IGF2 is parentally imprinted in human preimplantation embryos

The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome.

Journal of medical genetics·2003

Physical activity, hormone replacement therapy and plasma lipoprotein-lipid levels in postmenopausal women.

International journal of sports medicine·2003

Moderate physical activity is associated with higher bone mineral density in postmenopausal women.

Journal of the American Geriatrics Society·2002

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.

Journal of medical genetics·2001

Obesity gene variant and elite endurance performance.

Metabolism: clinical and experimental·2001

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

Nature genetics·2001

Plasticity of human microglia and brain perivascular macrophages in aging and Alzheimer's disease.

Nature genetics·2026

Prevalence and chronology of colibactin-associated mutational processes and their microbiome spectra in Japanese colorectal cancer.

Nature genetics·2026

High-resolution promoter interaction analysis implicates genes involved in activation of type 3 innate lymphoid cells in immune disease risk.

Nature genetics·2026

Mapping enhancer-gene regulatory interactions from single-cell data.

Nature genetics·2026

Diversity and evolution of chromatin regulatory states across eukaryotes.

Nature genetics·2026

Gene mutant dosage is associated with prognosis and metastatic tropism in 60,000 clinical cancer samples.

Nature genetics·2026

LIMK1 and PKM as Integratively Identified Transcriptomic Signatures in Inflammatory Bowel Disease.

Omics : a journal of integrative biology·2026

[Diagnosis and Treatment Experience in a Case of Visceral Leishmaniasis Co-infected with HIV].

Mikrobiyoloji bulteni·2026

Anatomical variations in internal jugular vein splitting patterns: a theoretical framework for a classification system.

Anatomy & cell biology·2026

Idiopathic pulmonary fibrosis and interleukins: a bibliometric analysis [1999-2025].

Journal of thoracic disease·2026

FGF21 in idiopathic pulmonary fibrosis: mechanistic insights, translational potential, and unresolved questions.

Journal of thoracic disease·2026

The value of serum biomarkers in the management of interstitial lung disease in patients with connective tissue disease: a protocol for an observational study.

Journal of thoracic disease·2026

Related Experiment Videos

IGF2 is parentally imprinted in human preimplantation embryos

Related Concept Videos

The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome.

Physical activity, hormone replacement therapy and plasma lipoprotein-lipid levels in postmenopausal women.

Moderate physical activity is associated with higher bone mineral density in postmenopausal women.

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.

Obesity gene variant and elite endurance performance.

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

Plasticity of human microglia and brain perivascular macrophages in aging and Alzheimer's disease.

Prevalence and chronology of colibactin-associated mutational processes and their microbiome spectra in Japanese colorectal cancer.

High-resolution promoter interaction analysis implicates genes involved in activation of type 3 innate lymphoid cells in immune disease risk.

Mapping enhancer-gene regulatory interactions from single-cell data.

Diversity and evolution of chromatin regulatory states across eukaryotes.

Gene mutant dosage is associated with prognosis and metastatic tropism in 60,000 clinical cancer samples.

LIMK1 and PKM as Integratively Identified Transcriptomic Signatures in Inflammatory Bowel Disease.

[Diagnosis and Treatment Experience in a Case of Visceral Leishmaniasis Co-infected with HIV].

Anatomical variations in internal jugular vein splitting patterns: a theoretical framework for a classification system.

Idiopathic pulmonary fibrosis and interleukins: a bibliometric analysis [1999-2025].

FGF21 in idiopathic pulmonary fibrosis: mechanistic insights, translational potential, and unresolved questions.

The value of serum biomarkers in the management of interstitial lung disease in patients with connective tissue disease: a protocol for an observational study.

Related Experiment Videos

IGF2 is parentally imprinted in human preimplantation embryos

Related Concept Videos

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