Esanov rustam (51 resultados)

Condición: New.

Taschenbuch. Condición: Neu. DNA Hydroxymethylation in Non-coding Repeat Expansion Disorders | Rustam Esanov | Taschenbuch | 132 S. | Englisch | 2017 | Scholars' Press | EAN 9783330653122 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. …

Paperback. Condición: Brand New. 132 pages. 8.66x5.91x0.30 inches. In Stock.

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

Condición: New.

Condición: New.

Condición: New.

Taschenbuch. Condición: Neu. Hydroxyméthylation de l'ADN dans les troubles liés à l'expansion des répétitions non codantes | Rustam Esanov | Taschenbuch | Einband - flex.(Paperback) | Französisch | 2024 | Editions Notre Savoir | EAN 9786208407094 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. …

Taschenbuch. Condición: Neu. Idrossimetilazione del DNA nei disturbi da espansione delle ripetizioni non codificanti | Rustam Esanov | Taschenbuch | Einband - flex.(Paperback) | Italienisch | 2024 | Edizioni Sapienza | EAN 9786208407100 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. …

Taschenbuch. Condición: Neu. Hidroximetilação do ADN em doenças de expansão de repetições não codificantes | Rustam Esanov | Taschenbuch | Einband - flex.(Paperback) | Portugiesisch | 2024 | Edições Nosso Conhecimento | EAN 9786208407117 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

Taschenbuch. Condición: Neu. DNA-Hydroxymethylierung bei nicht-kodierenden Repeat-Expansionsstörungen | Rustam Esanov | Taschenbuch | 116 S. | Deutsch | 2024 | Verlag Unser Wissen | EAN 9786208407063 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu. …

Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -My research is focused on the repeat expansion disorders, a family of disorders that result from the repetitive microsatellite sequence within the gene. In particular, this thesis investigates two non-coding repeat expansion disorders: C9orf72-associated Amyotrophic Lateral Sclerosis (C9-ALS) and the Fragile X Syndrome (FXS). Our group was the first to report the presence of 5-hydroxymethylcytosine, a novel epigenetic mark and active DNA demethylation intermediate, at the expanded loci of patients with C9-ALS and FXS. 132 pp. Englisch.…

PAP. Condición: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

Condición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Esanov RustamRustam grew up in Ashgabat, Turkmenistan and attended Fatih University in Istanbul, Turkey to study biology. During his PhD at the University of Miami, he characterized novel epigenetic abnormalities associated with the .…

PAP. Condición: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

Taschenbuch. Condición: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - My research is focused on the repeat expansion disorders, a family of disorders that result from the repetitive microsatellite sequence within the gene. In particular, this thesis investigates two non-coding repeat expansion disorders: C9orf72-associated Amyotrophic Lateral Sclerosis (C9-ALS) and the Fragile X Syndrome (FXS). Our group was the first to report the presence of 5-hydroxymethylcytosine, a novel epigenetic mark and active DNA demethylation intermediate, at the expanded loci of patients with C9-ALS and FXS.…

Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 116 pp. Spanisch.

Taschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -My research is focused on the repeat expansion disorders, a family of disorders that result from the repetitive microsatellite sequence within the gene. In particular, this thesis investigates two non-coding repeat expansion disorders: C9orf72-associated Amyotrophic Lateral Sclerosis (C9-ALS) and the Fragile X Syndrome (FXS). Our group was the first to report the presence of 5-hydroxymethylcytosine, a novel epigenetic mark and active DNA demethylation intermediate, at the expanded loci of patients with C9-ALS and FXS.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 132 pp. Englisch.…

Taschenbuch. Condición: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Mi investigación se centra en los trastornos por expansión de repeticiones, una familia de trastornos que resultan de la secuencia repetitiva de microsatélites dentro del gen. En particular, esta tesis investiga dos trastornos de expansión de repeticiones no codificantes: La esclerosis lateral amiotrófica asociada a C9orf72 (C9-ALS) y el síndrome del cromosoma X frágil (FXS). Nuestro grupo fue el primero en informar de la presencia de 5-hidroximetilcitosina, una nueva marca epigenética e intermediario activo de la desmetilación del ADN, en los loci expandidos de pacientes con C9-ALS y FXS.…

Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 116 pp. Französisch.

Taschenbuch. Condición: Neu. Hidroximetilación del ADN en los trastornos por expansión de repeticiones no codificantes | Rustam Esanov | Taschenbuch | Spanisch | 2024 | Ediciones Nuestro Conocimiento | EAN 9786208407070 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu Print on Demand. …

Taschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Mi investigación se centra en los trastornos por expansión de repeticiones, una familia de trastornos que resultan de la secuencia repetitiva de microsatélites dentro del gen. En particular, esta tesis investiga dos trastornos de expansión de repeticiones no codificantes: La esclerosis lateral amiotrófica asociada a C9orf72 (C9-ALS) y el síndrome del cromosoma X frágil (FXS). Nuestro grupo fue el primero en informar de la presencia de 5-hidroximetilcitosina, una nueva marca epigenética e intermediario activo de la desmetilación del ADN, en los loci expandidos de pacientes con C9-ALS y FXS.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 116 pp. Spanisch.…

PAP. Condición: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

PAP. Condición: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

PAP. Condición: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

PAP. Condición: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

PAP. Condición: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

PAP. Condición: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

Condición: New. Print on Demand.

Condición: New. Print on Demand.