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...embryo catalogue.jpg|thumb|alt=Orts Llorca Madrid embryo catalogue|Madrid embryo catalogue]] The human embryo histology collection was started in 1935 by Professor Orts-Llorca (1905-199

...opment olfactory and related structures in staged human embryos from the [[Carnegie Collection]]. ...es has been established from the serially sectioned human embryos of the [[Carnegie Collection]], from stage {{CS11}} to stage {{CS23}}.

| Broman, 1936 8 Bryce, 1924 (M'Intyre) || 8 | Carnegie No. 763 || 8?

[[File:Ziegler_model_05.jpg|thumb|An example of a Ziegler embryo model.]] His son, Friedrich Ziegler (- 1936), continued the modelling company.

| valign=top|[[File:Stage5 bf11L.jpg|alt=Human embryo Carnegie stage 5|400px]] Implantation completed, inner cell mass, bilaminar embryo, trophoblast development, no villous development. See also [[#Events|Events

...graphy also came into play, seen mainly associated with embryos within the Carnegie collection. [[File:Auzoux_model_workshop.jpg|alt=Auzoux embryo model workshop|400px]]

Department of EmbryologyThe Carnegie Institution Of Washington, Baltimore, Maryland ...empt was made to recover a specimen comparable to the youngest known human embryo.

==Appendix 1 - Embryos In The Carnegie Collection== The Carnegie specimens of stages 2-23 are listed in the following tables.

...e:Mark_Hill.jpg|50px|left]] This historic 1945 paper by Hertig describes [[Carnegie Collection]] early human extra-embryonic development in [[week 2]]. The his ...d of Obstetrics, Harvard Medical School, and the Department of Embryology, Carnegie Institution of Washington, Baltimore.

The embryo is now 1.0 - 1.5 mm in size. {{Carnegie stage 8 links}}

{{Carnegie stage 1 links}} {{Carnegie stage 2 links}}

...blood development, including the fact that the red corpuscles in the early embryo are nucleated and that the later cells lack a nucleus. Specific informatio ...red blood cells begins to be evident during the second month in the human embryo and (2) that few nucleated red cells are found by the middle of the third m

| The bilaminar ({{epiblast}} and {{hypoblast}}) embryo is now about 0.2 mm diameter in size. The three extra embryonic spaces (amn {{Carnegie stage 6 links}}

[[File:Human Carnegie stage 10-23.jpg|thumb|300px|Carnegie Embryos]] ...collection numbering also incorporated the Blechschmidt embryo collection (Carnegie Nos. 10315-10434 ) in 1972, the collection embryos have now been returned t

The author wishes to thank Dr. G. L. Streeter of the Carnegie Institution of Washington at Baltimore for the privilege of studying a larg ...rom the spinal accessory cell column in the upper cervical cord of a human embryo (no. 1433B). Camera lucida drawing. Pyridine silver preparation. X 750,

Human crown rump length Probable age ' Method of embryo no. in millimeters in weeks preparation H. 1360 17 7 Pyridine silver H. 119 ...’08) has shown that the motor elements in the brain stem of a 10 mm. human embryo form a continuous column which extends from the spinal cord into the medull

...t. This study used human embryos from the [[Harvard Collection]] and the [[Carnegie Collection]] ...n the development of the human adrenal cortex from its inception until the embryo has grown to a length of 20 mm. Special attention has been given to the gen

...e developing orgamsm This can be expressed by saying that structure in the embryo is frequently antecedent to function Although It IS obvious that no defimte ...as a marked retarding effect on developmental reparative changes (du Nouy, 1936).

* '''Contributions to Embryology''' - [[Book_-_Contributions_to_Embryology|Carnegie Institution of Washington Series]] A historic series of papers published by the Carnegie Institution of Washington early in the 20th Century.

