G Hoganson
Overview
Explore the profile of G Hoganson including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
17
Citations
272
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Koch R, Burton B, Hoganson G, Peterson R, Rhead W, Rouse B, et al.
J Inherit Metab Dis
. 2002 Nov;
25(5):333-46.
PMID: 12408183
During 1967-1983, the Maternal and Child Health Division of the Public Health Services funded a collaborative study of 211 newborn infants identified on newborn screening as having phenylketonuria (PKU). Subsequently,...
2.
Aronovich E, Carmichael K, Morizono H, Koutlas I, Deanching M, Hoganson G, et al.
Genomics
. 2000 Aug;
68(1):80-4.
PMID: 10950929
Heparan sulfate sulfamidase (HSS) is a lysosomal exohydrolase that, when deficient, results in intralysosomal accumulation of heparan sulfate and the clinical phenotype of Sanfilippo syndrome type A. The first animal...
3.
Pegoraro E, Marks H, Garcia C, Crawford T, Mancias P, Connolly A, et al.
Neurology
. 1998 Jul;
51(1):101-10.
PMID: 9674786
Objective: To determine the number of primary laminin alpha2 gene mutations and to conduct genotype/phenotype correlation in a cohort of laminin alpha2-deficient congenital muscular dystrophy patients. Background: Congenital muscular dystrophies...
4.
Souri M, Aoyama T, Hoganson G, Hashimoto T
FEBS Lett
. 1998 May;
426(2):187-90.
PMID: 9599005
This paper describes the process of dimer assembly of mitochondrial very-long-chain acyl-CoA dehydrogenase (VLCAD) subunit. Mature VLCAD is a homodimer of a 70-kDa protein associated with the mitochondrial membrane. Newly...
5.
Oldridge M, Lunt P, Zackai E, McDonald-McGinn D, Muenke M, Moloney D, et al.
Hum Mol Genet
. 1997 Jan;
6(1):137-43.
PMID: 9002682
Dominantly acting, allelic mutations of the fibroblast growth factor receptor 2 (FGFR2) gene have been described in five craniosynostosis syndromes. In Apert syndrome, characterised by syndactyly of the hands and...
6.
Santolaya J, Farolan M, Czapar J, Kambich M, Hauselman E, Hoganson G
Fetal Diagn Ther
. 1994 May;
9(3):170-4.
PMID: 8060512
We report the clinical and pathologic findings of 2 siblings affected with congenital nephrotic syndrome (CNS). The parents were a nonconsanguineous Mexican couple. The first sibling was born at term...
7.
Fukao T, Yamaguchi S, Wakazono A, Orii T, Hoganson G, Hashimoto T
J Clin Invest
. 1994 Mar;
93(3):1035-41.
PMID: 7907600
We identified a novel exonic mutation which causes exon skipping in the mitochondrial acetoacetyl-CoA thiolase (T2) gene from a girl with T2 deficiency (GK07). GK07 is a compound heterozygote; the...
8.
Hoar D, Field L, Beards F, Hoganson G, Rollnick B, Hoo J
Am J Med Genet
. 1992 Jan;
42(2):170-2.
PMID: 1733165
Detailed physical mapping of oto-palato-digital (OPD) syndrome gene on the X-chromosome was attempted on a family of 3 generations with 2 affected men. Although the result remains statistically non-significant, it...
9.
Eisenstein R, Hoganson G, Miller R, HARPER A
J Inherit Metab Dis
. 1991 Jan;
14(1):37-44.
PMID: 1861457
The abundance and phosphorylation state of the polypeptide constituents of the human branched-chain 2-oxo acid dehydrogenase complex were examined in mitochondria from normal and maple syrup urine disease (MSUD) fibroblasts....
10.
Surowy C, Hoganson G, Gosink J, Strunk K, Spritz R
Gene
. 1990 Jun;
90(2):299-302.
PMID: 2119325
We have isolated cDNA clones encoding the human RD protein, which is closely related to several known nuclear RNA-binding proteins. The RD protein contains a 60-amino acid (aa) tract consisting...