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Search Results - Bhagwat, Pranjali
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ABCD1 and X‐linked adrenoleukodystrophy: A disease with a markedly variable phenotype showing conserved neurobiology in animal models
by
Manor, Joshua
,
Chung, Hyunglok
,
Bhagwat, Pranjali K.
,
Wangler, Michael F.
Published in
Journal of neuroscience research
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A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins
by
Guichard, Annabel
,
Lu, Shenzhao
,
Kanca, Oguz
,
Bressan, Daniel
,
Huang, Yan
,
Ma, Mengqi
,
Sanz Juste, Sara
,
Andrews, Jonathan C.
,
Jay, Kristy L.
,
Sneider, Marketta
,
Schwartz, Ruth
,
Huang, Mei-Chu
,
Bei, Danqing
,
Pan, Hongling
,
Ma, Liwen
,
Lin, Wen-Wen
,
Auradkar, Ankush
,
Bhagwat, Pranjali
,
Park, Soo
,
Wan, Kenneth H.
,
Ohsako, Takashi
,
Takano-Shimizu, Toshiyuki
,
Celniker, Susan E.
,
Wangler, Michael F.
,
Yamamoto, Shinya
,
Bellen, Hugo J.
,
Bier, Ethan
Published in
Cell reports (Cambridge)
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De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures
by
Assia Batzir, Nurit
,
Bhagwat, Pranjali K
,
Eble, Tanya N
,
Liu, Pengfei
,
Eng, Christine M
,
Elsea, Sarah H
,
Robak, Laurie A
,
Scaglia, Fernando
,
Goldman, Alica M
,
Dhar, Shweta U
,
Wangler, Michael F
Published in
Cold Spring Harbor molecular case studies
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Abcd1
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Adrenoleukodystrophy
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Adrenoleukodystrophy - Genetics
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