E-LIB Suche - Ergebnisse für: Mohamoud, Hussein Sheikh

1

A missense mutation in TRAPPC6A leads to build-up of the pr..:

Mohamoud, Hussein Sheikh ; Ahmed, Saleem ; Jelani, Musharraf...
Scientific Reports. 8 (2018) 1 - p. , 2018

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

2

Whole exome sequencing reveals a homozygous SGCB variant in..:

Tariq, Muhammad ; Latif, Muhammad ; Inam, Memona...
Gene Reports. 22 (2021) - p. 101014 , 2021

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

3

A mutation in the major autophagy gene, WIPI2, associated w..:

Jelani, Musharraf ; Dooley, Hannah C. ; Gubas, Andrea...
Brain. 142 (2019) 5 - p. 1242-1254 , 2019

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

4

Whole-exome sequencing reveals a recurrent mutation in the ..:

Alkhiary, Yaser Mohammad ; Jelani, Musharraf ; Almramhi, Mona Mohammad...
Saudi Journal of Biological Sciences. 23 (2016) 5 - p. 571-576 , 2016

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

5

The alkylglycerol monooxygenase (AGMO) gene previously invo..:

Alrayes, Nuha ; Mohamoud, Hussein Sheikh Ali ; Ahmed, Saleem...
Journal of the Neurological Sciences. 363 (2016) - p. 240-244 , 2016

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

6

A novel homozygous PTH1R variant identified through whole-e..:

Jelani, Musharraf ; Kang, Changsoo ; Mohamoud, Hussein Sheikh Ali...
Archives of Oral Biology. 67 (2016) - p. 28-33 , 2016

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

7

Novel nonsense mutation in the PTRF gene underlies congenit..:

Jelani, Musharraf ; Ahmed, Saleem ; Almramhi, Mona Mohammad...
European Journal of Medical Genetics. 58 (2015) 4 - p. 216-221 , 2015

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

8

Exome analysis identified a novel missense mutation in the ..:

Ahmed, Saleem ; Jelani, Musharraf ; Alrayes, Nuha...
Journal of the Neurological Sciences. 353 (2015) 1-2 - p. 149-154 , 2015

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

9

Truncating mutation in intracellular phospholipase A1 gene ..:

Alrayes, Nuha ; Mohamoud, Hussein Sheikh Ali ; Jelani, Musharraf...
BMC Research Notes. 8 (2015) 1 - p. , 2015

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

10

The Microbial Pathology of Neu5Ac and Gal Epitopes:

Hussain, Muhammad Ramzan Manwar ; Asfour, Hani ; Yasir, Muhammad...
Journal of Carbohydrate Chemistry. 32 (2013) 3 - p. 169-183 , 2013

Link: https://doi.org/10.1080/..

11

P2: Finetuning of the genotype-phenotype correlation in Cri..:

Mul, Adri ; Man, Hai-Yen ; Mathijssen, Inge B....
European Journal of Medical Genetics. 48 (2005) 4 - p. 448-449 , 2005

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

12

Detection of genetic alterations in gastric cancer patients..:

Bibi, Fehmida ; Ali, Isse ; Naseer, Muhammad Imran...
PLOS ONE. 13 (2018) 9 - p. e0202576 , 2018

Link: https://doi.org/10.1371/..

13

First ComprehensiveIn SilicoAnalysis of the Functional and ..:

Ali Mohamoud, Hussein Sheikh ; Manwar Hussain, Muhammad Ramzan ; El-Harouni, Ashraf A....
Computational and Mathematical Methods in Medicine. 2014 (2014) - p. 1-15 , 2014

Link: https://doi.org/10.1155/..

14

From Genes to Health – Challenges and Opportunities:

Manwar Hussain, Muhammad Ramzan ; Khan, Asifullah ; Ali Mohamoud, Hussein Sheikh
Frontiers in Pediatrics. 2 (2014) - p. , 2014

Link: https://doi.org/10.3389/..

15

A missense mutation in TRAPPC6A leads to build-up of the pr..:

Mohamoud, Hussein Sheikh ; Ahmed, Saleem ; Jelani, Musharraf...
Mohamoud , H S , Ahmed , S , Jelani , M , Alrayes , N , Childs , K , Vadgama , N , Almramhi , M M , Al-Aama , J Y , Goodbourn , S & Nasir , J 2018 , ' A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features ' , Scientific Reports , vol. 8 , no. 1 , 2053 (2018) , pp. 1-9 . https://doi.org/10.1038/s41598-018-20658-w. , 2018

Link: https://pure.northampton..