嗅覚. 嗅覚. 嗅覚する. 独占的な受容体である.

Same author

Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society·2017

Same author

A role for TENM1 mutations in congenital general anosmia.

Clinical genetics·2016

Same author

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum.

Clinical genetics·2015

Same author

Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome.

Clinical genetics·2014

Same author

Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics·2009

Same author

Further evidence for association of the RGS2 gene with antipsychotic-induced parkinsonism: protective role of a functional polymorphism in the 3'-untranslated region.

The pharmacogenomics journal·2008

Same journal

Incoming US science academy chief vows to 'double down' on research.

Nature·2026

Same journal

Author Correction: Synthesis of enantioenriched atropisomers by biocatalytic deracemization.

Nature·2026

Same journal

Electrodeposited self-assembled molecules for perovskite photovoltaics.

Nature·2026

Same journal

Neutrino's nursery found: the 'Shadow Blaster'.

Nature·2026

Same journal

Dementia risk in middle-aged people linked to a blood protein.

Nature·2026

Same journal

Daily briefing: What's really happening with trust in science.

Nature·2026

関連する実験動画

嗅覚. 嗅覚. 嗅覚する. 独占的な受容体である.

関連する概念動画

Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin.

A role for TENM1 mutations in congenital general anosmia.

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum.

Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome.

Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.

Further evidence for association of the RGS2 gene with antipsychotic-induced parkinsonism: protective role of a functional polymorphism in the 3'-untranslated region.

Incoming US science academy chief vows to 'double down' on research.

Author Correction: Synthesis of enantioenriched atropisomers by biocatalytic deracemization.

Electrodeposited self-assembled molecules for perovskite photovoltaics.

Neutrino's nursery found: the 'Shadow Blaster'.

Dementia risk in middle-aged people linked to a blood protein.

Daily briefing: What's really happening with trust in science.

関連する実験動画

嗅覚. 嗅覚. 嗅覚する. 独占的な受容体である.

関連する概念動画

関連記事

Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin.

A role for TENM1 mutations in congenital general anosmia.

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum.

Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome.

Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.

Further evidence for association of the RGS2 gene with antipsychotic-induced parkinsonism: protective role of a functional polymorphism in the 3'-untranslated region.

Incoming US science academy chief vows to 'double down' on research.

Author Correction: Synthesis of enantioenriched atropisomers by biocatalytic deracemization.

Electrodeposited self-assembled molecules for perovskite photovoltaics.

Neutrino's nursery found: the 'Shadow Blaster'.

Dementia risk in middle-aged people linked to a blood protein.

Daily briefing: What's really happening with trust in science.