Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 13

1.

Proteomics identification and characterization of MbovP730 as a potential DIVA antigen of Mycoplasma bovis.

Khan FA, Zhao G, Guo Y, Faisal M, Chao J, Chen X, He C, Menghwar H, Dad R, Zubair M, Hu C, Chen Y, Chen H, Rui Z, Guo A.

Oncotarget. 2017 Nov 2;9(47):28322-28336. doi: 10.18632/oncotarget.22265. eCollection 2018 Jun 19.

2.

Chorea-acanthocytosis: Homozygous 1-kb deletion in VPS13A detected by whole-genome sequencing.

Walker S, Dad R, Thiruvahindrapuram B, Ullah MI, Ahmad A, Hassan MJ, Scherer SW, Minassian BA.

Neurol Genet. 2018 May 18;4(3):e242. doi: 10.1212/NXG.0000000000000242. eCollection 2018 Jun.

3.

Mechanism of pattern recognition receptors (PRRs) and host pathogen interplay in bovine mastitis.

Bhattarai D, Worku T, Dad R, Rehman ZU, Gong X, Zhang S.

Microb Pathog. 2018 Apr 7;120:64-70. doi: 10.1016/j.micpath.2018.04.010. [Epub ahead of print] Review.

PMID:
29635052
4.

Knockdown of melatonin receptor 1 and induction of follicle-stimulating hormone on the regulation of mouse granulosa cell function.

Talpur HS, Worku T, Rehman ZU, Dad R, Bhattarai D, Bano I, Farmanullah, Liang A, He C, Yang L.

Reprod Biol. 2017 Dec;17(4):380-388. doi: 10.1016/j.repbio.2017.10.005. Epub 2017 Oct 31.

PMID:
29097083
5.

Hyperventilation-athetosis in ASXL3 deficiency (Bainbridge-Ropers) syndrome.

Dad R, Walker S, Scherer SW, Hassan MJ, Kang SY, Minassian BA.

Neurol Genet. 2017 Sep 22;3(5):e189. doi: 10.1212/NXG.0000000000000189. eCollection 2017 Oct. No abstract available.

6.

Role and mechanism of AMH in the regulation of Sertoli cells in mice.

Rehman ZU, Worku T, Davis JS, Talpur HS, Bhattarai D, Kadariya I, Hua G, Cao J, Dad R, Farmanullah, Hussain T, Yang L.

J Steroid Biochem Mol Biol. 2017 Nov;174:133-140. doi: 10.1016/j.jsbmb.2017.08.011. Epub 2017 Aug 26.

PMID:
28851672
7.

Polyamines: therapeutic perspectives in oxidative stress and inflammatory diseases.

Hussain T, Tan B, Ren W, Rahu N, Dad R, Kalhoro DH, Yin Y.

Amino Acids. 2017 Sep;49(9):1457-1468. doi: 10.1007/s00726-017-2447-9. Epub 2017 Jul 21. Review.

PMID:
28733904
8.

Febrile ataxia and myokymia broaden the SPG26 hereditary spastic paraplegia phenotype.

Dad R, Walker S, Scherer SW, Hassan MJ, Alghamdi MD, Minassian BA, Alkhater RA.

Neurol Genet. 2017 May 23;3(3):e156. doi: 10.1212/NXG.0000000000000156. eCollection 2017 Jun. No abstract available.

9.

Structural annotation of Beta-1,4-N-acetyl galactosaminyltransferase 1 (B4GALNT1) causing Hereditary Spastic Paraplegia 26.

Dad R, Malik U, Javed A, Minassian BA, Hassan MJ.

Gene. 2017 Aug 30;626:258-263. doi: 10.1016/j.gene.2017.05.041. Epub 2017 May 20.

PMID:
28536081
10.

Corrigendum to "Clinical and genetic studies in patients with Lafora disease from Pakistan"[J. Neurol. Sci. 373 (2017) 263-267].

Ahmad A, Dad R, Ullah MI, Baig TA, Ahmad IN, Nasir A, Hübner CA, Hassan MJ.

J Neurol Sci. 2017 Apr 15;375:281. doi: 10.1016/j.jns.2017.02.010. Epub 2017 Feb 12. No abstract available.

PMID:
28320149
11.

Association of MAP4K4 gene single nucleotide polymorphism with mastitis and milk traits in Chinese Holstein cattle.

Bhattarai D, Chen X, Ur Rehman Z, Hao X, Ullah F, Dad R, Talpur HS, Kadariya I, Cui L, Fan M, Zhang S.

J Dairy Res. 2017 Feb;84(1):76-79. doi: 10.1017/S0022029916000832.

PMID:
28252361
12.

Clinical and genetic studies in patients with Lafora disease from Pakistan.

Ahmad A, Dad R, Ullah MI, Baig TA, Ahmad IN, Nasir A, Hübner CA, Hassan MJ.

J Neurol Sci. 2017 Feb 15;373:263-267. doi: 10.1016/j.jns.2017.01.010. Epub 2017 Jan 4. Erratum in: J Neurol Sci. 2017 Apr 15;375:281.

PMID:
28131202
13.

Biallelic truncating SCN9A mutation identified in four families with congenital insensitivity to pain from Pakistan.

Sawal HA, Harripaul R, Mikhailov A, Dad R, Ayub M, Jawad Hassan M, Vincent JB.

Clin Genet. 2016 Dec;90(6):563-565. doi: 10.1111/cge.12860. Epub 2016 Oct 17.

PMID:
27747863

Supplemental Content

Support Center