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Showing 1–50 of 128 results

Advanced filters: Author: S Huet Clear advanced filters

First evidence of coexistence of Pseudo Pelger Huet anomaly and balanced translocation in a two decades retrospectively exposed human subject

Rajesh Kumar Chaurasia
Ranjana S. Pathak
Balvinder K. Sapra
ResearchOpen Access11 Aug 2025
Scientific Reports

Volume: 15, P: 1-9
A neonate with the Pelger–Huët anomaly, cleft lip and palate, and agenesis of the corpus callosum, with a chromosomal microdeletion involving 1q41 to 1q42.12

R D Christensen
H M Yaish
Research28 Feb 2012
Journal of Perinatology

Volume: 32, P: 238-240
New system for assessing the prognosis of refractory anemia patients

A Matsuda
I Jinnai
M Tomonaga
Research03 Nov 1999
Leukemia

Volume: 13, P: 1727-1734
Refractory anemia with severe dysplasia: clinical significance of morphological features in refractory anemia

A Matsuda
I Jinnai
K Hirashima
Research08 May 1998
Leukemia

Volume: 12, P: 482-485
Comings and goings

Frank Gonzalez-Crussi
Books & Arts30 Sept 1993
Nature

Volume: 365, P: 399-400
Prospective study to analyze the yield and clinical impact of trio exome sequencing in 137 Indian children with autism spectrum disorder

Shruti Bajaj
Shreya Gandhi
Anaita Udwadia Hegde
Research21 Aug 2025
Journal of Human Genetics

P: 1-14
Control of 5S RNA synthesis in Xenopus laevis

PETER J. FORD
TOM MATHIESON
Research03 Jun 1976
Nature

Volume: 261, P: 433-435
Myelodysplastic/myeloproliferative neoplasms-unclassifiable with isolated isochromosome 17q represents a distinct clinico-biologic subset: a multi-institutional collaborative study from the Bone Marrow Pathology Group

Rashmi Kanagal-Shamanna
Attilio Orazi
Carlos Bueso-Ramos
Research13 Nov 2021
Modern Pathology

Volume: 35, P: 470-479
White blood cell left shift in a neonate: a case of mistaken identity

I S I Mohamed
R J Wynn
S Lakshminrusimha
Research25 May 2006
Journal of Perinatology

Volume: 26, P: 378-380
Author Correction: Deterministic and reconfigurable graph state generation with a single solid-state quantum emitter

H. Huet
P. R. Ramesh
P. Senellart
Amendments and CorrectionsOpen Access19 Jun 2025
Nature Communications

Volume: 16, P: 1
Wild Swine of Palawan and the Philippines

A. H. EVERETT
Research05 Mar 1891
Nature

Volume: 43, P: 416
Amino-Acids in the Hæmolymph of the Dragon-fly Nymph, Aeschna cyanea

RICHARD RAPER
JOHN SHAW
Research25 Dec 1948
Nature

Volume: 162, P: 999
Identification of self peptides bound to purified HLA-B27

T. S. Jardetzky
W. S. Lane
D. C. Wiley
Research26 Sept 1991
Nature

Volume: 353, P: 326-329
The structure of HLA-B27 reveals nonamer self-peptides bound in an extended conformation

D. R. Madden
J. C. Gorga
D. C. Wiley
Research26 Sept 1991
Nature

Volume: 353, P: 321-325
Haptotaxis and the Mechanism of Cell Motility

S. B. CARTER
Research21 Jan 1967
Nature

Volume: 213, P: 256-260
Deterministic and reconfigurable graph state generation with a single solid-state quantum emitter

Quantum emitters have recently been identified as efficient sources of graph states, which are entangled states crucial for photonic quantum computation. Here the authors demonstrate deterministic and reconfigurable generation of caterpillar graph states using a semiconductor quantum dot in a cavity.

H. Huet
P. R. Ramesh
P. Senellart
ResearchOpen Access09 May 2025
Nature Communications

Volume: 16, P: 1-8
Ezh2 loss promotes development of myelodysplastic syndrome but attenuates its predisposition to leukaemic transformation

Mutations in the EZH2 gene are found in myelodysplastic syndrome (MDS) and are often accompanied by mutations in RUNX1. Here, the authors develop a mouse model of MDS and show that EZH2loss enhances the RUNX1-mediated MDS pathology.

Goro Sashida
Hironori Harada
Atsushi Iwama
Research23 Jun 2014
Nature Communications

Volume: 5, P: 1-14
Ubiquitination of hnRNPA1 by TRAF6 links chronic innate immune signaling with myelodysplasia

Starczynowski and colleagues show that overexpression of TRAF6 in HSCs induces ubiquitination of the RNA-binding protein hnRNPA1 and alternative splicing of Arhgap1, which accounts for the hematopoietic defects in myelodysplastic syndromes.

