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N Schweitzer

Showing results (31-40 of 39) with videos related to

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Acta Gastro-Enterologica Belgica|February 17, 2015
Long-lasting tumour response to sorafenib therapy in advanced hepatocellular carcinomaM M Kirstein, N Schweitzer, S Schmidt, et al.
American Journal of Medical Genetics|June 28, 2001
Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3D N Schweitzer, J M Graham, R S Lachman, et al.
American Journal of Medical Genetics. Part A|June 15, 2011
Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palateTrilochan Sahoo, Aaron Theisen, Pedro A Sanchez-Lara, et al.
Immunity|March 1, 1997
B7-1 and B7-2 have overlapping, critical roles in immunoglobulin class switching and germinal center formationF Borriello, M P Sethna, S D Boyd, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|August 19, 2024
Genetic Testing in Craniofacial Care: Development of Algorithms for Testing Patients with Orofacial Clefting, Branchial Arch Anomalies, and CraniosynostosisEmily R Gallagher, Penny Chow, Maria R Mills, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|April 29, 2011
The temporal structure of feeding behaviorBert J Tolkamp, David J Allcroft, Juan P Barrio, et al.
Leukemia|October 2, 2013
Histone deacetylase inhibitors induce apoptosis in myeloid leukemia by suppressing autophagyM V Stankov, M El Khatib, B Kumar Thakur, et al.
Molecular Genetics & Genomic Medicine|September 14, 2021
Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanismsMegan Yabumoto, Jessica Kianmahd, Meghna Singh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2022
Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalitiesElisa Cali, Mohnish Suri, Marcello Scala, et al.
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Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Acta Gastro-Enterologica Belgica|February 17, 2015
Long-lasting tumour response to sorafenib therapy in advanced hepatocellular carcinomaM M Kirstein, N Schweitzer, S Schmidt, et al.
American Journal of Medical Genetics|June 28, 2001
Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3D N Schweitzer, J M Graham, R S Lachman, et al.
American Journal of Medical Genetics. Part A|June 15, 2011
Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palateTrilochan Sahoo, Aaron Theisen, Pedro A Sanchez-Lara, et al.
Immunity|March 1, 1997
B7-1 and B7-2 have overlapping, critical roles in immunoglobulin class switching and germinal center formationF Borriello, M P Sethna, S D Boyd, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|August 19, 2024
Genetic Testing in Craniofacial Care: Development of Algorithms for Testing Patients with Orofacial Clefting, Branchial Arch Anomalies, and CraniosynostosisEmily R Gallagher, Penny Chow, Maria R Mills, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|April 29, 2011
The temporal structure of feeding behaviorBert J Tolkamp, David J Allcroft, Juan P Barrio, et al.
Leukemia|October 2, 2013
Histone deacetylase inhibitors induce apoptosis in myeloid leukemia by suppressing autophagyM V Stankov, M El Khatib, B Kumar Thakur, et al.
Molecular Genetics & Genomic Medicine|September 14, 2021
Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanismsMegan Yabumoto, Jessica Kianmahd, Meghna Singh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2022
Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalitiesElisa Cali, Mohnish Suri, Marcello Scala, et al.
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