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GENE (2013)
Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population
Ayda Khalfallah et al.
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Phenotype of the First Otosclerosis Family Linked to OTSC10
Nicole J. D. Weegerink et al.
LARYNGOSCOPE (2011)
Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia
Ayda Khalfallah et al.
ANNALS OF HUMAN GENETICS (2010)
Lack of association between SNP rs3914132 of the RELN gene and otosclerosis in India
S. Priyadarshi et al.
GENETICS AND MOLECULAR RESEARCH (2010)
The Genetics of otosclerosis
Megan Ealy et al.
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Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations
Isabelle Schrauwen et al.
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Santiago Rodriguez et al.
AMERICAN JOURNAL OF EPIDEMIOLOGY (2009)
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Isabelle Schrauwen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Autism and Nonsyndromic Mental Retardation Associated with a De Novo Mutation in the NLGN4X Gene Promoter Causing an Increased Expression Level
Hussein Daoud et al.
BIOLOGICAL PSYCHIATRY (2009)
Role of 5 '- and 3 '-untranslated regions of mRNAs in human diseases
Sangeeta Chatterjee et al.
BIOLOGY OF THE CELL (2009)
An overview of the etiology of otosclerosis
Konstantinos Markou et al.
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY (2009)
Functional impact of sequence variation in the promoter region of TGFB1
Jasmine Healy et al.
INTERNATIONAL JOURNAL OF CANCER (2009)
Normal Bone Anatomy and Physiology
Bart Clarke
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2008)
Gene expression analysis of human otosclerotic stapedial footplates
Megan Ealy et al.
HEARING RESEARCH (2008)
A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9
Insaf Bel Hadj Ali et al.
HUMAN GENETICS (2008)
Association of bone morphogenetic proteins with otosclerosis
Isabelle Schrauwen et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2008)
The coding polymorphism T263I in TGF-β1 is associated with otosclerosis in two independent populations
Melissa Thys et al.
HUMAN MOLECULAR GENETICS (2007)
Association of TGFβ1, TNFα, CCR2 and CCR5 gene polymorphisms in type-2 diabetes and renal insufficiency among Asian Indians
Pushplata Prasad et al.
BMC MEDICAL GENETICS (2007)
A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1
Melissa Thys et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2007)
Transforming growth factor beta 1 (TGFB1) gene polymorphisms and risk of advanced colorectal adenoma
Sonja I. Berndt et al.
CARCINOGENESIS (2007)
Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locus
Z Brownstein et al.
ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY (2006)
TGFβ1 haplotypes and asthma in Indian populations
K Nagpal et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2005)
Transforming growth factor-β1 promoter polymorphism C-509T is associated with asthma
ES Silverman et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2004)
Roles of stromal cell RANKL, OPG, and M-CSF expression in biphasic TGF-β regulation of osteoclast differentiation
M Karst et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2004)
A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22-24
K Van Den Bogaert et al.
JOURNAL OF MEDICAL GENETICS (2004)
Linkage of otosclerosis to a third locus (OTSC3) on human chromosome 6p21.3-22.3
W Chen et al.
JOURNAL OF MEDICAL GENETICS (2002)
Transforming growth factor β affects osteoclast differentiation via direct and indirect actions
JMW Quinn et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2001)
Association of the C-509→T polymorphism, alone or in combination with the T869→C polymorphism, of the transforming growth factor-β1 gene with bone mineral density and genetic susceptibility to osteoporosis in Japanese women
Y Yamada et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2001)
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36
K Van den Bogaert et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)