{{Carnegie stage 7 links}} =The Chorion and Endometrium of the Embryo H.R.1=

[[Carnegie stage 5]] ...asures approximately 0.1-0.2 mm in diameter. The significant dimensions of Carnegie specimens of stage 5 are listed in Table 5-1. The external and internal dia

[[File:Stage_22_image_085.jpg|thumb|300px|Developing Human Spleen ([[Carnegie stage 22|stage 22]])]] .... The spleen's haematopoietic function (blood cell formation) is lost with embryo development and lymphoid precursor cells migrate into the developing organ.

{{Carnegie stage 5 links}} ..., the terminology employed by Ramsey (1938) in her description of the Yale embryo will be used. Thus we are able to recognize central cytotrophoblast, periph

...al origin, are very early differentiated from the otic vesicle in the 7 mm embryo as a medial diverticular projection (Bast, Anson and Gardner, ’47). This ...and Gardner (’47) pointed out that the sac overlies the sinus in the 50 mm embryo.

By A. M. Hain (Carnegie Research Fellow), The Institute of Animal Genetics, Edinburgh University, ...y defrayed by grants (to A.M.H.) from the Medical Research Council and the Carnegie Trust for the Universities of Scotland.

...and 13'''{{#pmid:26995337|PMID26995337}} "We selected 37 human embryos at Carnegie Stage (CS) {{CS11}}-{{CS13}} (28-33 days after fertilization) and three-dim Human embryo small intestine secondary loops (week 7 to 8).{{#pmid:26297675|PMID26297675

[[Carnegie stage 8]] ...: the primitive pit, the notochordal canal, and the neurenteric canal. The embryo is presomitic, i.e., somites are not yet visible.

...ed into the [[Carnegie Collection]] as [[:Category:Carnegie Embryo 8819|'''embryo no. 8819''']]. {{Carnegie stage 6 links}}

...nitil tract Most of the sperms are dead withm a peiwsd of four da\-s fCaia 1936) and m most mammals ...the zona pelluci a or may even be found in the perivitellme space (Pincus, 1936), but they take no part in future development.

| [[File:Mark_Hill.jpg|90px|left]] This 1936 paper by Hain describes abnormal development of the {{rat}} {{renal}} syste By A. M. Hain (Carnegie Research Fellow), Institute of Animal Genetics, University of Edinburgh,

...y Atlas of the 13-mm. Pig Embryo. (Prefaced by younger stages of the chick embryo.) The Wistar Institute Press, Philadelphia, iv & 104 pp. Corner, G. W., 1915. The corpus luteum of pregnancy as it is in swine. Carnegie Inst., Contrib. to E-mbryoL, Vol. 2, pp. 69-94.

[[Carnegie stage 18]] ...d than the similar group of the preceding stage, shown in figure 17-2. The embryo of stage 18 is larger and has advanced in the coalescence of its body regio

...by grants from the Penrose Fund of the American Philosophical Society, the Carnegie Corporationof New York and the University of Pittsburgh. Publication no. 7, ...on is Von K6lliker’s (1882 and 1883) description of the bulb in an 8-weeks embryo. The microscopic structure of the olfactory bulb in adult man, however, exc

...left]] This is equivalent to the later Carnegie staging system of embryo [[Carnegie stage 7]]. {{Carnegie stage 7 links}}

[[Carnegie stage 6]] ...ncidence of sex chromatin in the trophoblast and chorionic mesoblast of an embryo (No. {{CE7801}}) of stage 6, and in the chorionic mesoblast and umbilical v

...he total number of somatic segments represented in the average ii mm human embryo (the time of maximum number) is 42 to 44 (fit, 391) The first occipital (Ar In a human embryo of about 5 mm the cells of the ventro-medial portion of, for example, the f

...pment of the trachea and esophagus and includes several embryos from the [[Carnegie Collection]]. Department Of Embryology, Carnegie Institution Of Washington, Baltimore, Maryland

...are not Carnegie stages, use the embryo CRL to approximately convert to [[Carnegie Stages]]. ...bryology_15|Historic - Urogenital Development]] | [[Carnegie Embryos]] | [[Carnegie Collection]]

