[Technics of genetic recombination and the human chromosomal map]

Placental expression of the obesity-associated gene FTO is reduced by fetal growth restriction but not by macrosomia in rats and humans.

Journal of developmental origins of health and disease·2014

Maternal environment and the reproductive function of the offspring.

Theriogenology·2012

[Epigenetics, interface between environment and genes: role in complex diseases].

Revue medicale de Liege·2012

Child health, developmental plasticity, and epigenetic programming.

Endocrine reviews·2010

Placental BDNF/TrkB signaling system is modulated by fetal growth disturbances in rat and human.

Placenta·2010

Nutritional developmental epigenomics: immediate and long-lasting effects.

The Proceedings of the Nutrition Society·2010

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Annales de genetique·2004

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Annales de genetique·2004

Large duplication 4q25-q34 with mild clinical effect.

Annales de genetique·2004

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Annales de genetique·2004

Partial trisomy 8q and partial monosomy 18p: a case report.

Annales de genetique·2004

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Annales de genetique·2004

Chromosome movements in meiotic prophase: regulatory mechanisms and biological roles.

Frontiers in cell and developmental biology·2026

Nuclear diversity in Charophyceae revealed by fluorescence staining and its implications for genome size estimation.

Planta·2026

SANS ankyrin repeats mediate non-classical nuclear import and dictate distinct pathogenic mechanisms.

The FEBS journal·2026

Bone marrow-inspired DLL1-presenting microparticles enhance asymmetric division and maintenance of mouse hematopoietic stem and progenitor cells.

Stem cell reports·2026

Partial trisomy of 1q42.1 and 8q24.3 deletion: a family history.

Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo·2026

A Novel Hemizygous CDX4 Missense Variant Identified in a Taiwanese Man with Severe Teratozoospermia.

Medicina (Kaunas, Lithuania)·2026

Related Experiment Videos

[Technics of genetic recombination and the human chromosomal map]

Related Concept Videos

Placental expression of the obesity-associated gene FTO is reduced by fetal growth restriction but not by macrosomia in rats and humans.

Maternal environment and the reproductive function of the offspring.

[Epigenetics, interface between environment and genes: role in complex diseases].

Child health, developmental plasticity, and epigenetic programming.

Placental BDNF/TrkB signaling system is modulated by fetal growth disturbances in rat and human.

Nutritional developmental epigenomics: immediate and long-lasting effects.

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Large duplication 4q25-q34 with mild clinical effect.

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Partial trisomy 8q and partial monosomy 18p: a case report.

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Chromosome movements in meiotic prophase: regulatory mechanisms and biological roles.

Nuclear diversity in Charophyceae revealed by fluorescence staining and its implications for genome size estimation.

SANS ankyrin repeats mediate non-classical nuclear import and dictate distinct pathogenic mechanisms.

Bone marrow-inspired DLL1-presenting microparticles enhance asymmetric division and maintenance of mouse hematopoietic stem and progenitor cells.

Partial trisomy of 1q42.1 and 8q24.3 deletion: a family history.

A Novel Hemizygous CDX4 Missense Variant Identified in a Taiwanese Man with Severe Teratozoospermia.

Related Experiment Videos

[Technics of genetic recombination and the human chromosomal map]

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