Mouse Timeline Detailed
|Embryology - 6 Oct 2015 Translate|
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- 1 Introduction
- 2 Week 1
- 3 Week 2
- 4 Week 3
- 5 Postnatal
- 6 Species Stages Comparison
- 7 Timed Pregnancy
- 8 References
- 9 External Links
- 10 Glossary Links
This page is organised to show a detailed day by day development of sytems and features with approximate timing of key events. The staging by "days" relate to in the female presence of a vaginal plug indicating that the mating occurred, see timed pregnancy.
Theiler Stages divides mouse development into 26 prenatal and 2 postnatal stages. 
Downs and Davies Stages is a more recent (1993) staging of gastrulating mouse embryos by morphological landmarks in the dissecting microscope.
- Mouse Links: Introduction | Mouse Stages | Mouse Timeline | Mouse Timeline Detailed | Mouse Estrous Cycle | Mouse Knockout | Movie - Cephalic Plexus | ANAT2341 Project (2009) | Category:Mouse
- Mouse Stages: E1 | E2.5 | E3 | E3.5 | E4.5 | E7.0 | E7.5 | E8.0 | E8.5 | E9.0 | E9.5 | E10 | E10.5 | E11 | E11.5 | E12 | E12.5 | E13 | E13.5 | E14 | E14.5 | E15 | E15.5 | E16 | E16.5 | E17 | E18 | E18.5 | E19 | E20 | Timeline | About timed pregnancy
- Note these Carnegie stages are only approximate day timings for average of embryos.
- Links: Carnegie Stage Comparison
R O'Rahilly Early human development and the chief sources of information on staged human embryos. Eur. J. Obstet. Gynecol. Reprod. Biol.: 1979, 9(4);273-80 PubMed 400868
Rat Witschi, E. (1962) Development: Rat. In: Growth Including Reproduction and Morphological Development. Altman, P. L. , and D. S. Dittmer, ed. Fed. Am. Soc. Exp. Biol., Washington DC, pp. 304-314.
Day 1 (E1.0)
Theiler Stage 1 - Fertilization
Theiler Stage 2 - Dividing egg stage 2-4 cells. Zona pellucida present. First cleavage occurs at about 24 hours. Embryonic age = 1 dpc (range 1-2.5 dpc)
Day 2 (E2.0)
Theiler Stage 3 - Morula (early to fully compacted) 4-16 cells. Zona pellucida present. Usually found in the oviduct towards the utero-tubal junction. Embryonic age = 2 dpc (range 1-3.5 dpc)
Day 3 (E3.0)
Theiler Stage 4 - Blastocyst (ICM apparent) 16-40 compacted cells. Zona pellucida present. Embryo progresses from morula to the blastocyst. Early evidence of the blastocoelic cavity.
In the blastocyst stage (zona-intact) there is a distinct inner cell mass and an outer layer of trophectoderm cells. Usually located in the uterine lumen. Embryonic age = 3 dpc (range 2-4 dpc)
Day 4 (E4.0)
Theiler Stage 5 - Blastocyst (Zona pellucida absent) Zona free blastocyst. Invariably located within the uterine lumen.
Embryonic age = 4 dpc (range 3-5.5 dpc)
Theiler Stage 6 - Attachment of blastocyst. Blastocyst implants, first evidence of embryonic endoderm cells covering the blastocoelic surface of the inner cell mass. Embryonic age = 4.5 dpc (range 4-5.5 dpc)
Day 5 (E5.0)
Theiler Stage 7 - Implantation and formation of egg cylinder. Ectoplacental cone appears. Rapid increase in the number of inner cell mass cells leading to the formation of the epiblast with subsequent growth to form the egg cylinder. The proximal or visceral cells (opposite side from the trophoblastic cap) are cuboidal in shape. Primary endoderm lines the mural trophectoderm. Embryonic age = 5 dpc (range 4.5-6 dpc)
Differentiation of egg cylinder. Implantation site 2x3mm.The maternal tissue is invaded by trophoblast (primary) giant cells and the ectoplacental cone is invaded by maternal blood. Differentiation of the egg cylinder into embryonic and extra-embryonic regions and the formation of the pro-amniotic cavity. Reichert's membrane, which is non-cellular and secreted by the distal endoderm, first appears. Embryonic age = 6 dpc (range 5-6.5 dpc)
Day 5 (E5.5)
E5.5 Nodal signaling from the epiblast induces distal visceral endoderm (DVE) formation that will establish embryo anterior–posterior axis.