=A Presomite Human Embryo (Shaw): The Implantation= ...ed account of the structure of the intrachorionic rudiment of the ‘ Shaw ’ embryo. The present communication provides a more detailed account of the chorioni

=A Presomite Human Embryo (Shaw): The Implantation= ...ed account of the structure of the intrachorionic rudiment of the ‘ Shaw ’ embryo. The present communication provides a more detailed account of the chorioni

...indicate the absence of pouches. Weller (30) described a two somite human embryo which according to his description possessed the first pharyngeal pouch. Th Corner (4) described the foregut of a 10-somite human embryo, as being compressed dorso-ventrally with the anterior end immediately unde

[[Carnegie stage 17]] ...ecisely of the size of the chorionic sac than of the size of the contained embryo. If the manifestly abnormal chorions be omitted, none has a greatest diamet

...reaction of Bennett (1940) and the plasmal reaction as described by Lison (1936) were applied to representative cases. Plain sections, both untreated and s ...ltttea associated with 7‘/3- and 9‘/3-day normal pregnancies respectively (Carnegie nos. {{CE8020}}, {{CE8215}}). Unfortunately, these sections, which were sta

...to tissues that are lost during development. It includes several of the [[Carnegie Collection]] embryos in the figures. ...thology, Harvard Medical School, Boston, and the Department of Embryology, Carnegie Institution of Washington, Baltimore.

...use of the intrinsic nature of the subject, for the functions of which the embryo or fetus is capable at various times are determined by the growth of the ne ...representation, then, allows us to observe the general growth picture from embryo to adult, and gives us a basis upon which to establish a more detailed anal

...ot readily released under the action of estrogen alone (Lendrum and Hisaw, 1936; Engle Burford and Elder, 1936; Fish, Young and

...s a description of the development of the human adrenal gland using many [[Carnegie Collection]] embryos. Note that this describes the neural crest contributio ...seriated, well preserved, and adequately stained material available in the Carnegie Embryological Collection, in Baltimore, Maryland, made a complete histologi

...pear very early in development as specialized region (otic placode) on the embryo surface that sinks into the mesenchyme to form a vesicle (otic vesicle = ot * stage 13/14 embryo (shown below) the otic placode has sunk from the surface ectoderm to form a

...pear very early in development as specialized region (otic placode) on the embryo surface that sinks into the mesenchyme to form a vesicle (otic vesicle = ot * stage 13/14 embryo (shown below) the otic placode has sunk from the surface ectoderm to form a

...viously primitive character was seen in the thoracic cord of a 5—mm. human embryo, it seemed worth While to examine the suitable younger specimens available ...by grants from the Penrose Fund of the American Philosophical Society, the Carnegie Corporation of New York and the University of Pittsburgh.

=Part V - The Care of the Developing Embryo= ...embryonic membranes, and in many species, the retention of the developing embryo within either maternal or paternal body structures (Chap. 22).

...ry of Natural Products Related to Phenanthrene, by L. F. Fieser, New York, 1936; Sterols and Related Compounds, by E. Friedmann, Cambridge, England, 1937; ...hed by L. B. Clark and W. N. Hess, "Swarming of the Atlantic Palolo W6rm," Carnegie Institution of Washington^ Publication d'^l).. Papers from the Tortugas Lab

...mative cells, i.e., all the cells enter directly into the formation of the embryo's body. ...organforming areas which later enter into the formation of the body of the embryo; auxiliary or non-formative tissue has no part in its composition. All coel

...logue.jpg|200px|alt=Orts Llorca Madrid embryo catalogue|Orts Llorca Madrid embryo catalogue|left]] ...dentally, in the University of Valencia, during the Spanish Civil War from 1936-1939) and, later on, at the Faculty of Medicine of Madrid (Complutense Univ

....jpg|90px|left]] This historic 1941 paper by Gilmour describes early human embryo blood formation. ....065 x 0.045 mm. Age about 16 days, probably slightly younger than Peters’ embryo (1899).

