Search Results - "Bridoux, Marie"
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Proton Pump Inhibitors and Cancer: Current State of Play
Published in Frontiers in pharmacology (14-03-2022)“…Proton pump inhibitors (PPIs) are one of the most widely used drugs worldwide and are overprescribed in patients with cancer; there is increasing evidence of…”
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Loss-of-Function Mutations in the Human Ortholog of Chlamydomonas reinhardtii ODA7 Disrupt Dynein Arm Assembly and Cause Primary Ciliary Dyskinesia
Published in American journal of human genetics (11-12-2009)“…Cilia and flagella are evolutionarily conserved structures that play various physiological roles in diverse cell types. Defects in motile cilia result in…”
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3
common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia
Published in Proceedings of the National Academy of Sciences - PNAS (27-02-2007)“…Thioredoxins belong to a large family of enzymatic proteins that function as general protein disulfide reductases, therefore participating in several cellular…”
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Heterozygous Mutation Disrupting the SPAG16 Gene Results in Biochemical Instability of Central Apparatus Components of the Human Sperm Axoneme
Published in Biology of reproduction (01-11-2007)“…The SPAG16 gene encodes two major transcripts, one for the 71-kDa SPAG16L, which is the orthologue of the Chlamydomonas rheinhardtii central apparatus protein…”
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Loss-of-Function Mutations in a Human Gene Related to Chlamydomonas reinhardtii Dynein IC78 Result in Primary Ciliary Dyskinesia
Published in American journal of human genetics (01-12-1999)“…Primary ciliary dyskinesia (PCD) is a group of heterogeneous disorders of unknown origin, usually inherited as an autosomal recessive trait. Its phenotype is…”
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The human dynein intermediate chain 2 gene (DNAI2) : cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia
Published in Human genetics (01-12-2000)“…Primary ciliary dyskinesia (PCD) is an autosomal recessive disease characterized by chronic sinusitis and bronchiectasis, and usually associated with…”
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Mutations of DNAI1 in Primary Ciliary Dyskinesia: Evidence of Founder Effect in a Common Mutation
Published in American journal of respiratory and critical care medicine (15-10-2006)“…Primary ciliary dyskinesia (PCD) is a rare, usually autosomal recessive, genetic disorder characterized by ciliary dysfunction, sino-pulmonary disease, and…”
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Effects of Proton Pump Inhibitors Intake During Chemoradiotherapy for Rectal Cancer: a Retrospective Cohort Study
Published in Journal of gastrointestinal cancer (01-06-2023)“…Purpose Proton pump inhibitors (PPIs) are one of the most widely used drugs worldwide and are involved in several drug interactions. Recently, several studies…”
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9
Preserving bone in cancers of the elderly: A necessity
Published in Joint, bone, spine : revue du rhumatisme (01-07-2023)“…[Display omitted] •Given the frequency and burden of bone events in elderly cancer patients, collaboration between rheumatologists, oncologists and…”
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A Heterozygous Mutation Disrupting the SPAG16 Gene Results in Biochemical Instability of Central Apparatus Components of the Human Sperm Axoneme1
Published in Biology of reproduction (01-11-2007)“…The SPAG16 gene encodes two major transcripts, one for the 71-kDa SPAG16L, which is the orthologue of the Chlamydomonas rheinhardtii central apparatus protein…”
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11
Préservation de la santé osseuse dans le cancer de la personne âgée : une nécessité
Published in Revue du rhumatisme (Ed. française : 1993) (01-03-2024)“…[Display omitted] La survenue de fractures osseuses est fréquente dans la population âgée et chez les patients atteints d’un cancer, en particulier ceux qui…”
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Isolation and Expression of the Human hPF20 Gene Orthologous to Chlamydomonas pf20
Published in American journal of respiratory cell and molecular biology (01-03-2002)“…Primary ciliary dyskinesia (PCD) is a heterogeneous congenital disorder characterized by bronchiectasis and chronic sinusitis, sometimes associated with situs…”
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Isolation and Expression of the Human hPF20 Gene Orthologous to Chlamydomonas pf20 . Evaluation as a Candidate for Axonemal Defects of Respiratory Cilia and Sperm Flagella
Published in American journal of respiratory cell and molecular biology (01-03-2002)“…Primary ciliary dyskinesia (PCD) is a heterogeneous congenital disorder characterized by bronchiectasis and chronic sinusitis, sometimes associated with situs…”
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Splicing of Juvenile and Adult Tau mRNA Variants is Regulated by Thyroid Hormone
Published in Proceedings of the National Academy of Sciences - PNAS (01-05-1991)“…The effect of thyroid hormone on the expression of tau transcripts was studied during postnatal brain development. The level of tau mRNA was only slightly…”
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A Heterozygous Mutation Disrupting the SPAG16 Gene Results in Biochemical Instability of Central Apparatus Components of the Human Sperm Axoneme1
Published in Biology of reproduction (01-11-2007)“…The SPAG16 gene encodes two major transcripts, one for the 71-kDa SPAG16L, which is the orthologue of the Chlamydomonas rheinhardtii central apparatus protein…”
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16
Predictive factors for compliance with transanal irrigation for the treatment of defecation disorders
Published in World journal of gastroenterology : WJG (21-03-2017)“…AIM To investigate compliance with transanal irrigation(TAI) one year after a training session and to identify predictive factors for compliance.METHODS The…”
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Regulation by thyroid hormone of microtubule assembly and neuronal differentiation
Published in Neurochemical research (01-09-1991)“…In this review we examine successively: 1) the major effects of thyroid hormone deficiency seen during brain development with special emphasis on the changes…”
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Protein synthesis in astrocytes: 'spontaneous' and cyclic AMP-induced differentiation
Published in Developmental neuroscience (1986)“…Primary cultures of mouse astrocytes have been used to study astroglial protein synthesis during 'in vitro' differentiation. Spontaneous age-related…”
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