Search Results

PORCN gene mutations and the protean nature of focal dermal hypoplasia

Authors: Clements, S.E.; Mellerio, J.E.; Holden, S.T.; McCauley, J.; McGrath, J.A.

Source: British Journal of Dermatology, Volume 160, Number 5, May 2009 , pp. 1103-1109(7)

Publisher: Blackwell Publishing

Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region

Authors: Froyen, Guy; Bauters, Marijke; Boyle, Jackie; Esch, Hilde; Govaerts, Karen; Bokhoven, Hans; Ropers, Hans-Hilger; Moraine, Claude; Chelly, Jamel; Fryns, Jean-Pierre; Marynen, Peter; Gecz, Jozef; Turner, Gillian

Source: Human Genetics, Volume 121, Number 5, June 2007 , pp. 539-547(9)

Publisher: Springer

Compound haplotypes at Xp11.23 and human population growth in Eurasia

Authors: S. Alonso; J. A. L. Armour

Source: Annals of Human Genetics, Volume 68, Number 5, September 2004 , pp. 428-437(10)

Publisher: Blackwell Publishing

Progress in Monoamine Oxidase (MAO) Research in Relation to Genetic Engineering

Author: Nagatsu T.

Source: Neurotoxicology, Volume 25, Number 1, January 2004 , pp. 11-20(10)

Publisher: Elsevier

A highly conserved human gene encoding a novel member of WD-repeat family of proteins (WDR13)

Authors: Singh B.N.; Suresh A.; UmaPrasad G.; Subramanian S.; Sultana M.; Goel S.; Kumar S.; Singh L.

Source: Genomics, Volume 81, Number 3, March 2003 , pp. 315-328(14)

Publisher: Elsevier

ARTICLE
Gene Expression Profiles of BRCA1-Linked, BRCA2-Linked, and Sporadic Ovarian Cancers

Authors: Jazaeri A.A.; Yee C.J.; Sotiriou C.; Brantley K.R.; Boyd J.; Liu E.T.

Source: Journal of the National Cancer Institute, Volume 94, Number 13, 3 July 2002 , pp. 990-1000(11)

Publisher: Oxford University Press

Structure, Function, and Tissue Expression Pattern of Human SN2, a Subtype of the Amino Acid Transport System N

Authors: Nakanishi T.; Sugawara M.; Huang W.; Martindale R.G.; Leibach F.H.; Ganapathy M.E.; Prasad P.D.; Ganapathy V.

Source: Biochemical and Biophysical Research Communications, Volume 281, Number 5, 16 March 2001 , pp. 1343-1348(6)

Publisher: Elsevier

The Wiskott-Aldrich Syndrome Gene as a Candidate Gene for Atopic Dermatitis

Authors: Bradley M.; Söderhäll C.; Wahlgren C.-F.; Luthman H.; Nordenskjöld M.; Kockum I.

Source: Acta Dermato-Venereologica, Volume 81, Number 5, 1 November 2001 , pp. 340-342(3)

Publisher: Informa Healthcare

Structure, Function, and Tissue Expression Pattern of Human SN2, a Subtype of the Amino Acid Transport System N

Authors: Nakanishi T.; Sugawara M.; Huang W.; Martindale R.G.; Leibach F.H.; Ganapathy M.E.; Prasad P.D.; Ganapathy V.

Source: Biochemical and Biophysical Research Communications, Volume 281, Number 5, March 2001 , pp. 1343-1348(6)

Publisher: Academic Press

Isolation and Characterization of a Calcium Channel Gene, Cacna1f, the Murine Orthologue of the Gene for Incomplete X-Linked Congenital Stationary Night Blindness

Authors: Naylor M.J.; Rancourt D.E.; Bech-Hansen N.T.

Source: Genomics, Volume 66, Number 3, 15 June 2000 , pp. 324-327(4)

Publisher: Elsevier

Gene regulation of Wiskott-Aldrich syndrome protein and the human homolog of the Drosophila Su(var)3-9: WASP and SUV39H1, two adjacent genes at Xp11.23

Authors: Hagemann^a T.L.; Mares^b D.; Kwan^b S.-P.

Source: Biochimica et Biophysica Acta (BBA)/Gene Structure and Expression, Volume 1493, Number 3, 2 October 2000 , pp. 368-372(5)

Publisher: Elsevier

Isolation and Characterization of a Calcium Channel Gene, Cacna1f, the Murine Orthologue of the Gene for Incomplete X-Linked Congenital Stationary Night Blindness

Authors: Naylor M.J.; Rancourt D.E.; Bech-Hansen N.T.

Source: Genomics, Volume 66, Number 3, June 2000 , pp. 324-327(4)

Publisher: Academic Press

Genetic and structural characterization of the human mitochondrial inner membrane translocase

Authors: Bauer M.F.; Gempel K.; Reichert A.S.; Rappold G.A.; Lichtner P.; Gerbitz K.-D.; Neupert W.; Brunner M.; Hofmann S.

Source: Journal of Molecular Biology, Volume 289, Number 1, 28 May 1999 , pp. 69-82(14)

Publisher: Elsevier

Genetic and Structural Characterization of the Human Mitochondrial Inner Membrane Translocase

Authors: Bauer M.F.; Gempel K.; Reichert A.S.; Rappold G.A.; Lichtner P.; Gerbitz K-D.; Neupert W.; Brunner M.; Hofmann S.

Source: Journal of Molecular Biology, Volume 289, Number 1, May 1999 , pp. 69-82(14)

Publisher: Academic Press

Construction of a 1.5-Mb Bacterial Artificial Chromosome Contig in Xp11.23, a Region of High Gene Content

Authors: Boycott K.M.; Zahorchak R.J.; Summer C.G.; Boycott N.P.; Kotak V.; Russell C.G.; Bech-Hansen N.T.

Source: Genomics, Volume 48, Number 3, 15 March 1998 , pp. 369-372(4)

Publisher: Elsevier

Construction of a 1.5-Mb Bacterial Artificial Chromosome Contig in Xp11.23, a Region of High Gene Content

Authors: Boycott K.M.; Zahorchak R.J.; Summer C.G.; Boycott N.P.; Kotak V.; Russell C.G.; Bech-Hansen N.T.

Source: Genomics, Volume 48, Number 3, March 1998 , pp. 369-372(4)

Publisher: Academic Press

A Novel Gene, DXS8237E, Lies within 20 kb Upstream of UBE1 in Xp11.23 and Has a Different X Inactivation Status

Authors: Coleman M.P.; Ambrose H.J.; Carrel L.; Nemeth A.H.; Willard H.F.; Davies K.E.

Source: Genomics, Volume 31, Number 1, January 1996 , pp. 135-138(4)

Publisher: Academic Press

Comparative Mapping Identifies the Fusion Point of an Ancient Mammalian X-Autosomal Rearrangement

Authors: Wilcox S.A.; Watson J.M.; Spencer J.A.; Graves J.A.M.

Source: Genomics, Volume 35, Number 1, July 1996 , pp. 66-70(5)

Publisher: Academic Press