LINKAGE ANALYSIS OF 3 CLONED DNA-SEQUENCES, DXS294, CDR AND DXS105, IN X-LINKED RECESSIVE HYPOPARATHYROID FAMILIES

LINKAGE ANALYSIS OF 3 CLONED DNA-SEQUENCES, DXS294, CDR AND DXS105, IN X-LINKED RECESSIVE HYPOPARATHYROID FAMILIES

Sonraí bibleagrafaíochta
Príomhchruthaitheoirí:	Thakker, R, Wooding, C, Parkinson, D, Blake, D, Whyte, M, Davies, K
Formáid:	Journal article
Foilsithe / Cruthaithe:	1991

Míreanna comhchosúla

Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families.
de réir: Thakker, R, et al.
Foilsithe / Cruthaithe: (1990)

DXS106 AND DXS559 FLANK THE X-LINKED DYSTONIA-PARKINSONISM LOCUS, DYT3
de réir: Wagner, T, et al.
Foilsithe / Cruthaithe: (1994)

Primers for the dinucleotide repeat at the DXS453 locus also recognizes the DXS983 locus.
de réir: Rider, S, et al.
Foilsithe / Cruthaithe: (1993)

PRIMERS FOR THE DINUCLEOTIDE REPEAT AT THE DXS453 LOCUS ALSO RECOGNIZES THE DXS983 LOCUS
de réir: Rider, S, et al.
Foilsithe / Cruthaithe: (1993)

DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3).
de réir: Müller, U, et al.
Foilsithe / Cruthaithe: (1994)

Dinucleotide repeat polymorphisms from DXS106 and DXS227 YACs using a two stage approach.
de réir: Fairweather, N, et al.
Foilsithe / Cruthaithe: (1993)

Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies.
de réir: Thakker, R, et al.
Foilsithe / Cruthaithe: (1990)

Genetic analysis of DXS101and DXS6807 short tandem repeat (X-STR) in samples of Iraqi Arab male population
de réir: Hayder Allawi Khaleefah, et al.
Foilsithe / Cruthaithe: (2020-12-01)

Cloning and expression characterisation of LiDXS2 gene in Oriental Lily (Lilium 'Sorbonne')
de réir: Yu Jiaxuan, et al.
Foilsithe / Cruthaithe: (2025-01-01)

The evolution of radio sources in the UKIDSS-DXS-XMM-LSS field
de réir: McAlpine, K, et al.
Foilsithe / Cruthaithe: (2011)

MAPPING OF THE X-LINKED IDIOPATHIC HYPOPARATHYROID GENE TO XQ26-XQ27 BY LINKAGE STUDIES
de réir: Thakker, R, et al.
Foilsithe / Cruthaithe: (1989)

Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.
de réir: Pook, M, et al.
Foilsithe / Cruthaithe: (1993)

The discovery of a massive supercluster at z=0.9 in the UKIDSS DXS
de réir: Swinbank, A, et al.
Foilsithe / Cruthaithe: (2007)

Recombination with pERT87 (DXS164) in families with X-linked muscular dystrophy.
de réir: Fischbeck, K, et al.
Foilsithe / Cruthaithe: (1986)

Genetic mapping studies of the X-linked recessive hypoparathyroid gene on the X chromosome (Xq27).
de réir: Dixon, P, et al.
Foilsithe / Cruthaithe: (1996)

Layer by layer encapsulation of PRM/DXS/neutravidin and antibody on calcium carbonate core
de réir: Liaw, Zi Yen.
Foilsithe / Cruthaithe: (2009)

Identification of Inhibitors of the Anti-Infective Target DXS Using Dynamic Combinatorial Chemistry
de réir: Ravindra P. Jumde, et al.
Foilsithe / Cruthaithe: (2019-08-01)

Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146.
de réir: Fisher, S, et al.
Foilsithe / Cruthaithe: (1995)

Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.
de réir: Trump, D, et al.
Foilsithe / Cruthaithe: (1998)

中国汉族群体DXS101 位点的多态性
de réir: 吕德坚, et al.
Foilsithe / Cruthaithe: (2001-01-01)

