Nature Search

Distinguishing benign from pathogenic duplications involving GPR101 and VGLL1-adjacent enhancers in the clinical setting with the bioinformatic tool POSTRE

Giampaolo Trivellin
Víctor Sánchez-Gaya
Adrian F. Daly
ResearchOpen Access15 Jan 2026
npj Genomic Medicine

P: 1-12
RETRACTED ARTICLE: High expression of PKA regulatory subunit 1A protein is related to proliferation of human melanoma cells

G Mantovani
S Bondioni
A Spada
Research01 Oct 2007
Oncogene

Volume: 27, P: 1834-1843
Retraction Note: High expression of PKA regulatory subunit 1A protein is related to proliferation of human melanoma cells

G. Mantovani
S. Bondioni
A. Spada
Amendments and Corrections28 Jul 2025
Oncogene

Volume: 44, P: 3040
Epilepsy and brain abnormalities in mice lacking the Otx1 gene

Dario Acampora
Sylvie Mazan
Antonio Simeone
Research01 Oct 1996
Nature Genetics

Volume: 14, P: 218-222
A human homoeo box gene specifically expressed in spinal cord during embryonic development

A. Simeone
F. Mavilio
C. Peschle
Research24 Apr 1986
Nature

Volume: 320, P: 763-765
59 Analysis of N-Ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissues

A Lolascon
A Lania
S Cutillo
Research01 Sept 1990
Pediatric Research

Volume: 28, P: 287
Mechanisms of Disease: mutations of G proteins and G-protein-coupled receptors in endocrine diseases

Many hormones use G-protein-coupled receptors and G proteins in the target cell to transduce their signals. A range of disease-causing mutations have been characterized that mimic states of hormone deficiency or excess. This Review describes these mutations, and their resultant clinical and biochemical features.

Andrea G Lania
Giovanna Mantovani
Anna Spada
Reviews01 Dec 2006
Nature Clinical Practice Endocrinology & Metabolism

Volume: 2, P: 681-693
Molecular analysis of α-thalassemia in Nepal: correlation with malaria endemicity

Y. Sakai
S. Kobayashi
Y. Fukumaki
Research01 May 2000
Journal of Human Genetics

Volume: 45, P: 127-132
ID1 and ID2 are retinoic acid responsive genes and induce a G0/G1 accumulation in acute promyelocytic leukemia cells

J Nigten
M C Breems-de Ridder
J H Jansen
Research03 Mar 2005
Leukemia

Volume: 19, P: 799-805
Skeletal disorders associated with the growth hormone–insulin-like growth factor 1 axis

The growth hormone (GH)–insulin-like growth factor 1 (IGF1) axis regulates bone remodelling and metabolism. This Review highlights the pathophysiological and clinical aspects of skeletal fragility associated with perturbations in the GH–IGF1 axis such as GH deficiency, anorexia nervosa, ageing and acromegaly.

Gherardo Mazziotti
Andrea G. Lania
Ernesto Canalis
Reviews14 Mar 2022
Nature Reviews Endocrinology

Volume: 18, P: 353-365
Erratum: miR-194-5p/BCLAF1 deregulation in AML tumorigenesis

C Dell'Aversana
C Giorgio
L Altucci
Amendments and Corrections22 Dec 2017
Leukemia

Volume: 32, P: 573
miR-194-5p/BCLAF1 deregulation in AML tumorigenesis

C Dell'Aversana
C Giorgio
L Altucci
ResearchOpen Access20 Feb 2017
Leukemia

Volume: 31, P: 2315-2325
Dopamine D₂ receptor gene polymorphisms and response to cabergoline therapy in patients with prolactin-secreting pituitary adenomas

M Filopanti
A M Barbieri
A Spada
Research11 Mar 2008
The Pharmacogenomics Journal

Volume: 8, P: 357-363

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Distinguishing benign from pathogenic duplications involving GPR101 and VGLL1-adjacent enhancers in the clinical setting with the bioinformatic tool POSTRE

RETRACTED ARTICLE: High expression of PKA regulatory subunit 1A protein is related to proliferation of human melanoma cells

Retraction Note: High expression of PKA regulatory subunit 1A protein is related to proliferation of human melanoma cells

Epilepsy and brain abnormalities in mice lacking the Otx1 gene

A human homoeo box gene specifically expressed in spinal cord during embryonic development

59 Analysis of N-Ras gene mutations in medulloblastomas by polymerase chain reaction and oligonucleotide probes in formalin-fixed, paraffin-embedded tissues

Mechanisms of Disease: mutations of G proteins and G-protein-coupled receptors in endocrine diseases

Molecular analysis of α-thalassemia in Nepal: correlation with malaria endemicity

ID1 and ID2 are retinoic acid responsive genes and induce a G0/G1 accumulation in acute promyelocytic leukemia cells

Skeletal disorders associated with the growth hormone–insulin-like growth factor 1 axis

Erratum: miR-194-5p/BCLAF1 deregulation in AML tumorigenesis

miR-194-5p/BCLAF1 deregulation in AML tumorigenesis

Dopamine D₂ receptor gene polymorphisms and response to cabergoline therapy in patients with prolactin-secreting pituitary adenomas

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