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The Journal of Organic Chemistry
|
August 22, 2020
Stereochemical Inversion of Rim-Differentiated Pillar[5]arene Molecular Swings
Ke Du, Paul Demay-Drouhard, Kushal Samanta, et al.
Seminars in Thoracic and Cardiovascular Surgery
|
January 4, 2017
The Integrated Comprehensive Care Program: A Novel Home Care Initiative After Major Thoracic Surgery
Yaron Shargall, Wael C Hanna, Laura Schneider, et al.
Endocrinology
|
June 30, 2000
Deficient mineralization of intramembranous bone in vitamin D-24-hydroxylase-ablated mice is due to elevated 1,25-dihydroxyvitamin D and not to the absence of 24,25-dihydroxyvitamin D
R St-Arnaud, A Arabian, R Travers, et al.
Journal of Medical Genetics
|
October 9, 2010
Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing
Karen Gaudon, Isabelle Pénisson-Besnier, Brigitte Chabrol, et al.
Emerging Microbes & Infections
|
March 25, 2025
Genomic islands and molecular mechanisms relating to drug-resistance in <i>Clostridioides</i> (<i>Clostridium</i>) <i>difficile</i> PCR ribotype 176
Krutova Marcela, Kovarovic Vojtech, Brajerova Marie, et al.
Circulation Research
|
February 19, 1999
Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome
N Neyroud, P Richard, N Vignier, et al.
Archives of Neurology
|
May 19, 2004
Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variant
Eugenio Mercuri, Maja Poppe, Ros Quinlivan, et al.
The Journal of Physical Chemistry Letters
|
March 4, 2016
The Use of Mn(II) Bound to His-tags as Genetically Encodable Spin-Label for Nanometric Distance Determination in Proteins
H Y Vincent Ching, Florencia C Mascali, Hélène C Bertrand, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1988
Comparison of basal and adrenocorticotropin-stimulated plasma 21-deoxycortisol and 17-hydroxyprogesterone values as biological markers of late-onset adrenal hyperplasia
J Fiet, B Gueux, M Gourmelen, et al.
Neuromuscular Disorders : NMD
|
December 7, 2002
Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy
Michal Vytopil, Enzo Ricci, Antonio Dello Russo, et al.
Page
of 29
Search research articles
Search
Showing results (231-240 of 288) with videos related to
Sort By:
Page
of 29
The Journal of Organic Chemistry
|
August 22, 2020
Stereochemical Inversion of Rim-Differentiated Pillar[5]arene Molecular Swings
Ke Du, Paul Demay-Drouhard, Kushal Samanta, et al.
Seminars in Thoracic and Cardiovascular Surgery
|
January 4, 2017
The Integrated Comprehensive Care Program: A Novel Home Care Initiative After Major Thoracic Surgery
Yaron Shargall, Wael C Hanna, Laura Schneider, et al.
Endocrinology
|
June 30, 2000
Deficient mineralization of intramembranous bone in vitamin D-24-hydroxylase-ablated mice is due to elevated 1,25-dihydroxyvitamin D and not to the absence of 24,25-dihydroxyvitamin D
R St-Arnaud, A Arabian, R Travers, et al.
Journal of Medical Genetics
|
October 9, 2010
Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing
Karen Gaudon, Isabelle Pénisson-Besnier, Brigitte Chabrol, et al.
Emerging Microbes & Infections
|
March 25, 2025
Genomic islands and molecular mechanisms relating to drug-resistance in <i>Clostridioides</i> (<i>Clostridium</i>) <i>difficile</i> PCR ribotype 176
Krutova Marcela, Kovarovic Vojtech, Brajerova Marie, et al.
Circulation Research
|
February 19, 1999
Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome
N Neyroud, P Richard, N Vignier, et al.
Archives of Neurology
|
May 19, 2004
Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variant
Eugenio Mercuri, Maja Poppe, Ros Quinlivan, et al.
The Journal of Physical Chemistry Letters
|
March 4, 2016
The Use of Mn(II) Bound to His-tags as Genetically Encodable Spin-Label for Nanometric Distance Determination in Proteins
H Y Vincent Ching, Florencia C Mascali, Hélène C Bertrand, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1988
Comparison of basal and adrenocorticotropin-stimulated plasma 21-deoxycortisol and 17-hydroxyprogesterone values as biological markers of late-onset adrenal hyperplasia
J Fiet, B Gueux, M Gourmelen, et al.
Neuromuscular Disorders : NMD
|
December 7, 2002
Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy
Michal Vytopil, Enzo Ricci, Antonio Dello Russo, et al.
Page
of 29