Theiler Stage 8
Day 6 (E6.0)
Theiler Stage 9
Stage 9a Advanced Endometrial Reaction. Advanced egg-cylinder stage with the first evidence of an embryonic axis. Clear morphological distinction between the embryonic and extra-embryonic ectoderm. The ectoplacental cone is further invaded by maternal blood and the original lumen of the uterine crypt has disappeared. Equivalent Downs and Davies Stage : PS (pre-streak)
Stage 9b Advanced Endometrial Reaction. Late in this stage gastrulation begins, producing the first mesodermal cells. Equivalent Downs and Davies Stage : ES (early streak)
Day 6.5 (E6.5)
- Heart - earliest heart precursors are 50 founder cells located on both sides of the midline in the epiblast of early gastrula stage embryos 
Day 7 (E7.0)
Theiler Stage 10
Stage 10a Amnion. Tissue at the posterior end of the primitive streak bulges into the pro-amniotic cavity and forms the amniotic fold (Equivalent Downs and Davies stage: MS, mid-streak)
Stage 10b Amnion. In the mesoderm of the posterior amniotic fold small cavities coalesce to form a single cavity, the exocoelom Embryonic age = 7.0 dpc (range 6.5-7.5 dpc)
Stage 10c . Amnion. The allantoic bud first appears, gastrulation continues and the node becomes visible. Embryonic age = 7.0 dpc (range 6.5-7.5 dpc) (Equivalent Downs and Davies stages: MS - LS, mid-streak to late streak)
Day 7 (E7.5)
|E7.5 early bud||E7.5 late bud|
Theiler Stage 11
Stage 11a Neural Plate, Presomite stage The amniotic cavity is now sealed off into three distinct cavities - the amniotic cavity, the exocoelom and the ectoplacental cleft. The neural plate is defined anteriorly and the head process is developing. In the midline, subjacent to the neural groove, the notochodal plate is visible. Embryonic age = 7.5 dpc (range 7.25-8 dpc) Equivalent Downs and Davies stages: OB-EB (no allantoic bud to early allantoic bud); LB-EHF-LHF (late allantoic bud to early head fold to late head fold)
Stage 11b Neural Plate, Presomite stage. The allantoic bud elongates. Embryonic age = 7.5 dpc (range 7.25-8 dpc) . Equivalent Downs & Davies stages: OB-EB (no allantoic bud to early allantoic bud); LB-EHF-LHF (late allantoic bud to early head fold to late head fold)
Stage 11c Neural Plate, Presomite stage. The rostral part of the neural plate begins to enlarge to form the head folds. The neural groove is visible. Embryonic age = 7.5 dpc (range 7.25-8 dpc) Equivalent Downs and Davies stages: OB-EB (no allantoic bud to early allantoic bud); LB-EHF-LHF (late allantoic bud to early head fold to late head fold)
Stage11d Neural Plate, Presomite stage. Head folds continue to enlarge and the foregut pocket begins to form. Embryonic age = 7.5 dpc (range 7.25-8 dpc) ; LB-EHF-LHF (late allantoic bud to early head fold to late head fold) . Equivalent Downs & Davies stages: OB-EB (no allantoic bud to early allantoic bud)
- Heart - migration of anterior lateral plate mesoderm towards midline, forms a linear heart tube.
