HomeLiterature Search
Popular searches
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.

Barron(Martin J),McDonnell(Sinead T),Mackie(… Orphanet J Rare Dis 2009-01-27

...COL1A1 and COL1A2, underlie this condition. All other forms of DGI and DD, except DD-1, appear to result from mutations ...

Ectopic expression of interleukin-1 receptor type II enhances cell migration th…

Chang(Shih-Yu),Su(Pei-Fen),Lee(Te-Chang) Cytokine 2009-02-03

...COL1A1). However, depleting gene expression using small RNA interference specific to either pIL-1alpha or COL1A1, but no...

Medallion-like dermal dendrocyte hamartoma: the main diagnostic pitfall is cong…

Marque(M),Bessis(D),Pedeutour(F),Viseux(V),G… Br J Dermatol 2009-02-17

...COL1A1-PDGFB. We observed that the main diagnostic pitfall of medallion-like dermal dendrocyte hamartoma is atrophic con...

Absence of association between COL1A1 polymorphisms and high myopia in the Japa…

Nakanishi(Hideo),Yamada(Ryo),Gotoh(Norimoto)… Invest Ophthalmol Vis Sci 2009-02-06

The collagen type I alpha 1 (COL1A1) gene was recently reported to be associated with high myopia in the Japanese popula...

[Molecular diagnosis of osteogenesis imperfecta type I].

Galicka(Anna),Bielawski(Tomasz),Gindzieński(… Pol Merkur Lekarski 2009-03-19

...COL1A1 gene polymorphism.,In the group of 17 OI patients 11 were heterozygous for insertion of 4 bp in 3'UTR region of C...

Differential global and extra-cellular matrix focused gene expression patterns …

Kirwan(Ruaidhrí P),Wordinger(Robert J),Clark… Mol Vis 2009-04-17

...COL1A1), collagen type V (COL5A1), and collagen type XI (COL11A1). Downregulated ECM genes in POAG included fibulin 1 (F...

Connective tissue and related disorders and preterm birth: clues to genes contr…

Anum(E A),Hill(L D),Pandya(A),Strauss(J F) Placenta 2009-05-14

...COL1A1, COL1A2, TNXB, PLOD1, ADAMTS2, CRTAP, LEPRE1 and ZMPSTE24. Marfan syndrome, caused by FBN1 mutations, and polymor...

Chondroitin sulphate decreases collagen synthesis in normal and scleroderma fib…

Renard(Emmanuelle),Chadjichristos(Christos),… J Cell Mol Med 2009-03-25

...COL1A1 and COL1A2 in NF and SF. These glycosaminoglycan molecules repress COL1A1 gene transcription through a -112/-61 b...

CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.

Baldridge(Dustin),Schwarze(Ulrike),Morello(R… Hum Mutat 2009-01-08

Autosomal dominant osteogenesis imperfecta (OI) is caused by mutations in the genes (COL1A1 or COL1A2) encoding the chai...

Study of the association between polymorphisms of the COL1A1 gene and HBV-relat…

Zhao(Yun-Peng),Wang(Hao),Fang(Meng),Ji(Qiang… Dig Dis Sci 2009-03-09

...COL1A1 is crucial to the increased transcriptional activity. COL1A1 gene polymorphism might be associated with liver fib...

Previous 200 201 202 203 204 205 206 207 208 Next Vol. 204 / of 293

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]