F Tsien
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Explore the profile of F Tsien including associated specialties, affiliations and a list of published articles.
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12
Citations
182
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Recent Articles
1.
Kibe R, Zhang S, Guo D, Marrero L, Tsien F, Rodriguez P, et al.
Cell Death Differ
. 2012 Jan;
19(7):1139-51.
PMID: 22281704
Interleukin-7 (IL-7) is an essential T-cell survival cytokine. IL-7 receptor (IL-7Rα) deficiency severely impairs T-cell development due to substantial apoptosis. We hypothesized that IL-7Rα(null)-induced apoptosis is partially contributed by an...
2.
Morava E, Jackson K, Tsien F, Marble M
Genet Couns
. 2005 Jan;
15(4):449-53.
PMID: 15658621
Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac anomalies: Patients with trisomy (1)(q42-qter) present with psychomotor retardation, macrocephaly, occasional presence of facial capillary naevi,...
3.
Tsien F, Fiala E, Youn B, Long T, Laird P, Weissbecker K, et al.
Cytogenet Genome Res
. 2003 Feb;
98(1):13-21.
PMID: 12584436
Untreated cultures from normal chorionic villus (CV) or amniotic fluid-derived (AF) samples displayed dramatic cell passage-dependent increases in aberrations in the juxtacentromeric heterochromatin of chromosomes 1 or 16 (1qh or...
4.
Ehrlich M, Tsien F, Herrera D, BLACKMAN V, Roggenbuck J
J Med Genet
. 2002 Jan;
38(12):882-4.
PMID: 11768395
No abstract available.
5.
Ehrlich M, Buchanan K, Tsien F, Jiang G, Sun B, Uicker W, et al.
Hum Mol Genet
. 2001 Dec;
10(25):2917-31.
PMID: 11741835
ICF (immunodeficiency, centromeric region instability and facial anomalies) is a recessive disease caused by mutations in the DNA methyltransferase 3B gene (DNMT3B). Patients have immunodeficiency, chromosome 1 (Chr1) and Chr16...
6.
Tsien F, Sun B, Hopkins N, Vedanarayanan V, Figlewicz D, Winokur S, et al.
Mol Genet Metab
. 2001 Nov;
74(3):322-31.
PMID: 11708861
Facioscapulohumeral muscular dystrophy (FSHD) has an unusual molecular etiology. In a putatively heterochromatic subtelomeric region of each chromosome 4 homologue (4q35), unaffected individuals have 11 to about 95 tandem copies...
7.
Jackson K, Tsien F, Marble M
Am J Med Genet
. 2000 Dec;
95(3):229-32.
PMID: 11102928
We report on a patient with mosaicism for monosomy 18, a chromosomal abnormality that has been reported only once previously. The patient had cleft lip and palate and mild behavioral...
8.
Narayan A, Tsien F, Smeets D, Sawyer J, Fiala E, Sohn O, et al.
Cytogenet Cell Genet
. 2000 Jul;
89(1-2):121-8.
PMID: 10894953
The ICF syndrome (immunodeficiency, centromeric region instability, facial anomalies) is a unique DNA methylation deficiency disease diagnosed by an extraordinary collection of chromosomal anomalies specifically in the vicinity of the...
9.
Marble M, Morava E, Tsien F, Amedee R, Pierce M
Am J Med Genet
. 1998 Mar;
75(5):537.
PMID: 9489801
No abstract available.
10.
Gill J, Varela M, Tsien F, Krause J
Cancer Genet Cytogenet
. 1997 Apr;
94(2):85-7.
PMID: 9109932
The der(1)t(1;19)(p12;p11) has not been previously reported in myelodysplastic syndrome (MDS). Fluorescence in situ hybridization (FISH) using chromosome 1- and chromosome 19-specific probes, performed on the bone marrow (BM) cells...