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Rare earth elements mining investment: It is not all about China

Resources policy, 2017-09, Vol.53, p.66-76

2017

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The Knowledge Absorptive Capacity to Improve the Cooperation and Innovation in the Firm

Journal of industrial engineering and management, 2018-01, Vol.11 (2), p.290-307

2018

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Rare earth elements price forecasting by means of transgenic time series developed with ARIMA models

Resources policy, 2018-12, Vol.59, p.95-102

2018

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Okadaic acid toxin at sublethal dose produced cell proliferation in gastric and colon epithelial cell lines

Marine drugs, 2013-12, Vol.11 (12), p.4751-4760

2013

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Is Religiosity Related to Attitudes Toward Clinical Trials Participation?

Journal of cancer education, 2015-06, Vol.30 (2), p.220-224

2015

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Human NR5A1/SF-1 mutations show decreased activity on BDNF (brain-derived neurotrophic factor), an important regulator of energy balance: testing impact of novel SF-1 mutations beyond steroidogenesis

PloS one, 2014-08, Vol.9 (8), p.e104838-e104838

2014

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Hemizygosity at the NCF1 Gene in Patients with Williams-Beuren Syndrome Decreases Their Risk of Hypertension

American journal of human genetics, 2006-04, Vol.78 (4), p.533-542

2006

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Age and Gender Differences in Teen Relationship Violence

Journal of aggression, maltreatment & trauma, 2012-04, Vol.21 (3), p.351-364

2012

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Effect of Superior Ovarian Nerve and Plexus Nerve Sympathetic Denervation on Ovarian-Derived Infertility Provoked by Estradiol Exposure to Rats

Frontiers in physiology, 2019-04, Vol.10, p.349-349

2019

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Nerve Growth Factor: A Dual Activator of Noradrenergic and Cholinergic Systems of the Rat Ovary

Frontiers in endocrinology (Lausanne), 2021-02, Vol.12, p.636600-636600

2021

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Neosaxitoxin Inhibits the Expression of Inflammation Markers of the M1 Phenotype in Macrophages

Marine drugs, 2020-05, Vol.18 (6), p.283

2020

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Editorial: Teratogenesis: Experimental Models, Mechanisms and Clinical Findings in Humans

Frontiers in genetics, 2022-05, Vol.13, p.901400-901400

2022

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A novel immunomodulatory hemocyanin from the limpet Fissurella latimarginata promotes potent anti-tumor activity in melanoma

PloS one, 2014-01, Vol.9 (1), p.e87240-e87240

2014

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Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment

American journal of human genetics, 2012-11, Vol.91 (5), p.883-889

2012

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The Prevalence of Fetal Alcohol Spectrum Disorders in An American Indian Community

International journal of environmental research and public health, 2019-06, Vol.16 (12), p.2179

2019

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Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder

Human molecular genetics, 2009-05, Vol.18 (10), p.1795-1804

2009

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Cerebral arteriopathy associated with heterozygous Arg179Cys mutation in the ACTA2 gene: Report in 2 newborn siblings

Brain & development (Tokyo. 1979), 2017-01, Vol.39 (1), p.62-66

2017

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A neonatal case of vascular ring with Alagille syndrome

SAGE open medical case reports, 2023-01, Vol.11

2023

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Array-CGH in patients with Kabuki-like phenotype: identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration

BMC medical genetics, 2008-04, Vol.9 (1), p.27-27, Article 27

2008

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Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders

Molecular autism, 2015-04, Vol.6 (1), p.21-21, Article 21

2015

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Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease

Clinica chimica acta, 2014-11, Vol.437, p.88-92

2014

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Optimised low-dose multidetector CT protocol for children with cranial deformity

European radiology, 2013-08, Vol.23 (8), p.2279-2287

2013

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The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly

Human molecular genetics, 1999-12, Vol.8 (13), p.2479-2488

1999

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Association study of six candidate genes asymmetrically expressed in the two cerebral hemispheres suggests the involvement of BAIAP2 in autism

Journal of psychiatric research, 2011-02, Vol.45 (2), p.280-282

2011

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A review of the physical features of the fetal alcohol spectrum disorders

European journal of medical genetics, 2017-01, Vol.60 (1), p.55-64

2017

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Rare earth elements mining investment: It is not all about China

The Knowledge Absorptive Capacity to Improve the Cooperation and Innovation in the Firm

Rare earth elements price forecasting by means of transgenic time series developed with ARIMA models

Okadaic acid toxin at sublethal dose produced cell proliferation in gastric and colon epithelial cell lines

Is Religiosity Related to Attitudes Toward Clinical Trials Participation?

Human NR5A1/SF-1 mutations show decreased activity on BDNF (brain-derived neurotrophic factor), an important regulator of energy balance: testing impact of novel SF-1 mutations beyond steroidogenesis

Hemizygosity at the NCF1 Gene in Patients with Williams-Beuren Syndrome Decreases Their Risk of Hypertension

Age and Gender Differences in Teen Relationship Violence

Effect of Superior Ovarian Nerve and Plexus Nerve Sympathetic Denervation on Ovarian-Derived Infertility Provoked by Estradiol Exposure to Rats

Nerve Growth Factor: A Dual Activator of Noradrenergic and Cholinergic Systems of the Rat Ovary

Neosaxitoxin Inhibits the Expression of Inflammation Markers of the M1 Phenotype in Macrophages

Editorial: Teratogenesis: Experimental Models, Mechanisms and Clinical Findings in Humans

A novel immunomodulatory hemocyanin from the limpet Fissurella latimarginata promotes potent anti-tumor activity in melanoma

Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment

The Prevalence of Fetal Alcohol Spectrum Disorders in An American Indian Community

Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder

Cerebral arteriopathy associated with heterozygous Arg179Cys mutation in the ACTA2 gene: Report in 2 newborn siblings

A neonatal case of vascular ring with Alagille syndrome

Array-CGH in patients with Kabuki-like phenotype: identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration

Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders

Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease

Optimised low-dose multidetector CT protocol for children with cranial deformity

The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly

Association study of six candidate genes asymmetrically expressed in the two cerebral hemispheres suggests the involvement of BAIAP2 in autism

A review of the physical features of the fetal alcohol spectrum disorders

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