Salihi anam (38 risultati)

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Condizione: New. pp. 192.

Paperback. Condizione: Brand New. 164 pages. 8.66x5.91x0.37 inches. In Stock.

paperback. Condizione: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

paperback. Condizione: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Condizione: New.

Condizione: New.

Condizione: New.

Condizione: New.

Condizione: New.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Polycystic ovary syndrome (PCOS) is the most common, yet complex,endocrine disorder affecting women in their reproductive years. The etiology of PCOS is still unknown, yet, there is increasing evidence to support a major genetic basis, as the syndrome have strong familial predisposition. More than one gene were contributes to the heterogeneous phenotype and the clinical and biochemical presentation. Clinical phenotyping of PCOS involves determining the presence of clinical and/or biochemical androgen excess. The androstenedione is converted to estrogens by the action of aromatase enzyme which was encoded by cytochrome p450, family19 (CYP19) located on the long arm of chromosome 15. Several single nucleotide polymorphisms of the CYP19 gene were associated with variation in serum androgen concentrations among women; one of it is the SNP rs2414096. Most women with PCOS (obese or non-obese) suffer from insulin resistance. The insulin receptor is encoded by the INSR gene which is located at the chromosome 19. Several kinds of polymorphisms have been identified within INSR. Of these polymorphisms, most were single nucleotide polymorphism of the C/T SNP at His1058 in exon 17 of INSR. 164 pp. Englisch.…

Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Polycystic ovary syndrome (PCOS) is the most common, yet complex,endocrine disorder affecting women in their reproductive years. The etiology of PCOS is still unknown, yet, there is increasing evidence to support a major genetic basis, as the syndrome have strong familial predisposition. More than one gene were contributes to the heterogeneous phenotype and the clinical and biochemical presentation. Clinical phenotyping of PCOS involves determining the presence of clinical and/or biochemical androgen excess. The androstenedione is converted to estrogens by the action of aromatase enzyme which was encoded by cytochrome p450, family19 (CYP19) located on the long arm of chromosome 15. Several single nucleotide polymorphisms of the CYP19 gene were associated with variation in serum androgen concentrations among women; one of it is the SNP rs2414096. Most women with PCOS (obese or non-obese) suffer from insulin resistance. The insulin receptor is encoded by the INSR gene which is located at the chromosome 19. Several kinds of polymorphisms have been identified within INSR. Of these polymorphisms, most were single nucleotide polymorphism of the C/T SNP at His1058 in exon 17 of INSR.…

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Al-Obaidi ManalDr. Manal T. AL-Obaidy {M.B.CH.B, H.D(ART),Ph.D} Specialist physician in Assisted Reproductive Technologies. I am the director of infertility consultant clinic, and the Head of the clinical reproductive physiology dep.…

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Al - Azzawi LehadhDr.Lehadh Al-Azzawi has obtained her PhD degree in oral pathology in 2003.since she has worked in different projects in this fieldOSCC,salivary gland tumours and histologic evaluation of laser application in Dentis.…

Condizione: New. Print on Demand.

Condizione: New. Print on Demand pp. 192.

Condizione: New. PRINT ON DEMAND.

Condizione: New. PRINT ON DEMAND pp. 192.

Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Polycystic ovary syndrome (PCOS) is the most common, yet complex,endocrine disorder affecting women in their reproductive years. The etiology of PCOS is still unknown, yet, there is increasing evidence to support a major genetic basis, as the syndrome have strong familial predisposition. More than one gene were contributes to the heterogeneous phenotype and the clinical and biochemical presentation. Clinical phenotyping of PCOS involves determining the presence of clinical and/or biochemical androgen excess. The androstenedione is converted to estrogens by the action of aromatase enzyme which was encoded by cytochrome p450, family19 (CYP19) located on the long arm of chromosome 15. Several single nucleotide polymorphisms of the CYP19 gene were associated with variation in serum androgen concentrations among women; one of it is the SNP rs2414096. Most women with PCOS (obese or non-obese) suffer from insulin resistance. The insulin receptor is encoded by the INSR gene which is located at the chromosome 19. Several kinds of polymorphisms have been identified within INSR. Of these polymorphisms, most were single nucleotide polymorphism of the C/T SNP at His1058 in exon 17 of INSR.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 164 pp. Englisch.…

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Hameed MajidMajid Hameed, MBChB, MSc, PhD in Physiology,Lecturer in Physiology, College of Medicine, Alnahrain University, Baghdad, Iraq.With almost 50% of infertility attributed either wholly or in part to male issues, a compreh.…

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 136 pp. Spanisch.

Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - El síndrome de ovario poliquístico (SOP) es el trastorno endocrino más frecuente, aunque también uno de los más complejos, que afecta a las mujeres en edad fértil. La etiología del SOP sigue siendo desconocida; sin embargo, cada vez hay más pruebas que apuntan a una base genética importante, ya que el síndrome presenta una fuerte predisposición familiar. Varios genes contribuyen al fenotipo heterogéneo y a la presentación clínica y bioquímica. La caracterización fenotípica clínica del SOP implica determinar la presencia de un exceso de andrógenos clínico y/o bioquímico. La androstenediona se convierte en estrógenos por la acción de la enzima aromatasa, codificada por el citocromo P450, familia 19 (CYP19), situado en el brazo largo del cromosoma 15. Varios polimorfismos de un solo nucleótido del gen CYP19 se han asociado a variaciones en las concentraciones séricas de andrógenos entre las mujeres; uno de ellos es el SNP rs2414096. La mayoría de las mujeres con SOP (obesas o no obesas) padecen resistencia a la insulina. El receptor de insulina está codificado por el gen INSR, que se localiza en el cromosoma 19. Se han identificado varios tipos de polimorfismos dentro del INSR. De estos polimorfismos, la mayoría eran polimorfismos de un solo nucleótido del SNP C/T en His1058 en el exón 17 del INSR.…

Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware 136 pp. Spanisch.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 136 pp. Französisch.

Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware 136 pp. Französisch.

Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Le syndrome des ovaires polykystiques (SOPK) est le trouble endocrinien le plus fréquent, mais aussi le plus complexe, touchant les femmes en âge de procréer. L'étiologie du SOPK reste inconnue, mais de plus en plus d'éléments tendent à confirmer une composante génétique majeure, ce syndrome présentant en effet une forte prédisposition familiale. Plusieurs gènes contribuent au phénotype hétérogène ainsi qu'aux manifestations cliniques et biochimiques de la maladie. Le phénotypage clinique du SOPK consiste à déterminer la présence d'un excès d'androgènes clinique et/ou biochimique. L'androstènedione est convertie en oestrogènes par l'action de l'enzyme aromatase, codée par le gène du cytochrome P450, famille 19 (CYP19), situé sur le bras long du chromosome 15. Plusieurs polymorphismes nucléotidiques simples (SNP) du gène CYP19 ont été associés à des variations des concentrations sériques d'androgènes chez les femmes ; l'un d'entre eux est le SNP rs2414096. La plupart des femmes atteintes du SOPK (obèses ou non) souffrent d'insulinorésistance. Le récepteur de l'insuline est codé par le gène INSR, situé sur le chromosome 19. Plusieurs types de polymorphismes ont été identifiés au sein de l'INSR. Parmi ces polymorphismes, la plupart étaient des polymorphismes nucléotidiques simples (SNP) de type C/T au niveau de l'acide aminé His1058 dans l'exon 17 de l'INSR.…

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 132 pp. Polnisch.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 132 pp. Italienisch.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 132 pp. Portugiesisch.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 136 pp. Deutsch.