Nature Search

Fetal-Like Erythropoiesis during Recovery from Transient Erythroblastopenia of Childhood (TEC)

Michael P Link
Blanche P Alter
Research01 Jul 1981
Pediatric Research

Volume: 15, P: 1036-1039
A most Friendly meeting

BLANCHE ALTER
ALBERT DEISSEROTH
News & Views25 Dec 1975
Nature

Volume: 258, P: 663
Benefits for children with suspected cancer from routine whole-genome sequencing

In a cohort of 281 children with diagnosed or suspected cancer presenting to the NHS, implementing routine whole-genome sequencing provided clinical benefit in 29% of cases and led to change in management in 7% of patients.

Angus Hodder
Sarah M. Leiter
Sam Behjati
ResearchOpen Access02 Jul 2024
Nature Medicine

Volume: 30, P: 1905-1912
Genome-wide association study identifies multiple risk loci for renal cell carcinoma

Risk for renal cell carcinoma (RCC) is higher when there are first-degree family members with the disease. Here, Scelo and colleagues perform a genome-wide association meta-analysis and new genome-wide scan to identify seven new loci with significant RCC association.

Ghislaine Scelo
Mark P. Purdue
Stephen J. Chanock
ResearchOpen Access09 Jun 2017
Nature Communications

Volume: 8, P: 1-9
Dynamic analysis of geomaterials using microwave sensing

Jamie Blanche
Daniel Mitchell
Marc Desmulliez
ResearchOpen Access26 Mar 2024
Scientific Reports

Volume: 14, P: 1-17
(CAG)nCAA and GGN repeats in the human androgen receptor gene are not associated with prostate cancer in a French–German population

Lina Correa-Cerro
Gudrun Wöhr
Walther Vogel
Research05 May 1999
European Journal of Human Genetics

Volume: 7, P: 357-362
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25

A genome-wide association study for lung cancer finds that genetic sequences in the nicotinic acetylcholine receptor subunit gene cluster contribute susceptibility. Interestingly, this susceptibility is not related to smoking status or frequency, and seems to come from a change in an amino acid in the receptor itself.

Rayjean J. Hung
James D. McKay
Paul Brennan
Research03 Apr 2008
Nature

Volume: 452, P: 633-637
RED CELL SIZE HETEROGENEITY DURING ONDOGENY

Blanche P Alter
James D Goldberg
Richard L Berkowitz
Research01 Apr 1987
Pediatric Research

Volume: 21, P: 296
ERYTHROCYTE CHARACTERISTICS IN CHILDHOOD ACUTE LEUKEMIA

Blanche P Alter
Michael A Weiner
Michael B Harris
Research01 Apr 1987
Pediatric Research

Volume: 21, P: 296
Erythropoiesis is Distinct at Each Stage of Ontogeny

Rona S Weinberg
Liya He
Blanche P Alter
Research01 Feb 1992
Pediatric Research

Volume: 31, P: 170-175
504 REGULATION OF GLOBIN CHAIN SYNTHESIS IN NEONATES

Blanche P Alter
Arthur L Beaudet
Charles I Scott
Research01 Apr 1978
Pediatric Research

Volume: 12, P: 447
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

Iris Heid, Gonçalo Abecasis, Sudha Iyengar and colleagues report the results of a large genome-wide association meta-analysis of macular degeneration based on over 43,000 subjects. They identify 16 new risk loci, including some very rare coding variants.

Lars G Fritsche
Wilmar Igl
Iris M Heid
Research21 Dec 2015
Nature Genetics

Volume: 48, P: 134-143
505 SEPARATION OF FETAL AND ADULT ERYTHROCYTES BY SELECTIVE HEMOLYSIS: AN AID TO PERNTAL DIAGNOSIS OF HEMOGLOBINOPATHIES

Blanche P Alter
David G Nathan
Bernard G Forget
Research01 Apr 1978
Pediatric Research

Volume: 12, P: 448
Transient viral exposure drives functionally-coordinated humoral immune responses in HIV-1 post-treatment controllers

A rare sub-population of people living with HIV-1 experience long-lasting viral remission after interrupting antiretroviral therapy and are considered post-treatment controllers. Here the authors characterise the humoral immune response to HIV-1 in a cohort of post-treatment controllers.

