Suchergebnisse - "Qadree, Abdul K"

PubPharm (5)

1

Bloch-Sulzberger Syndrome : A Rare X-Linked Dominant Genetic Disorder in a Newborn

enthalten in: Cureus | 2023

von Vaghani, U. | Qadree, A. | Mehta, S. | +5

2

Bulbar onset amyotrophic lateral sclerosis with more evident symptoms in the left hemibody : a case report

enthalten in: Oxford medical case reports | 2023

von Chavan, M. | Singh, A. | Bathvar, P. | +3

ErratumIn: Oxf Med Case Reports. 2023 Jul 18;2023(7):omad077. - PMID 37484552

3

Structural and mutational analysis of member-specific STAT functions

enthalten in: Biochimica et biophysica acta. General subjects | 2022

von Erdogan, F. | Qadree, A. | Radu, T. | +8

4

Structural and functional consequences of the STAT5BN642H driver mutation

enthalten in: Nature communications | 2019

von de Araujo, E. | Erdogan, F. | Neubauer, H. | +21

5

A functional in vitro assay for screening inhibitors of STAT5B phosphorylation

enthalten in: Journal of pharmaceutical and biomedical analysis | 2019

von de Araujo, E. | Manaswiyoungkul, P. | Erdogan, F. | +6

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