Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure - Wikidata - awgldk - TriplyDB

Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure

Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure

http://www.wikidata.org/entity/Q28236974

about

Transcription factor FIGLA is mutated in patients with premature ovarian failure Bidirectional communication between oocytes and follicle cells: ensuring oocyte developmental competence Contemporary genetic technologies and female reproduction Genetics of the ovarian reserve Genetics of primary ovarian insufficiency: new developments and opportunities Insights into female germ cell biology: from in vivo development to in vitro derivations A Major Gene for Bovine Ovulation Rate Oocyte-somatic cell interactions in the human ovary-novel role of bone morphogenetic proteins and growth differentiation factors The genetics of premature ovarian failure: current perspectives Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes Oocyte-specific overexpression of mouse bone morphogenetic protein-15 leads to accelerated folliculogenesis and an early onset of acyclicity in transgenic mice.Meta-analysis of loci associated with age at natural menopause in African-American women Genomic markers of ovarian reserve Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform.Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency.The menstrual cycle: basic biology Impaired production of BMP-15 and GDF-9 mature proteins derived from proproteins WITH mutations in the proregion.Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.The fundamental role of bone morphogenetic protein 15 in ovarian function and its involvement in female fertility disorders.The genetic make-up of ovarian development and function: the focus on the transcription factor FOXL2.Integral role of GDF-9 and BMP-15 in ovarian function.Genome-wide association studies identify two novel BMP15 mutations responsible for an atypical hyperprolificacy phenotype in sheep Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure.Ovarian function in girls and women with GALT-deficiency galactosemia Intraovarian control of early folliculogenesis Single nucleotide polymorphisms in premature ovarian failure-associated genes in a Chinese Hui population.Replication of loci influencing ages at menarche and menopause in Hispanic women: the Women's Health Initiative SHARe Study Histone H2AFX Links Meiotic Chromosome Asynapsis to Prophase I Oocyte Loss in Mammals Association between BMP15 Gene Polymorphism and Reproduction Traits and Its Tissues Expression Characteristics in Chicken.Identification and characterization of canine growth differentiation factor-9 and its splicing variant.Phosphorylation of bone morphogenetic protein-15 and growth and differentiation factor-9 plays a critical role in determining agonistic or antagonistic functions.Growth differentiation factor 9:bone morphogenetic protein 15 heterodimers are potent regulators of ovarian functions.Dizygotic twinning.Role of Growth Differentiation Factor 9 and Bone Morphogenetic Protein 15 in Ovarian Function and Their Importance in Mammalian Female Fertility - A Review Revisiting oocyte-somatic cell interactions: in search of novel intrafollicular predictors and regulators of oocyte developmental competence.Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein Mutation analysis of exon1 of bone morphogenetic protein-15 gene in Iranian patients with polycystic ovarian syndrome.Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis

P2860

Q21710713-C30874EA-E875-41D5-B1A8-83BE3896BB32 Q24634160-EB16D67E-FA9E-4023-8EA7-1E49E9DC16B5 Q24635098-C58D97B9-D92C-4530-A247-CA006115A9C8 Q26777164-301053B0-78C9-4352-8A8B-4E4FBB5B2450 Q26798895-00B92E3D-F2BD-452E-AE69-64AB66A35844 Q27004698-53163BC7-BC82-4281-8DA2-4EBC0B18013F Q27304937-F7402BA0-29EF-476F-8ADC-BF12EF001941 Q28069613-7D125A5A-AC76-4C70-9FF5-DE8A5ED03A92 Q28084777-925D0983-4519-472B-9D35-CEC0215AB2D0 Q28306123-70CABC59-3178-4F72-88B9-0F2B8E8BA8D1 Q30439521-015D5CB6-4547-4EAD-BF27-10118A8A73CD Q33649334-7B027D4B-A15A-4142-B339-0BD18DF28EFD Q33705774-3F1EE99F-6852-4147-8471-74532BE36D8D Q33888318-2DA2C269-3391-4D17-9C3E-EBB2B243F02A Q33903951-7F91CDC1-4998-4231-995C-80F996DCA0E1 Q34032462-EB8322D6-60C0-4493-9EAC-3096D32F91FA Q34108150-D3E0BF24-0C17-47CA-B39A-7151B760E1C6 Q34200920-60CE9352-9D79-4470-B3B0-7B4AAD87A77A Q34427147-0F3E0884-C93F-4532-9DB3-4ECFDBFF7102 Q34539732-BC7FD219-136B-4E2D-A9FB-9DEDED997C03 Q34637927-788A7AE8-6C5C-41CD-AB16-3B69DBD1D2C9 Q34699842-9C3BB4EE-C62F-418A-9E6A-DD33D64016A3 Q34708642-6558C17C-F0F2-4929-BE52-0D6AE08E55E7 Q34714428-B9EB68EC-B379-44F8-A453-AAFAD2938989 Q35024088-21345D2D-0769-4B2B-B861-C97021571EBB Q35728984-A7348D85-E031-4189-BFCE-2FE3FA9C7F7F Q35771001-A6E40751-1DDA-4D73-B0D7-8EABCEECF7CE Q35824466-AC69482C-69C5-4E84-8367-7DD0689B444F Q35843408-8B69F15F-3EAE-4BB2-8497-6734C701306D Q36010170-B45C2A1F-AC44-49B1-ADAD-6A45A55BFD66 Q36415867-300A0D3D-1D93-492D-A21E-AB3008C2F9BD Q36637656-E23FBCFC-9BC1-4573-8170-2BCD0310AF2D Q37007519-2A6C68B0-4E70-4D19-A1D3-E54BA22C95A2 Q37064045-833AE7CC-E027-4920-8127-244690AFF966 Q37091054-AAE818FF-26CB-4E0F-A829-3C8ED65E473C Q37154012-FB481662-B1CE-4D88-BD56-4199733B2ADB Q37179550-1CE205CF-354E-48E4-AD20-ED15DEC77116 Q37241424-4BF747E3-85C4-4983-9ED5-6793248B9586 Q37291548-323920D8-19AE-446D-9B8D-56ED86531551 Q37377768-44513892-37A6-440A-92B5-1F0252898545

