Hashmi JA - Search Results

1

NR2F1 mediated down-regulation of osteoblast differentiation was rescued by bone morphogenetic protein-2 (BMP-2) in human MSC.

Manikandan M, Abuelreich S, Elsafadi M, Alsalman H, Almalak H, Siyal A, Hashmi JA, Aldahmash A, Kassem M, Alfayez M, Mahmood A. Manikandan M, et al. Among authors: hashmi ja. Differentiation. 2018 Nov-Dec;104:36-41. doi: 10.1016/j.diff.2018.10.003. Epub 2018 Oct 29. Differentiation. 2018. PMID: 30445268

2

Characterization of Cellular and Molecular Heterogeneity of Bone Marrow Stromal Cells.

Elsafadi M, Manikandan M, Atteya M, Hashmi JA, Iqbal Z, Aldahmash A, Alfayez M, Kassem M, Mahmood A. Elsafadi M, et al. Among authors: hashmi ja. Stem Cells Int. 2016;2016:9378081. doi: 10.1155/2016/9378081. Epub 2016 Aug 16. Stem Cells Int. 2016. PMID: 27610142 Free PMC article.

3

Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa.

Hashmi JA, Albarry MA, Almatrafi AM, Albalawi AM, Mahmood A, Basit S. Hashmi JA, et al. Congenit Anom (Kyoto). 2018 Jan;58(1):10-15. doi: 10.1111/cga.12225. Epub 2017 May 28. Congenit Anom (Kyoto). 2018. PMID: 28419563

4

TGFβ1-Induced Differentiation of Human Bone Marrow-Derived MSCs Is Mediated by Changes to the Actin Cytoskeleton.

Elsafadi M, Manikandan M, Almalki S, Mobarak M, Atteya M, Iqbal Z, Hashmi JA, Shaheen S, Alajez N, Alfayez M, Kassem M, Dawud RA, Mahmood A. Elsafadi M, et al. Among authors: hashmi ja. Stem Cells Int. 2018 Feb 15;2018:6913594. doi: 10.1155/2018/6913594. eCollection 2018. Stem Cells Int. 2018. PMID: 29535777 Free PMC article.

5

An 18 bps in-frame deletion mutation in RUNX2 gene is a population polymorphism rather than a pathogenic variant.

Hashmi JA, Almatrafi A, Latif M, Nasir A, Basit S. Hashmi JA, et al. Eur J Med Genet. 2019 Feb;62(2):124-128. doi: 10.1016/j.ejmg.2018.06.013. Epub 2018 Jun 28. Eur J Med Genet. 2019. PMID: 29960047

6

High frequency and poor prognosis of late childhood BCR-ABL-positive and MLL-AF4-positive ALL define the need for advanced molecular diagnostics and improved therapeutic strategies in pediatric B-ALL in Pakistan.

Iqbal Z, Akhtar T, Awan T, Aleem A, Sabir N, Rasool M, Absar M, Akram AM, Shammas MA, Shah IH, Khalid M, Taj AS, Jameel A, Alanazi A, Gill AT, Hashmi JA, Hussain A, Sabar MF, Khalid AM, Qazi MH, Karim S, Siddiqi MH, Mahmood A, Iqbal M, Saeed A, Irfan MI. Iqbal Z, et al. Among authors: hashmi ja. Mol Diagn Ther. 2015 Oct;19(5):277-87. doi: 10.1007/s40291-015-0149-0. Mol Diagn Ther. 2015. PMID: 26266519

7

High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families.

AlAyadhi LY, Hashmi JA, Iqbal M, Albalawi AM, Samman MI, Elamin NE, Bashir S, Basit S. AlAyadhi LY, et al. Among authors: hashmi ja. Neuroscience. 2016 Dec 17;339:561-570. doi: 10.1016/j.neuroscience.2016.10.030. Epub 2016 Oct 19. Neuroscience. 2016. PMID: 27771533

8

A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly.

Hashmi JA, Al-Harbi KM, Ramzan K, Albalawi AM, Mehmood A, Samman MI, Basit S. Hashmi JA, et al. Ann Saudi Med. 2016 Nov-Dec;36(6):391-396. doi: 10.5144/0256-4947.2016.391. Ann Saudi Med. 2016. PMID: 27920410 Free PMC article.

9

Whole exome sequencing identification of a novel insertion mutation in the phospholipase C ε‑1 gene in a family with steroid resistant inherited nephrotic syndrome.

Hashmi JA, Safar RA, Afzal S, Albalawi AM, Abdu-Samad F, Iqbal Z, Basit S. Hashmi JA, et al. Mol Med Rep. 2018 Dec;18(6):5095-5100. doi: 10.3892/mmr.2018.9528. Epub 2018 Oct 2. Mol Med Rep. 2018. PMID: 30280192

10

A Heterozygous Mutation in the Triple Helical Region of the Alpha 1 (II) Chain of the COL2A1 Protein Causes Non-Lethal Spondyloepiphyseal Dysplasia Congenita.

Almatrafi A, Alfadhli F, Khan YN, Afzal S, Hashmi JA, Ullah A, Albalawi AM, Basit S. Almatrafi A, et al. Among authors: hashmi ja. Genet Test Mol Biomarkers. 2019 May;23(5):310-315. doi: 10.1089/gtmb.2018.0301. Epub 2019 Mar 30. Genet Test Mol Biomarkers. 2019. PMID: 30932712

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