Muhammad Ahmer Jamil - Search Results

Year	Number of Results
2015	2
2019	1
2020	2
2021	1
2022	3
2023	1
2024	2

1

Exploring Diverse Coagulation Factor XIII Subunit Expression Datasets: A Bioinformatic Analysis.

Jamil MA, Singh S, El-Maarri O, Oldenburg J, Biswas A. Jamil MA, et al. Int J Mol Sci. 2022 Apr 25;23(9):4725. doi: 10.3390/ijms23094725. Int J Mol Sci. 2022. PMID: 35563115 Free PMC article.

2

Multifaceted pathomolecular mechanism of a VWF large deletion involved in the pathogenesis of severe VWD.

Yadegari H, Jamil MA, Müller J, Marquardt N, Rawley O, Budde U, El-Maarri O, Lillicrap D, Oldenburg J. Yadegari H, et al. Among authors: jamil ma. Blood Adv. 2022 Feb 8;6(3):1038-1053. doi: 10.1182/bloodadvances.2021005895. Blood Adv. 2022. PMID: 34861678 Free PMC article.

3

A Homozygous Deep Intronic Variant Causes Von Willebrand Factor Deficiency and Lack of Endothelial-Specific Secretory Organelles, Weibel-Palade Bodies.

Yadegari H, Jamil MA, Marquardt N, Oldenburg J. Yadegari H, et al. Among authors: jamil ma. Int J Mol Sci. 2022 Mar 13;23(6):3095. doi: 10.3390/ijms23063095. Int J Mol Sci. 2022. PMID: 35328514 Free PMC article.

4

Molecular Profiling of Liver Sinusoidal Endothelial Cells in Comparison to Hepatocytes: Reflection on Which Cell Type Should Be the Target for Gene Therapy.

El-Maarri O, Jamil MA, Oldenburg J. El-Maarri O, et al. Among authors: jamil ma. Hamostaseologie. 2020 Nov;40(S 01):S26-S31. doi: 10.1055/a-1282-2286. Epub 2020 Nov 13. Hamostaseologie. 2020. PMID: 33187005

5

Heterozygosity in factor XIII genes and the manifestation of mild inherited factor XIII deficiency.

Singh S, Pezeshkpoor B, Jamil MA, Dodt J, Sharma A, Ramar V, Ivaskevicius V, Hethershaw E, Philippou H, Pavlova A, Oldenburg J, Biswas A. Singh S, et al. Among authors: jamil ma. J Thromb Haemost. 2024 Feb;22(2):379-393. doi: 10.1016/j.jtha.2023.09.032. Epub 2023 Oct 12. J Thromb Haemost. 2024. PMID: 37832789

6

The role of microRNAs in defining LSECs cellular identity and in regulating F8 gene expression.

Jamil MA, Al-Rifai R, Nuesgen N, Altmüller J, Oldenburg J, El-Maarri O. Jamil MA, et al. Front Genet. 2024 Feb 19;15:1302685. doi: 10.3389/fgene.2024.1302685. eCollection 2024. Front Genet. 2024. PMID: 38440189 Free PMC article.

7

Molecular Analysis of Fetal and Adult Primary Human Liver Sinusoidal Endothelial Cells: A Comparison to Other Endothelial Cells.

Jamil MA, Singer H, Al-Rifai R, Nüsgen N, Rath M, Strauss S, Andreou I, Oldenburg J, El-Maarri O. Jamil MA, et al. Int J Mol Sci. 2020 Oct 21;21(20):7776. doi: 10.3390/ijms21207776. Int J Mol Sci. 2020. PMID: 33096636 Free PMC article.

8

DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations.

Sharma A, Jamil MA, Nuesgen N, Schreiner F, Priebe L, Hoffmann P, Herns S, Nöthen MM, Fröhlich H, Oldenburg J, Woelfle J, El-Maarri O. Sharma A, et al. Among authors: jamil ma. Clin Epigenetics. 2015 Jul 28;7(1):76. doi: 10.1186/s13148-015-0112-2. eCollection 2015. Clin Epigenetics. 2015. PMID: 26221191 Free PMC article.

9

Stratifying Cumulus Cell Samples Based on Molecular Profiling to Help Resolve Biomarker Discrepancies and to Predict Oocyte Developmental Competence.

El-Maarri O, Jamil MA, Köster M, Nüsgen N, Oldenburg J, Montag M, van der Ven H, van der Ven K. El-Maarri O, et al. Among authors: jamil ma. Int J Mol Sci. 2021 Jun 15;22(12):6377. doi: 10.3390/ijms22126377. Int J Mol Sci. 2021. PMID: 34203623 Free PMC article.

10

Inter-locus as well as intra-locus heterogeneity in LINE-1 promoter methylation in common human cancers suggests selective demethylation pressure at specific CpGs.

Nüsgen N, Goering W, Dauksa A, Biswas A, Jamil MA, Dimitriou I, Sharma A, Singer H, Fimmers R, Fröhlich H, Oldenburg J, Gulbinas A, Schulz WA, El-Maarri O. Nüsgen N, et al. Among authors: jamil ma. Clin Epigenetics. 2015 Mar 1;7(1):17. doi: 10.1186/s13148-015-0051-y. eCollection 2015. Clin Epigenetics. 2015. PMID: 25798207 Free PMC article.

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