Day 8 (E8.0)
Theiler Stage 12
Theiler Stage 12a - First Somites Unturned embryo with first appearance of somite pairs 1-4 somites. The allantois extends further into the exocoelom and the maxillary components of the 1st branchial arch become prominent. The preotic sulcus is visible in the 2-3 somite embryo. The cardiogenic plate begins to form and the foregut pocket is clearly visible. Embryonic age = 8 dpc (range 7.5-8.75 dpc) 1-7 somite pairs
Theiler Stage 12b - First Somites Unturned embryo with first appearance of somite pairs 5-7 somites. The headfolds are particularly prominent and neural closure occurs in the region of the 4th and 5th somites, extending in both directions from this site. The otic placode appears at 9 somite pairs stage (between E8.5 to 8.75). The optic placodes are first evident and become indented to form the optic pits. The heart rudiment develops rapidly. The allantois contacts the chorion at the end of this stage. Absent: The 2nd branchial arch and >7 somites. Embryonic age = 8 dpc (range 7.5-8.75 dpc) 1-7 somite pairs
Theiler Stage 13 - Turning of the embryo. This is a short period with turning initiated in embryos with 6-8 pairs of somites and usually completed in embryos with 14-16 pairs of somites. The first branchial arch has maxillary and mandibular components but the maxillary process is not visible until later (TS16). A second branchial arch is now evident. There is evidence of regionalisation of the heart and the neural tube is closed from a point opposite the outflow tract to the proximal part of the tail. Absent: 3rd branchial arch. Embryonic age = 8.5 dpc (range 8-9.25 dpc) 8-12 somite pairs
- Neural - Formation and closure of anterior neuropore. The rostral extremity of the neural tube closes in embryos with usually about 15-18 somite pairs and defines this stage. The otic pit becomes progressively more indented but not closed, the mandibular process of the 1st branchial arch is clearly visible. The 3rd branchial arch becomes visible late in the stage.
- Limb - An increasingly prominent ridge on the lateral body wall, approximately at the level of the 8th-12th somite, indicates the site of the future forelimb bud. Absent: forelimb bud. Embryonic age = 9 dpc (range 8.5-9.75 dpc) 13-20 somite pairs
- Heart - Heart tube undergoes looping at E8.5. The second heart field (pharyngeal mesoderm cells) contributes to parts of the right ventricle, the interventricular septum, the venous pole, and the base of the outflow tract.
Day 9 (E9.0)
Theiler Stage 14 - Formation of posterior neuropore, forelimb bud. The posterior neuropore forms and the condensation of the forelimb bud becomes apparent near the 8th-12th somite pairs. A distinct condensation of the hind limb bud appears just at the end of the stage.The forebrain vesicle subdivides into telencephalic and diencephalic vesicles. Absent: hindlimb bud, Rathke's pouch. Embryonic age = 9.5 dpc (range 9-10.25 dpc) 21-29 somite pairs
Theiler Stage 15 - Closure of posterior neuropore. Hind limb bud and tail bud. The hind limb bud becomes visible at the level of the 23rd-28th somites. The tail bud appears as a short stump and the 3rd and 4th branchial arches are distinctly concave. Rathke's pouch and the nasal processes start to form. At the end of this stage the posterior neuropore begins to close. Absent: thin and long tail. Embryonic age = 10 dpc (range 9.5-10.75 dpc) 30-34 somite pairs.
|Migration E9.0 | Quicktime||Migration E9.5 | Quicktime|
Mouse Stage E9.5 Specific Gene Expression
Day 10 (E10.0)
Theiler Stage 16
Theiler Stage 17 - Deep Lens Indentation The most obvious distinguishing features are the deepening of the lens pit, with a narrowing of its outer pore-like opening, and the first appearance of the physiological umbilical hernia. The 1st branchial arch is conspicuously divided into maxillary and mandibular components. There is advanced development of the brain tube and the tail elongates and thins. Absent: nasal pits. Embryonic age = 10.5 dpc (range 10-11.25 dpc) 35-39 somite pairs
Hearing and Balance - Formation of vestibular (otic) ganglion cells (E10-12) Afferent processes of vestibular ganglion cells invade the macula utricle and saccule and cristae of the semicircular canals (10.5)
|Neural Crest Development|
|Gastrointestinal Tract Development - differential gene expression of some selected markers during development (E10.5 and E13.5) of the mouse gastrointestinal tract.|
|Primordial germ cell migration Migration E10.5 | Quicktime|
- Heart - Cardiac neural crest cells migrate to the outflow tract and endocardial cushions to form the the outflow tract septum (systemic and pulmonary separation). 
