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1 - 12 de 12 resultados para “saadi khochbin”
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  • Epigenetics and Human Reproduction

    Edición de Sophie Rousseaux, Saadi Khochbin ...
    Series series Biomedical and Life Sciences (R0)
    Epigenetics is a rapidly expanding field in medical and biological research which concerns heritable traits that are not attributable to changes in the DNA sequence. Epigenetic mechanisms play key roles in many biological processes, and it has become clear that their disruption can gives rise to diverse pathologies in humans. Edited by preeminent experts, Sophie Rousseaux and Saadi Khochbin, this ... Leer más

    $188.09 USD

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  • Disorders of Thrombosis and Hemostasis in Pregnancy

    A Guide to Management

    Edición de Hannah Cohen, Patrick O'Brien ...
    Series series Medicine (R0)
    In this second edition of Disorders of Thrombosis and Hemostasis in Pregnancy - A Guide to Management the content has been thoroughly updated, with a particular focus on strengthening the management sections to ensure that advice on management represents state of the art. ... Leer más

    $89.99 USD

  • Gamete and Embryo-fetal Origins of Adult Diseases

    Edición de He-Feng Huang, Jian-Zhong Sheng ...
    Series series Medicine (R0)
    The book Gamete and Embryo-fetal Origins of Adult Diseases introduces various diseases resulting from the abnormal gametogenesis and embryo development, which manifests as growth retardation, birth defects, or increased susceptibility to chronic metabolic diseases such as diabetes, cardiovascular disease and cancer in childhood and adult life, even fertility disorders and the risk of ... Leer más

    $143.09 USD

  • Uniparental Disomy (UPD) in Clinical Genetics

    A Guide for Clinicians and Patients

    de Thomas Liehr, UNIQUE ...
    Series series Biomedical and Life Sciences (R0)
    This book focus on genetic diagnostics for Uniparental Disomy (UPD), a chromosomal disorder defined by the exceptional presence of a chromosome pair derived from only one parent, which leads to a group of rare diseases in humans. First the molecular and cytogenetic background of UPD is described in detail; subsequently, all available information of the various chromosomal origins and the latest ... Leer más

    $80.99 USD

  • Biomarkers for Endometriosis

    State of the Art

    Edición de Thomas D'Hooghe ...
    Series series Medicine (R0)
    This book presents an overview of the diagnostic performance of non- or semi-invasive tests for endometriosis in peripheral blood, endometrium, saliva, peritoneal fluid and urine. The value of existing and emerging systems biology technologies for biomarker development is addressed in several chapters on genetics, microarrays, proteomics and metabolomics. Although tests with high sensitivity and ... Leer más

    $89.99 USD

  • Practical Preimplantation Genetic Diagnosis

    de Anver Kuliev ...
    Series series Medicine (R0)
    Although treatment remains the major goal in the control of genetic disease, this is not yet a reality for most inherited conditions. In the absence of radical treatment, preimplantation genetic diagnosis (PGD) offers the answer to the control of these inherited conditions by predicting reproductive outcome. PGD is now entering its third decade as an established procedure for genetic and assisted ... Leer más

    $170.99 USD

  • Small Supernumerary Marker Chromosomes (sSMC)

    A Guide for Human Geneticists and Clinicians

    de Thomas Liehr, UNIQUE (Rare Chromosome Disorder Support Group) ...
    Series series Biomedical and Life Sciences (R0)
    Human beings normally have a total of 46 chromosomes, with each chromosome present twice, apart from the X and Y chromosomes in males. Some three million people worldwide, however, have 47 chromosomes: they have a small supernumerary marker chromosome (sSMC) in addition to the 46 normal ones. This sSMC can originate from any one of the 24 human chromosomes and can have different shapes. ... Leer más

    $80.99 USD

  • Living with HHT

    Understanding and Managing Your Hereditary Hemorrhagic Telangiectasia

    de Sara Palmer ...
    Series series A Johns Hopkins Press Health Book
    Everything you need to know about nosebleeds, arteriovenous malformations, and other symptoms of HHT.Hereditary Hemorrhagic Telangiectasia (HHT) is a rare genetic disorder that causes blood vessel abnormalities in the nose, skin, gastrointestinal tract, lungs, brain, and liver. Nosebleeds are the most common symptom of HHT, but abnormal vessels in other organs, if they are not diagnosed and ... Leer más

    $27.99 USD

  • Non-coding RNA and the Reproductive System

    Edición de Dagmar Wilhelm, Pascal Bernard ...
    Series series Biomedical and Life Sciences (R0)
    This book provides an overview of the role and function of regulatory RNAs that lack protein-coding potential in key reproductive tissues. This includes the role of small interfering RNAs (siRNAs), microRNAs (miRNAs), PIWI-interacting RNAs (piRNAs), small nucleolar RNAs (snoRNAs) and long non-coding RNAs (lncRNAs). Through clear, detailed and comprehensive debate, international leading experts ... Leer más

    $89.99 USD

  • Oocytes

    Maternal Information and Functions

    Edición de Malgorzata Kloc ...
    Series series Biomedical and Life Sciences (R0)
    This book combines the most recent knowledge on the maternal, i.e. oocyte/egg-specific, molecules and processes. The volume covers the most recent advances in a plethora of subjects such as: maternal transfer of immunity, localized RNAs functions and mechanisms of RNA localization, transcriptional repression of maternal messages, maternal inheritance and maternal role of CRISPR/Cas9-based genome ... Leer más

    $242.99 USD

  • Male Infertility: Understanding, Causes and Treatment

    Edición de RAJENDER SINGH, Kiran Singh ...
    Series series Biomedical and Life Sciences (R0)
    This book covers the latest research on male infertility. The topics discussed range from understanding the genetic basis of infertility, to its causes and treatment. Since infertility is also of great interest to the general public, the book also includes a detailed description of what infertility is and how one can understand the different types. Given the complex etiology of infertility, the ... Leer más

    $143.99 USD

  • Screening the Single Euploid Embryo

    Molecular Genetics in Reproductive Medicine

    Edición de E Scott Sills ...
    Series series Medicine (R0)
    Intended for readers with a background in fertility medicine as well as those less familiar with IVF, this comprehensive work presents an update on preimplantation genetic testing to enable single embryo transfer (SET). An international cast of contributors explains the treatment sequence—from ovulation induction to luteal support—aiming to transfer only one euploid embryo. Applications of ... Leer más

    $89.99 USD