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The Journal of Pathology. Clinical Research
|
March 15, 2022
Molecular profile of pure squamous cell carcinoma of the bladder identifies major roles for OSMR and YAP signalling
Carolyn D Hurst, Guo Cheng, Fiona M Platt, et al.
Genomics
|
February 1, 1993
Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B
V M Soares, L M Brzustowicz, P W Kleyn, et al.
Molecular Psychiatry
|
October 14, 2000
No genetic linkage or association between a functional promoter polymorphism in the monoamine oxidase-A gene and panic disorder
S P Hamilton, S L Slager, G A Heiman, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
September 1, 1996
Report of the Diabetic Foot and Amputation Group
M Edmonds, A Boulton, T Buckenham, et al.
Molecular Psychiatry
|
March 13, 2001
No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorder
S P Hamilton, S L Slager, L Helleby, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology
|
October 8, 2004
Corrigendum to "gender in obsessive-compulsive disorder: clinical and genetic findings" [Eur. Neuropsychopharmacol. 14 (2004) 105-113]
Christine Lochner, Sian M J Hemmings, Craig J Kinnear, et al.
Genome Research
|
September 5, 2024
A Bayesian framework for inferring dynamic intercellular interactions from time-series single-cell data
Cameron Park, Shouvik Mani, Nicolas Beltran-Velez, et al.
Ebiomedicine
|
June 23, 2015
The Effect of Mutations on Drug Sensitivity and Kinase Activity of Fibroblast Growth Factor Receptors: A Combined Experimental and Theoretical Study
Tom D Bunney, Shunzhou Wan, Nethaji Thiyagarajan, et al.
Ear and Hearing
|
January 28, 2020
Genes Implicated in Rare Congenital Inner Ear and Cochleovestibular Nerve Malformations
Elina Kari, Lorida Llaci, John L Go, et al.
Human Genetics
|
June 30, 2018
De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness
Isabelle Schrauwen, Elina Kari, Jacob Mattox, et al.
Page
of 69
Search research articles
Search
Showing results (451-460 of 688) with videos related to
Sort By:
Page
of 69
The Journal of Pathology. Clinical Research
|
March 15, 2022
Molecular profile of pure squamous cell carcinoma of the bladder identifies major roles for OSMR and YAP signalling
Carolyn D Hurst, Guo Cheng, Fiona M Platt, et al.
Genomics
|
February 1, 1993
Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B
V M Soares, L M Brzustowicz, P W Kleyn, et al.
Molecular Psychiatry
|
October 14, 2000
No genetic linkage or association between a functional promoter polymorphism in the monoamine oxidase-A gene and panic disorder
S P Hamilton, S L Slager, G A Heiman, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
September 1, 1996
Report of the Diabetic Foot and Amputation Group
M Edmonds, A Boulton, T Buckenham, et al.
Molecular Psychiatry
|
March 13, 2001
No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorder
S P Hamilton, S L Slager, L Helleby, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology
|
October 8, 2004
Corrigendum to "gender in obsessive-compulsive disorder: clinical and genetic findings" [Eur. Neuropsychopharmacol. 14 (2004) 105-113]
Christine Lochner, Sian M J Hemmings, Craig J Kinnear, et al.
Genome Research
|
September 5, 2024
A Bayesian framework for inferring dynamic intercellular interactions from time-series single-cell data
Cameron Park, Shouvik Mani, Nicolas Beltran-Velez, et al.
Ebiomedicine
|
June 23, 2015
The Effect of Mutations on Drug Sensitivity and Kinase Activity of Fibroblast Growth Factor Receptors: A Combined Experimental and Theoretical Study
Tom D Bunney, Shunzhou Wan, Nethaji Thiyagarajan, et al.
Ear and Hearing
|
January 28, 2020
Genes Implicated in Rare Congenital Inner Ear and Cochleovestibular Nerve Malformations
Elina Kari, Lorida Llaci, John L Go, et al.
Human Genetics
|
June 30, 2018
De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness
Isabelle Schrauwen, Elina Kari, Jacob Mattox, et al.
Page
of 69