Renal System Development - metanephric mesenchyme present, an area of intermediate mesoderm caudal to the mesonephros and adjacent to a widening of the ‘nephric duct, metanephric portion’ that gives rise to the metanephros.
Pecam 1 and Smooth muscle actin (SMA) staining
Mouse Stage E10.5 Specific Gene Expression
Day 11 (E11.0)
- Links: Category:Mouse E11
Theiler Stage 18
Theiler Stage 19
Closure of Lens Vesicle. The primary externally recognisable feature is the progressive closure of the lens vesicle. The somites in the cervical region are no longer visible and the rapid growth of the brain is striking. The nasal pits start to form. Absent: auditory hillocks, anterior footplate. Embryonic age = 11 dpc (range 10.5-11.25 dpc) 40-44 somite pairs
Palate Development - palatal shelves protrude from bilateral maxillary processes.
Day 11.5 (E11.5)
- Links: Category:Mouse E11.5 (TS19)
Stage 19 - Lens vesicle completely separated from surface. The lens vesicle becomes completely closed and detached from the ectoderm. The peripheral margins of the eye become well defined. The forelimbs are seen to be divided into two regions, the proximal part consisting of the future limb-girdle and 'arm' and the more peripheral part which forms a circular or paddle-shaped 'handplate' (anterior footplate). The medial and lateral margins of the otic pit are coming together reducing the entrance to a narrow slit and the auditory hillocks become visible. Absent: retinal pigmentation, signs of 'fingers'. Embryonic age = 11.5 dpc (range 11-12.25 dpc) 45-47 somite pairs
Gonad E11.5 - coelomic epithelium basement membrane is discontinuous, supporting cell migration. 11.2-11.4 - (somite 15-17 stages) coelomic epithelial cells of both sexes migrated into the gonad. In XY gonads, the migrating coelomic epithelial cells became Sertoli cells, as well as interstitial cells. This ability of the coelomic epithelium to give rise to Sertoli cells was developmentally regulated. 11.5-11.7 - (somite 18-20 stages) coelomic epithelial cells no longer became Sertoli cells. Instead, cells that migrated into the gonad stayed outside testis cords, in the interstitium. 
Aorta-Gonad-Mesonephros E11.5 - (AGM) region is a site of hematopoietic stem cell (HSC) development prior to colonisation of the embryonic liver.
Tooth Development - placode stage
Heart - Progressive septation of the outflow tract and septation of the atria and ventricles. 
Mouse Stage E11.5 Specific Gene Expression
Day 12 (E12.0)
Theiler Stage 20 - Earliest signs of fingers. The 'handplate' (anterior footplate) is no longer circular but develops angles which correspond to the future digits. The posterior footplate is also distinguishable from the lower part of the leg. It is possible to see the pigmentation of the pigmented layer of the retina through the transparent cornea. The tongue and brain vesicles are clearly visible. Absent:5 rows of whiskers, indented handplate. Embryonic age = 12 dpc (range 11.5-13 dpc) 48-51 somite pairs
Joints - 12.5 -13.5 interzone forms in cartilage of digits which is the precursor to synovial joint formation.
Tooth Development - 12.5 bud stage
Palate Development - E12.5-E14 palatal shelves grow vertically along the developing tongue.
Heart - E12.5 (TS21) Progressive septation of the outflow tract and initiation of atrioventricular canal septation.
