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Videos de Conceptos Relacionados

Animal Mitochondrial Genetics02:59

Animal Mitochondrial Genetics

Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
Genomic Imprinting and Inheritance02:30

Genomic Imprinting and Inheritance

Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
Meiosis vs. Mitosis02:57

Meiosis vs. Mitosis

Cell division is necessary for growth and reproduction in organisms. Mitosis aids cell growth and development by dividing somatic cells. In contrast, meiosis causes the division of germ cells and plays an essential role in sexual reproduction. Due to their unique functional requirements, mitosis and meiosis differ from each other in multiple aspects.
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
Cancer Prevention02:59

Cancer Prevention

Several factors can increase the risk of cancer in an individual. About 50% of cancer cases can be prevented by adopting a healthy lifestyle, regular exercise, eating healthy, and following a modest cancer prevention diet. Epidemiological studies have consistently shown that populations with vegetable and fruit-rich diets have reduced the incidence of cancer. On the other hand, populations who have a diet rich in animal fat, red meat, junk food, or high calories are predisposed to cancer.
Some...
Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
Development of the Oral Microbiota01:28

Development of the Oral Microbiota

The establishment of the oral microbiome begins before birth, challenging the long-held belief that the fetal oral cavity is sterile. The presence of oral microbes such as Streptococcus and Fusobacterium in amniotic fluid suggests that microbial exposure may occur in utero, potentially through translocation from the maternal oral or gastrointestinal tract. This early colonization primes the neonatal immune system and sets the stage for subsequent microbial succession. Maternal health,...

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Video Experimental Relacionado

Updated: Jun 24, 2026

FISH for Pre-implantation Genetic Diagnosis
07:34

FISH for Pre-implantation Genetic Diagnosis

Published on: February 24, 2011

La patogénesis y la genética de la preeclampsia.

J M Roberts1, D W Cooper

  • 1Magee-Womens Research Institute, Pittsburgh, PA, USA.

Lancet (London, England)
|February 24, 2001
PubMed
Resumen

La preeclampsia y la eclampsia son trastornos complejos del embarazo. La investigación se centra en las interacciones placentario-maternales, en el endotelio vascular, el estrés oxidativo y la genética para comprender estas condiciones.

Área de la Ciencia:

  • Obstetricia y Ginecología.
  • La medicina materno-fetal es una de ellas.
  • Genética La genética.

Sus antecedentes:

  • La preeclampsia y la eclampsia siguen siendo poco conocidas a pesar de una extensa investigación.
  • La causa principal es probablemente una aberración en la interacción del tejido placentario-materno.
  • Las desviaciones precisas de la fisiología normal del embarazo son todavía difíciles de alcanzar.

Objetivo del estudio:

  • Revisar el conocimiento actual de la preeclampsia y la eclampsia.
  • Para explorar los cambios fisiológicos involucrados en estas condiciones.
  • Identificar posibles factores genéticos que contribuyen a la susceptibilidad.

Principales métodos:

  • Revisión de la literatura que se centra en el endotelio vascular y el estrés oxidativo.

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  • Análisis de componentes genéticos en genotipos maternos y fetales.
  • Discusión del mapeo del genoma completo como una futura dirección de investigación.
  • Principales resultados:

    • La investigación actual hace hincapié en los roles de la disfunción del endotelio vascular y el estrés oxidativo.
    • Se reconoce la susceptibilidad genética, pero las contribuciones del genotipo materno y fetal no están claras.
    • El mapeo de todo el genoma se propone como un método para identificar los genes causantes.

    Conclusiones:

    • Comprender la preeclampsia y la eclampsia requiere una mayor investigación sobre las interacciones placentario-materna.
    • El endotelio vascular y el estrés oxidativo son áreas clave de enfoque.
    • La identificación de los determinantes genéticos es crucial para los avances futuros.