Results 121 to 130 of about 14,972 (184)

Very Late Extramedullary Relapse of Acute Myeloid Leukemia 13 Years After Allogeneic Transplant: A Case Report. [PDF]

Case Rep Hematol
von Aarburg Y, Beerlage A, Juskevicius D, Rütsche C, Dirks J, Grobholz R, Hartmann B, Mathew R, Leonards K, Gerull S.   +9 more
europepmc   +1 more source

Zero-shot prediction of drug responses using biologically informed neural networks trained on phosphoproteomic timeseries. [PDF]

PLoS Comput Biol
Antonopoulos K, Nordenstorm O, Nilsson A.   +2 more
europepmc   +1 more source

<i>PTPN11</i> mutations define a rare but highly adverse subset of myelodysplastic syndromes. [PDF]

Haematologica
Bazinet A, Bataller A, Montalban-Bravo G, Chien K, Sasaki K, Jen WY, Swaminathan M, Kadia T, DiNardo C, Ravandi F, Garcia-Manero G, Kantarjian H.   +11 more
europepmc   +1 more source

Case Report: Genomic characterization of a rare skull-base plasmacytoma. [PDF]

Front Oncol
Alanya H, Kasturi S, Yalcin K, Gultekin B, Kumar D, Samuel N, Figuera DS, Mishra-Gorur K, Gunel M, Erson-Omay EZ, Omay SB.   +10 more
europepmc   +1 more source

Linear epidermal naevus associated with a novel mosaic heterozygous PTPN11 variant. [PDF]

Br J Dermatol
Jiang X, Chen TX, Hu R, Mortlock RD, Ko C, Choate KA.   +5 more
europepmc   +1 more source

Innate immune mechanisms hijacked by leukemia-initiating stem cells for selective advantage and immune evasion in Ptpn11-associated JMML. [PDF]

Cell Rep
Zheng H, Zhao P, Tan Z, Yu WM, Werner J, Stieglitz E, Porter CC, Chandrakasan S, Wechsler DS, Mendez-Ferrer S, Qu CK.   +10 more
europepmc   +1 more source

Inherited variants in autosomal dominant disease genes are a significant cause of fetal structural anomalies. [PDF]

J Med Genet
Graham SA, McCabe A, Harrison V, Castleman J, Doyle S, Allen S.   +5 more
europepmc   +1 more source

Durable remission despite transplantation with active disease in therapy-related NUP98::TOP1-rearranged acute myeloid leukemia. [PDF]

Ann Hematol
Cimino G, Sembenico R, Zorutti F, Saldi S, Caridi M, Cardinali V, Sciabolacci S, Crescenzi B, Matteucci C, La Starza R, Pucciarini A, Zei T, Iacucci Ostini R, Aristei C, Carotti A, Mecucci C, Ruggeri L, Martelli MP, Pierini A.   +18 more
europepmc   +1 more source

Noonan syndrome with <i>PTPN11</i> gene variant presenting as isolated short stature: a case report. [PDF]

Transl Pediatr
Peng J, Huang T, Wang Q, Liu B, Qin L, Yao Y.   +5 more
europepmc   +1 more source

Clinical characteristics, genomic profiling, treatments, and outcomes of Langerhans cell sarcoma. [PDF]

Orphanet J Rare Dis
Lang M, Zheng XJ, Chang L, Zhou DB, Zhang W, Cao XX.   +5 more
europepmc   +1 more source