Search research articles
Contact Us
Filters
Showing results (381-390 of 386) with videos related to
Page
of 39
Sort By:
You have reached the last page of results.
This site can display upto 386 results.
Science Translational Medicine
|
November 16, 2022
Visualization of exhaled breath metabolites reveals distinct diagnostic signatures for acute cardiorespiratory breathlessness
Wadah Ibrahim, Michael J Wilde, Rebecca L Cordell, et al.
Nature Food
|
May 2, 2023
A natural mutation in Pisum sativum L. (pea) alters starch assembly and improves glucose homeostasis in humans
Katerina Petropoulou, Louise J Salt, Cathrina H Edwards, et al.
Seminars in Hematology
|
December 6, 2001
Use of recombinant factor VIIa (NovoSeven) in patients with Glanzmann thrombasthenia
M C Poon, R d'Oiron, I Hann, et al.
Nature
|
August 14, 2012
HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle
Matthew A Deardorff, Masashige Bando, Ryuichiro Nakato, et al.
Human Molecular Genetics
|
January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
Frank J Kaiser, Morad Ansari, Diana Braunholz, et al.
American Journal of Medical Genetics. Part A
|
June 28, 2023
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms
Maninder Kaur, Justin Blair, Batsal Devkota, et al.
Page
of 39
Search research articles
Search
Showing results (381-390 of 386) with videos related to
Sort By:
Page
of 39
You have reached the last page of results.
This site can display upto 386 results.
Science Translational Medicine
|
November 16, 2022
Visualization of exhaled breath metabolites reveals distinct diagnostic signatures for acute cardiorespiratory breathlessness
Wadah Ibrahim, Michael J Wilde, Rebecca L Cordell, et al.
Nature Food
|
May 2, 2023
A natural mutation in Pisum sativum L. (pea) alters starch assembly and improves glucose homeostasis in humans
Katerina Petropoulou, Louise J Salt, Cathrina H Edwards, et al.
Seminars in Hematology
|
December 6, 2001
Use of recombinant factor VIIa (NovoSeven) in patients with Glanzmann thrombasthenia
M C Poon, R d'Oiron, I Hann, et al.
Nature
|
August 14, 2012
HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle
Matthew A Deardorff, Masashige Bando, Ryuichiro Nakato, et al.
Human Molecular Genetics
|
January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
Frank J Kaiser, Morad Ansari, Diana Braunholz, et al.
American Journal of Medical Genetics. Part A
|
June 28, 2023
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms
Maninder Kaur, Justin Blair, Batsal Devkota, et al.
Page
of 39