Nature Search

Les Explosifs modernes

J. S. S. B.
Books & Arts22 Jun 1911
Nature

Volume: 86, P: 546-547
Survey of wheelchair athletic injuries: common patterns and prevention

Kathleen A Curtis
Deborah A Dillon
Research01 Jun 1985
Spinal Cord

Volume: 23, P: 170-175
Near-ultraviolet and visible spectrophotometry of comet Halley from Vega 2

G. Moreels
M. Gogoshev
V. Vanyšek
Research15 May 1986
Nature

Volume: 321, P: 271-273
Fetal Control of Calcium Transport across the Rat Placenta

N R Robinson
C P Sibley
R D H Boyd
Research01 Aug 1989
Pediatric Research

Volume: 26, P: 109-115
Single-cell multi-omics identifies chronic inflammation as a driver of TP53-mutant leukemic evolution

Single-cell multi-omic analyses show that chronic inflammation contributes to myeloproliferative neoplasm transformation to secondary acute myeloid leukemia by enhancing tumor protein 53 (TP53) mutant cell fitness and genetic evolution.

Alba Rodriguez-Meira
Ruggiero Norfo
Adam J. Mead
ResearchOpen Access04 Sept 2023
Nature Genetics

Volume: 55, P: 1531-1541
Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization

Nephrophthisis (NPH) is a common manifestation of ciliopathy diseases. Here the authors identify mutations in intraflagellar transport 54 (IFT54) in patients with NPH and discover an extra-ciliary role for IFT54 in regulating cytoplasmic microtubule dynamics, that contributes to the pathophysiology of this disease.

Albane A. Bizet
Anita Becker-Heck
Sophie Saunier
ResearchOpen Access21 Oct 2015
Nature Communications

Volume: 6, P: 1-14
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection

Yanick J Crow
Andrea Leitch
Andrew P Jackson
Research16 Jul 2006
Nature Genetics

Volume: 38, P: 910-916
Assembly Pheromone(s) in the Soft Tick Argas persicus (Oken)

M. G. LEAHY
R. VANDEHEY
R. GALUN
Research21 Dec 1973
Nature

Volume: 246, P: 515-517
Association analysis of polymorphisms in the prepronociceptin gene and schizophrenia

K. Imai
S. Harada
T. Suzuki
Research01 Aug 2001
Journal of Human Genetics

Volume: 46, P: 442-447
p73 is over-expressed in vulval cancer principally as the Δ2 isoform

J O'Nions
L A Brooks
T Crook
ResearchOpen Access13 Nov 2001
British Journal of Cancer

Volume: 85, P: 1551-1556
Mutation analysis of P73 and TP53 in Merkel cell carcinoma

M Van Gele
M Kaghad
F Speleman
ResearchOpen Access20 Jan 2000
British Journal of Cancer

Volume: 82, P: 823-826
A common p73 polymorphism is associated with a reduced incidence of oesophageal carcinoma

B M Ryan
R McManus
D Kelleher
ResearchOpen Access13 Nov 2001
British Journal of Cancer

Volume: 85, P: 1499-1503
Absence of mutation of the p73 gene localized at chromosome 1p36.3 in hepatocellular carcinoma

M Mihara
Y Nimura
A Nakagawara
ResearchOpen Access11 Dec 1998
British Journal of Cancer

Volume: 79, P: 164-167
Impact of sentinel node biopsy on long-term quality of life in breast cancer patients

E De Gournay
A Guyomard
T S Dabakuyo-Yonli
ResearchOpen Access29 Oct 2013
British Journal of Cancer

Volume: 109, P: 2783-2791
Calbindin-D_9K Gene Expression in Rat Chorioallantoic Placenta Is Not Regulated by 1,25-Dihydroxyvitamin D₃

J D Glazier
E B Mawer
C P Sibley
Research01 Jun 1995
Pediatric Research

Volume: 37, P: 720-725
The important balance between cytokines derived from type 1 and type 2 helper T cells in the control of graft-versus-host disease

J Tanaka
M Imamura
M Asaka
Research01 Mar 1997
Bone Marrow Transplantation

Volume: 19, P: 571-576
T-bet expression in intratumoral lymphoid structures after neoadjuvant trastuzumab plus docetaxel for HER2-overexpressing breast carcinoma predicts survival

S Ladoire
L Arnould
F Ghiringhelli
ResearchOpen Access12 Jul 2011
British Journal of Cancer

Volume: 105, P: 366-371
Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1

Birgitte Lane and colleagues show that Ferguson-Smith disease, an autosomal dominant skin cancer condition characterized by the development of multiple self-healing tumors, is caused by a disease-specific spectrum of mutations in TGFBR1.