Luis M. Molinos-Albert
Valérie Lorin
Laetitia Laine
ResearchOpen Access11 Apr 2022
Nature Communications

Volume: 13, P: 1-17
2023 International Rome consensus for the nomenclature of Sjögren disease

In this Consensus Statement, an international group of experts and patient representatives validates and endorses the transition from the term ‘Sjögren syndrome’ to ‘Sjögren disease’, and issue several additional recommendations regarding the nomenclature of this disorder.

Manuel Ramos-Casals
Alan N. Baer
Arjan Vissink
Reviews10 Jun 2025
Nature Reviews Rheumatology

Volume: 21, P: 426-437
Correction: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

Corine Bertolotto
Fabienne Lesueur
Brigitte Bressac-de Paillerets
Amendments and Corrections02 Dec 2015
Nature

Volume: 531, P: 126
887 CONGENITAL DYSERYTHROPOIETIC ANEMIA (CDA) WITH KARYORRHEXIS

Joel A Brochstein
Salvatore Siena
Blanche P Alter
Research01 Apr 1985
Pediatric Research

Volume: 19, P: 258
The SND proteins constitute an alternative targeting route to the endoplasmic reticulum

Experiments in yeast cells show that three proteins—Snd1, Snd2 and Snd3—provide an alternative pathway for targeting of cellular proteins to the endoplasmic reticulum.

Naama Aviram
Tslil Ast
Maya Schuldiner
Research30 Nov 2016
Nature

Volume: 540, P: 134-138
Crystal structure of RecBCD enzyme reveals a machine for processing DNA breaks

Martin R. Singleton
Mark S. Dillingham
Dale B. Wigley
Research11 Nov 2004
Nature

Volume: 432, P: 187-193
Interleukin-1β-mediated induction of Cox-2 in the CNS contributes to inflammatory pain hypersensitivity

Tarek A. Samad
Kimberly A. Moore
Clifford J. Woolf
Research22 Mar 2001
Nature

Volume: 410, P: 471-475
1257 STORAGE OF TERM PLACENTAL BLOOD FOR AUTOTRANSFUSION

Joseph M Brandes
Eugene F Roth Jr.
Paul D Berk
Research01 Apr 1981
Pediatric Research

Volume: 15, P: 652
Use of Erythropoietin in Stable Preterm Infants (1000-1500 grams) to Reduce Erythrocyte Transfusions † 1374

Alagappan Alagappan
Blanche P Alter
Michael H Malloy
Research01 Apr 1998
Pediatric Research

Volume: 43, P: 235
Telomere shortening and loss of self-renewal in dyskeratosis congenita induced pluripotent stem cells

Luis F. Z. Batista
Matthew F. Pech
Steven E. Artandi
Research22 May 2011
Nature

Volume: 474, P: 399-402
Determination of the relative contribution of three genes–the cystic fibrosis transmembrane conductance regulator gene, the cationic trypsinogen gene, and the pancreatic secretory trypsin inhibitor gene–to the etiology of idiopathic chronic pancreatitis

Marie-Pierre Audrézet
Jian-Min Chen
Claude Férec
Research05 Apr 2002
European Journal of Human Genetics

Volume: 10, P: 100-106
Expression of RMRP RNA is regulated in chondrocyte hypertrophy and determines chondrogenic differentiation

Mandy M. F. Steinbusch
Marjolein M. J. Caron
Tim J. M. Welting
ResearchOpen Access25 Jul 2017
Scientific Reports

Volume: 7, P: 1-15
Crystal structure of the integral membrane diacylglycerol kinase

This study presents the crystal structures of three functional forms of diacylglycerol kinase, an integral membrane protein that catalyses a crucial step in oligosaccharide and lipopolysaccharide synthesis and assembly; these X-ray structures are markedly different from the only other structure available for this unique kinase that was solved using solution NMR.

