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Forabosco

Showing results (221-230 of 243) with videos related to

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Neurobiology of Aging|July 17, 2013
Insights into TREM2 biology by network analysis of human brain gene expression dataPaola Forabosco, Adaikalavan Ramasamy, Daniah Trabzuni, et al.
Clinical Genetics|March 22, 2001
Analysis of candidate genes for intrinsic neuropathy in a family with chronic idiopathic intestinal pseudo-obstructionR De Giorgio, M Seri, R Cogliandro, et al.
BMC Developmental Biology|June 23, 2009
Foxl2 functions in sex determination and histogenesis throughout mouse ovary developmentJosé Elias Garcia-Ortiz, Emanuele Pelosi, Shakib Omari, et al.
Frontiers in Immunology|April 17, 2024
Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq datasetPaola Forabosco, Mauro Pala, Francesca Crobu, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2C Lo Nigro, R Cusano, M Scaranari, et al.
Human Mutation|February 12, 2000
Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. OnlineL Flagiello, V Cirigliano, M Strazzullo, et al.
Journal of Medical Genetics|November 25, 2003
Linkage of ulcerative colitis to the pericentromeric region of chromosome 16 in Italian inflammatory bowel disease families is independent of the presence of common CARD15 mutationsV Annese, A Latiano, O Palmieri, et al.
Journal of Medical Genetics|June 19, 2002
SHOX point mutations and deletions in Leri-Weill dyschondrosteosisC Falcinelli, L Iughetti, A Percesepe, et al.
American Journal of Human Genetics|May 13, 2003
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolateFernando Gianfrancesco, Teresa Esposito, Maria Neve Ombra, et al.
American Journal of Human Genetics|February 11, 1999
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophyM Seri, R Cusano, P Forabosco, et al.
Pageof 25

Showing results (221-230 of 243) with videos related to

Sort By:
Pageof 25
Neurobiology of Aging|July 17, 2013
Insights into TREM2 biology by network analysis of human brain gene expression dataPaola Forabosco, Adaikalavan Ramasamy, Daniah Trabzuni, et al.
Clinical Genetics|March 22, 2001
Analysis of candidate genes for intrinsic neuropathy in a family with chronic idiopathic intestinal pseudo-obstructionR De Giorgio, M Seri, R Cogliandro, et al.
BMC Developmental Biology|June 23, 2009
Foxl2 functions in sex determination and histogenesis throughout mouse ovary developmentJosé Elias Garcia-Ortiz, Emanuele Pelosi, Shakib Omari, et al.
Frontiers in Immunology|April 17, 2024
Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq datasetPaola Forabosco, Mauro Pala, Francesca Crobu, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2C Lo Nigro, R Cusano, M Scaranari, et al.
Human Mutation|February 12, 2000
Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. OnlineL Flagiello, V Cirigliano, M Strazzullo, et al.
Journal of Medical Genetics|November 25, 2003
Linkage of ulcerative colitis to the pericentromeric region of chromosome 16 in Italian inflammatory bowel disease families is independent of the presence of common CARD15 mutationsV Annese, A Latiano, O Palmieri, et al.
Journal of Medical Genetics|June 19, 2002
SHOX point mutations and deletions in Leri-Weill dyschondrosteosisC Falcinelli, L Iughetti, A Percesepe, et al.
American Journal of Human Genetics|May 13, 2003
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolateFernando Gianfrancesco, Teresa Esposito, Maria Neve Ombra, et al.
American Journal of Human Genetics|February 11, 1999
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophyM Seri, R Cusano, P Forabosco, et al.
Pageof 25