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25篇 您的检索式：作者名="Bastepe"

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	题名	作者	年代	出处	被引量
1	DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis显示文摘	Lorenz-Depiereux B Bastepe M Benet-Pages A Amyere M Wagenstaller J Muller-Barth U Badenhoop K Kaiser SM Rittmaster RS Shlossberg AH Olivares JL Loris C Ramos FJ Glorieux F Vikkula M Juppner H Strom TM		0，，11：	1
2	Phenotypie and molecular genetic aspects of psendohypoparathyroidism type Ib in a Greek kindred: evidence for enhanced uric acid excretion due to parathyroid hormone resistance显示文摘	Laspa E Bastepe M Juppner H	2004	J Clin Endocrinol Metab2004，89，12：	1
3	DMP1 mutations in autosomal recessive hypophosphatemia implicate a bonematrix protein in the regulation of phosphate homeo-stasis显示文摘	Lorenz-Depiereux B Bastepe M Benet-Pages A	2006	Nat Genet2006，3，8：	1
4	Gsalpha enhances commitment of mesenchymal progenitors to the osteoblast lineage but restrains osteoblast differentiation in mice显示文摘	Wu JY Aarnisalo P Bastepe M	2011	J Clin Invest2011，121，9：	1
5	Inherited hypophosphatemic disorders in children and the evolving mechanisms of phosphate regulation显示文摘	Bastepe M Juppner H	2008	Rev Endocr Metab Disord2008，9，2：	1
6	Gsalpha enhances commitment of mesenchymal progenitors to the osteoblast lineage but restrains osteoblast differentiation in mice显示文摘	Wu JY Aarnisalo P Bastepe M		0，，09：	1
7	DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis 显示文摘	Lorenz- Depiereux B Bastepe M Benet- Pages A	2006	Nat Genet2006，3，8：	1
8	DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis显示文摘	Lorenz DB Bastepe M Benet PA	2006	Nat Genet2006，8，11：	1
9	Cyclic AMP phosphodiesterases in human lymphocytes显示文摘	Sheth S B Chaganti K Bastepe M	1997	Br J Haemato 11997，99，：	1
10	The GNAS locus and pseudohypoparathyroidism显示文摘	Bastepe M	2008	Adv Exp Med Biol2008，626，：	1
11	Th? GNAS locus and pseudohypoparathyroidism显示文摘	Bastepe M	2008	Adv Exp Med Biol2008，626，：	1
12	Molecular diagnosis of pseudohypoarathyroidism type 1b in a family with presumed paroxysmal dyskinesia显示文摘	Mahmud FH Linglart A Bastepe M	2005	Pediatries2005，115，2：	1
13	GNAS locus and pseudohypoparathyroidism 显示文摘	Bastepe M Jtippner H	2005	Horm Res2005，63，2：	1
14	Phenotypic and molecular genetic aspects of pseudohypoparathyroidism type Ib in a Greek Kindred:evidence for enhanced uric acid excretion due to parathyroid hormone resistance显示文摘	Laspa E Bastepe M Jppner H	2004	J Clin Endocrin Metab2004，89，12：	1
15	Similar clinical and laboratory findings in patients with symptomatic autosomal dominant and sporadic pseudohypoparathyroidism type Ib despite different epigenetic changes at the GNAS locus显示文摘	Linglart A Bastepe M Juppner H	2007	Clin Endocrinol(Oxf)2007，67，6：	1
16	Molecular diagnosis of pseudohypoparathyroidism type Ib in a family with presumed paroxysmal dyskinesia显示文摘	Mahmud FH Linglart A Bastepe M	2005	Pediatrics2005，115，2：	1
17	Inherited hypophosphatemie disorders in children and the evolving mechanisms of phosphate regulation 显示文摘	Bastepe M Juppner H	2008	Rev Endocr Metab Disord2008，9，2：	1
18	Pater- nal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib ( PHP- Ib) 显示文摘	BASTEPE M ALTUG- TEBER O AGARWAL C	2011	Bone2011，48，3：	1
19	The GNAS locus and pseudohypoparathyroidism显示文摘	Bastepe M	2008	Adv Exp Med Biol2008，626，：	1
20	The GNAS locus: quintessential complex gene encoding Gsa, XLαs, and other imprinted transcripts显示文摘	Murat Bastepe	2007	Current Ge nomics2007，8，：	1

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