(Q24322076)

GOA release 2020-03-11

limb development

1 reference

SPARC related modular calcium binding 1

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Yoshinori Tsurusaki

23

Yoshinori

Tsurusaki

1 reference

20 October 2023

Hirotomo Saitsu

28

Hirotomo

Saitsu

1 reference

20 October 2023

19

Norio Niikawa

Norio

Niikawa

1 reference

20 October 2023

22

Koh-Ichiro Yoshiura

Koh-Ichiro

Yoshiura

1 reference

20 October 2023

18

Takeshi Mizuguchi

Takeshi

Mizuguchi

1 reference

20 October 2023

20

Fumiki Hirahara

Fumiki

Hirahara

1 reference

20 October 2023

25

Noriko Miyake

Noriko

Miyake

1 reference

20 October 2023

14

Shiro

Ikegawa

Shiro Ikegawa

1 reference

20 October 2023

13

Tatsuya Furuichi

Tatsuya

Furuichi

1 reference

20 October 2023

16

Satoko Miyatake

Satoko

Miyatake

1 reference

20 October 2023

Ippei Okada

1

Ippei

Okada

1 reference

20 October 2023

Haruka Hamanoue

2

Haruka

Hamanoue

1 reference

20 October 2023

Koji Terada

3

Koji

Terada

1 reference

20 October 2023

Takaya Tohma

4

Takaya

Tohma

1 reference

20 October 2023

Andre Megarbane

5

Andre

Megarbane

1 reference

20 October 2023

Eliane Chouery

6

Eliane

Chouery

1 reference

20 October 2023

Joelle Abou-Ghoch

7

Joelle

Abou-Ghoch

1 reference

20 October 2023

Nadine Jalkh

8

Nadine

Jalkh

1 reference

20 October 2023

Ozgur Cogulu

9

Ozgur

Cogulu

1 reference

20 October 2023

Ferda Ozkinay

10

Ferda

Ozkinay

1 reference

20 October 2023

Kyoji Horie

11

Kyoji

Horie

1 reference

20 October 2023

Junji Takeda

12

Junji

Takeda

1 reference

20 October 2023

Kiyomi Nishiyama

15

Kiyomi

Nishiyama

1 reference

20 October 2023

Akira Nishimura

17

Akira

Nishimura

1 reference

20 October 2023

Tadashi Kaname

21

Tadashi

Kaname

1 reference

20 October 2023

Hiroshi Doi

24

Hiroshi

Doi

1 reference

20 October 2023

Takahisa Furukawa

26

Takahisa

Furukawa

1 reference

20 October 2023

Naomichi Matsumoto

27

Naomichi

Matsumoto

1 reference

American Journal of Human Genetics

20 October 2023

language of work or name

English

0 references

publication date

7 January 2011

0 references

published in

0 references

volume

88

0 references

issue

1

0 references

page(s)

30-41

0 references

cites work

Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Microarray analysis of Foxa2 mutant mouse embryos reveals novel gene expression and inductive roles for the gastrula organizer and its derivatives

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

GDF6, a novel locus for a spectrum of ocular developmental anomalies

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Heterozygous mutations of OTX2 cause severe ocular malformations

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

BMP4 is essential for lens induction in the mouse embryo

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Gremlin is the BMP antagonist required for maintenance of Shh and Fgf signals during limb patterning

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Loss-of-function mutations of CHST14 in a new type of Ehlers-Danlos syndrome.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Vertebrate limb bud development: moving towards integrative analysis of organogenesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Essential mesenchymal role of small GTPase Rac1 in interdigital programmed cell death during limb development.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Loss of Tbx2 delays optic vesicle invagination leading to small optic cups.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Formin1 disruption confers oligodactylism and alters Bmp signaling

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Bone morphogenetic protein signaling in limb outgrowth and patterning

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Anophthalmos with limb anomalies (Waardenburg opththalmo-acromelic syndrome): report of a new Italian case with renal anomaly and review.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Molecular mechanisms of optic vesicle development: complexities, ambiguities and controversies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Matricellular proteins: extracellular modulators of cell function

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Development of retinal ganglion cell structure and function

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Ophthalmo-acromelic syndrome: report and review

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Sequential changes of programmed cell death in developing fetal mouse limbs and its possible roles in limb morphogenesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Secreted modular calcium-binding protein-1 localization during mouse embryogenesis.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Bone morphogenetic protein 7 (BMP7) mutations are associated with variable ocular, brain, ear, palate, and skeletal anomalies

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Spatial and temporal expression of folate-binding protein 1 (Fbp1) is closely associated with anterior neural tube closure in mice

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Characterization of SMOC-1, a novel modular calcium-binding protein in basement membranes

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

Mouse Wnt genes exhibit discrete domains of expression in the early embryonic CNS and limb buds.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3014372

A locus for ophthalmo-acromelic syndrome mapped to 10p11.23

29 November 2018

1 reference

12 December 2020

Waardenburg anophthalmia syndrome: report and review

1 reference

12 December 2020

Ophthalmo-acromelic syndrome (Waardenburg) with split hand and polydactyly

1 reference

12 December 2020

Region-specific saturation germline mutagenesis in mice using the Sleeping Beauty transposon system

1 reference

12 December 2020

Ophthalmo-acromelic syndrome: report of a case with vertebral anomalies

1 reference

12 December 2020

10.1016/J.AJHG.2010.11.012

Identifiers

DOI

0 references

Fatcat ID

release_2rtve7efwjbhhf2kclxolmakle

0 references

PMC publication ID

3014372

0 references