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Showing results (431-440 of 536) with videos related to

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Matrix Biology : Journal of the International Society for Matrix Biology|March 5, 2026
Observations of dystrophic epidermolysis bullosa patients with collagen VII NC2 truncation provide new insights into anchoring fibril assemblyNeha S Momin, I Sinem Bagci, John A Dolorito, et al.
Psychology, Health & Medicine|April 15, 2011
The psychological impact of facial changes in sclerodermaKavit Amin, A Clarke, B Sivakumar, et al.
Human Molecular Genetics|December 1, 1995
Oncogenic conversion of a novel orphan nuclear receptor by chromosome translocationY Labelle, J Zucman, G Stenman, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 16, 1994
Mapping of Ras-related GTP-binding proteins by GTP overlay following two-dimensional gel electrophoresisL A Huber, O Ullrich, Y Takai, et al.
JAAD International|May 14, 2023
Mapping the burden of severe forms of epidermolysis bullosa - Implications for patient managementJemima E Mellerio, Dimitra Kiritsi, M Peter Marinkovich, et al.
Human Molecular Genetics|April 1, 1995
Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplificationH Caron, M Peter, P van Sluis, et al.
Physical Chemistry Chemical Physics : PCCP|October 15, 2014
Tin doping speeds up hole transfer during light-driven water oxidation at hematite photoanodesHalina K Dunn, Johann M Feckl, Alexander Müller, et al.
Pediatric Dermatology|March 22, 2021
Clinical characteristics associated with increased wound size in patients with recessive dystrophic epidermolysis bullosaDaniel C Solis, Emily S Gorell, Claudia Teng, et al.
Pediatric Dermatology|September 13, 2021
Patient-reported outcomes and quality of life in dominant dystrophic epidermolysis bullosa: A global cross-sectional surveyShivali Fulchand, Nicole Harris, Shufeng Li, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1996
CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiencyS Geley, K Kapelari, K Jöhrer, et al.
Pageof 54

Showing results (431-440 of 536) with videos related to

Sort By:
Pageof 54
Matrix Biology : Journal of the International Society for Matrix Biology|March 5, 2026
Observations of dystrophic epidermolysis bullosa patients with collagen VII NC2 truncation provide new insights into anchoring fibril assemblyNeha S Momin, I Sinem Bagci, John A Dolorito, et al.
Psychology, Health & Medicine|April 15, 2011
The psychological impact of facial changes in sclerodermaKavit Amin, A Clarke, B Sivakumar, et al.
Human Molecular Genetics|December 1, 1995
Oncogenic conversion of a novel orphan nuclear receptor by chromosome translocationY Labelle, J Zucman, G Stenman, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 16, 1994
Mapping of Ras-related GTP-binding proteins by GTP overlay following two-dimensional gel electrophoresisL A Huber, O Ullrich, Y Takai, et al.
JAAD International|May 14, 2023
Mapping the burden of severe forms of epidermolysis bullosa - Implications for patient managementJemima E Mellerio, Dimitra Kiritsi, M Peter Marinkovich, et al.
Human Molecular Genetics|April 1, 1995
Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplificationH Caron, M Peter, P van Sluis, et al.
Physical Chemistry Chemical Physics : PCCP|October 15, 2014
Tin doping speeds up hole transfer during light-driven water oxidation at hematite photoanodesHalina K Dunn, Johann M Feckl, Alexander Müller, et al.
Pediatric Dermatology|March 22, 2021
Clinical characteristics associated with increased wound size in patients with recessive dystrophic epidermolysis bullosaDaniel C Solis, Emily S Gorell, Claudia Teng, et al.
Pediatric Dermatology|September 13, 2021
Patient-reported outcomes and quality of life in dominant dystrophic epidermolysis bullosa: A global cross-sectional surveyShivali Fulchand, Nicole Harris, Shufeng Li, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1996
CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiencyS Geley, K Kapelari, K Jöhrer, et al.
Pageof 54