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Nurnberg

Showing results (101-110 of 111) with videos related to

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Nature Genetics|May 10, 2006
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4John A Sayer, Edgar A Otto, John F O'Toole, et al.
American Journal of Human Genetics|April 17, 2007
Haploinsufficiency of TCF4 causes syndromal mental retardation with intermittent hyperventilation (Pitt-Hopkins syndrome)Christiane Zweier, Maarit M Peippo, Juliane Hoyer, et al.
Plos Genetics|May 29, 2015
Coronary Artery Disease Associated Transcription Factor TCF21 Regulates Smooth Muscle Precursor Cells That Contribute to the Fibrous CapSylvia T Nurnberg, Karen Cheng, Azad Raiesdana, et al.
Genomics Data|June 20, 2015
Coronary Artery Disease Associated Transcription Factor TCF21 Regulates Smooth Muscle Precursor Cells that Contribute to the Fibrous CapS T Nurnberg, K Cheng, A Raiesdana, et al.
American Journal of Human Genetics|May 16, 2007
RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesityDagan Jenkins, Dominik Seelow, Fernanda S Jehee, et al.
Plos Genetics|January 10, 2020
Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseasesSylvia T Nurnberg, Marie A Guerraty, Robert C Wirka, et al.
American Journal of Human Genetics|October 13, 2006
Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvementMartin Konrad, Andre Schaller, Dominik Seelow, et al.
The Journal of Clinical Investigation|February 25, 2010
Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathyJohn F O'Toole, Yangjian Liu, Erica E Davis, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|March 14, 2024
Student ultrasound education - current views and controversiesChristoph F Dietrich, Roxana Lucia Sirli, Gregor Barth, et al.
Cell|August 7, 2012
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signalingMoumita Chaki, Rannar Airik, Amiya K Ghosh, et al.
Pageof 12

Showing results (101-110 of 111) with videos related to

Sort By:
Pageof 12
Nature Genetics|May 10, 2006
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4John A Sayer, Edgar A Otto, John F O'Toole, et al.
American Journal of Human Genetics|April 17, 2007
Haploinsufficiency of TCF4 causes syndromal mental retardation with intermittent hyperventilation (Pitt-Hopkins syndrome)Christiane Zweier, Maarit M Peippo, Juliane Hoyer, et al.
Plos Genetics|May 29, 2015
Coronary Artery Disease Associated Transcription Factor TCF21 Regulates Smooth Muscle Precursor Cells That Contribute to the Fibrous CapSylvia T Nurnberg, Karen Cheng, Azad Raiesdana, et al.
Genomics Data|June 20, 2015
Coronary Artery Disease Associated Transcription Factor TCF21 Regulates Smooth Muscle Precursor Cells that Contribute to the Fibrous CapS T Nurnberg, K Cheng, A Raiesdana, et al.
American Journal of Human Genetics|May 16, 2007
RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesityDagan Jenkins, Dominik Seelow, Fernanda S Jehee, et al.
Plos Genetics|January 10, 2020
Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseasesSylvia T Nurnberg, Marie A Guerraty, Robert C Wirka, et al.
American Journal of Human Genetics|October 13, 2006
Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvementMartin Konrad, Andre Schaller, Dominik Seelow, et al.
The Journal of Clinical Investigation|February 25, 2010
Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathyJohn F O'Toole, Yangjian Liu, Erica E Davis, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|March 14, 2024
Student ultrasound education - current views and controversiesChristoph F Dietrich, Roxana Lucia Sirli, Gregor Barth, et al.
Cell|August 7, 2012
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signalingMoumita Chaki, Rannar Airik, Amiya K Ghosh, et al.
Pageof 12