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G Merla

Showing results (11-20 of 18) with videos related to

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Cell Death & Disease|February 22, 2014
Expression of base excision repair key factors and miR17 in familial and sporadic breast cancerS De Summa, R Pinto, B Pilato, et al.
Journal of Medical Genetics|July 5, 2005
Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletionsC Howald, G Merla, M C Digilio, et al.
The EMBO Journal|May 2, 2001
The tripartite motif family identifies cell compartmentsA Reymond, G Meroni, A Fantozzi, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Identifying individuals at risk for surgical supravalvar aortic stenosis by polygenic risk score with graded phenotypingD Liu, C B Mervis, M D Levin, et al.
Oncogene|November 1, 2001
Amplification and overexpression of PRUNE in human sarcomas and breast carcinomas-a possible mechanism for altering the nm23-H1 activityA Forus, A D'Angelo, J Henriksen, et al.
Science Advances|May 25, 2019
Autophagy induction in atrophic muscle cells requires ULK1 activation by TRIM32 through unanchored K63-linked polyubiquitin chainsM Di Rienzo, M Antonioli, C Fusco, et al.
Clinical Genetics|January 17, 2013
MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype studyP Makrythanasis, B W van Bon, M Steehouwer, et al.
Genetics in Medicine Open|December 13, 2024
<i>ARID1B</i>-related disorder in 87 adults: Natural history and self-sustainabilityP J van der Sluijs, M Gösgens, A J M Dingemans, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Cell Death & Disease|February 22, 2014
Expression of base excision repair key factors and miR17 in familial and sporadic breast cancerS De Summa, R Pinto, B Pilato, et al.
Journal of Medical Genetics|July 5, 2005
Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletionsC Howald, G Merla, M C Digilio, et al.
The EMBO Journal|May 2, 2001
The tripartite motif family identifies cell compartmentsA Reymond, G Meroni, A Fantozzi, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Identifying individuals at risk for surgical supravalvar aortic stenosis by polygenic risk score with graded phenotypingD Liu, C B Mervis, M D Levin, et al.
Oncogene|November 1, 2001
Amplification and overexpression of PRUNE in human sarcomas and breast carcinomas-a possible mechanism for altering the nm23-H1 activityA Forus, A D'Angelo, J Henriksen, et al.
Science Advances|May 25, 2019
Autophagy induction in atrophic muscle cells requires ULK1 activation by TRIM32 through unanchored K63-linked polyubiquitin chainsM Di Rienzo, M Antonioli, C Fusco, et al.
Clinical Genetics|January 17, 2013
MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype studyP Makrythanasis, B W van Bon, M Steehouwer, et al.
Genetics in Medicine Open|December 13, 2024
<i>ARID1B</i>-related disorder in 87 adults: Natural history and self-sustainabilityP J van der Sluijs, M Gösgens, A J M Dingemans, et al.
Pageof 2