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Mutations in the novel protocadherin PCDH15 cause usher syndrome type 1F

Human molecular genetics, 2001-08, Vol.10 (16), p.1709-1718

2001

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The DFNA10 Phenotype

Annals of otology, rhinology & laryngology, 2001-09, Vol.110 (9), p.861-866

2001

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Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus

Human molecular genetics, 2001-02, Vol.10 (3), p.195-200

2001

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Upper aerodigestive tract squamous dysplasia: correlation with p16, p53, pRb, and Ki-67 expression

Archives of pathology & laboratory medicine (1976), 2006-09, Vol.130 (9), p.1309-1314

2006

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Two Sites of Head and Neck Squamous Cell Carcinoma: Utility of Loss of Heterozygosity

Annals of otology, rhinology & laryngology, 2008-08, Vol.117 (8), p.591-593

2008

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Localization of the Usher Syndrome Type ID Gene (Ush1D) to Chromosome 10

Human molecular genetics, 1996-10, Vol.5 (10), p.1689-1692

1996

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AP-2 participates in the transcriptional control of the amyloid precursor protein (APP) gene in oral squamous cell carcinoma

Experimental and molecular pathology, 2007-10, Vol.83 (2), p.277-282

2007

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The DFNA 10 phenotype

Annals of otology, rhinology & laryngology, 2001-09, Vol.110 (9), p.861

2001

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A Gene for Autosomal Dominant Late-Onset Progressive Non-Syndromic Hearing Loss, DFNA10, Maps to Chromosome 6

Human molecular genetics, 1996-06, Vol.5 (6), p.853-856

1996

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A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus

Human molecular genetics, 1995-12, Vol.4 (12), p.2391-2394

1995

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fs(1)Yb is required for ovary follicle cell differentiation in Drosophila melanogaster and has genetic interactions with the Notch group of neurogenic genes

Genetics (Austin), 1995-05, Vol.140 (1), p.207-217

1995

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Physical mapping of the deafness gene DFNA 10

Otolaryngology-head and neck surgery, 1999-08, Vol.121 (2), p.P80-P80

1999

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Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment

Human genetics, 2000-07, Vol.107 (1), p.7-11

2000

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54: Tobacco Use and Postoperative Complications in Head and Neck Surgery

Otolaryngology-head and neck surgery, 1996-08, Vol.115 (2), p.P178-P178

1996

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Passage to India: The search for genes causing autosomal recessive nonsyndromic hearing loss

Otolaryngology-head and neck surgery, 1998-03, Vol.118 (3), p.333-337

1998

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Tobacco use and postoperative complications in head and neck surgery

Otolaryngology-head and neck surgery, 1996, Vol.115 (2), p.P178-P178

1996

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Passage to India: The Search for Genes Causing Autosomal Recessive Nonsyndromic Hearing Loss

Otolaryngology-head and neck surgery, 1998-03, Vol.118 (3), p.333-337

1998

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DFNA10/EYA4--the clinical picture

Advances in oto-rhino-laryngology, 2002, Vol.61, p.73-78

2002

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Genetic characterization of small ovaries, a gene required in the soma for the development of the Drosophila ovary and the female germline

Genetics (Austin), 1995-03, Vol.139 (3), p.1309-1320

1995

Volltextzugriff (PDF)

New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p

American journal of medical genetics, 1997-09, Vol.71 (4), p.467-471

1997

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Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31

American journal of medical genetics, 1998-06, Vol.78 (2), p.107-113

1998

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Essential role of mitochondrial energy metabolism in Foxp3+ T‐regulatory cell function and allograft survival

The FASEB journal, 2015-06, Vol.29 (6), p.2315-2326

2015

Volltextzugriff (PDF)

Improving Nitrogen Use Efficiency Through Overexpression of Alanine Aminotransferase in Rice, Wheat, and Barley

Frontiers in plant science, 2021-01, Vol.12, p.628521

2021

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Higher airborne pollen concentrations correlated with increased SARS-CoV-2 infection rates, as evidenced from 31 countries across the globe

Proceedings of the National Academy of Sciences - PNAS, 2021-03, Vol.118 (12)

2021

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Ear, Auditive Nerve, Cochleovestibular Tract, Facial Nerve: Diseases, Semeiology
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Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

Mutations in the novel protocadherin PCDH15 cause usher syndrome type 1F

The DFNA10 Phenotype

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus

Upper aerodigestive tract squamous dysplasia: correlation with p16, p53, pRb, and Ki-67 expression

Two Sites of Head and Neck Squamous Cell Carcinoma: Utility of Loss of Heterozygosity

Localization of the Usher Syndrome Type ID Gene (Ush1D) to Chromosome 10

AP-2 participates in the transcriptional control of the amyloid precursor protein (APP) gene in oral squamous cell carcinoma

The DFNA 10 phenotype

A Gene for Autosomal Dominant Late-Onset Progressive Non-Syndromic Hearing Loss, DFNA10, Maps to Chromosome 6

A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus

fs(1)Yb is required for ovary follicle cell differentiation in Drosophila melanogaster and has genetic interactions with the Notch group of neurogenic genes

Physical mapping of the deafness gene DFNA 10

Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment

54: Tobacco Use and Postoperative Complications in Head and Neck Surgery

Passage to India: The search for genes causing autosomal recessive nonsyndromic hearing loss

Tobacco use and postoperative complications in head and neck surgery

Passage to India: The Search for Genes Causing Autosomal Recessive Nonsyndromic Hearing Loss

DFNA10/EYA4--the clinical picture

Genetic characterization of small ovaries, a gene required in the soma for the development of the Drosophila ovary and the female germline

New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p

Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31

Essential role of mitochondrial energy metabolism in Foxp3+ T‐regulatory cell function and allograft survival

Improving Nitrogen Use Efficiency Through Overexpression of Alanine Aminotransferase in Rice, Wheat, and Barley

Higher airborne pollen concentrations correlated with increased SARS-CoV-2 infection rates, as evidenced from 31 countries across the globe

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