...and blastulation appear normal. However, gastrulation is abortive, and the embryo soon dies (Moore, '41, '46, '47). ===6. Relation of Early Cleavage Planes to the Antero-posterior Axis of the Embryo===

...s thesis by Stewart describes development of the blood supply to the human embryo basal ganglia. =The Development of the Blood Supply to the Human Embryo Basal Ganglia=

===3. Basic Structure of the Vertebrate Skin in the Embryo=== In the embryo of the shark, chick, and mammal, the single-layered condition of the primit

...f the Carnegie Institution of Washington. The uterus in which this 11 -day embryo has attached itself is in the typical progestational phase, as shown by the Carl G. Hartman, Time of Ovulation in Women. Baltimore, 1936.

...oker from the Penrose Fund of the American Philosophical Society, from the Carnegie Corporation of New York, and from the University of Pittsburgh. ...lar components in the thoracic portion of the spinal cord of a 55-cm. calf embryo. He corroborated the findings of Ramon y Cajal in general but declared tha

embryo (Heuser and Streeter, 1941 ; Hertig (Pincus, 1936), Krebs' solution (Black,

Carnegie Institution Of Washington, Department Of Embryology, The Johns Hopkins Univ in the embryo is controlled by a hormone,

Fuss, A. 1911. Uber extraregioniaire Geschlechtzellen bei einem Menschhchen Embryo von vier wochen. Anat. Am. 39, 407. Gregory, P. W. 1930. The early embryology of the rabbit. Carnegie Inst. Wash. Contrib. to Embryol. 21, 141.

...ed follicle, but which have usually completely disappeared by the time the embryo begins to implant in the uterus In some species true luteal cells are added ...man> \crtcbrnc. (bird, ferrets, etc see Bissonnettc 1932 nnd 1935 Marslnll 1936) cm ironmental conditions, for cxamp e h«ht ma% act reBcxI) b% \\a> of the

...atic system. Lymph hearts are present also in the tail region of the chick embryo. ...cal tubes begin to form, one set on either side of the median plane of the embryo (fig. 3 32 A and B). Simultaneous with the formation of these primitive, su

ribs in a 30-mm. CR embryo, for some cervical and upper and of the tympanic annulus of a 42—mm. CR embryo by Mall

the embryo of the mouse and rabbit is lower embryo, until the sprouting of the primary

...dly number of which have appeared from the Department of Embryology of the Carnegie Institution of Washington. ...generosity of Dr. Carl G. Hartman from the Department of Embryology of the Carnegie Institution. These three macaque monkeys (Macaca mulatta) were killed on th

...evident as a protuberance (see His-Ziegler model of brain of 13.6mm human embryo). As the brain enlarges, the pallium envelops the basal ganglia and the tha Ariins Kaprers, C. U., G. C. Huser anp E. C. Crospy 1936 The comparative anatomy of the nervous system of vertebrates, including man

1936). Recently, Bruce and East (1956) the development of the embryo.

namely, is there a separate germinal plasm set apart in the early embryo which used to refer to those germ cells which possibly segregate early in the embryo,

embryo without the cooperation of the female, and whether the result is male enlarged compartment where the egg or developing embryo may be retained.

structural relationships between the developing embryo and the uterus. These comprise a succession of stages of placental metabolic demands of the developing embryo and fetus.

...h he believed was the essential element in that it contained the preformed embryo in an intangible way. That is, the sperm animalcule of the ram contains a l ...rged capsule is soon formed which assumes the size and shape of the future embryo at the time of hatching (fig. 123). (See Tavolga, '50.) In the brook lampre

Staff Member, Department of Embryology, Carnegie Institution Of Washington. Baltimore. Maryland Burrows, 1936; Van Drinnnolen, 1945), viviparous fish (Clark, 1950), and insects