[A novel allelic variation of serotonin transporter gene polymorphism in anorexia nervosa]

Structure analysis of a class II transposon encoding the mercury resistance of the Gram-positive Bacterium bacillus megaterium MB1, a strain isolated from minamata bay, Japan.

Gene·1999

p53 mutations in tumor and non-tumor tissues of thorotrast recipients: a model for cellular selection during radiation carcinogenesis in the liver.

Carcinogenesis·1999

Bcl-2 family proteins regulate the release of apoptogenic cytochrome c by the mitochondrial channel VDAC.

Nature·1999

[Effectiveness of hypoallergenic rice-by cast analysis].

Arerugi = [Allergy]·1999

Hodgkin disease with subsequent transformation to CD30 positive non-hodgkin lymphoma in six patients.

Cancer·1999

Absence of G-protein activation by mu-opioid receptor agonists in the spinal cord of mu-opioid receptor knockout mice.

British journal of pharmacology·1999

[Successful treatment with topiramate in a case of idiopathic intracranial hypertension refractory to acetazolamide].

No to hattatsu = Brain and development·2018

[Clinical characteristics of early juvenile GM2 gangliosidosis: a case report].

No to hattatsu = Brain and development·2018

[Non-invasive positive pressure ventilation during the management of severe spinal muscular atrophy type I].

No to hattatsu = Brain and development·2018

[Ictal arterial spin labeling MRI findings in two cases of acute confusional migraine].

No to hattatsu = Brain and development·2018

[A case of West syndrome with a deletion at chromosome 2q24.3-q31.3].

No to hattatsu = Brain and development·2018

[Irreversible cerebral ischemia caused by febrile status epilepticus in Sturge-Weber syndrome type III].

No to hattatsu = Brain and development·2018

A Regulator SNP Affecting the Transcription Factor SP1 Binding Site in the PIK3R3 Gene Contributes to Noise-Induced Hearing Loss Risk.

Human mutation·2026

Neuropsychiatry genetics in Africa.

Nature communications·2026

Genetic findings in a Turkish clinical cohort with hereditary Parkinson's disease.

Neurogenetics·2026

Caregiver's perspectives toward genome sequencing in children with neurodevelopmental disorders: Integrating genomic information into pediatric care.

Current problems in pediatric and adolescent health care·2026

Father and son with a pathogenic variant c.614dup p.(Gln206Thrfs*20) in the NR5A1 gene: a case report.

Frontiers in pediatrics·2026

Pediatric Spinal Cord Astrocytoma With Granular Cell-Like Morphology and KIAA1549::BRAF Fusion.

Neuropathology : official journal of the Japanese Society of Neuropathology·2026

Related Experiment Videos

[A novel allelic variation of serotonin transporter gene polymorphism in anorexia nervosa]

Related Concept Videos

Structure analysis of a class II transposon encoding the mercury resistance of the Gram-positive Bacterium bacillus megaterium MB1, a strain isolated from minamata bay, Japan.

p53 mutations in tumor and non-tumor tissues of thorotrast recipients: a model for cellular selection during radiation carcinogenesis in the liver.

Bcl-2 family proteins regulate the release of apoptogenic cytochrome c by the mitochondrial channel VDAC.

[Effectiveness of hypoallergenic rice-by cast analysis].

Hodgkin disease with subsequent transformation to CD30 positive non-hodgkin lymphoma in six patients.

Absence of G-protein activation by mu-opioid receptor agonists in the spinal cord of mu-opioid receptor knockout mice.

[Successful treatment with topiramate in a case of idiopathic intracranial hypertension refractory to acetazolamide].

[Clinical characteristics of early juvenile GM2 gangliosidosis: a case report].

[Non-invasive positive pressure ventilation during the management of severe spinal muscular atrophy type I].

[Ictal arterial spin labeling MRI findings in two cases of acute confusional migraine].

[A case of West syndrome with a deletion at chromosome 2q24.3-q31.3].

[Irreversible cerebral ischemia caused by febrile status epilepticus in Sturge-Weber syndrome type III].

A Regulator SNP Affecting the Transcription Factor SP1 Binding Site in the PIK3R3 Gene Contributes to Noise-Induced Hearing Loss Risk.

Neuropsychiatry genetics in Africa.

Genetic findings in a Turkish clinical cohort with hereditary Parkinson's disease.

Caregiver's perspectives toward genome sequencing in children with neurodevelopmental disorders: Integrating genomic information into pediatric care.

Father and son with a pathogenic variant c.614dup p.(Gln206Thrfs*20) in the NR5A1 gene: a case report.

Pediatric Spinal Cord Astrocytoma With Granular Cell-Like Morphology and KIAA1549::BRAF Fusion.

Related Experiment Videos

[A novel allelic variation of serotonin transporter gene polymorphism in anorexia nervosa]

Related Concept Videos

Related Articles