P2860

Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure

http://www.wikidata.org/entity/Q28236974

description

2006 nî lūn-bûn

@nan

2006 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի մայիսին հրատարակված գիտական հոդված

@hy

2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu

name

Mutations and sequence variant ...... with premature ovarian failure

@ast

Mutations and sequence variant ...... with premature ovarian failure

@en

Mutations and sequence variant ...... with premature ovarian failure

@nl

type

label

Mutations and sequence variant ...... with premature ovarian failure

@ast

Mutations and sequence variant ...... with premature ovarian failure

@en

Mutations and sequence variant ...... with premature ovarian failure

@nl

prefLabel

Mutations and sequence variant ...... with premature ovarian failure

@ast

Mutations and sequence variant ...... with premature ovarian failure

@en

Mutations and sequence variant ...... with premature ovarian failure

@nl

P1433

Q28236974-5FAB15F7-09F2-4E43-AF09-F6DB9C75514F

P1476

Q28236974-5D5C47CB-888C-4020-B8AE-EB514365DCB4

P2093

Q28236974-0723B27A-CCBE-4456-B1CF-E26D3DA8618E

Q28236974-10AEC9E1-8463-41E5-9738-224C8CD3A518

Q28236974-2A538697-B018-4DDB-B303-0199F4FF7D35

Q28236974-2B9A6DF1-1354-4343-B363-C6BE010605F6

Q28236974-2C8B6150-3667-4C76-AF4C-6DB28861DBEB

Q28236974-39BD9132-1075-4479-9640-36DC1ABA0C5B

Q28236974-5334F75D-F26E-4554-A9C4-D446D226B8A9

Q28236974-7F81F6D2-F6F5-48B1-AB29-A1B7B496FF29

Q28236974-810FB5E8-3166-407D-B17D-9C7D51B40746

Q28236974-97709353-648F-4BFC-B2DB-9BC60E137BE1

P304

Q28236974-A1194966-7CEA-4867-8FEF-B4ADB2B28F26

P31

Q28236974-C03DF963-262F-41B0-B651-B3CE45235255

P3181

Q28236974-6846FC52-931C-4491-8AB3-4D8AA6E1DA20

P356

Q28236974-CA30CFF4-B9DF-47B6-87F6-9E46CC1B44D8

P407

Q28236974-7B4C2103-7F67-45BE-B4D3-EB88E68C35BA

P433

Q28236974-8F55CF96-FCEB-45BC-B72C-7D945D2EB4F2

P478

Q28236974-45D50884-B1B8-479B-84A4-428485879D61

P50

Q28236974-2701CB17-1BD6-4893-A3B2-6251E0FB45CD

Q28236974-F70816F8-B5D6-4E60-9A6F-B10C8BF31093

Q28236974-FDB19F05-5354-41DC-9B4B-371D2F90298C

P577

Q28236974-52DD79B2-B920-427E-B7AE-A48A31CD3C40

P5875

Q28236974-E58BE41F-E1D5-40FA-A1EF-8397A289A7DC

P698

Q28236974-55AAEAA0-37E2-4EDE-BC4A-184DAB22AC53

P921

Q28236974-F8DCAFF5-91B7-486E-A375-ED3A30547252

P3181

P356

P1433

European Journal of Endocrinology

P1476

Mutations and sequence variant ...... with premature ovarian failure

@en

P2093

Anne Bachelot

http://www.w3.org/2001/XMLSchema#string

Anne-Céline Reyss

http://www.w3.org/2001/XMLSchema#string

Frederique Kuttenn

http://www.w3.org/2001/XMLSchema#string

Kristiina Aittomaki

http://www.w3.org/2001/XMLSchema#string

Laetitia Jacquesson

http://www.w3.org/2001/XMLSchema#string

Luke Jeffery

http://www.w3.org/2001/XMLSchema#string

Marc Fellous

http://www.w3.org/2001/XMLSchema#string

Nathalie Bourcigaux

http://www.w3.org/2001/XMLSchema#string

Olli Ritvos

http://www.w3.org/2001/XMLSchema#string

Philippe Bouchard

http://www.w3.org/2001/XMLSchema#string

P304

739-744

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

1324575

http://www.w3.org/2001/XMLSchema#string

P356

10.1530/EJE.1.02135

http://www.w3.org/2001/XMLSchema#string

P407

P433

5

http://www.w3.org/2001/XMLSchema#string

P478

154

http://www.w3.org/2001/XMLSchema#string

P50

Nathalie Massin

Didier Dewailly

P577

2006-05-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

7136283

http://www.w3.org/2001/XMLSchema#string

P698

16645022

http://www.w3.org/2001/XMLSchema#string

P921