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Abdul K Qadree

Showing results (1-10 of 5) with videos related to

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Oxford Medical Case Reports|June 1, 2023
Bulbar onset amyotrophic lateral sclerosis with more evident symptoms in the left hemibody: a case reportManisha Chavan, Ajay Singh, Pinank K Bathvar, et al.
Cureus|December 18, 2023
Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a NewbornUtsav P Vaghani, Abdul K Qadree, Sarang Mehta, et al.
Journal of Pharmaceutical and Biomedical Analysis|September 18, 2018
A functional in vitro assay for screening inhibitors of STAT5B phosphorylationElvin D de Araujo, Pimyupa Manaswiyoungkul, Fettah Erdogan, et al.
Biochimica Et Biophysica Acta. General Subjects|November 14, 2021
Structural and mutational analysis of member-specific STAT functionsFettah Erdogan, Abdul K Qadree, Tudor B Radu, et al.
Nature Communications|June 9, 2019
Structural and functional consequences of the STAT5B<sup>N642H</sup> driver mutationElvin D de Araujo, Fettah Erdogan, Heidi A Neubauer, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Oxford Medical Case Reports|June 1, 2023
Bulbar onset amyotrophic lateral sclerosis with more evident symptoms in the left hemibody: a case reportManisha Chavan, Ajay Singh, Pinank K Bathvar, et al.
Cureus|December 18, 2023
Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a NewbornUtsav P Vaghani, Abdul K Qadree, Sarang Mehta, et al.
Journal of Pharmaceutical and Biomedical Analysis|September 18, 2018
A functional in vitro assay for screening inhibitors of STAT5B phosphorylationElvin D de Araujo, Pimyupa Manaswiyoungkul, Fettah Erdogan, et al.
Biochimica Et Biophysica Acta. General Subjects|November 14, 2021
Structural and mutational analysis of member-specific STAT functionsFettah Erdogan, Abdul K Qadree, Tudor B Radu, et al.
Nature Communications|June 9, 2019
Structural and functional consequences of the STAT5B<sup>N642H</sup> driver mutationElvin D de Araujo, Fettah Erdogan, Heidi A Neubauer, et al.
Pageof 1