遺伝学. 遺伝学について. 壊れた心臓を設計する.

Same author

Absence of the vagus nerve in the stomach of Tbx1-/- mutant mice.

Neurogastroenterology and motility·2010

Same author

Molecular study of 33 families with Fraser syndrome new data and mutation review.

American journal of medical genetics. Part A·2008

Same author

Mutations in SRD5B1 (AKR1D1), the gene encoding delta(4)-3-oxosteroid 5beta-reductase, in hepatitis and liver failure in infancy.

Gut·2003

Same author

A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13.

Journal of medical genetics·2003

Same author

Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13.

Journal of medical genetics·2002

Same author

Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p.

Journal of molecular medicine (Berlin, Germany)·2002

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

遺伝学. 遺伝学について. 壊れた心臓を設計する.

関連する概念動画

Absence of the vagus nerve in the stomach of Tbx1-/- mutant mice.

Molecular study of 33 families with Fraser syndrome new data and mutation review.

Mutations in SRD5B1 (AKR1D1), the gene encoding delta(4)-3-oxosteroid 5beta-reductase, in hepatitis and liver failure in infancy.

A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13.

Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13.

Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p.

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

遺伝学. 遺伝学について. 壊れた心臓を設計する.

関連する概念動画

関連記事

Absence of the vagus nerve in the stomach of Tbx1-/- mutant mice.

Molecular study of 33 families with Fraser syndrome new data and mutation review.

Mutations in SRD5B1 (AKR1D1), the gene encoding delta(4)-3-oxosteroid 5beta-reductase, in hepatitis and liver failure in infancy.

A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13.

Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13.

Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p.

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.