Search Results - Qadree, Abdul

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  1. 1
    Composite adverse outcomes in obstetric studies: a systematic review

    Composite adverse outcomes in obstetric studies: a systematic review by Herman, Dylan, Lor, Kar Yee, Qadree, Abdul, Horn, Daphne, D'Souza, Rohan

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  2. 2
    Structural and mutational analysis of member-specific STAT functions

    Structural and mutational analysis of member-specific STAT functions by Erdogan, Fettah, Qadree, Abdul K., Radu, Tudor B., Orlova, Anna, de Araujo, Elvin D., Israelian, Johan, Valent, Peter, Mustjoki, Satu M., Herling, Marco, Moriggl, Richard, Gunning, Patrick T.

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  3. 3
    A functional in vitro assay for screening inhibitors of STAT5B phosphorylation

    A functional in vitro assay for screening inhibitors of STAT5B phosphorylation by de Araujo, Elvin D., Manaswiyoungkul, Pimyupa, Erdogan, Fettah, Qadree, Abdul K., Sina, Diana, Tin, Gary, Toutah, Krimo, Yuen, Karen, Gunning, Patrick T.

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  4. 4
    Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn

    Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn by Vaghani, Utsav P, Qadree, Abdul K, Mehta, Sarang, Chaudhary, Nileshkumar S, Sharma, Kriti, Chaudhary, Sachin M, Kelechi, Anasonye E, Bano, Kausar

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  5. 5
    JAK‐STAT core cancer pathway: An integrative cancer interactome analysis

    JAK‐STAT core cancer pathway: An integrative cancer interactome analysis by Erdogan, Fettah, Radu, Tudor Bogdan, Orlova, Anna, Qadree, Abdul Khawazak, Araujo, Elvin Dominic, Israelian, Johan, Valent, Peter, Mustjoki, Satu M., Herling, Marco, Moriggl, Richard, Gunning, Patrick Thomas

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  6. 6
    Structural and utational nalysis of ember-pecific STAT unctions

    Structural and utational nalysis of ember-pecific STAT unctions by Erdogan, Fettah, Qadree, Abdul K., Radu, Tudor B., Orlova, Anna, de Araujo, Elvin D., Israelian, Johan, Valent, Peter, Mustjoki, Satu M., Herling, Marco, Moriggl, Richard, Gunning, Patrick T.

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  7. 7
    Bulbar onset amyotrophic lateral sclerosis with more evident symptoms in the left hemibody: a case report

    Bulbar onset amyotrophic lateral sclerosis with more evident symptoms in the left hemibody: a case report by Chavan, Manisha, Singh, Ajay, Bathvar, Pinank K, Mehta, Sarang T, Qadree, Abdul K, Dhakal, Sandesh

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  8. 8
    Structural and functional consequences of the STAT5BN642H driver mutation

    Structural and functional consequences of the STAT5BN642H driver mutation by de Araujo, Elvin D., Erdogan, Fettah, Neubauer, Heidi A., Meneksedag-Erol, Deniz, Manaswiyoungkul, Pimyupa, Eram, Mohammad S., Seo, Hyuk-Soo, Qadree, Abdul K., Israelian, Johan, Orlova, Anna, Suske, Tobias, Pham, Ha T. T., Boersma, Auke, Tangermann, Simone, Kenner, Lukas, Rülicke, Thomas, Dong, Aiping, Ravichandran, Manimekalai, Brown, Peter J., Audette, Gerald F., Rauscher, Sarah, Dhe-Paganon, Sirano, Moriggl, Richard, Gunning, Patrick T.

    Published in Nature communications
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  9. 9
    Structural and functional consequences of the STAT5B N642H driver mutation

    Structural and functional consequences of the STAT5B N642H driver mutation by de Araujo, Elvin D, Erdogan, Fettah, Neubauer, Heidi A, Meneksedag-Erol, Deniz, Manaswiyoungkul, Pimyupa, Eram, Mohammad S, Seo, Hyuk-Soo, Qadree, Abdul K, Israelian, Johan, Orlova, Anna, Suske, Tobias, Pham, Ha T T, Boersma, Auke, Tangermann, Simone, Kenner, Lukas, Rülicke, Thomas, Dong, Aiping, Ravichandran, Manimekalai, Brown, Peter J, Audette, Gerald F, Rauscher, Sarah, Dhe-Paganon, Sirano, Moriggl, Richard, Gunning, Patrick T

    Published in Nature communications
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  10. 10
    Bulbar onset amyotrophic lateral sclerosis with more evident symptoms in the left hemibody: a case report

    Bulbar onset amyotrophic lateral sclerosis with more evident symptoms in the left hemibody: a case report by Chavan, Manisha, Singh, Ajay, Bathvar, Pinank K, Mehta, Sarang T, Qadree, Abdul K, Dhakal, Sandesh

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  11. 11
    Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn

    Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn by Vaghani, Utsav P, Qadree, Abdul K, Mehta, Sarang, Chaudhary, Nileshkumar S, Sharma, Kriti, Chaudhary, Sachin M, Kelechi, Anasonye E, Bano, Kausar

    Published in Cureus
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