Literature DB >> 30358901

MPP1/p55 gene deletion in a hemophilia A patient with ectrodactyly and severe developmental defects.

Daniel I Fritz1,2, Toshihiko Hanada1, Yunzhe Lu1, J Martin Johnston3, Athar H Chishti1,2.   

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Year:  2018        PMID： 30358901     DOI： 10.1002/ajh.25323

Source DB:  PubMed          Journal:  Am J Hematol        ISSN： 0361-8609            Impact factor:   10.047


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  2 in total

1.  Phospho-PTM proteomic discovery of novel EPO- modulated kinases and phosphatases, including PTPN18 as a positive regulator of EPOR/JAK2 Signaling.

Authors:  Matthew A Held; Emily Greenfest-Allen; Su Su; Christian J Stoeckert; Matthew P Stokes; Don M Wojchowski
Journal:  Cell Signal       Date:  2020-02-03       Impact factor: 4.315

2.  Bleeding Post Constriction Ring Release Surgery Causing Lower Limb Ischemia in an Infant with Undetected Hemophilia B.

Authors:  S Raja Sabapathy; Monusha Mohan; G Venkateswaran; Shashi Ranjani
Journal:  Indian J Plast Surg       Date:  2021-06-10
  2 in total

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