Mouse Stage E12.5 Specific Gene Expression
Day 13 (E13.0)
Theiler Stage 21 - Anterior footplate indented, marked pinna. The distal borders of the anterior and posterior footplates are now indented and the digit widths and locations can be discerned. The 'elbow' and 'wrist' are now identifiable. The pinna rapidly develops and forms a crest at right angles to the head. Five rows of vibrissae are visible as well as a prominant hair follicle over the eye and another over the ear. The lens vesicle has lost its lumen. The physiological umbilical hernia is prominent. Absent: hair follicles, distally separate fingers. Embryonic age = 13 dpc (range 12.5-14) 52-55 somite pairs
Ovary - E13.5-16.5 ovarian cord structure formation required for oocyte development
Liver - E13.5-15.5 single layer of hepatoblasts forms close to the portal mesenchyme (ductal plate) and expresses bile duct-specific cytokeratins. By E16.5, the ductal plate partially becomes bi-layered and, around E17.5, enters a phase of profound remodeling during which time focal dilations appear between the two cell layers.
Gastrointestinal tract - differential gene expression of some selected markers during development (E10.5 and E13.5) of the mouse gastrointestinal tract.
Heart - E13.5 (TS22) Bilaterally asymmetrical aortic arch system, completely septated outflow tract and ventricles and remodeling of the atrioventricular cushions.
Mouse Stage E13.5 Specific Gene Expression
Day 14 (E14.0)
- Links: Category:Mouse E14
Theiler Stage 22 - Fingers separate distally. Individual 'fingers' are visible in the anterior footplate and there are deep indentations between the 'toes' which are not yet separated.The long bones of the limbs are present and there are hair follicles in the pectoral, pelvic and trunk regions. The pinna is turned forwards and the umbilical hernia is conspicuous. Absent: hair follicles in the cephalic region. Embryonic age = 14 dpc (range 13.5-15 dpc) 56-60 somite pairs
Tooth Development - cap stage
Palate Development - E14.5 palatal shelves elevate, meet, and fuse at the midline, to form an intact palate shelf.
Heart - E14.5 (TS23) Atrial septation complete. 
Day 15 (E15.0)
Theiler Stage 23 Toes separate. The 'toes' separate and are clearly divergent, not becoming parallel until later. Hair follicles are present in the cephalic region but not at the periphery of the vibrissae. The pinna covers more than half of the external auditory meatus and the eyelids are still open. Absent: nail primordia, 'fingers' 2-5 parallel. Embryonic age = 15 dpc >60 somite pairs
Tooth Development - bell stage
Day 16 (E16.0)
Theiler Stage 24 Reposition of umbilical hernia 'Fingers' 2-5 are nearly parallel. Nail primordia are visible on the 'toes'. The eyelids have fused in most cases by the end of the stage and the pinna almost completely covers the external auditory meatus. The umbilical hernia is disappearing and there is a corresponding increase in the size of the peritoneal sac. Absent: 'fingers' and 'toes' joined together. Embryonic age = 16 dpc > 60 Somite pairs
Heart - E15.5 (TS24) - E18.5 (TS27) Definitive external prenatal configuration achieved, Atrioventricular valve leaflets are being modified, Coronary arteries are being modified. 
Liver - E16.5 ductal plate becomes partially bi-layered.
Day 17 (E17.0)
Day 18 (E18.0)
Theiler Stage 26
Long whiskers The whiskers that were present at stage 25 are definitely longer and the skin has thickened. The pinna is larger and such that virtually none of the lumen of the auditory meatus is visible. The eyes are barely visible through the closed eyelids. Embryonic age = 18 dpc
Mammary Development - E18.5 elongating duct has now grown into the fat pad and has branched into a small ductal system. Cells of the mammary mesenchyme have formed the nipple, which is made of specialized epidermal cells. Reviewed
Day 19 (E19.0)
Theiler Stage 27
Theiler Stage 28 New born Mouse
Day 20 (E20.0)
Day 21 (E21.0)
- Uterine adenogenesis - uterine gland buds develop between postnatal day (PND) 5 to 7.
Species Stages Comparison
The table below gives an approximate comparison of human, mouse and rat embryos based upon Carnegie staging.
- Presence of the vaginal plug indicates that the mating occurred.
- Assumes that fertilization takes place around midnight during a 7pm to 5am dark cycle.
- Check for vaginal plugs early in the morning, because they fall out or are no longer detectable ~12 hours or sooner after mating.
- Noon of the day on which the vaginal plug is found the embryos are aged "0.5 dpc" (days post coitum).
