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GJB2
Results: 11

#	Item
1	Ausprägung der Innenohrschwerhörigkeit bei Patienten mit Mutationen im GJB2-Gen Diana Arweiler-Harbeck1, Sven Saleik1, Patrick Munder1, Judith Arnolds1, Stefan Lang1, Bernd Wollnik3, Dagmar Wieczorek2, Alma Kuechler2 1 Add to Reading List Source URL: www.egms.de - Date: 2015-04-23 18:56:34
2	Microsoft Word - 3 R.S.R. Add to Reading List Source URL: www.ata.org.tn Language: English - Date: 2011-02-22 05:31:54 Nonsyndromic deafness Biology Genetics Sensorineural hearing loss Health GJB2 GJB6 Philosophy of biology Mutation Deafness Mitochondrial diseases Channelopathy
3	PL-ISSNprint), ISSNonline) Ó Institute of Systematics and Evolution of Animals, PAS, Kraków, 2014 Folia Biologica (Kraków), vol), No 4 doi:fb62_4.367 Add to Reading List Source URL: www.isez.pan.krakow.pl Language: English - Date: 2014-12-23 05:21:52 Zoology Developmental biology Organs Pelvis Connexin Placentation Trophoblast GJB2 Uterus Anatomy Biology Female reproductive system
4	Temozolomide resistance in glioblastoma cells occurs partly through epidermal growth factor receptor-mediated induction of connexin 43 Add to Reading List Source URL: www.nature.com Language: English - Date: 2014-03-27 10:59:45 Brain tumor Glioblastoma multiforme Epidermal growth factor receptor GJB2 Connexin Carcinogenesis Temozolomide Cell signaling Cetuximab Biology Medicine Chemistry
5	The n e w e ng l a n d j o u r na l of Add to Reading List Source URL: www.infanthearing.org Language: English - Date: 2010-04-22 17:51:15 Otolaryngology Otology Sensorineural hearing loss Mitochondrial diseases Hearing impairment Syndromes GJB2 KCNQ4 Congenital hearing loss Deafness Health Medicine
6	Associations between GJB2, Mitochondrial 12S rRNA, SLC26A4 Mutations, and Hearing Loss among Three Ethnicities Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Deafness DNA Mitochondrial diseases Channelopathy Nonsyndromic deafness MT-RNR1 Sensorineural hearing loss Uyghur people GJB2 Genetics Biology Philosophy of biology
7	A Novel Homozygous Mutation in the EC1/EC2 Interaction Domain of the Gap Junction Complex Connexon 26 Leads to Profound Hearing Impairment Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Integral membrane proteins Connexin Deafness GJB2 Gap junction GJB6 Connexon GJB3 Chromosome 13 Biology Cell biology Genodermatoses
8	CpGPAP: CpG island predictor analysis platform Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Apoptosis Auditory system Immune system Integral membrane proteins Caspase 3 GJB2 Connexin Organ of Corti Caspase Biology Cell biology Programmed cell death
9	Visio-hearing loss[removed]edits.vsd Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English GJB6 GJB2 Screening Audiology Maternal and Child Health Bureau Medical genetics Connexin Medicine Medical specialties Medical tests
10	Biochem. J[removed], 375–385 (Printed in Great Britain) 375 Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Immunology Immunologic tests Biotechnology Connexin GJB2 Immunoprecipitation Antibody Protein L Epitope mapping Biology Immune system Glycoproteins