Molecular genetics of cranial nerve development in mouse

2001 ◽  
Vol 2 (9) ◽  
pp. 611-623 ◽  
Author(s):  
Sabine P. Cordes
Keyword(s):  
Molecular Genetics ◽  
Cranial Nerve ◽  
Nerve Development

scholarly journals Cranial Nerve Development Requires Co-Ordinated Shh and Canonical Wnt Signaling

PLoS ONE ◽  
2015 ◽  
Vol 10 (3) ◽  
pp. e0120821 ◽  
Author(s):  
Hiroshi Kurosaka ◽  
Paul A. Trainor ◽  
Margot Leroux-Berger ◽  
Angelo Iulianella
Keyword(s):  
Wnt Signaling ◽  
Cranial Nerve ◽  
Canonical Wnt Signaling ◽  
Nerve Development ◽  
Canonical Wnt

Exposure to low concentrations of nicotine during cranial nerve development inhibits apoptosis and causes cellular hypertrophy in the ventral oculomotor nuclei of the chick embryo

2004 ◽  
Vol 1000 (1-2) ◽  
pp. 123-133 ◽  
Author(s):  
John J. Wielgus ◽  
L. Corbin Downey ◽  
Katelyn W. Ewald ◽  
Melissa E. Hatley ◽  
Kathleen C. Wilson ◽  
...  
Keyword(s):  
Chick Embryo ◽  
Cranial Nerve ◽  
Cellular Hypertrophy ◽  
Low Concentrations ◽  
Nerve Development ◽  
Oculomotor Nuclei

scholarly journals Dynamic expression of transcription factor Brn3b during mouse cranial nerve development

2015 ◽  
Vol 524 (5) ◽  
pp. 1033-1061 ◽  
Author(s):  
Szilard Sajgo ◽  
Seid Ali ◽  
Octavian Popescu ◽  
Tudor Constantin Badea
Keyword(s):  
Transcription Factor ◽  
Cranial Nerve ◽  
Dynamic Expression ◽  
Nerve Development

scholarly journals Retrolabyrinthine syndromes of tumoral etiology – acoustic neuroma

2015 ◽  
Vol 62 (4) ◽  
pp. 363-366
Author(s):  
Corneliu Toader ◽  
◽  
Mioriţa Toader ◽  
Iolanda Vivisenco ◽  
Mircea Drăghici ◽  
...  
Keyword(s):  
Acoustic Neuroma ◽  
Cranial Nerve ◽  
Benign Tumor ◽  
Important Place ◽  
Early Stages ◽  
Nerve Development ◽  
Age Range

Among retrolabyrinthine syndromes of tumoral etiology, acoustic neuroma ranks the most important place, being a benign tumor, but with malignant evolution. It is more common in women and occurs predominantly in the age range 20-60 years old. It is usually unilateral and only about 4% of cases are bilateral. Portmann et al, quoting Nager, say that certain peculiarities of the cranial nerve development explain the intracanalicular location of the neuroma at the beginning. Being a tumor with a very serious prognosis, acoustic neuroma needs to be diagnosed in very early stages, when it can be surgically removed.

scholarly journals Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome

2013 ◽  
Vol 7 (2) ◽  
pp. 245-257 ◽  
Author(s):  
B. A. Karpinski ◽  
T. M. Maynard ◽  
M. S. Fralish ◽  
S. Nuwayhid ◽  
I. E. Zohn ◽  
...  
Keyword(s):  
Mouse Model ◽  
Cranial Nerve ◽  
Deletion Syndrome ◽  
22Q11 Deletion ◽  
22Q11 Deletion Syndrome ◽  
Nerve Development

scholarly journals Nav2 is necessary for cranial nerve development and blood pressure regulation

2010 ◽  
Vol 5 (1) ◽  
pp. 6 ◽  
Author(s):  
Elizabeth M McNeill ◽  
Kenneth P Roos ◽  
Dieder Moechars ◽  
Margaret Clagett-Dame
Keyword(s):  
Blood Pressure ◽  
Cranial Nerve ◽  
Blood Pressure Regulation ◽  
Pressure Regulation ◽  
Nerve Development

Introduction

1978 ◽  
Vol 36 (3) ◽  
pp. 543-544
Author(s):  
W. Bernard
Keyword(s):  
Molecular Weight ◽  
Electron Microscope ◽  
Nucleic Acid ◽  
Gene Mapping ◽  
Molecular Genetics ◽  
Cell Biology ◽  
Gene Activity ◽  
Close Connection ◽  
Basic Information ◽  
Simple Systems

In comparison to many other fields of ultrastructural research in Cell Biology, the successful exploration of genes and gene activity with the electron microscope in higher organisms is a late conquest. Nucleic acid molecules of Prokaryotes could be successfully visualized already since the early sixties, thanks to the Kleinschmidt spreading technique - and much basic information was obtained concerning the shape, length, molecular weight of viral, mitochondrial and chloroplast nucleic acid. Later, additonal methods revealed denaturation profiles, distinction between single and double strandedness and the use of heteroduplexes-led to gene mapping of relatively simple systems carried out in close connection with other methods of molecular genetics.

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