نتایج جستجو برای: numb chin syndrome

تعداد نتایج: 625728  

Journal: :Neuron 1995
Ming Guo Ethan Bier Lily Yeh Jan Yuh Nung Jan

Asymmetric cell divisions allow a sensory organ precursor (SOP) cell to generate a neuron and its support cells in the Drosophila PNS. We demonstrate a role of tramtrack (ttk), previously identified as a zinc finger-containing putative transcription factor, in the determination of different daughter cell fates. Both loss of function and overexpression of ttk affect the fates of the SOP progeny....

Journal: :Genes & development 1998
A Carmena B Murugasu-Oei D Menon F Jiménez W Chia

Each larval hemisegment comprises approximately 30 uniquely specified somatic muscles. These derive from muscle founders that arise as distinct sibling pairs from the division of muscle progenitor cells. We have analyzed the progenitor cell divisions of three mesodermal lineages that generate muscle (and pericardial cell) founders. Our results show that Inscuteable and Numb proteins are localiz...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2001
L Susini B J Passer N Amzallag-Elbaz T Juven-Gershon S Prieur N Privat M Tuynder M C Gendron A Israël R Amson M Oren A Telerman

The Drosophila Seven in absentia (Sina) gene product originally was described as a protein that controls cell fate decisions during eye development. Its mammalian homolog, Siah-1, recently was found to be involved in p53-dependent and -independent pathways of apoptosis and G(1) arrest. We report that Siah-1 interacts directly with and promotes the degradation of the cell fate regulator Numb. Si...

Journal: :Developmental cell 2012
Ozren Bogdanović Mariana Delfino-Machín María Nicolás-Pérez María P Gavilán Inês Gago-Rodrigues Ana Fernández-Miñán Concepción Lillo Rosa M Ríos Joachim Wittbrodt Juan R Martínez-Morales

Polarized trafficking of adhesion receptors plays a pivotal role in controlling cellular behavior during morphogenesis. Particularly, clathrin-dependent endocytosis of integrins has long been acknowledged as essential for cell migration. However, little is known about the contribution of integrin trafficking to epithelial tissue morphogenesis. Here we show how the transmembrane protein Opo, pre...

2015
Shasha Qi Xingbo Zhao Mingjiang Li Xiaohui Zhang Zhenzhen Lu Chunrun Yang Chunhua Zhang Hui Zhang Na Zhang

BACKGROUND Epithelial mesenchymal transition (EMT) is involved in the pathogenesis of adenomyosis, and Notch signaling is crucial to EMT. The objective of this study was to explore Notch1/Numb/Snail signaling in adenomyosis. METHODS The expression levels of the members of the Notch1/Numb/Snail signaling cascade in normal endometria (proliferative phase: n = 15; secretory phase: n = 15; postme...

Journal: :iranian red crescent medical journal 0
besa gacaferri lumezi department of physiology and immunology, university clinical center of kosovo, pristina, kosovo; department of physiology and immunology, university clinical center of kosovo, bulevardi i deshmoreve p.n. 10 000, prishtina, kosovo. tel/fax: +37-744186036 aferdita goci child and adolescent mental health center, university clinical center of kosovo, pristina, kosovo violeta lokaj department of physiology and immunology, university clinical center of kosovo, pristina, kosovo hatixhe latifi department of physiology and immunology, university clinical center of kosovo, pristina, kosovo natyra karahoda department of physiology and immunology, university clinical center of kosovo, pristina, kosovo ganimete minci department of physiology and immunology, university clinical center of kosovo, pristina, kosovo

discussion: establishing the etiology, using the evidence–based strategies to improve hirsutism, and treating the underlying disorder, are essential for proper management of women with hirsutism. case presentation: the case was a 17-year-old female with severe hirsutism, oligomenorrhea, and obesity. she was evaluated to identify the etiology and diagnosed as a case of polycystic ovarian syndrom...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1997
A Destee F Cassim L Defebvre J D Guieu

Hereditary chin trembling is a rare autosomal dominant disease often considered as an "essential tremor variant". The clinical and neurophysiological data obtained in a new white family lead to the suggestion that this abnormal involuntary movement is a focal variant of hereditary essential myoclonus.

1937
Min Sein

My own motor driver, a Mahommedan male, aged about 27, came running to me one day about March 1933 in great terror holding a handkerchief to his chin, which was soaking wet with blood. He said he had suddenly discovered blood oozing out of his chin and had tried to stop it but in vain. The handkerchief was soaked in about 15 minutes. On examination after cleaning the part I found a bead of bloo...

2016
Pratik Thacker Pramod Kumar

BACKGROUND Excessive hair on the face is a significant cause for distress amongst women. Permanent hair reduction methods including lasers and pulsed light devices are increasingly being used. AIMS The aim of this study is to evaluate the efficacy and safety of near infrared pulsed light source for permanent hair reduction in women seeking treatment for excessive hair growth on the upper lip ...

Journal: :Development 1997
M Ruiz Gómez M Bate

Terminal divisions of myogenic lineages in the Drosophila embryo generate sibling myoblasts that found larval muscles or form precursors of adult muscles. Alternative fates adopted by sibling myoblasts are associated with distinct patterns of gene expression. Genes expressed in the progenitor cell are maintained in one sibling and repressed in the other. These differences depend on an asymmetri...

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