E-LIB Suche - Ergebnisse für: Doubaj, Yassamine

1

MG132 Induces Progerin Clearance and Improves Disease Pheno..:

Harhouri, Karim ; Cau, Pierre ; Casey, Frank...
Cells. 11 (2022) 4 - p. 610 , 2022

2

Mutational spectrum of BRCA1/2 genes in Moroccan patients w..:

Elalaoui, Siham Chafai ; Laarabi, Fatima Zohra ; Afif, Lamiae...
Breast Cancer Research and Treatment. 194 (2022) 1 - p. 187-198 , 2022

Link: https://doi.org/10.1007/..

3

Clinical, cytogenetic and molecular findings in nine Morocc..:

Doubaj, Yassamine ; Zrhidri, Abdelali ; Elalaoui, Siham Chafai...
Pan African Medical Journal. 39 (2021) - p. , 2021

Link: https://doi.org/10.11604..

4

Hutchinson‐Gilford Progeria syndrome: Report of the first T..:

Guedenon, Koffi M. ; Doubaj, Yassamine ; Akolly, Djatougbe A. E....
American Journal of Medical Genetics Part A. 182 (2020) 6 - p. 1316-1320 , 2020

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

5

High frequency of the recurrent c.1310_1313delAAGA BRCA2 mu..:

Laarabi, Fatima-Zahra ; Ratbi, Ilham ; Elalaoui, Siham Chafai...
BMC Research Notes. 10 (2017) 1 - p. , 2017

Link: https://doi.org/10.1186/..

6

CHARGE syndrome: a recurrent hotspot of mutations in CHD7 I..:

Legendre, Marine ; Rodriguez - Ballesteros, Montserrat ; Rossi, Massimiliano...
European Journal of Human Genetics. 26 (2017) 2 - p. 287-292 , 2017

Link: https://doi.org/10.1038/..

7

A novel frameshift mutation in the XPC gene in a Moroccan p..:

Doubaj, Yassamine ; Smaili, Wiam ; Laarabi, Fatima-Zahra.
Journal of Medical Case Reports. 11 (2017) 1 - p. , 2017

Link: https://doi.org/10.1186/..

8

Novel splice site mutation in CNNM4 gene in a family with J..:

Cherkaoui Jaouad, Imane ; Lyahyai, Jaber ; Guaoua, Soukaina...
European Journal of Medical Genetics. 60 (2017) 5 - p. 239-244 , 2017

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

9

Antisense-Based Progerin Downregulation in HGPS-Like Patien..:

Harhouri, Karim ; Navarro, Claire ; Baquerre, Camille...
Cells. 5 (2016) 3 - p. 31 , 2016

Link: https://doi.org/10.3390/..

10

An inherited LMNA gene mutation in atypical Progeria syndro..:

Doubaj, Yassamine ; De Sandre‐Giovannoli, Annachiara ; Vera, Esteves‐Vieira...
American Journal of Medical Genetics Part A. 158A (2012) 11 - p. 2881-2887 , 2012

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

11

Carrier frequency of the recurrent mutation c.1643_1644delT..:

DOUBAJ, Yassamine ; LAARABI, Fatima‐Zahra ; CHAFAI ELALAOUI, Siham..
The Journal of Dermatology. 39 (2011) 4 - p. 382-384 , 2011

Link: https://doi.org/10.1111/..

12

MG132 Induces Progerin Clearance and Improves Disease Pheno..:

Harhouri, Karim ; Cau, Pierre ; Casey, Frank...
info:eu-repo/semantics/altIdentifier/doi/10.3390/cells11040610. , 2022

Link: https://hal.science/hal-..

13

CHARGE syndrome: a recurrent hotspot of mutations in CHD7 I..:

Legendre, Marine ; Rodriguez - Ballesteros, Montserrat ; Rossi, Massimiliano...
boreal:219927. , 2018

Link: http://hdl.handle.net/20..

14

CHARGE syndrome: a recurrent hotspot of mutations in CHD7 I..:

Legendre, Marine ; Rodriguez - Ballesteros, Montserrat ; Rossi, Massimiliano...
boreal:219927. , 2018

Link: http://hdl.handle.net/20..

15

Antisense-Based Progerin Downregulation in HGPS-Like Patien..:

Harhouri, Karim ; Navarro, Claire ; Baquerre, Camille...
info:eu-repo/semantics/altIdentifier/doi/10.3390/cells5030031. , 2016

Link: https://amu.hal.science/..