- Noon on the next day, the embryos are 1.5 dpc, and so on.
- The House Mouse: Atlas of Mouse Development by Theiler Springer-Verlag, NY (1972, 1989). | online book
- K M Downs, T Davies Staging of gastrulating mouse embryos by morphological landmarks in the dissecting microscope. Development: 1993, 118(4);1255-66 PubMed 8269852 | Development
- Cindy C Lu, Elizabeth J Robertson Multiple roles for Nodal in the epiblast of the mouse embryo in the establishment of anterior-posterior patterning. Dev. Biol.: 2004, 273(1);149-59 PubMed 15302604
- P P Tam, M Parameswaran, S J Kinder, R P Weinberger The allocation of epiblast cells to the embryonic heart and other mesodermal lineages: the role of ingression and tissue movement during gastrulation. Development: 1997, 124(9);1631-42 PubMed 9165112
- Liqin Cao, Hiroshi Shitara, Michihiko Sugimoto, Jun-Ichi Hayashi, Kuniya Abe, Hiromichi Yonekawa New evidence confirms that the mitochondrial bottleneck is generated without reduction of mitochondrial DNA content in early primordial germ cells of mice. PLoS Genet.: 2009, 5(12);e1000756 PubMed 19997484 | PMC2777314 | PLoS Genet.
- Margaret Buckingham, Sigolène Meilhac, Stéphane Zaffran Building the mammalian heart from two sources of myocardial cells. Nat. Rev. Genet.: 2005, 6(11);826-35 PubMed 16304598
- Richard L Mort, Leonard Hay, Ian J Jackson Ex vivo live imaging of melanoblast migration in embryonic mouse skin. Pigment Cell Melanoma Res: 2010, 23(2);299-301 PubMed 20067551 | PMC2859249
- Leila Taher, Nicole M Collette, Deepa Murugesh, Evan Maxwell, Ivan Ovcharenko, Gabriela G Loots Global gene expression analysis of murine limb development. PLoS ONE: 2011, 6(12);e28358 PubMed 22174793 | PMC3235105 | PLoS One.
- April E Ronca, Bernd Fritzsch, Laura L Bruce, Jeffrey R Alberts Orbital spaceflight during pregnancy shapes function of mammalian vestibular system. Behav. Neurosci.: 2008, 122(1);224-32 PubMed 18298265
- Makoto Matsuyama, Shinichi Aizawa, Akihiko Shimono Sfrp controls apicobasal polarity and oriented cell division in developing gut epithelium. PLoS Genet.: 2009, 5(3);e1000427 PubMed 19300477 | PLoS Genet.
- X Jiang, D H Rowitch, P Soriano, A P McMahon, H M Sucov Fate of the mammalian cardiac neural crest. Development: 2000, 127(8);1607-16 PubMed 10725237
- Melissa H Little, Jane Brennan, Kylie Georgas, Jamie A Davies, Duncan R Davidson, Richard A Baldock, Annemiek Beverdam, John F Bertram, Blanche Capel, Han Sheng Chiu, Dave Clements, Luise Cullen-McEwen, Jean Fleming, Thierry Gilbert, Doris Herzlinger, Derek Houghton, Matt H Kaufman, Elena Kleymenova, Peter A Koopman, Alfor G Lewis, Andrew P McMahon, Cathy L Mendelsohn, Eleanor K Mitchell, Bree A Rumballe, Derina E Sweeney, M Todd Valerius, Gen Yamada, Yiya Yang, Jing Yu A high-resolution anatomical ontology of the developing murine genitourinary tract. Gene Expr. Patterns: 2007, 7(6);680-99 PubMed 17452023 | PMC2117077
- Qingqing Wang, Ning Zhao, Simone Kennard, Brenda Lilly Notch2 and Notch3 function together to regulate vascular smooth muscle development. PLoS ONE: 2012, 7(5);e37365 PubMed 22615991 | PMC3355134 | PLoS ONE
- Steven C Munger, Anirudh Natarajan, Loren L Looger, Uwe Ohler, Blanche Capel Fine time course expression analysis identifies cascades of activation and repression and maps a putative regulator of mammalian sex determination. PLoS Genet.: 2013, 9(7);e1003630 PubMed 23874228 | PLoS Genet.
