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Scholar Results 1 - 10 of about 101 related to Fan: A missense mutation in PTCH2 underlies dominantly inherited NBCCS in a Chinese family. (0.11 sec) 

A missense mutation in PTCH2 underlies dominantly inherited NBCCS in a Chinese family


Z Fan, J Li, J Du, H Zhang, Y Shen, CY Wang … - British Medical Journal, 2008 - jmg.bmj.com
ABSTRACT Background: Naevoid basal cell carcinoma syndrome (NBCCS) is a
pleiotropic, autosomal dominant disease. Growing evidence suggests that the
disorder may result from mutations in genes of the Sonic hedgehog (Shh) ...
Cited by 7 - Related articles - BL Direct - All 5 versions

GLI2-specific transcriptional activation of the bone morphogenetic protein/activin antagonist …

- jbc.org
T Eichberger, A Kaser, C Pixner, C Schmid, S … - Journal of Biological Chemistry, 2008 - ASBMB
Hedgehog (HH) signaling in the epidermis is primarily mediated by the zinc
finger transcription factors GLI1 and GLI2. Exquisite regulation of HH/GLI
signaling is crucial for proper specification of the epidermal lineage and ...
Cited by 4 - Related articles - All 6 versions

Hedgehog signaling: Iguana debuts as a nuclear gatekeeper


SA Vokes, AP McMahon - Current Biology, 2004 - Elsevier
The Hedgehog (Hh) pathway is one of the preeminent modes of molecular signaling
in the developing embryo, and is highly conserved in organisms ranging from
Drosophila to humans. The vast repertoire of tissues affected by Hh include ...
Cited by 7 - Related articles - All 7 versions

Disruption of Smad4 in odontoblasts causes multiple keratocystic odontogenic tumors and …


Y Gao, G Yang, T Weng, J Du, X Wang, J … - Molecular and Cellular Biology, 2009 - Am Soc Microbiol
Keratocystic odontogenic tumors (KCOTs) are cystic epithelial neoplasias with a
high recurrence rate. However, the molecular mechanisms underlying the
initiation and progression of KCOTs are still largely unknown. Here, we ...
Related articles - All 3 versions

Xeroderma pigmentosum skin: an immune privilege site for tumor development


K Abid, F El Mezni, MR Kamoun, B Fazaa, R … - Journal of Cutaneous Pathology, 2009 - interscience.wiley.com
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[CITATION] A susceptibility locus on 1p32-1p34 for congenital macrostomia in a Chinese family and …


Z Fan, J Du, H Liu, H Zhang, AA Dlugosz, … - American Journal of Medical Genetics Part C: Seminars … - interscience.wiley.com
It is also possible that your web browser is not configured or not able to
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degraded, the site should continue to be functional. We recommend using the ...
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[CITATION] A susceptibility locus on 1p32-1p34 for congenital macrostomia in a Chinese family and …


Z Fan, J Du, H Liu - American Journal of Medical Genetics Part A, 2009 - Wiley Subscription Services, Inc., A Wiley Company …
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Hedgehog Target Genes: Mechanisms of Carcinogenesis Induced by Aberrant Hedgehog …


Y Katoh, M Katoh - Current Molecular Medicine, 2009 - ingentaconnect.com
1M & M Medical Bioinformatics, Hongo 113-0033, Japan; 2Genetics and Cell Biology
Section, National Cancer Center, Tokyo 104-0045, Japan Abstract: Hedgehog
signaling is aberrantly activated in glioma, medulloblastoma, basal cell ...
Related articles

[PDF] Mutational Analyses of the Tumor Suppressor Gene PATCHED1


E Lindström - diss.kib.ki.se
Page 1. From the Department of Biosciences and Nutrition Karolinska Institutet,
Stockholm, Sweden Mutational Analyses of the Tumor Suppressor Gene PATCHED1 ...
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Gorlin Syndrome Patient with Large Deletion in 9q22. 32–q22. 33 Detected by Quantitative …


V Musani, M Cretnik, M Situm, A Basta- … - Dermatology, 2009 - content.karger.com
Background: Gorlin syndrome is a rare autosomal-dominant disorder characterized
by a wide range of developmental abnormalities and various tumors. The syndrome
is caused by mutations in PTCH1, a tumor suppressor gene located at ...
Related articles - All 4 versions


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