Ph1


Also found in: Acronyms.

Ph1

Abbreviation for Philadelphia chromosome.
References in periodicals archive ?
These initial results support the hypothesis that GO inhibition has the potential to reduce and possibly normalize levels of hepatic oxalate production, thus potentially halting PH1 disease progression.
PH1 is an autosomal recessive metabolic condition caused by a congenital deficiency of alanine-glyoxylate aminotransferase (AGT), a hepatic peroxisomal enzyme.
Professional astronomers have since confirmed the existence of PH1 and its four suns, but Jek and Gagliano are credited with the find.
Age at Urinary Age at first oxalate, inclusion, symptoms, mmol/mol Patient years years Symptoms creatinine (a) 1 59 2 UNI (b) 60 2 85 34 U 80 3 55 51 UNR 70 4 40 31 UNR 200 5 63 48 UI 130 6 69 50 UE 100 Patient Comorbidity Diagnosis 1 PH1 2 IH 3 Sb SH 4 Cd SH 5 Sb,Cd SH 6 Sb SH (a) Reference value, 0-54 mmol/mol creatinine.
Seeds are either black or black with white stripes with a respective 1000-seed weight of 43, 43, 69, 33, 31, 29, and 35 g for PH1 through PH7.
The test with the highest sensitivity for the diagnosis of PH1 is analysis of AGT activity in a liver biopsy sample.
Syracuse teaches you to look beyond your horizons and be more creative, unlike most Navy schools that teach you the technical side," said PH1 Steve Vanderwerff, a Syracuse graduate from the Motion Media Specialist Program in 1996.
Supply of spare parts for the speedometers as par of a project for the rehabilitation of the PH1 French made metro units operating on the Cairo Metro first line.
Donations to the charity can be sent to: Fairways home of rest for retired working horses, c/o Fairways Business Centre, 1 Watergate, Perth PH1 5TF.
PH1 is a rare, inherited genetic disorder of the AGXT gene in the liver which causes excess oxalate production.
Import of mechanical spare parts required for the rehabilitation of the PH1 French made metro trains operating on the Cairo Metro first line .