Mosig, Rebecca A., Dowling, Oonagh, DiFeo, Analisa, Ramirez, Maria Celeste M., Parker, Ian C., Abe, Etsuko, ...
The ‘vanishing bone’ or inherited osteolysis/arthritis syndromes represent a heterogeneous group of skeletal disorders characterized by mineralization defects of affected bones and joints....
Kirschenbaum, Alexander, Liu, Xin-Hua, Yao, Shen, Narla, Goutham, Friedman, Scott L., Martignetti, John A., ...
The majority of human prostate cancers arise from the peripheral zone. Prostate epithelial stem cells have been localized to the basal epithelial cell compartment. In addition, basal cells have been...
Yang, Tao, Martignetti, John A., Massa, Stephen M., Longo, Frank M.
Regulation of cell proliferation by protein tyrosine phosphatases (PTPs) suggests that PTPs are important tumor suppressor genes. The gene encoding the leukocyte common-antigen-related (LAR) PTP...
Heath, Karen E., Campos-Barros, Angel, Toren, Amos, Rozenfeld-Granot, Galit, Carlsson, Lena E., Savige, Judy, ...
May-Hegglin anomaly (MHA) and Fechtner (FTNS) and Sebastian (SBS) syndromes are autosomal dominant platelet disorders that share macrothrombocytopenia and characteristic leukocyte inclusions. FTNS...
The Gene for May-Hegglin Anomaly Localizes to a
Martignetti, John A., Heath, Karen E., Harris, Juliette, Bizzaro, Nicola, Savoia, Anna, Balduini, Carlo L., ...
The May-Hegglin anomaly (MHA) is an autosomal dominant platelet disorder of unknown etiology. It is characterized by thrombocytopenia, giant platelets, and leukocyte inclusion bodies, and affected...
Dowling, Oonagh, Difeo, Analisa, Ramirez, Maria C., Tukel, Turgut, Narla, Goutham, Bonafe, Luisa, ...
Juvenile hyaline fibromatosis (JHF) and infantile systemic hyalinosis (ISH) are autosomal recessive syndromes of unknown etiology characterized by multiple, recurring subcutaneous tumors, gingival...
Heath, Karen E., Campos-Barros, Angel, Toren, Amos, Rozenfeld-Granot, Galit, Carlsson, Lena E., Savige, Judy, ...
May-Hegglin anomaly (MHA) and Fechtner (FTNS) and Sebastian (SBS) syndromes are autosomal dominant platelet disorders that share macrothrombocytopenia and characteristic leukocyte inclusions. FTNS...
The Gene for May-Hegglin Anomaly Localizes to a
Martignetti, John A., Heath, Karen E., Harris, Juliette, Bizzaro, Nicola, Savoia, Anna, Balduini, Carlo L., ...
The May-Hegglin anomaly (MHA) is an autosomal dominant platelet disorder of unknown etiology. It is characterized by thrombocytopenia, giant platelets, and leukocyte inclusion bodies, and affected...
KLF6-SV1 overexpression accelerates human and mouse prostate cancer progression and metastasis
Narla, Goutham, DiFeo, Analisa, Fernandez, Yolanda, Dhanasekaran, Saravana, Huang, Fei, Sangodkar, Jaya, ...
Metastatic prostate cancer (PCa) is one of the leading causes of death from cancer in men. The molecular mechanisms underlying the transition from localized tumor to hormone-refractory metastatic PCa...