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Co-authors
(31)
David H. K. Chui
4
Martin H. Steinberg
3
Hong-Yuan Luo
3
Ross C. Hardison
1
Lalana Nuntakarn
1
Journals
(5)
Hemoglobin
2
CLIN GENET
1
EUR J HAEMATOL
1
PEDIATR BLOOD CANCER
1
MOL CELL BIOL
1
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Authors
Raveen K. Basran
Raveen K. Basran,Physiology,Genetics & Genealogy,Molecular Biology
Edit
Raveen K. Basran
Publications:
6
|
Citations:
10
Fields:
Physiology
,
Genetics & Genealogy
,
Molecular Biology
View FAQ about top research areas and Fields of study
Collaborated with
31 co-authors
from 2007 to 2010
|
Cited by
64 authors
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Annual
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Publications
(6)
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Novel intragenic deletion in OPHN1 in a family causing XLMR with cerebellar hypoplasia and distinctive facial appearance
(
Citations: 2
)
M Al-Owain
,
N Kaya
,
H Al-Zaidan
,
N Al-Hashmi
,
A Al-Bakheet
,
M Al-Muhaizea
,
A Chedrawi
,
RK Basran
,
A Milunsky
Journal:
Clinical Genetics - CLIN GENET
, pp. no-no, 2010
A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA1 binding motif is associated with elevated hemoglobin F
(
Citations: 6
)
Zhiyi Chen
,
Hong-Yuan Luo
,
Raveen K. Basran
,
Tien-Huei Hsu
,
Daniel W. H. Mang
,
Lalana Nuntakarn
,
Cathy G. Rosenfield
,
George P. Patrinos
,
Ross C. Hardison
,
Martin H. Steinberg
,
David H. K. Chui
Journal:
Molecular and Cellular Biology - MOL CELL BIOL
, vol. 28, no. 13, pp. 4386-4393, 2008
β-thalassemia intermedia due to compound heterozygosity for two β-globin gene promoter mutations, including a novel TATA box deletion
(
Citations: 1
)
Raveen K. Basran
,
Ulrike M. Reiss
,
Hong-yuan Luo
,
Russell E. Ware
,
David H. K. Chui
Journal:
Pediatric Blood & Cancer - PEDIATR BLOOD CANCER
, vol. 50, no. 2, pp. 363-366, 2008
THE Hb S/β + Thalassemia Phenotype Demonstrates that the IVS-I (−2) (A>C) Mutation is a Mild βThalassemia Allele
Markus Schmugge
,
John S. Waye
,
Raveen K. Basran
,
Karin Zurbriggen
,
Hannes Frischknecht
Journal:
Hemoglobin
, vol. 32, no. 3, pp. 303-307, 2008
Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb ?-globin gene deletion
(
Citations: 1
)
B. Anders R. Andersson
,
Mikaela E. L. Wering
,
Hong-Yuan Luo
,
Raveen K. Basran
,
Martin H. Steinberg
,
Hedy P. Smith
,
David H. K. Chui
Journal:
European Journal of Haematology - EUR J HAEMATOL
, vol. 78, no. 1, pp. 82-85, 2007
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Citations
(10 times by 10 publications)
Eos Negatively Regulates Human γ-globin Gene Transcription during Erythroid Differentiation
Hai-Chuan Yu
,
Hua-Lu Zhao
,
Zhi-Kui Wu
,
Jun-Wu Zhang
Journal:
PLOS One
, vol. 6, no. 7, 2011
X-linked disorders with cerebellar dysgenesis
Ginevra Zanni
,
Enrico S Bertini
Journal:
Orphanet Journal of Rare Diseases - ORPHANET J RARE DIS
, vol. 6, no. 1, pp. 1-11, 2011
NuRD mediates activating and repressive functions of GATA1 and FOG1 during blood development
(
Citations: 7
)
Annarita Miccio
,
Yuhuan Wang
,
Wei Hong
,
Gregory D Gregory
,
Hongxin Wang
,
Xiang Yu
,
John K Choi
,
Suresh Shelat
,
Wei Tong
,
Mortimer Poncz
,
Gerd A Blobel
Journal:
Embo Journal - EMBO J
, vol. 29, no. 2, pp. 442-456, 2010
BCL11A represses HBG transcription in K562 cells
(
Citations: 11
)
Zhiyi Chen
,
Hong-yuan Luo
,
Martin H. Steinberg
,
David H. K. Chui
Journal:
Blood Cells Molecules and Diseases - BLOOD CELLS MOLECULES DIS
, vol. 42, no. 2, pp. 144-149, 2009
Role of STAT3 and GATA1 interactions in γ-globin gene expression
(
Citations: 5
)
Xiao Yao
,
Sirisha Kodeboyina
,
Li Liu
,
James Dzandu
,
Jose Sangerman
,
Solomon F. Ofori-Acquah
,
Betty S. Pace
Journal:
Experimental Hematology - EXP HEMATOL
, vol. 37, no. 8, pp. 889-900, 2009
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