Jing Fang
Lyndsey C Bolanos
Daniel T Starczynowski
Research26 Dec 2016
Nature Immunology

Volume: 18, P: 236-245
Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes

Christoph Klein and colleagues identify loss-of-function mutations in SMARCD2 (BAF60b) that lead to neutropenia, specific granule deficiency and myelodysplasia. They show that SMARCD2 controls differentiation of myeloid–erythroid progenitor cells through interaction with CEBPɛ and that reduced SMARCD2 levels cause transcription and chromatin alterations in acute myeloid leukemia cells.

Maximilian Witzel
Daniel Petersheim
Christoph Klein
Research03 Apr 2017
Nature Genetics

Volume: 49, P: 742-752
Morphological subtyping of acute myeloid leukemia with maturation (AML-M2): homogeneous pink-colored cytoplasm of mature neutrophils is most characteristic of AML-M2 with t(8;21)

H Nakamura
K Kuriyama
M Tomonaga
Research01 May 1997
Leukemia

Volume: 11, P: 651-655
Biological Half-life of Mouse Transferrins

J. WATKINS
D. E. H. TEE
OLWYNNE TARLOW
Research12 Nov 1966
Nature

Volume: 212, P: 706-707
Elastin peptides regulate HT-1080 fibrosarcoma cell migration and invasion through an Hsp90-dependent mechanism

M Donet
S Brassart-Pasco
B Brassart
ResearchOpen Access29 May 2014
British Journal of Cancer

Volume: 111, P: 139-148
Defining clinical subgroups and genotype–phenotype correlations in NBAS-associated disease across 110 patients

Christian Staufner
Bianca Peters
Dominic Lenz
Research25 Nov 2019
Genetics in Medicine

Volume: 22, P: 610-621
Forbidden Lines from Atomic Sulphur

J. W. McCONKEY
D. J. BURNS
L. HERMAN
Research01 Dec 1964
Nature

Volume: 204, P: 1180
A Method of obtaining Glochidia

G. P. DARNELL-SMITH
Research06 Jul 1893
Nature

Volume: 48, P: 223
Acute myeloid leukemia (AML) having evolved from essential thrombocythemia (ET): distinctive chromosome abnormalities in patients treated with pipobroman or hydroxyurea

P Bernasconi
M Boni
C Bernasconi
Research02 Oct 2002
Leukemia

Volume: 16, P: 2078-2083
Minerals in the Livers of Protein Deficient Rats

F. GAUDIN-HARDING
D. ROBIN
M. PINTA
Research12 Nov 1966
Nature

Volume: 212, P: 707-708
Statistical Studies of Evolution

C. A. F. PANTIN
Research01 Apr 1922
Nature

Volume: 109, P: 413
P-glycoprotein overexpression cannot explain the complete doxorubicin-resistance phenotype in rat glioblastoma cell lines

S Huet
B Schott
J Robert
Research01 Apr 1992
British Journal of Cancer

Volume: 65, P: 538-544
Insertion of E. coli photoreactivating enzyme into V79 hamster cells

Betsy M. Sutherland
S. G. Hausrath
Research31 Jul 1980
Nature

Volume: 286, P: 510-511
Stimulation of RNA synthesis in isolated nuclei by an insulin-induced factor in liver

Agnes Horvat
Research28 Aug 1980
Nature

Volume: 286, P: 906-908
Complete fusion of a transposon and herpesvirus created the Teratorn mobile element in medaka fish

Teratorn is a large mobile genetic element originally identified in the small teleost fish medaka. Here, the authors show that Teratorn is derived from the fusion of a piggyBac superfamily DNA transposon and an alloherpesvirus and that it is widely found across teleost fish.

Yusuke Inoue
Tomonori Saga
Hiroyuki Takeda
ResearchOpen Access15 Sept 2017
Nature Communications

Volume: 8, P: 1-14
CHD6 has poly(ADP-ribose)- and DNA-binding domains and regulates PARP1/2-trapping inhibitor sensitivity via abasic site repair

Discovering molecular pathways that sensitize cells to poly(ADP-ribose) polymerase (PARP)- trapping inhibitors is important for anti-cancer therapy. Here, the authors report that inactivation of the CHD6 chromatin remodelling enzyme sensitizes cells to PARP inhibitors via reduced abasic site repair, PARP-1 accumulation on chromatin, and replication stress.

