Zobrazeno 1 - 10
of 30
pro vyhledávání: '"G W, Hall"'
Autor:
Fiona Ryan, C. Noakes, Paul Q. Thomas, N. Curry, G. W. Hall, P. Bignell, Helen Stewart, Nicholas Rogers, A. Azriyanti, Mehul T. Dattani, KS Alatzoglou, D Saunders, A. S. Littooij
Publikováno v:
The Journal of clinical endocrinology and metabolism. 99(12)
SOX3 is an early developmental transcription factor involved in pituitary development. In humans, over- and underdosage of SOX3 is associated with X-linked hypopituitarism with variable phenotypes ranging from isolated GH deficiency (GHD) to panhypop
Publikováno v:
Blood. 92:3428-3435
A common β-thalassemia mutation in Asian populations is the C → T substitution at position 654 of intron 2, which leads to the activation of two cryptic splicing sites and the incorporation of 73 extra nucleotides into the mutant mRNA. Like most
Publikováno v:
Annals of the New York Academy of Sciences. 850:436-441
Publikováno v:
The Shock and Vibration Digest. 28:12-17
A method to measure rotary motion during dynamic loading of a complex human joint has been developed. Magnetohydrodynamic angular rate sensors are mounted to rigid links on either side of the joint and are employed to measure angular velocities about
Publikováno v:
SPIE Proceedings.
"Closed field" magnetron (CFM) sputtering offers a flexible and high throughput deposition process for optical coatings and thin films required in display technologies. CFM sputtering uses two or more different metal targets to deposit multilayers co
Autor:
G W, Hall
Publikováno v:
British journal of haematology. 112(4)
Publikováno v:
Ethnicitydisease. 10(2)
To examine the impact of family environment, morbidity, and socioeconomic status (SES) on coping strategies in families of children with sickle cell disease.A cross-sectional study.The study sample consisted of 40 mothers, 24 fathers, 40 patients, an
Autor:
G W, Hall
Publikováno v:
Journal of refractive surgery (Thorofare, N.J. : 1995). 12(7)
Publikováno v:
Blood. 83(8)
We present in vivo evidence that there is no reduction in beta-mRNA accumulation in patients with nonsense codons in the terminal exon of the beta-globin gene. Using reverse transcriptase/polymerase chain reaction (RT-PCR), beta-globin cDNA was isola
Autor:
G W, Hall, S L, Thein, A C, Newland, M, Chisholm, J, Traeger-Synodinos, E, Kanavakis, C, Kattamis, D R, Higgs
Publikováno v:
British journal of haematology. 85(3)
We have identified three individuals of Greek or Greek Cypriot origin with an atypical form of HbH disease characterized by a severe hypochromic microcytic anaemia associated with relatively small amounts of HbH in the peripheral blood. Molecular ana