Dianfan Li
Joseph A. Lyons
Martin Caffrey
Research15 May 2013
Nature

Volume: 497, P: 521-524
Functional Screening Identifies MicroRNAs as Multi-Cellular Regulators of Heart Failure

Robin Verjans
Wouter J. A. Derks
Stephane Heymans
ResearchOpen Access15 Apr 2019
Scientific Reports

Volume: 9, P: 1-15
Bone mineral density in patients with inherited bone marrow failure syndromes

Roopa Kanakatti Shankar
Neelam Giri
Blanche P Alter
Research31 May 2017
Pediatric Research

Volume: 82, P: 458-464
Pseudomonas Aeruginosa Virulence Factors Delay Airway Epithelial Wound Repair by Altering the Actin Cytoskeleton and Inducing Overactivation of Epithelial Matrix Metalloproteinase–2

Sophie de Bentzmann
Myriam Polette
Edith Puchelle
Research01 Feb 2000
Laboratory Investigation

Volume: 80, P: 209-219
Heritability, phenotypic and genetic correlations of size and shape of Drosophila mediopunctata wings

Blanche Christine Bitner-Mathé
Louis Bernard Klaczko
Research01 Dec 1999
Heredity

Volume: 83, P: 688-696
Research participant interest in primary, secondary, and incidental genomic findings

Jennifer T. Loud
Renee C. Bremer
Sharon A. Savage
Research21 Apr 2016
Genetics in Medicine

Volume: 18, P: 1218-1225
Long-Term Impairment in the Neurochemical Activity of the Sympathoadrenal System after Neonatal Hypoxia in the Rat

Valerie Soulier
Julie Peyronnet
Yvette Dalmaz
Research01 Jul 1997
Pediatric Research

Volume: 42, P: 30-38
Identifying robust communities and multi-community nodes by combining top-down and bottom-up approaches to clustering

Chris Gaiteri
Mingming Chen
Vitalina Komashko
ResearchOpen Access09 Nov 2015
Scientific Reports

Volume: 5, P: 1-14
A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Tobias Strunz
Susette Lauwen
Bernhard H. F. Weber
ResearchOpen Access31 Jan 2020
Scientific Reports

Volume: 10, P: 1-16
Effects of eight neuropsychiatric copy number variants on human brain structure

Claudia Modenato
Kuldeep Kumar
Sébastien Jacquemont
ResearchOpen Access20 Jul 2021
Translational Psychiatry

Volume: 11, P: 1-10
The Lim1 oncogene as a new therapeutic target for metastatic human renal cell carcinoma

Imène Hamaidi
Catherine Coquard
Thierry Massfelder
Research03 Aug 2018
Oncogene

Volume: 38, P: 60-72
Clostridium difficile clade 3 (RT023) have a modified cell surface and contain a large transposable island with novel cargo

Helen Alexandra Shaw
Ladan Khodadoost
Brendan W. Wren
ResearchOpen Access25 Oct 2019
Scientific Reports

Volume: 9, P: 1-12
Ubiquitin signalling in DNA replication and repair

Monoubiquitylation and polyubiquitylation by Lys63-linked chains contribute to three different pathways related to the maintenance of genome integrity that are responsible for the processing of DNA double-strand breaks, the repair of interstrand cross links and the bypass of lesions during DNA replication.

Helle D. Ulrich
Helen Walden
Reviews16 Jun 2010
Nature Reviews Molecular Cell Biology

Volume: 11, P: 479-489
Establishment of the first WHO international genetic reference panel for Prader Willi and Angelman syndromes

Jennifer Boyle
Malcolm Hawkins
J Ross Hawkins
Research18 May 2011
European Journal of Human Genetics

Volume: 19, P: 857-864
Shwachman Diamond syndrome: narrow genotypic spectrum and variable clinical features

Ashley S. Thompson
Neelam Giri
Lisa J. McReynolds
Research23 Mar 2022
Pediatric Research

Volume: 92, P: 1671-1680
Acceleration of clear cell renal cell carcinoma growth in mice following bevacizumab/Avastin treatment: the role of CXCL cytokines

R Grepin
M Guyot
G Pages
Research12 Sept 2011
Oncogene

Volume: 31, P: 1683-1694
Comparative studies on cellular gene regulation by HIV-1 based vectors: implications for quality control of vector production

Y Zhao
S Azam
R Thorpe
Research18 Nov 2004
Gene Therapy

Volume: 12, P: 311-319
Guidelines for the welfare and use of animals in cancer research

P Workman
E O Aboagye
S A Eccles
ReviewsOpen Access25 May 2010
British Journal of Cancer

Volume: 102, P: 1555-1577
Guidelines for the use of cell lines in biomedical research

R J Geraghty
A Capes-Davis
M Vias
ReviewsOpen Access12 Aug 2014
British Journal of Cancer

Volume: 111, P: 1021-1046

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