Luc Provencher
Wilson Nartey
Aaron A. Goodarzi
ResearchOpen Access25 Jan 2025
Nature Communications

Volume: 16, P: 1-24
Selective proteolysis defines two DNA binding domains in yeast transcription factor τ

N. Marzouki
S. Camier
A. Sentenac
Research11 Sept 1986
Nature

Volume: 323, P: 176-178
Genetic evidence equating SRY and the testis-determining factor

Philippe Berta
J. Boss Hawkins
Marc Fellous
Research29 Nov 1990
Nature

Volume: 348, P: 448-450
Human aminopeptidase N is a receptor for human coronavirus 229E

Curtis L. Yeager
Richard A. Ashmun
Kathryn V. Holmes
Research04 Jun 1992
Nature

Volume: 357, P: 420-422
A nucleoprotein peptide of influenza A virus stimulates assembly of HLA-B27 class I heavy chains and β₂-micro-globulin translated in vitro

Sune Kvist
Ute Hamann
Research29 Nov 1990
Nature

Volume: 348, P: 446-448
Effect of cortisol, prolactin and ADH on the amniotic membrane

M. S. MANKU
J. P. MTABAJI
D. F. HORROBIN
Research06 Nov 1975
Nature

Volume: 258, P: 78-80
Potent neutralizing nanobodies resist convergent circulating variants of SARS-CoV-2 by targeting diverse and conserved epitopes

Highly potent neutralizing nanobodies (Nbs) are of great interest as potential COVID-19 therapeutics. Here, the authors show that potent neutralizing Nbs targeting the receptor binding domain (RBD) of the SARS-CoV-2 spike protein are also effective against convergent variants of concern of the virus. They determine eight Nb-bound spike protein cryo-EM structures, classify the binding epitopes of the Nbs and discuss their neutralization mechanisms.

Dapeng Sun
Zhe Sang
Yi Shi
ResearchOpen Access03 Aug 2021
Nature Communications

Volume: 12, P: 1-14
Leukaemogenesis induced by an activating β-catenin mutation in osteoblasts

A mouse model shows that osteoblast activating β-catenin mutations alone are sufficient to initiate the development of acute myeloid leukaemia acting through increased Notch signalling.

Aruna Kode
John S. Manavalan
Stavroula Kousteni
Research15 Jan 2014
Nature

Volume: 506, P: 240-244
CHD7 and 53BP1 regulate distinct pathways for the re-ligation of DNA double-strand breaks

Chromatin is dynamically remodeled in response to DNA damage in favour of repair. Here the authors reveal how the chromatin remodeler CHD7 and chromatin binding protein 53BP1 regulate distinct DNA repair pathways.

Magdalena B. Rother
Stefania Pellegrino
Haico van Attikum
ResearchOpen Access13 Nov 2020
Nature Communications

Volume: 11, P: 1-19
Clinical diagnosis of genetic disorders at both single-nucleotide and chromosomal levels based on BGISEQ-500 platform

Yanqiu Liu
Liangwei Mao
Xiaoming Wei
ResearchOpen Access22 May 2023
Human Genome Variation

Volume: 10, P: 1-43
Human laminopathies: nuclei gone genetically awry

Intense investigation of the laminopathies has revised the traditional structural view of the nuclear lamina, highlighting crucial roles in processes including gene regulation and differentiation. This research has also led to a range of promising therapies for these rare diseases.

Brian C. Capell
Francis S. Collins
Reviews01 Dec 2006
Nature Reviews Genetics

Volume: 7, P: 940-952
Classification of GBA1 variants and their impact on Parkinson’s disease: an in silico score analysis

Aymeric Lanore
Christelle Tesson
Eva Camgrand
ResearchOpen Access02 Aug 2025
npj Parkinson's Disease

Volume: 11, P: 1-14
Gene flow favours local adaptation under habitat choice in ciliate microcosms

Theory predicts that gene flow hinders local adaptation, unless it is coupled with habitat choice. Here, the authors show that dispersal with habitat choice favours local adaptation in ciliate microcosms.

Staffan Jacob
Delphine Legrand
Jean Clobert
Research14 Aug 2017
Nature Ecology & Evolution

Volume: 1, P: 1407-1410
Fundamentals of Physics

J. S. DOWKER
Books & Arts03 Oct 1970
Nature

Volume: 228, P: 95-96
Evaluation of Parameters of Folic Acid and Vitamin B₁₂ Deficiency in Patients with Iron Deficiency Anemia

P Vossough
S Leikin
G Gautier
Research01 May 1968
Pediatric Research

Volume: 2, P: 179-186
The International Institute of Bibliography

S. C. BRADFORD
News03 Nov 1928
Nature

Volume: 122, P: 710
Early presence of Homo sapiens in Southeast Asia by 86–68 kyr at Tam Pà Ling, Northern Laos

Here the authors report new human fossils from Tam Pà Ling cave, Laos, consisting of a cranial and a tibial fragment, dated to 68–86 thousand years ago. This find confirms that Homo sapiens were present in Southeast Asia by this time and the shape of the fossils indicates they may have descended from non-local populations.

Sarah E. Freidline
Kira E. Westaway
Fabrice Demeter
ResearchOpen Access13 Jun 2023
Nature Communications

Volume: 14, P: 1-21
Maintenance of the functional integrity of mouse hematopoiesis by EED and promotion of leukemogenesis by EED haploinsufficiency

Kenichiro Ikeda
Takeshi Ueda
Hiroaki Honda
ResearchOpen Access19 Jul 2016
Scientific Reports

Volume: 6, P: 1-13

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