192-201
Correction: ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs

Marina T. DiStefano
Sarah E. Hemphill
Keijan Zhang
Amendments and Corrections22 May 2019
Genetics in Medicine

Volume: 21, P: 2409
Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Lance H. Rodan
Rebecca C. Spillmann
Vandana Shashi
Amendments and Corrections14 Sept 2021
Genetics in Medicine

Volume: 23, P: 2016
Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Sacha Ferdinandusse
Kirsty McWalter
Frédéric M. Vaz
Amendments and CorrectionsOpen Access19 Oct 2021
Genetics in Medicine

Volume: 23, P: 2467

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