David R Goudie
Mariella D'Alessandro
E Birgitte Lane
Research27 Feb 2011
Nature Genetics

Volume: 43, P: 365-369
Transcriptional dysregulation of the p73L / p63 / p51 / p40 / KET gene in human squamous cell carcinomas: expression of Δ Np73L, a novel dominant-negative isoform, and loss of expression of the potential tumour suppressor p51

M Senoo
I Tsuchiya
S Habu
ResearchOpen Access01 May 2001
British Journal of Cancer

Volume: 84, P: 1235-1241
AIF-mediated caspase-independent necroptosis requires ATM and DNA-PK-induced histone H2AX Ser139 phosphorylation

M Baritaud
L Cabon
S A Susin
ResearchOpen Access13 Sept 2012
Cell Death & Disease

Volume: 3, P: e390
Radiation-induced G₁ arrest is not defective in fibroblasts from Li-Fraumeni families without TP53 mutations

J M Boyle
M J Greaves
J M Varley
ResearchOpen Access12 Mar 1999
British Journal of Cancer

Volume: 79, P: 1657-1664
Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival

G Ragnarsson
G Eiriksdottir
S Ingvarsson
ResearchOpen Access26 Feb 1999
British Journal of Cancer

Volume: 79, P: 1468-1474
BID regulates AIF-mediated caspase-independent necroptosis by promoting BAX activation

L Cabon
P Galán-Malo
S A Susin
Research08 Jul 2011
Cell Death & Differentiation

Volume: 19, P: 245-256
The expression of p73 is increased in lung cancer, independent of p53 gene alteration

Y Tokuchi
T Hashimoto
E Tsuchiya
ResearchOpen Access25 Jun 1999
British Journal of Cancer

Volume: 80, P: 1623-1629
318 Maternal LPS Enhances Excitotoxic Brain Lesions in Newborn Rats

C Rousset
P Gressens
E Saliba
Research01 Aug 2005
Pediatric Research

Volume: 58, P: 409
319 Maternal LPS Treatment Induces Apoptosis and White Matter Lesions in Newborn Rat Brain

C Rousset
S Cantagrel
E Saliba
Research01 Aug 2005
Pediatric Research

Volume: 58, P: 409
Differences in epitope accessibility of p53 monoclonal antibodies suggest at least three conformations or states of protein binding of p53 protein in human tumor cell lines

Mary K Danks
David O Whipple
Linda C Harris
Research03 Aug 1998
Cell Death & Differentiation

Volume: 5, P: 678-686
Reduced Symptoms of Inattention after Dietary Omega-3 Fatty Acid Supplementation in Boys with and without Attention Deficit/Hyperactivity Disorder

Dienke J Bos
Bob Oranje
Sarah Durston
ResearchOpen Access19 Mar 2015
Neuropsychopharmacology

Volume: 40, P: 2298-2306
p53 family genes: structural comparison, expression and mutation

S Ikawa
A Nakagawara
Y Ikawa
Reviews13 Nov 1999
Cell Death & Differentiation

Volume: 6, P: 1154-1161
Toxic iron species in lower-risk myelodysplastic syndrome patients: course of disease and effects on outcome

Marlijn Hoeks
Tim Bagguley
L. Bond
ResearchOpen Access18 Sept 2020
Leukemia

Volume: 35, P: 1745-1750
Heterozygous deletion of the LRFN2 gene is associated with working memory deficits

Julien Thevenon
Céline Souchay
Laurence Faivre
Research21 Oct 2015
European Journal of Human Genetics

Volume: 24, P: 911-918
Long-term follow-up confirms the benefit of all-trans retinoic acid in acute promyelocytic leukemia

P Fenaux
S Chevret
L Degos
Research04 Aug 2000
Leukemia

Volume: 14, P: 1371-1377
Long-term outcome with pentostatin treatment in hairy cell leukemia patients. A French retrospective study of 238 patients

F Maloisel
L Benboubker
S Castaigne
Research03 Jan 2003
Leukemia

Volume: 17, P: 45-51
Extramedullary relapse in acute promyelocytic leukemia treated with all-trans retinoic acid and chemotherapy

S de Botton
M A Sanz
P Fenaux
Research24 Nov 2005
Leukemia

Volume: 20, P: 35-41
Age, JAK2^V617F and SF3B1 mutations are the main predicting factors for survival in refractory anaemia with ring sideroblasts and marked thrombocytosis

J Broséus
T Alpermann
S Schnittger
Research18 Apr 2013
Leukemia

Volume: 27, P: 1826-1831
Early onset of chemotherapy can reduce the incidence of ATRA syndrome in newly diagnosed acute promyelocytic leukemia (APL) with low white blood cell counts: results from APL 93 trial

S de Botton
S Chevret
P Fenaux
Research18 Feb 2003
Leukemia

Volume: 17, P: 339-342
Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma

Maroulio Pertesi
Maxime Vallée
Charles Dumontet
ResearchOpen Access09 Apr 2019
Leukemia

Volume: 33, P: 2324-2330
Minor clone provides a reservoir for relapse in multiple myeloma

F Magrangeas
H Avet-Loiseau
S Minvielle
Research09 Aug 2012
Leukemia

Volume: 27, P: 473-481
Identification of New Prognosis Factors from the Clinical and Epidemiologic Analysis of a Registry of 229 Diamond-Blackfan Anemia Patients

Thiébaut-Noël Willig
Charlotte M Niemeyer
Narla Mohandas
Research01 Nov 1999
Pediatric Research

Volume: 46, P: 553
Prognostic implication of FLT3 and Ras gene mutations in patients with acute promyelocytic leukemia (APL): a retrospective study from the European APL Group

C Callens
S Chevret
H Dombret
Research12 May 2005
Leukemia

Volume: 19, P: 1153-1160
Low rate of calreticulin mutations in refractory anaemia with ring sideroblasts and marked thrombocytosis

J Broséus
E Lippert
F Girodon
Correspondence30 Jan 2014
Leukemia

Volume: 28, P: 1374-1376

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