- J Karl, B Capel Sertoli cells of the mouse testis originate from the coelomic epithelium. Dev. Biol.: 1998, 203(2);323-33 PubMed 9808783
- Erin Taylor, Samir Taoudi, Alexander Medvinsky Hematopoietic stem cell activity in the aorta-gonad-mesonephros region enhances after mid-day 11 of mouse development. Int. J. Dev. Biol.: 2010, 54(6-7);1055-60 PubMed 20711982
- Gertraud W Robinson Cooperation of signalling pathways in embryonic mammary gland development. Nat. Rev. Genet.: 2007, 8(12);963-72 PubMed 18007652
- Saija M Savolainen, Julie F Foley, Susan A Elmore Histology atlas of the developing mouse heart with emphasis on E11.5 to E18.5. Toxicol Pathol: 2009, 37(4);395-414 PubMed 19359541 | PMC2773446 | Toxicol Pathol.
- Cory R Nicholas, Kelly M Haston, Renee A Reijo Pera Intact fetal ovarian cord formation promotes mouse oocyte survival and development. BMC Dev. Biol.: 2010, 10;2 PubMed 20064216
- Makoto Matsuyama, Shinichi Aizawa, Akihiko Shimono Sfrp controls apicobasal polarity and oriented cell division in developing gut epithelium. PLoS Genet.: 2009, 5(3);e1000427 PubMed 19300477 | PLoS Genet.
- Takashi Ozaki, Kunio Nagashima, Takashi Kusakabe, Kennichi Kakudo, Shioko Kimura Development of thyroid gland and ultimobranchial body cyst is independent of p63. Lab. Invest.: 2011, 91(1);138-46 PubMed 20697379
- Mark F Vondenhoff, Serge A van de Pavert, Miriam E Dillard, Mascha Greuter, Gera Goverse, Guillermo Oliver, Reina E Mebius Lymph sacs are not required for the initiation of lymph node formation. Development: 2009, 136(1);29-34 PubMed 19060331
- Laurent Chorro, Aurélien Sarde, Mei Li, Kevin J Woollard, Pierre Chambon, Bernard Malissen, Adrien Kissenpfennig, Jean-Baptiste Barbaroux, Richard Groves, Frédéric Geissmann Langerhans cell (LC) proliferation mediates neonatal development, homeostasis, and inflammation-associated expansion of the epidermal LC network. J. Exp. Med.: 2009, 206(13);3089-100 PubMed 19995948 | J Exp Med.
- Shelton DN, Fornalik H, Neff T, Park SY, Bender D, et al. (2012) The Role of LEF1 in Endometrial Gland Formation and Carcinogenesis. PLoS ONE 7(7): e40312. doi:10.1371/journal.pone.0040312
- R O'Rahilly Early human development and the chief sources of information on staged human embryos. Eur. J. Obstet. Gynecol. Reprod. Biol.: 1979, 9(4);273-80 PubMed 400868
- Witschi, E. (1962) Development: Rat. In: Growth Including Reproduction and Morphological Development. Altman, P. L. , and D. S. Dittmer, ed. Fed. Am. Soc. Exp. Biol., Washington DC, pp. 304-314.
External Links Notice - The dynamic nature of the internet may mean that some of these listed links may no longer function. If the link no longer works search the web with the link text or name.
- Edinburgh Mouse Atlas of Gene Expression - Edinburgh Mouse Atlas of Gene Expression- Appendix 4 Theiler Staging | The Edinburgh Mouse Atlas: Staging Criteria | Standard Anatomical Nomenclature
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Cite this page: Hill, M.A. (2015) Embryology Mouse Timeline Detailed. Retrieved October 6, 2015, from https://embryology.med.unsw.edu.au/embryology/index.php/Mouse_Timeline_Detailed
- © Dr Mark Hill 2015, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G