E-LIB Suche - Ergebnisse für: Azzi, Salah

1

Genetic disruption of the oncogenic HMGA2–PLAG1–IGF2 pathwa..:

Abi Habib, Walid ; Brioude, Frédéric ; Edouard, Thomas...
Genetics in Medicine. 20 (2018) 2 - p. 250-258 , 2018

2

Chromosome 14q32.2 Imprinted Region Disruption as an Altern..:

Geoffron, Sophie ; Abi Habib, Walid ; Chantot-Bastaraud, Sandra...
The Journal of Clinical Endocrinology & Metabolism. 103 (2018) 7 - p. 2436-2446 , 2018

Link: https://doi.org/10.1210/..

3

Beckwith–Wiedemann and Russell–Silver Syndromes: from new m..:

Azzi, Salah ; Abi Habib, Walid ; Netchine, Irene
Current Opinion in Endocrinology, Diabetes & Obesity. 21 (2014) 1 - p. 30-38 , 2014

Link: https://doi.org/10.1097/..

4

Extensive investigation of the IGF2/H19 imprinting control ..:

Abi Habib, Walid ; Azzi, Salah ; Brioude, Frédéric...
Human Molecular Genetics. 23 (2014) 21 - p. 5763-5773 , 2014

Link: https://doi.org/10.1093/..

5

Epigenetic Anomalies in Childhood Growth Disorders:

, In: Recent Advances in Growth Research: Nutritional, Molecular and Endocrine Perspectives; Nestlé Nutrition Institute Workshop Series,

Netchine, Irène ; Rossignol, Sylvie ; Azzi, Salah. - p. 65-73 , 2013

Link: https://doi.org/10.1159/..

6

Degree of methylation ofZAC1(PLAGL1) is associated with pre..:

Azzi, Salah ; Sas, Theo CJ ; Koudou, Yves...
Epigenetics. 9 (2013) 3 - p. 338-345 , 2013

Link: https://doi.org/10.4161/..

7

SNP arrays in Beckwith–Wiedemann syndrome: An improved diag..:

Keren, Boris ; Chantot-Bastaraud, Sandra ; Brioude, Frédéric...
European Journal of Medical Genetics. 56 (2013) 10 - p. 546-550 , 2013

Link: https://doi.org/10.1016/..

8

Imprinted Anomalies in Fetal and Childhood Growth Disorders..:

, In: Developmental Biology of GH Secretion, Growth and Treatment; Endocrine Development,

Netchine, Irène ; Rossignol, Sylvie ; Azzi, Salah.. - p. 60-70 , 2012

Link: https://doi.org/10.1159/..

9

IGF1 molecular anomalies demonstrate its critical role in f..:

Netchine, Irène ; Azzi, Salah ; Le Bouc, Yves.
Best Practice & Research Clinical Endocrinology & Metabolism. 25 (2011) 1 - p. 181-190 , 2011

Link: https://doi.org/10.1016/..

10

Lessons from imprinted multilocus loss of methylation in hu..:

Azzi, Salah ; Rossignol, Sylvie ; Le Bouc, Yves.
Epigenetics. 5 (2010) 5 - p. 373-377 , 2010

Link: https://doi.org/10.4161/..

11

Partial Primary Deficiency of Insulin-Like Growth Factor (I..:

Netchine, Irène ; Azzi, Salah ; Houang, Muriel...
The Journal of Clinical Endocrinology & Metabolism. 94 (2009) 10 - p. 3913-3921 , 2009

Link: https://doi.org/10.1210/..

12

Analysis of the IGF2/H19 imprinting control region uncovers..:

Demars, Julie ; Shmela, Mansur Ennuri ; Rossignol, Sylvie...
Human Molecular Genetics. 19 (2009) 5 - p. 803-814 , 2009

Link: https://doi.org/10.1093/..

13

Multilocus methylation analysis in a large cohort of 11p15-..:

Azzi, Salah ; Rossignol, Sylvie ; Steunou, Virginie...
Human Molecular Genetics. 18 (2009) 24 - p. 4724-4733 , 2009

Link: https://doi.org/10.1093/..

14

11p15 Imprinting Center Region 1 Loss of Methylation Is a C..:

Netchine, Irène ; Rossignol, Sylvie ; Dufourg, Marie-Noëlle...
The Journal of Clinical Endocrinology & Metabolism. 92 (2007) 8 - p. 3148-3154 , 2007

Link: https://doi.org/10.1210/..

15

Possible association between complex congenital heart defec..:

Ghanim, Mustafa ; Rossignol, Sylvie ; Delobel, Bruno...
American Journal of Medical Genetics Part A. 161 (2013) 3 - p. 572-577 , 2013

Link: https://doi.org/10.1002/..