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M Doss

Showing results (151-160 of 180) with videos related to

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Human Genetics|December 22, 1998
Exon 1 donor splice site mutations in the porphobilinogen deaminase gene in the non-erythroid variant form of acute intermittent porphyriaH Puy, U Gross, J C Deybach, et al.
Klinische Wochenschrift|December 15, 1980
[Hereditary and non-hereditary form of chronic hepatic porphyria: different behaviour of uroporphyrinogen decarboxylase in liver and erythrocytes (author's transl)]M Doss, R von Tiepermann, D Look, et al.
Molecular and Cellular Probes|February 5, 2000
New mutations of the hydroxymethylbilane synthase gene in German patients with acute intermittent porphyriaU Gross, H Puy, M Doss, et al.
Annals of Surgical Oncology|October 18, 2025
ASO Visual Abstract: Disaggregating Asian American and Pacific Islander Subpopulations in Esophageal Cancer-Stage, Histology, and SurvivalShawn M Doss, Vatsala Kapoor, Ryan Brownlee, et al.
HGG Advances|November 8, 2025
Exon-skipping due to bi-allelic splice site mutations in the neurodevelopmental disease gene LNPKRose M Doss, Sara A Wirth, Jonathan W Pitsch, et al.
Annals of Surgical Oncology|September 25, 2025
Disaggregating Asian American and Pacific Islander Subpopulations in Esophageal Cancer: Stage, Histology, and SurvivalShawn M Doss, Vatsala Kapoor, Ryan Brownlee, et al.
Genes|February 26, 2025
Mosaicism in Short Tandem Repeat Disorders: A Clinical PerspectiveRose M Doss, Susana Lopez-Ignacio, Anna Dischler, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
A molecular, enzymatic and clinical study in a family with hereditary coproporphyriaU Gross, H Puy, U Meissauer, et al.
Klinische Wochenschrift|June 15, 1982
Persistent protoporphyrinemia in hereditary porphobilinogen synthase (delta-aminolevulinic acid dehydrase) deficiency under low lead exposure. A new molecular basis for the pathogenesis of lead intoxicationM Doss, U Becker, F Sixel, et al.
Peerj|August 30, 2023
Characterization of endoplasmic reticulum-associated degradation in the human fungal pathogen <i>Candida albicans</i>Ellen M Doss, Joshua M Moore, Bryce H Harman, et al.
Pageof 18

Showing results (151-160 of 180) with videos related to

Sort By:
Pageof 18
Human Genetics|December 22, 1998
Exon 1 donor splice site mutations in the porphobilinogen deaminase gene in the non-erythroid variant form of acute intermittent porphyriaH Puy, U Gross, J C Deybach, et al.
Klinische Wochenschrift|December 15, 1980
[Hereditary and non-hereditary form of chronic hepatic porphyria: different behaviour of uroporphyrinogen decarboxylase in liver and erythrocytes (author's transl)]M Doss, R von Tiepermann, D Look, et al.
Molecular and Cellular Probes|February 5, 2000
New mutations of the hydroxymethylbilane synthase gene in German patients with acute intermittent porphyriaU Gross, H Puy, M Doss, et al.
Annals of Surgical Oncology|October 18, 2025
ASO Visual Abstract: Disaggregating Asian American and Pacific Islander Subpopulations in Esophageal Cancer-Stage, Histology, and SurvivalShawn M Doss, Vatsala Kapoor, Ryan Brownlee, et al.
HGG Advances|November 8, 2025
Exon-skipping due to bi-allelic splice site mutations in the neurodevelopmental disease gene LNPKRose M Doss, Sara A Wirth, Jonathan W Pitsch, et al.
Annals of Surgical Oncology|September 25, 2025
Disaggregating Asian American and Pacific Islander Subpopulations in Esophageal Cancer: Stage, Histology, and SurvivalShawn M Doss, Vatsala Kapoor, Ryan Brownlee, et al.
Genes|February 26, 2025
Mosaicism in Short Tandem Repeat Disorders: A Clinical PerspectiveRose M Doss, Susana Lopez-Ignacio, Anna Dischler, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
A molecular, enzymatic and clinical study in a family with hereditary coproporphyriaU Gross, H Puy, U Meissauer, et al.
Klinische Wochenschrift|June 15, 1982
Persistent protoporphyrinemia in hereditary porphobilinogen synthase (delta-aminolevulinic acid dehydrase) deficiency under low lead exposure. A new molecular basis for the pathogenesis of lead intoxicationM Doss, U Becker, F Sixel, et al.
Peerj|August 30, 2023
Characterization of endoplasmic reticulum-associated degradation in the human fungal pathogen <i>Candida albicans</i>Ellen M Doss, Joshua M Moore, Bryce H Harman, et al.
Pageof 18