A 2-Mb YAC contig encompassing three loci (DXF34, DXS14, and DXS390) that lie between Xp11.2 translocation breakpoints associated with incontinentia pigmenti type 1.
de réir: Reed, V, et al.
Foilsithe / Cruthaithe: (1994)

Molecular Cloning and Functional Analysis of <i>DXS</i> and <i>FPS</i> Genes from <i>Zanthoxylum bungeanum</i> Maxim
de réir: Lu Tian, et al.
Foilsithe / Cruthaithe: (2022-06-01)

New candidate genes for X-linked recessive hypoparathyroidism.
de réir: Mumm, S, et al.
Foilsithe / Cruthaithe: (1999)

Integrated profiling identifies DXS253E as a potential prognostic marker in colorectal cancer
de réir: Pu Xing, et al.
Foilsithe / Cruthaithe: (2024-06-01)

A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism.
de réir: Parkinson, D, et al.
Foilsithe / Cruthaithe: (1992)

Overexpression of SrDXS1 and SrKAH enhances steviol glycosides content in transgenic Stevia plants
de réir: Junshi Zheng, et al.
Foilsithe / Cruthaithe: (2019-01-01)

Excavating the functionally crucial active-site residues of the DXS protein of Bacillus subtilis by exploring its closest homologues
de réir: Ashish Runthala, et al.
Foilsithe / Cruthaithe: (2020-11-01)

Overexpression of LiDXS and LiDXR From Lily (Lilium ‘Siberia’) Enhances the Terpenoid Content in Tobacco Flowers
de réir: Tengxun Zhang, et al.
Foilsithe / Cruthaithe: (2018-07-01)

Isolation of DNTR polymorphisms from yeast artificial chromosomes encompassing X chromosomal loci PGK1 and DXS56.
de réir: Graeber, M, et al.
Foilsithe / Cruthaithe: (1992)

Functional Identification and Regulatory Active Site Screening of the <i>DfDXS</i> Gene of <i>Dryopteris fragrans</i>
de réir: Hanxu Zhao, et al.
Foilsithe / Cruthaithe: (2024-09-01)

Physical map of the Xq27 candidate region for X-linked recessive hypoparathyroidism in two kindreds merged by mitochondrial DNA analysis
de réir: Mumm, S, et al.
Foilsithe / Cruthaithe: (1996)

Engineering of Recombinant Poplar Deoxy-D-Xylulose-5-Phosphate Synthase (PtDXS) by Site-Directed Mutagenesis Improves Its Activity.
de réir: Aparajita Banerjee, et al.
Foilsithe / Cruthaithe: (2016-01-01)

Correction: Engineering of Recombinant Poplar Deoxy-D-Xylulose-5-Phosphate Synthase (PtDXS) by Site-Directed Mutagenesis Improves Its Activity.
de réir: Aparajita Banerjee, et al.
Foilsithe / Cruthaithe: (2016-01-01)

mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation.
de réir: Mumm, S, et al.
Foilsithe / Cruthaithe: (1997)

Karakterisasi alga hijau Dunaliella sp. dan isolat sianobakteria serta deteksi gen DXS penyandi enzim kunci biosintesis karotenoid
de réir: , KUSUMANINGRUM, Hermin Pancasakti, et al.
Foilsithe / Cruthaithe: (2008)

2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes.
de réir: Lafrenière, R, et al.
Foilsithe / Cruthaithe: (1993)

SmDXS5, acting as a molecular valve, plays a key regulatory role in the primary and secondary metabolism of tanshinones in Salvia miltiorrhiza
de réir: Da-chuan Zhang, et al.
Foilsithe / Cruthaithe: (2022-11-01)

X-linked recessive hypoparathyroidism is caused by a molecular deletional-insertion involving chromosomes Xq27 and 2p25.
de réir: Bowl, MR, et al.
Foilsithe / Cruthaithe: (2001)

A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status.
de réir: Coleman, M, et al.
Foilsithe / Cruthaithe: (1996)

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.
de réir: Scheinman, S, et al.
Foilsithe / Cruthaithe: (1993)